| geneid | 64324 |
|---|---|
| ensemblid | ENSG00000165671.22 |
| hgncid | 14234 |
| symbol | NSD1 |
| name | nuclear receptor binding SET domain protein 1 |
| refseq_nuc | NM_022455.5 |
| refseq_prot | NP_071900.2 |
| ensembl_nuc | ENST00000439151.7 |
| ensembl_prot | ENSP00000395929.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 177133773 |
| end | 177300213 |
| strand | + |
| ver | v1.2 |
| region | chr5:177133773-177300213 |
| region5000 | chr5:177128773-177305213 |
| regionname0 | NSD1_chr5_177133773_177300213 |
| regionname5000 | NSD1_chr5_177128773_177305213 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2696 | 179 | 61 | 36 | 51 | 8 | 21 | 36 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002 | 0/0 | 2696 | 80 | 5 | 13 | 53 | 2 | 7 | 38 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003 | 0/0 | 2696 | 10 | 3 | 1 | 2 | 0 | 4 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004 | 0/0 | 2696 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0005 | 0/0 | 2696 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0006 | 0/0 | 2696 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0007 | 0/0 | 2696 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0008 | 0/0 | 2696 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0009 | 0/0 | 2696 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0010 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0011 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0012 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0013 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0014 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0015 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0016 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0017 | 0/0 | 2696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0018 | 0/0 | 2696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 8091 | 109 | 19 | 24 | 49 | 4 | 12 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0002 | 0/0 | 8091 | 76 | 5 | 13 | 49 | 2 | 7 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0003 | 0/0 | 8091 | 26 | 24 | 2 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0004 | 0/0 | 8091 | 17 | 1 | 10 | 0 | 2 | 4 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0005 | 0/0 | 8091 | 15 | 13 | 0 | 0 | 2 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0006 | 0/0 | 8091 | 9 | 3 | 1 | 1 | 0 | 4 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0007 | 0/0 | 8091 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0008 | 0/0 | 8091 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0009 | 0/0 | 8091 | 4 | 0 | 0 | 2 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0010 | 0/0 | 8091 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0011 | 0/0 | 8091 | 2 | 0 | 0 | 0 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0012 | 0/0 | 8091 | 2 | 1 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0013 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0014 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0015 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0016 | 0/0 | 8091 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0017 | 0/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0018 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0019 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0020 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0021 | 1/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0022 | 0/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0023 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0024 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0025 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0026 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0027 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0028 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0029 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0030 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0031 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0032 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0033 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0034 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| c0035 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4953 | 38 | 3 | 4 | 24 | 1 | 6 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0002 | 0/1 | 4952 | 28 | 12 | 6 | 1 | 4 | 4 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0003 | 1/0 | 4952 | 25 | 2 | 6 | 15 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0004 | 0/0 | 4952 | 17 | 0 | 5 | 9 | 1 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0005 | 0/0 | 4953 | 14 | 9 | 4 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0006 | 0/0 | 4954 | 13 | 9 | 2 | 1 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0007 | 0/0 | 4949 | 12 | 11 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0008 | 0/0 | 4951 | 11 | 0 | 3 | 6 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0009 | 0/0 | 4952 | 9 | 3 | 1 | 2 | 0 | 3 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0010 | 0/0 | 4952 | 9 | 0 | 0 | 9 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0011 | 0/0 | 4951 | 8 | 5 | 1 | 0 | 1 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0012 | 0/0 | 4953 | 7 | 1 | 2 | 1 | 0 | 3 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0013 | 0/0 | 4953 | 6 | 0 | 2 | 2 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0014 | 0/0 | 4954 | 5 | 1 | 2 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0015 | 0/0 | 4952 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0016 | 0/0 | 4951 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0017 | 0/0 | 4953 | 3 | 0 | 1 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0018 | 0/0 | 4952 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0019 | 0/0 | 4954 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0020 | 0/0 | 4951 | 3 | 1 | 0 | 1 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0021 | 0/0 | 4952 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0022 | 0/0 | 4953 | 3 | 1 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0023 | 0/0 | 4953 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0024 | 0/0 | 4953 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0025 | 0/0 | 4953 | 2 | 0 | 1 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0026 | 0/0 | 4951 | 2 | 0 | 0 | 0 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0027 | 0/0 | 4952 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0028 | 0/0 | 4953 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0029 | 0/0 | 4953 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0030 | 0/0 | 4952 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0031 | 0/0 | 4952 | 2 | 0 | 1 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0032 | 0/0 | 4955 | 2 | 0 | 1 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0033 | 0/0 | 4951 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0034 | 0/0 | 4952 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0035 | 0/0 | 4951 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0036 | 0/0 | 4953 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0037 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0038 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0039 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0040 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0041 | 0/0 | 4953 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0042 | 0/0 | 4955 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0043 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0044 | 0/0 | 4952 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0045 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0046 | 0/0 | 4952 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0047 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0048 | 0/0 | 4952 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0049 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0050 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0051 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0052 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0053 | 0/0 | 4952 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0054 | 0/0 | 4951 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0055 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0056 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0057 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0058 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0059 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0060 | 0/0 | 4954 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0061 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0062 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0063 | 0/0 | 4953 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0064 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0065 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0066 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0067 | 0/0 | 4954 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0068 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0069 | 0/0 | 4955 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0070 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0071 | 0/0 | 4953 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0072 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0073 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0074 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0075 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0076 | 0/0 | 4953 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0077 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0078 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| t0079 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 8091 | 109 | 19 | 24 | 49 | 4 | 12 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003 | 0/0 | 8091 | 26 | 24 | 2 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004 | 0/0 | 8091 | 17 | 1 | 10 | 0 | 2 | 4 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005 | 0/0 | 8091 | 15 | 13 | 0 | 0 | 2 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0009 | 0/0 | 8091 | 4 | 0 | 0 | 2 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0011 | 0/0 | 8091 | 2 | 0 | 0 | 0 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0014 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0021 | 1/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0022 | 0/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0024 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0033 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002 | 0/0 | 8091 | 76 | 5 | 13 | 49 | 2 | 7 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0016 | 0/0 | 8091 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0027 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0034 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003c0006 | 0/0 | 8091 | 9 | 3 | 1 | 1 | 0 | 4 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003c0031 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0013 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0017 | 0/0 | 8091 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0026 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0029 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0005c0007 | 0/0 | 8091 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0006c0008 | 0/0 | 8091 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0007c0010 | 0/0 | 8091 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0008c0015 | 0/0 | 8091 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0009c0012 | 0/0 | 8091 | 2 | 1 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0010c0025 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0011c0028 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0012c0032 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0013c0023 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0014c0030 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0015c0020 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0016c0018 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0017c0035 | 0/0 | 8091 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0018c0019 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 13042 | 9 | 2 | 3 | 0 | 3 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0004 | 0/0 | 13042 | 16 | 0 | 5 | 8 | 1 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0005 | 0/0 | 13043 | 8 | 5 | 3 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0006 | 0/0 | 13044 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0007 | 0/0 | 13039 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0008 | 0/0 | 13041 | 10 | 0 | 3 | 5 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0010 | 0/0 | 13042 | 9 | 0 | 0 | 9 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0011 | 0/0 | 13041 | 3 | 2 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0012 | 0/0 | 13043 | 2 | 0 | 0 | 1 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0013 | 0/0 | 13043 | 5 | 0 | 2 | 1 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0017 | 0/0 | 13043 | 3 | 0 | 1 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0018 | 0/0 | 13042 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0023 | 0/0 | 13043 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0024 | 0/0 | 13043 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0025 | 0/0 | 13043 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0026 | 0/0 | 13041 | 2 | 0 | 0 | 0 | 0 | 2 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0029 | 0/0 | 13043 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0030 | 0/0 | 13042 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0032 | 0/0 | 13045 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0033 | 0/0 | 13041 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0034 | 0/0 | 13042 | 2 | 0 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0036 | 0/0 | 13043 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0043 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0044 | 0/0 | 13042 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0045 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0046 | 0/0 | 13042 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0048 | 0/0 | 13042 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0053 | 0/0 | 13042 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0054 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0055 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0059 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0063 | 0/0 | 13043 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0066 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0067 | 0/0 | 13044 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0072 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0073 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0074 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0075 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0001t0078 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0002 | 0/0 | 13042 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0007 | 0/0 | 13039 | 11 | 10 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0011 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0016 | 0/0 | 13041 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0027 | 0/0 | 13042 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0028 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0049 | 0/0 | 13039 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0050 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0051 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0052 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0068 | 0/0 | 13040 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0003t0077 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0002 | 0/0 | 13042 | 6 | 0 | 3 | 0 | 0 | 3 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0005 | 0/0 | 13043 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0006 | 0/0 | 13044 | 2 | 0 | 2 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0011 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0012 | 0/0 | 13043 | 3 | 0 | 2 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0031 | 0/0 | 13042 | 2 | 0 | 1 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0035 | 0/0 | 13041 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0004t0056 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0002 | 0/0 | 13042 | 2 | 1 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0005 | 0/0 | 13043 | 5 | 4 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0006 | 0/0 | 13044 | 5 | 5 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0038 | 0/0 | 13044 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0057 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0005t0058 | 0/0 | 13044 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0009t0002 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0009t0006 | 0/0 | 13044 | 2 | 0 | 0 | 1 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0009t0032 | 0/0 | 13045 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0011t0002 | 0/0 | 13042 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0011t0012 | 0/0 | 13043 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0014t0002 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0014t0012 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0021t0003 | 1/0 | 13042 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0022t0011 | 0/0 | 13041 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0024t0002 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0001c0033t0037 | 0/0 | 13045 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0001 | 0/0 | 13043 | 36 | 2 | 4 | 23 | 1 | 6 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0003 | 0/0 | 13042 | 21 | 1 | 6 | 13 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0014 | 0/0 | 13044 | 5 | 1 | 2 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0019 | 0/0 | 13044 | 3 | 0 | 0 | 3 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0020 | 0/0 | 13041 | 2 | 0 | 0 | 1 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0022 | 0/0 | 13043 | 3 | 1 | 0 | 2 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0039 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0042 | 0/0 | 13045 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0069 | 0/0 | 13045 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0070 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0076 | 0/0 | 13043 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0002t0079 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0016t0003 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0016t0040 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0027t0001 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0002c0034t0047 | 0/0 | 13044 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003c0006t0009 | 0/0 | 13042 | 8 | 3 | 1 | 1 | 0 | 3 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003c0006t0071 | 0/0 | 13043 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0003c0031t0009 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0013t0001 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0013t0020 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0017t0041 | 0/0 | 13043 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0026t0003 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0004c0029t0065 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0005c0007t0015 | 0/0 | 13042 | 4 | 4 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0006c0008t0021 | 0/0 | 13042 | 3 | 3 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0006c0008t0062 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0007c0010t0002 | 0/0 | 13042 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0007c0010t0011 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0008c0015t0002 | 0/0 | 13042 | 2 | 2 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0009c0012t0060 | 0/0 | 13044 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0009c0012t0061 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0010c0025t0028 | 0/0 | 13043 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0011c0028t0003 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0012c0032t0011 | 0/0 | 13041 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0013c0023t0013 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0014c0030t0064 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0015c0020t0008 | 0/0 | 13041 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0016c0018t0004 | 0/0 | 13042 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0017c0035t0025 | 0/0 | 13043 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| a0018c0019t0002 | 0/0 | 13042 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | copy fasta | chr5 | 177128773 | 177305213 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0008g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0011g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0012g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0013g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0013g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0013g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0017g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0017g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0018g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0018g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0023g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0023g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0023g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0024g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0024g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0025g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0026g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0026g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0029g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0029g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0030g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0030g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0032g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0033g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0033g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0034g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0034g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0036g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0043g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0044g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0045g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0046g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0048g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0053g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0054g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0055g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0059g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0063g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0066g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0067g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0072g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0073g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0074g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0075g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0001t0078g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0016g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0027g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0028g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0049g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0050g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0051g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0052g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0068g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0003t0077g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0011g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0012g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0012g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0012g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0031g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0031g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0035g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0004t0056g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0038g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0057g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0005t0058g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0009t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0009t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0009t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0009t0032g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0011t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0011t0012g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0014t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0014t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0021t0003g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0022t0011g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0024t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0001c0033t0037g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0014g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0014g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0014g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0019g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0019g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0020g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0020g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0022g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0022g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0039g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0042g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0069g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0070g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0076g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0002t0079g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0016t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0016t0040g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0027t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0002c0034t0047g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0006t0071g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0003c0031t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0004c0013t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0004c0013t0020g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0004c0017t0041g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0004c0026t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0004c0029t0065g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0005c0007t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0005c0007t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0005c0007t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0005c0007t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0006c0008t0021g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0006c0008t0021g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0006c0008t0021g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0006c0008t0062g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0007c0010t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0007c0010t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0007c0010t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0008c0015t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0008c0015t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0009c0012t0060g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0009c0012t0061g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0010c0025t0028g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0011c0028t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0012c0032t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0013c0023t0013g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0014c0030t0064g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0015c0020t0008g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0016c0018t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0017c0035t0025g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| a0018c0019t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0011 | g0219 | EUR | GBR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00099 | hp2 | a0002 | c0002 | t0020 | g0001 | EUR | GBR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00280 | hp1 | a0001 | c0004 | t0031 | g0169 | EUR | FIN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0209 | EUR | FIN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | FIN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | FIN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00408 | hp1 | a0001 | c0001 | t0017 | g0217 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00423 | hp2 | a0001 | c0001 | t0024 | g0243 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00597 | hp1 | a0013 | c0023 | t0013 | g0273 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00597 | hp2 | a0002 | c0002 | t0042 | g0036 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00609 | hp2 | a0001 | c0001 | t0059 | g0218 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00642 | hp1 | a0001 | c0004 | t0012 | g0259 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00642 | hp2 | a0001 | c0001 | t0032 | g0155 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | CHS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00733 | hp1 | a0003 | c0006 | t0009 | g0165 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00733 | hp2 | a0002 | c0002 | t0003 | g0044 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0227 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG00738 | hp2 | a0001 | c0001 | t0048 | g0198 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01069 | hp2 | a0001 | c0004 | t0006 | g0225 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0045 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01071 | hp1 | a0001 | c0004 | t0006 | g0224 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0207 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0083 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0295 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0174 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0226 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01106 | hp2 | a0001 | c0001 | t0067 | g0278 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01109 | hp1 | a0002 | c0002 | t0014 | g0029 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01109 | hp2 | a0001 | c0003 | t0068 | g0137 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01167 | hp1 | a0001 | c0003 | t0007 | g0128 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01167 | hp2 | a0001 | c0004 | t0035 | g0233 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01175 | hp2 | a0002 | c0002 | t0014 | g0039 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01192 | hp2 | a0001 | c0004 | t0005 | g0277 | AMR | PUR | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01255 | hp1 | a0001 | c0004 | t0031 | g0268 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01256 | hp1 | a0002 | c0002 | t0076 | g0035 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01256 | hp2 | a0001 | c0001 | t0011 | g0173 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01257 | hp2 | a0001 | c0001 | t0053 | g0266 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0267 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01261 | hp2 | a0001 | c0004 | t0012 | g0162 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0294 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01496 | hp2 | a0001 | c0001 | t0025 | g0190 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | IBS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01515 | hp2 | a0001 | c0005 | t0002 | g0007 | EUR | IBS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01517 | hp1 | a0001 | c0005 | t0005 | g0008 | EUR | IBS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01884 | hp1 | a0001 | c0001 | t0078 | g0237 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01884 | hp2 | a0001 | c0005 | t0006 | g0298 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01891 | hp1 | a0001 | c0005 | t0058 | g0024 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01891 | hp2 | a0001 | c0003 | t0007 | g0124 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0250 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0183 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0055 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02004 | hp2 | a0001 | c0004 | t0002 | g0272 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02015 | hp1 | a0003 | c0006 | t0009 | g0163 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02015 | hp2 | a0001 | c0001 | t0054 | g0271 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0197 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02027 | hp2 | a0002 | c0002 | t0079 | g0032 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02055 | hp1 | a0001 | c0005 | t0006 | g0019 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0157 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02071 | hp2 | a0001 | c0009 | t0002 | g0257 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02074 | hp1 | a0001 | c0001 | t0013 | g0234 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02074 | hp2 | a0002 | c0002 | t0019 | g0086 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02129 | hp2 | a0001 | c0001 | t0033 | g0172 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02135 | hp1 | a0001 | c0001 | t0012 | g0248 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02135 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02145 | hp1 | a0001 | c0033 | t0037 | g0262 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02145 | hp2 | a0012 | c0032 | t0011 | g0109 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0270 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CDX | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02155 | hp2 | a0001 | c0001 | t0008 | g0239 | EAS | CDX | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02165 | hp1 | a0002 | c0016 | t0003 | g0068 | EAS | CDX | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02165 | hp2 | a0001 | c0001 | t0055 | g0214 | EAS | CDX | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02257 | hp2 | a0001 | c0003 | t0007 | g0123 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0066 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0276 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02280 | hp1 | a0009 | c0012 | t0061 | g0140 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02300 | hp1 | a0001 | c0001 | t0046 | g0244 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02451 | hp1 | a0004 | c0013 | t0001 | g0105 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02451 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02523 | hp1 | a0001 | c0001 | t0075 | g0184 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02523 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | KHV | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02572 | hp1 | a0001 | c0003 | t0028 | g0136 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02602 | hp2 | a0001 | c0009 | t0032 | g0258 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02615 | hp1 | a0001 | c0005 | t0006 | g0021 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02615 | hp2 | a0003 | c0006 | t0009 | g0166 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02622 | hp1 | a0001 | c0003 | t0007 | g0126 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02622 | hp2 | a0003 | c0006 | t0009 | g0160 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02630 | hp1 | a0006 | c0008 | t0021 | g0145 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0236 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02647 | hp2 | a0001 | c0024 | t0002 | g0009 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02683 | hp2 | a0001 | c0001 | t0026 | g0246 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0189 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0231 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02717 | hp1 | a0001 | c0005 | t0005 | g0017 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0191 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02723 | hp1 | a0001 | c0003 | t0007 | g0125 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02738 | hp1 | a0009 | c0012 | t0060 | g0141 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0161 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02809 | hp1 | a0008 | c0015 | t0002 | g0131 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02809 | hp2 | a0001 | c0003 | t0051 | g0120 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02818 | hp2 | a0005 | c0007 | t0015 | g0006 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02886 | hp1 | a0006 | c0008 | t0021 | g0142 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02886 | hp2 | a0001 | c0001 | t0018 | g0192 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02896 | hp1 | a0001 | c0005 | t0005 | g0016 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02896 | hp2 | a0006 | c0008 | t0062 | g0144 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02897 | hp1 | a0006 | c0008 | t0021 | g0143 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02897 | hp2 | a0008 | c0015 | t0002 | g0116 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02922 | hp1 | a0007 | c0010 | t0011 | g0011 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02965 | hp1 | a0001 | c0001 | t0045 | g0287 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02965 | hp2 | a0001 | c0003 | t0049 | g0111 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02976 | hp1 | a0018 | c0019 | t0002 | g0265 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02976 | hp2 | a0005 | c0007 | t0015 | g0004 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0038 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03017 | hp2 | a0001 | c0009 | t0006 | g0168 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03041 | hp1 | a0001 | c0003 | t0007 | g0122 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03041 | hp2 | a0001 | c0003 | t0027 | g0121 | AFR | GWD | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03098 | hp1 | a0001 | c0003 | t0050 | g0110 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03098 | hp2 | a0005 | c0007 | t0015 | g0005 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03130 | hp1 | a0010 | c0025 | t0028 | g0115 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03130 | hp2 | a0001 | c0003 | t0007 | g0113 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03139 | hp1 | a0001 | c0003 | t0052 | g0129 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03139 | hp2 | a0001 | c0014 | t0012 | g0026 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03195 | hp1 | a0001 | c0003 | t0016 | g0114 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03195 | hp2 | a0001 | c0005 | t0006 | g0022 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0133 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03209 | hp2 | a0001 | c0001 | t0018 | g0238 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03225 | hp1 | a0001 | c0003 | t0007 | g0112 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03225 | hp2 | a0007 | c0010 | t0002 | g0010 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03239 | hp1 | a0001 | c0004 | t0002 | g0229 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03239 | hp2 | a0001 | c0001 | t0063 | g0296 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03453 | hp1 | a0001 | c0005 | t0057 | g0020 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03453 | hp2 | a0001 | c0003 | t0027 | g0119 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03486 | hp1 | a0001 | c0014 | t0002 | g0027 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03486 | hp2 | a0001 | c0003 | t0077 | g0108 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03490 | hp1 | a0003 | c0006 | t0009 | g0158 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03490 | hp2 | a0001 | c0001 | t0026 | g0201 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0188 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03491 | hp2 | a0003 | c0006 | t0071 | g0159 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03516 | hp1 | a0002 | c0002 | t0022 | g0087 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03516 | hp2 | a0007 | c0010 | t0002 | g0012 | AFR | ESN | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03579 | hp2 | a0001 | c0003 | t0007 | g0134 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03654 | hp1 | a0001 | c0001 | t0013 | g0177 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03654 | hp2 | a0001 | c0011 | t0002 | g0228 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03688 | hp1 | a0001 | c0004 | t0012 | g0263 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03710 | hp1 | a0003 | c0006 | t0009 | g0013 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0196 | SAS | PJL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03927 | hp1 | a0001 | c0001 | t0036 | g0199 | SAS | BEB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03927 | hp2 | a0004 | c0017 | t0041 | g0260 | SAS | BEB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04115 | hp1 | a0003 | c0006 | t0009 | g0164 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04115 | hp2 | a0001 | c0001 | t0044 | g0253 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | BEB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | BEB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04204 | hp1 | a0001 | c0004 | t0002 | g0220 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04228 | hp1 | a0001 | c0011 | t0012 | g0297 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | STU | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18522 | hp1 | a0001 | c0003 | t0016 | g0118 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18522 | hp2 | a0001 | c0005 | t0002 | g0015 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18612 | hp1 | a0001 | c0001 | t0017 | g0213 | EAS | CHB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | CHB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18747 | hp1 | a0001 | c0009 | t0006 | g0222 | EAS | CHB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | CHB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18906 | hp1 | a0005 | c0007 | t0015 | g0003 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18906 | hp2 | a0001 | c0005 | t0005 | g0018 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18941 | hp1 | a0001 | c0001 | t0023 | g0181 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18941 | hp2 | a0002 | c0027 | t0001 | g0099 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18943 | hp1 | a0016 | c0018 | t0004 | g0194 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18943 | hp2 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18944 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18944 | hp2 | a0001 | c0001 | t0010 | g0211 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18946 | hp1 | a0001 | c0001 | t0034 | g0290 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18946 | hp2 | a0002 | c0002 | t0069 | g0107 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18947 | hp2 | a0001 | c0001 | t0010 | g0212 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18950 | hp1 | a0001 | c0001 | t0023 | g0200 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0091 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0208 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18967 | hp1 | a0001 | c0001 | t0073 | g0251 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18967 | hp2 | a0002 | c0016 | t0040 | g0069 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18969 | hp1 | a0001 | c0001 | t0030 | g0282 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18970 | hp1 | a0002 | c0002 | t0019 | g0081 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18970 | hp2 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18971 | hp2 | a0001 | c0001 | t0023 | g0150 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18974 | hp1 | a0001 | c0001 | t0072 | g0152 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18975 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18975 | hp2 | a0003 | c0031 | t0009 | g0154 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18977 | hp1 | a0001 | c0001 | t0010 | g0264 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0255 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18981 | hp1 | a0017 | c0035 | t0025 | g0221 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18981 | hp2 | a0002 | c0002 | t0014 | g0071 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18984 | hp2 | a0011 | c0028 | t0003 | g0101 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18985 | hp1 | a0002 | c0002 | t0039 | g0040 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18989 | hp2 | a0001 | c0001 | t0010 | g0216 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18990 | hp2 | a0001 | c0001 | t0034 | g0235 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18991 | hp1 | a0002 | c0002 | t0022 | g0102 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18991 | hp2 | a0001 | c0001 | t0066 | g0283 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18993 | hp1 | a0002 | c0002 | t0019 | g0074 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18993 | hp2 | a0001 | c0001 | t0030 | g0280 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA18999 | hp2 | a0002 | c0002 | t0020 | g0049 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19000 | hp1 | a0001 | c0001 | t0024 | g0156 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19002 | hp1 | a0015 | c0020 | t0008 | g0275 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19005 | hp1 | a0001 | c0001 | t0074 | g0215 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19005 | hp2 | a0002 | c0034 | t0047 | g0093 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19009 | hp1 | a0002 | c0002 | t0070 | g0097 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19009 | hp2 | a0001 | c0001 | t0033 | g0176 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19011 | hp1 | a0002 | c0002 | t0022 | g0076 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19012 | hp2 | a0002 | c0002 | t0014 | g0072 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19030 | hp1 | a0001 | c0003 | t0011 | g0135 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19030 | hp2 | a0001 | c0005 | t0038 | g0025 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19043 | hp2 | a0004 | c0029 | t0065 | g0146 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19060 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19062 | hp2 | a0001 | c0001 | t0043 | g0291 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19067 | hp1 | a0001 | c0001 | t0029 | g0285 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19076 | hp1 | a0014 | c0030 | t0064 | g0153 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19076 | hp2 | a0001 | c0001 | t0029 | g0284 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19088 | hp1 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19088 | hp2 | a0001 | c0001 | t0008 | g0182 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19091 | hp2 | a0001 | c0001 | t0024 | g0195 | EAS | JPT | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19240 | hp1 | a0001 | c0003 | t0007 | g0127 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | YRI | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ASW | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0179 | AFR | ASW | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0279 | SAS | GIH | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA20905 | hp2 | a0001 | c0022 | t0011 | g0171 | SAS | GIH | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | CLM | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02109 | hp1 | a0003 | c0006 | t0009 | g0167 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02109 | hp2 | a0001 | c0003 | t0007 | g0132 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02486 | hp1 | a0002 | c0002 | t0014 | g0073 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02486 | hp2 | a0001 | c0005 | t0006 | g0023 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02559 | hp1 | a0001 | c0003 | t0016 | g0117 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG02559 | hp2 | a0001 | c0004 | t0056 | g0261 | AFR | ACB | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0130 | AFR | MSL | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG06807 | hp1 | a0004 | c0026 | t0003 | g0104 | AFR | USA | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | USA | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0289 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| NA21309 | hp2 | a0004 | c0013 | t0020 | g0103 | AFR | LWK | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0247 | REF | REF | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| homoSapiens_grch38 | hp1 | a0001 | c0021 | t0003 | g0206 | REF | REF | NSD1_chr5_177128773_177305213 | NSD1 | chr5 | 177128773 | 177305213 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177135863
|
C | T | 1 | a0008 | 2 | HG02809.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.760C>T | p.Leu254Phe | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 957/13042 | 760/8091 | 254/2696 | chr5 | 177135863 | ||
| chr5:177209973
|
G | A | 1 | a0010 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.1574G>A | p.Arg525Gln | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1771/13042 | 1574/8091 | 525/2696 | chr5 | 177209973 | ||
| chr5:177210089
|
G | T | 1 | a0006 | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.1690G>T | p.Ala564Ser | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1887/13042 | 1690/8091 | 564/2696 | chr5 | 177210089 | ||
| chr5:177210239
|
G | T | 2 | a0002a0011 | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
missense_variant | MODERATE | c.1840G>T | p.Val614Leu | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2037/13042 | 1840/8091 | 614/2696 | chr5 | 177210239 | ||
| chr5:177210470
|
G | A | 1 | a0009 | 2 | HG02280.hp1 HG02738.hp1 |
missense_variant | MODERATE | c.2071G>A | p.Ala691Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2268/13042 | 2071/8091 | 691/2696 | chr5 | 177210470 | ||
| chr5:177210575
|
T | C | 4 | a0002a0004a0009others(1): Show | 88 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
missense_variant | MODERATE | c.2176T>C | p.Ser726Pro | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2373/13042 | 2176/8091 | 726/2696 | chr5 | 177210575 | ||
| chr5:177210849
|
C | T | 1 | a0012 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2450C>T | p.Ser817Phe | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2647/13042 | 2450/8091 | 817/2696 | chr5 | 177210849 | ||
| chr5:177211505
|
G | C | 3 | a0005a0006a0009 | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
missense_variant | MODERATE | c.3106G>C | p.Ala1036Pro | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 3303/13042 | 3106/8091 | 1036/2696 | chr5 | 177211505 | ||
| chr5:177211691
|
A | G | 1 | a0013 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.3292A>G | p.Thr1098Ala | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 3489/13042 | 3292/8091 | 1098/2696 | chr5 | 177211691 | ||
| chr5:177257077
|
A | G | 1 | a0007 | 3 | HG02922.hp1 HG03225.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.4892A>G | p.Lys1631Arg | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/23 | 5089/13042 | 4892/8091 | 1631/2696 | chr5 | 177257077 | ||
| chr5:177294118
|
G | A | 5 | a0003a0005a0006others(2): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
missense_variant | MODERATE | c.6750G>A | p.Met2250Ile | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 6947/13042 | 6750/8091 | 2250/2696 | chr5 | 177294118 | ||
| chr5:177294150
|
T | C | 5 | a0003a0005a0006others(2): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
missense_variant | MODERATE | c.6782T>C | p.Met2261Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 6979/13042 | 6782/8091 | 2261/2696 | chr5 | 177294150 | ||
| chr5:177294513
|
C | T | 1 | a0015 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.7145C>T | p.Thr2382Ile | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7342/13042 | 7145/8091 | 2382/2696 | chr5 | 177294513 | ||
| chr5:177294782
|
C | T | 1 | a0018 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.7414C>T | p.Pro2472Ser | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7611/13042 | 7414/8091 | 2472/2696 | chr5 | 177294782 | ||
| chr5:177295004
|
G | A | 2 | a0003a0014 | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
missense_variant | MODERATE | c.7636G>A | p.Ala2546Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7833/13042 | 7636/8091 | 2546/2696 | chr5 | 177295004 | ||
| chr5:177295013
|
T | A | 1 | a0014 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.7645T>A | p.Tyr2549Asn | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7842/13042 | 7645/8091 | 2549/2696 | chr5 | 177295013 | ||
| chr5:177295148
|
G | A | 1 | a0011 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.7780G>A | p.Ala2594Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7977/13042 | 7780/8091 | 2594/2696 | chr5 | 177295148 | ||
| chr5:177295377
|
A | T | 1 | a0017 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.8009A>T | p.Asp2670Val | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 8206/13042 | 8009/8091 | 2670/2696 | chr5 | 177295377 | ||
| chr5:177295418
|
G | A | 1 | a0016 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.8050G>A | p.Ala2684Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 8247/13042 | 8050/8091 | 2684/2696 | chr5 | 177295418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177135442
|
C | T | 2 | a0001c0009a0017c0035 | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
synonymous_variant | LOW | c.339C>T | p.Cys113Cys | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 536/13042 | 339/8091 | 113/2696 | chr5 | 177135442 | ||
| chr5:177135583
|
C | T | 1 | a0002c0016 | 2 | HG02165.hp1 NA18967.hp2 |
synonymous_variant | LOW | c.480C>T | p.Asp160Asp | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 677/13042 | 480/8091 | 160/2696 | chr5 | 177135583 | ||
| chr5:177135871
|
C | T | 1 | a0002c0034 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.768C>T | p.Ala256Ala | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 965/13042 | 768/8091 | 256/2696 | chr5 | 177135871 | ||
| chr5:177135949
|
A | C | 1 | a0001c0033 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.846A>C | p.Pro282Pro | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 1043/13042 | 846/8091 | 282/2696 | chr5 | 177135949 | ||
| chr5:177209881
|
C | T | 22 | a0001c0003a0001c0005a0001c0014others(19): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
synonymous_variant | LOW | c.1482C>T | p.Cys494Cys | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1679/13042 | 1482/8091 | 494/2696 | chr5 | 177209881 | ||
| chr5:177209914
|
T | C | 2 | a0001c0024a0007c0010 | 4 | HG02647.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.1515T>C | p.Asn505Asn | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1712/13042 | 1515/8091 | 505/2696 | chr5 | 177209914 | ||
| chr5:177210034
|
G | A | 1 | a0004c0026 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1635G>A | p.Thr545Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1832/13042 | 1635/8091 | 545/2696 | chr5 | 177210034 | ||
| chr5:177210148
|
G | A | 5 | a0002c0002a0002c0016a0002c0027others(2): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
synonymous_variant | LOW | c.1749G>A | p.Glu583Glu | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1946/13042 | 1749/8091 | 583/2696 | chr5 | 177210148 | ||
| chr5:177210191
|
T | C | 1 | a0001c0011 | 2 | HG03654.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.1792T>C | p.Leu598Leu | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 1989/13042 | 1792/8091 | 598/2696 | chr5 | 177210191 | ||
| chr5:177210379
|
C | T | 1 | a0001c0014 | 2 | HG03139.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1980C>T | p.Asn660Asn | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2177/13042 | 1980/8091 | 660/2696 | chr5 | 177210379 | ||
| chr5:177210568
|
C | T | 1 | a0006c0008 | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
synonymous_variant | LOW | c.2169C>T | p.Thr723Thr | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 2366/13042 | 2169/8091 | 723/2696 | chr5 | 177210568 | ||
| chr5:177211729
|
C | T | 1 | a0001c0022 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.3330C>T | p.Phe1110Phe | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 3527/13042 | 3330/8091 | 1110/2696 | chr5 | 177211729 | ||
| chr5:177212104
|
T | C | 7 | a0001c0005a0001c0014a0001c0024others(4): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
synonymous_variant | LOW | c.3705T>C | p.Asn1235Asn | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/23 | 3902/13042 | 3705/8091 | 1235/2696 | chr5 | 177212104 | ||
| chr5:177294043
|
A | C | 1 | a0003c0031 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.6675A>C | p.Pro2225Pro | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 6872/13042 | 6675/8091 | 2225/2696 | chr5 | 177294043 | ||
| chr5:177294197
|
T | C | 30 | a0001c0001a0001c0003a0001c0004others(27): Show | 217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
synonymous_variant | LOW | c.6829T>C | p.Leu2277Leu | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7026/13042 | 6829/8091 | 2277/2696 | chr5 | 177294197 | ||
| chr5:177294271
|
G | C | 4 | a0001c0004a0001c0011a0001c0022others(1): Show | 21 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(18): Show |
synonymous_variant | LOW | c.6903G>C | p.Gly2301Gly | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 7100/13042 | 6903/8091 | 2301/2696 | chr5 | 177294271 | ||
| chr5:177295301
|
C | T | 1 | a0004c0029 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.7933C>T | p.Leu2645Leu | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 8130/13042 | 7933/8091 | 2645/2696 | chr5 | 177295301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177133783
|
C | T | 1 | a0002c0002t0079 | 1 | HG02027.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/23 | 1321 | chr5 | 177133783 | |||||
| chr5:177133820
|
C | A | 1 | a0001c0004t0035 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/23 | 1284 | chr5 | 177133820 | |||||
| chr5:177133843
|
A | AG | 9 | a0001c0001t0025a0001c0001t0036a0001c0005t0038others(6): Show | 9 | HG00597.hp2 HG01496.hp2 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-121dupG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/23 | 1254 | INFO_REALIGN_3_PRIME | chr5 | 177133843 | ||||
| chr5:177133939
|
G | A | 1 | a0001c0001t0043 | 1 | NA19062.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/23 | 1165 | chr5 | 177133939 | |||||
| chr5:177135096
|
G | A | 1 | a0001c0001t0044 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/23 | 8 | chr5 | 177135096 | |||||
| chr5:177295630
|
G | C | 1 | a0001c0001t0045 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 171 | chr5 | 177295630 | |||||
| chr5:177295866
|
G | A | 2 | a0001c0001t0026a0001c0001t0046 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*407G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 407 | chr5 | 177295866 | |||||
| chr5:177295874
|
G | T | 1 | a0001c0001t0078 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 415 | chr5 | 177295874 | |||||
| chr5:177296259
|
G | A | 1 | a0005c0007t0015 | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 800 | chr5 | 177296259 | |||||
| chr5:177296512
|
C | A | 1 | a0002c0034t0047 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 1053 | chr5 | 177296512 | |||||
| chr5:177296575
|
G | A | 1 | a0001c0001t0048 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1116G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 1116 | chr5 | 177296575 | |||||
| chr5:177296633
|
A | G | 1 | a0001c0003t0077 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 1174 | chr5 | 177296633 | |||||
| chr5:177296679
|
T | C | 7 | a0001c0003t0016a0001c0003t0027a0001c0003t0028others(4): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1220T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 1220 | chr5 | 177296679 | |||||
| chr5:177297056
|
G | A | 7 | a0001c0003t0016a0001c0003t0027a0001c0003t0028others(4): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1597G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 1597 | chr5 | 177297056 | |||||
| chr5:177297506
|
G | A | 1 | a0001c0003t0052 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2047 | chr5 | 177297506 | |||||
| chr5:177297514
|
G | T | 1 | a0002c0002t0076 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2055G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2055 | chr5 | 177297514 | |||||
| chr5:177297589
|
A | C | 1 | a0001c0001t0075 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2130A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2130 | chr5 | 177297589 | |||||
| chr5:177297644
|
A | G | 9 | a0001c0001t0010a0001c0001t0023a0001c0001t0024others(6): Show | 23 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2185A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2185 | chr5 | 177297644 | |||||
| chr5:177297659
|
T | TG | 23 | a0001c0001t0012a0001c0001t0013a0001c0001t0032others(20): Show | 36 | HG00597.hp1 HG00597.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2208dupG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2209 | INFO_REALIGN_3_PRIME | chr5 | 177297659 | ||||
| chr5:177297668
|
C | G | 1 | a0001c0003t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2209C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2209 | chr5 | 177297668 | |||||
| chr5:177297907
|
C | T | 1 | a0004c0029t0065 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2448C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2448 | chr5 | 177297907 | |||||
| chr5:177298230
|
A | T | 1 | a0014c0030t0064 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2771A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 2771 | chr5 | 177298230 | |||||
| chr5:177298600
|
G | A | 1 | a0001c0003t0049 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3141G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3141 | chr5 | 177298600 | |||||
| chr5:177298738
|
G | T | 2 | a0001c0001t0024a0001c0001t0034 | 5 | HG00423.hp2 NA18946.hp1 NA18990.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3279 | chr5 | 177298738 | |||||
| chr5:177298750
|
A | G | 1 | a0001c0001t0063 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3291A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3291 | chr5 | 177298750 | |||||
| chr5:177298797
|
A | C | 9 | a0003c0006t0009a0003c0006t0071a0003c0031t0009others(6): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3338A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3338 | chr5 | 177298797 | |||||
| chr5:177298885
|
T | A | 1 | a0001c0001t0053 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3426T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3426 | chr5 | 177298885 | |||||
| chr5:177298954
|
A | G | 4 | a0003c0006t0009a0003c0006t0071a0003c0031t0009others(1): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3495A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3495 | chr5 | 177298954 | |||||
| chr5:177299001
|
T | C | 95 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(92): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*3542T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3542 | chr5 | 177299001 | |||||
| chr5:177299212
|
C | T | 2 | a0006c0008t0021a0006c0008t0062 | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3753C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3753 | chr5 | 177299212 | |||||
| chr5:177299286
|
T | C | 2 | a0001c0001t0043a0001c0001t0054 | 2 | HG02015.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3827T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 3827 | chr5 | 177299286 | |||||
| chr5:177299460
|
C | T | 1 | a0001c0001t0059 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4001C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4001 | chr5 | 177299460 | |||||
| chr5:177299486
|
T | C | 2 | a0009c0012t0060a0009c0012t0061 | 2 | HG02280.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4027T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4027 | chr5 | 177299486 | |||||
| chr5:177299634
|
G | A | 30 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(27): Show | 77 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*4175G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4175 | chr5 | 177299634 | |||||
| chr5:177299658
|
T | G | 2 | a0001c0004t0031a0001c0004t0056 | 3 | HG00280.hp1 HG01255.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4199T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4199 | chr5 | 177299658 | |||||
| chr5:177299790
|
C | G | 1 | a0001c0001t0018 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4331C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4331 | chr5 | 177299790 | |||||
| chr5:177299999
|
T | TA | 3 | a0001c0001t0029a0001c0001t0030a0001c0001t0066 | 5 | NA18969.hp1 NA18991.hp2 NA18993.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4541dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4542 | INFO_REALIGN_3_PRIME | chr5 | 177299999 | ||||
| chr5:177300057
|
G | GC | 23 | a0001c0001t0005a0001c0001t0017a0001c0001t0023others(20): Show | 79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4611dupC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4612 | INFO_REALIGN_3_PRIME | chr5 | 177300057 | ||||
| chr5:177300057
|
G | GCC | 14 | a0001c0001t0006a0001c0001t0032a0001c0001t0055others(11): Show | 25 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4610_*4611dupCC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4612 | INFO_REALIGN_3_PRIME | chr5 | 177300057 | ||||
| chr5:177300057
|
GC | G | 20 | a0001c0001t0008a0001c0001t0011a0001c0001t0026others(17): Show | 37 | HG00099.hp1 HG00099.hp2 HG01081.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4611delC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4611 | INFO_REALIGN_3_PRIME | chr5 | 177300057 | ||||
| chr5:177300057
|
GCCC | G | 4 | a0001c0001t0007a0001c0003t0007a0001c0003t0049others(1): Show | 14 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4609_*4611delCCC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4609 | INFO_REALIGN_3_PRIME | chr5 | 177300057 | ||||
| chr5:177300071
|
G | A | 1 | a0001c0005t0057 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4612G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4612 | chr5 | 177300071 | |||||
| chr5:177300147
|
C | A | 1 | a0001c0005t0058 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4688C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 23/23 | 4688 | chr5 | 177300147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177133989
|
G | T | 1 | a0001c0005t0006g0298 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+37G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177133989 | ||||||
| chr5:177134112
|
T | C | 147 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-18+160T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134112 | ||||||
| chr5:177134458
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+506C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134458 | ||||||
| chr5:177134470
|
C | T | 1 | a0001c0011t0012g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-18+518C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134470 | ||||||
| chr5:177134701
|
C | T | 4 | a0001c0001t0002g0293a0001c0001t0005g0295a0001c0001t0017g0294others(1): Show | 4 | HG01081.hp1 HG01496.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-386C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134701 | ||||||
| chr5:177134742
|
G | C | 1 | a0002c0002t0020g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17-345G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134742 | ||||||
| chr5:177134747
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-340C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134747 | ||||||
| chr5:177134760
|
G | A | 1 | a0002c0002t0003g0002 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-17-327G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134760 | ||||||
| chr5:177134771
|
T | C | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-17-316T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134771 | ||||||
| chr5:177134902
|
G | A | 1 | a0001c0005t0006g0298 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-185G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134902 | ||||||
| chr5:177134981
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-17-106A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 1/22 | chr5 | 177134981 | ||||||
| chr5:177136078
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+48A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177136078 | ||||||
| chr5:177136329
|
T | TA | 12 | a0001c0001t0002g0149a0001c0001t0023g0150a0005c0007t0015g0003others(9): Show | 12 | HG01517.hp2 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+315dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177136329 | |||||
| chr5:177136329
|
TA | T | 8 | a0001c0001t0002g0288a0001c0001t0007g0289a0001c0001t0034g0290others(5): Show | 8 | HG01070.hp1 HG02965.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+315delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177136329 | |||||
| chr5:177136398
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+368T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177136398 | ||||||
| chr5:177136697
|
A | G | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.927+667A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177136697 | ||||||
| chr5:177136903
|
C | T | 1 | a0001c0003t0068g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.927+873C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177136903 | ||||||
| chr5:177137074
|
G | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+1044G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137074 | ||||||
| chr5:177137188
|
G | A | 95 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(92): Show | 95 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.927+1158G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137188 | ||||||
| chr5:177137193
|
T | G | 1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.927+1163T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137193 | ||||||
| chr5:177137375
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+1345C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137375 | ||||||
| chr5:177137485
|
G | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+1455G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137485 | ||||||
| chr5:177137554
|
C | T | 6 | a0001c0001t0004g0281a0001c0001t0029g0284a0001c0001t0029g0285others(3): Show | 6 | NA18942.hp1 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+1524C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137554 | ||||||
| chr5:177137662
|
C | T | 1 | a0002c0002t0069g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.927+1632C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137662 | ||||||
| chr5:177137780
|
G | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+1750G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137780 | ||||||
| chr5:177137829
|
G | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+1799G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177137829 | ||||||
| chr5:177138090
|
C | A | 9 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(6): Show | 9 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+2060C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138090 | ||||||
| chr5:177138090
|
CAAAA | C | 13 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.927+2064_927+2067d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177138090 | |||||
| chr5:177138093
|
A | C | 1 | a0002c0002t0003g0106 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.927+2063A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138093 | ||||||
| chr5:177138094
|
A | C | 5 | a0001c0001t0013g0279a0001c0001t0067g0278a0001c0014t0002g0027others(2): Show | 5 | HG01106.hp2 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+2064A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138094 | ||||||
| chr5:177138094
|
AAAAC | A | 87 | a0001c0001t0008g0151a0001c0005t0002g0007a0001c0005t0005g0008others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.927+2084_927+2087d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177138094 | |||||
| chr5:177138114
|
C | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+2084C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138114 | ||||||
| chr5:177138208
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.927+2178G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138208 | ||||||
| chr5:177138444
|
C | T | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.927+2414C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177138444 | ||||||
| chr5:177138645
|
A | AT | 13 | a0001c0001t0004g0269a0001c0001t0004g0274a0001c0001t0004g0276others(10): Show | 13 | HG00597.hp1 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+2626dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177138645 | |||||
| chr5:177139207
|
C | T | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+3177C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177139207 | ||||||
| chr5:177139223
|
C | T | 1 | a0009c0012t0060g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+3193C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177139223 | ||||||
| chr5:177139228
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+3198G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177139228 | ||||||
| chr5:177139254
|
G | GA | 86 | a0001c0001t0030g0280a0001c0001t0072g0152a0001c0003t0077g0108others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.927+3235dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177139254 | |||||
| chr5:177139444
|
C | CA | 15 | a0001c0001t0011g0157a0001c0001t0024g0156a0001c0001t0032g0155others(12): Show | 15 | HG00642.hp2 HG01109.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+3431dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177139444 | |||||
| chr5:177139444
|
CA | C | 14 | a0001c0001t0010g0264a0002c0027t0001g0099a0005c0007t0015g0003others(11): Show | 14 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.927+3431delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177139444 | |||||
| chr5:177139514
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+3484G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177139514 | ||||||
| chr5:177139850
|
A | C | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+3820A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177139850 | ||||||
| chr5:177139941
|
C | CA | 35 | a0001c0001t0012g0161a0001c0003t0007g0112a0001c0003t0049g0111others(32): Show | 35 | HG00733.hp1 HG01261.hp2 HG01515.hp2 others(32): Show |
intron_variant | MODIFIER | c.927+3926dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177139941 | |||||
| chr5:177139941
|
CA | C | 11 | a0002c0002t0022g0102a0002c0002t0069g0107a0004c0029t0065g0146others(8): Show | 11 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+3926delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177139941 | |||||
| chr5:177140191
|
T | C | 1 | a0001c0001t0004g0281 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.927+4161T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177140191 | ||||||
| chr5:177140229
|
G | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.927+4199G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177140229 | ||||||
| chr5:177140682
|
T | C | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.927+4652T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177140682 | ||||||
| chr5:177140911
|
A | G | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.927+4881A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177140911 | ||||||
| chr5:177140993
|
T | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+4963T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177140993 | ||||||
| chr5:177141121
|
C | G | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+5091C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141121 | ||||||
| chr5:177141299
|
C | T | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.927+5269C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141299 | ||||||
| chr5:177141313
|
C | T | 1 | a0001c0004t0012g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.927+5283C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141313 | ||||||
| chr5:177141314
|
G | A | 1 | a0002c0002t0079g0032 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.927+5284G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141314 | ||||||
| chr5:177141319
|
C | CT | 82 | a0001c0001t0002g0247a0001c0001t0002g0249a0001c0001t0004g0240others(79): Show | 82 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.927+5318dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177141319 | |||||
| chr5:177141319
|
C | CTT | 7 | a0001c0001t0011g0157a0001c0001t0029g0285a0001c0003t0028g0136others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+5317_927+5318d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177141319 | |||||
| chr5:177141319
|
CT | C | 10 | a0001c0001t0005g0147a0001c0001t0053g0266a0001c0003t0007g0113others(7): Show | 10 | HG00323.hp2 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+5318delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177141319 | |||||
| chr5:177141319
|
CTTTTTTT others(4): Show |
C | 3 | a0004c0013t0020g0103a0004c0026t0003g0104a0012c0032t0011g0109 | 3 | HG02145.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+5308_927+5318d others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177141319 | |||||
| chr5:177141319
|
CTTTTTTT others(5): Show |
C | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+5307_927+5318d others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177141319 | |||||
| chr5:177141333
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+5303T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141333 | ||||||
| chr5:177141342
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+5312T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141342 | ||||||
| chr5:177141407
|
G | A | 4 | a0001c0001t0008g0170a0001c0004t0031g0169a0001c0004t0056g0261others(1): Show | 4 | HG00280.hp1 HG01255.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+5377G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141407 | ||||||
| chr5:177141462
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+5432C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141462 | ||||||
| chr5:177141519
|
G | C | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.927+5489G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141519 | ||||||
| chr5:177141558
|
A | G | 186 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0005g0147others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.927+5528A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141558 | ||||||
| chr5:177141916
|
C | T | 1 | a0001c0001t0059g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+5886C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177141916 | ||||||
| chr5:177142126
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+6096G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177142126 | ||||||
| chr5:177142187
|
T | C | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.927+6157T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177142187 | ||||||
| chr5:177142263
|
T | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+6233T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177142263 | ||||||
| chr5:177142625
|
T | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+6595T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177142625 | ||||||
| chr5:177143021
|
C | T | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.927+6991C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143021 | ||||||
| chr5:177143040
|
T | C | 1 | a0002c0002t0042g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.927+7010T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143040 | ||||||
| chr5:177143130
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.927+7100G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143130 | ||||||
| chr5:177143281
|
A | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+7251A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143281 | ||||||
| chr5:177143356
|
C | T | 1 | a0001c0022t0011g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.927+7326C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143356 | ||||||
| chr5:177143382
|
T | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+7352T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143382 | ||||||
| chr5:177143736
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+7706G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143736 | ||||||
| chr5:177143781
|
A | C | 1 | a0002c0002t0022g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.927+7751A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143781 | ||||||
| chr5:177143783
|
C | CT | 16 | a0001c0001t0004g0252a0001c0001t0004g0254a0001c0001t0004g0256others(13): Show | 16 | HG00408.hp1 HG01175.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+7774dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177143783 | |||||
| chr5:177143783
|
CT | C | 69 | a0001c0001t0002g0149a0001c0001t0004g0223a0001c0001t0004g0230others(66): Show | 69 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.927+7774delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177143783 | |||||
| chr5:177143783
|
CTT | C | 85 | a0001c0003t0007g0122a0001c0003t0049g0111a0001c0004t0011g0219others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.927+7773_927+7774d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177143783 | |||||
| chr5:177143847
|
C | T | 1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.927+7817C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143847 | ||||||
| chr5:177143916
|
G | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+7886G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143916 | ||||||
| chr5:177143925
|
A | G | 1 | a0001c0001t0043g0291 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.927+7895A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177143925 | ||||||
| chr5:177144070
|
A | G | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+8040A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144070 | ||||||
| chr5:177144081
|
C | T | 4 | a0001c0001t0010g0208a0001c0001t0023g0150a0001c0001t0072g0152others(1): Show | 4 | NA18954.hp1 NA18967.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+8051C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144081 | ||||||
| chr5:177144220
|
GT | G | 22 | a0001c0001t0011g0173a0001c0003t0002g0130a0001c0003t0002g0133others(19): Show | 22 | HG01109.hp2 HG01167.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.927+8203delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177144220 | |||||
| chr5:177144241
|
A | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+8211A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144241 | ||||||
| chr5:177144320
|
G | A | 2 | a0004c0013t0020g0103a0004c0026t0003g0104 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+8290G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144320 | ||||||
| chr5:177144382
|
GT | G | 276 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.927+8363delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177144382 | |||||
| chr5:177144504
|
T | C | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.927+8474T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144504 | ||||||
| chr5:177144523
|
G | T | 7 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+8493G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144523 | ||||||
| chr5:177144807
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+8777C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144807 | ||||||
| chr5:177144809
|
C | T | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+8779C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144809 | ||||||
| chr5:177144988
|
T | G | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.927+8958T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177144988 | ||||||
| chr5:177145015
|
G | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+8985G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145015 | ||||||
| chr5:177145084
|
C | CA | 19 | a0001c0001t0002g0203a0001c0001t0005g0148a0001c0001t0008g0174others(16): Show | 19 | HG00597.hp2 HG01081.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.927+9072dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177145084 | |||||
| chr5:177145084
|
CA | C | 37 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(34): Show | 37 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(34): Show |
intron_variant | MODIFIER | c.927+9072delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177145084 | |||||
| chr5:177145223
|
T | C | 1 | a0001c0003t0011g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+9193T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145223 | ||||||
| chr5:177145281
|
A | AT | 32 | a0001c0001t0004g0202a0001c0001t0004g0223a0001c0001t0004g0230others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.927+9267dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177145281 | |||||
| chr5:177145488
|
T | C | 2 | a0002c0002t0003g0038a0002c0002t0020g0001 | 2 | HG00099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.927+9458T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145488 | ||||||
| chr5:177145521
|
C | T | 1 | a0004c0026t0003g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+9491C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145521 | ||||||
| chr5:177145554
|
G | A | 1 | a0001c0001t0013g0234 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.927+9524G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145554 | ||||||
| chr5:177145624
|
A | G | 3 | a0001c0004t0002g0220a0001c0004t0002g0231a0004c0017t0041g0260 | 3 | HG02698.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.927+9594A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145624 | ||||||
| chr5:177145769
|
G | A | 8 | a0001c0001t0002g0247a0001c0001t0002g0293a0001c0001t0005g0295others(5): Show | 8 | HG01081.hp1 HG01256.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+9739G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145769 | ||||||
| chr5:177145832
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+9802C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145832 | ||||||
| chr5:177145862
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+9832C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177145862 | ||||||
| chr5:177145908
|
C | CA | 248 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.927+9896dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177145908 | |||||
| chr5:177145908
|
C | CAA | 20 | a0001c0001t0002g0204a0001c0001t0011g0157a0001c0001t0013g0234others(17): Show | 20 | HG01175.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+9895_927+9896d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177145908 | |||||
| chr5:177146205
|
G | GT | 33 | a0001c0001t0002g0293a0001c0001t0004g0196a0001c0001t0004g0202others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.927+10193dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177146205 | |||||
| chr5:177146205
|
GT | G | 123 | a0001c0001t0010g0264a0001c0003t0002g0130a0001c0003t0007g0113others(120): Show | 123 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.927+10193delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177146205 | |||||
| chr5:177146223
|
T | G | 1 | a0002c0002t0001g0090 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.927+10193T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146223 | ||||||
| chr5:177146224
|
G | T | 1 | a0002c0002t0001g0090 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.927+10194G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146224 | ||||||
| chr5:177146275
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+10245G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146275 | ||||||
| chr5:177146312
|
TCTC | T | 7 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0124others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+10285_927+1028 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177146312 | |||||
| chr5:177146446
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+10416C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146446 | ||||||
| chr5:177146451
|
G | A | 3 | a0001c0001t0011g0157a0001c0001t0011g0236a0001c0001t0078g0237 | 3 | HG01884.hp1 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.927+10421G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146451 | ||||||
| chr5:177146668
|
T | C | 1 | a0001c0001t0006g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.927+10638T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146668 | ||||||
| chr5:177146703
|
C | T | 1 | a0001c0009t0006g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.927+10673C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146703 | ||||||
| chr5:177146847
|
T | TA | 12 | a0001c0001t0010g0264a0004c0029t0065g0146a0005c0007t0015g0003others(9): Show | 12 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+10827dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177146847 | |||||
| chr5:177146857
|
A | T | 1 | a0001c0001t0072g0152 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.927+10827A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146857 | ||||||
| chr5:177146994
|
A | G | 1 | a0002c0002t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+10964A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177146994 | ||||||
| chr5:177147006
|
CA | C | 246 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.927+10992delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177147006 | |||||
| chr5:177147087
|
A | G | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.927+11057A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147087 | ||||||
| chr5:177147186
|
C | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+11156C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147186 | ||||||
| chr5:177147218
|
A | G | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.927+11188A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147218 | ||||||
| chr5:177147245
|
A | G | 5 | a0001c0001t0024g0156a0001c0001t0024g0195a0001c0001t0024g0243others(2): Show | 5 | HG00423.hp2 NA18946.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+11215A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147245 | ||||||
| chr5:177147254
|
T | C | 5 | a0001c0001t0004g0196a0001c0001t0008g0174a0001c0001t0013g0177others(2): Show | 5 | HG01081.hp2 HG01106.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+11224T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147254 | ||||||
| chr5:177147497
|
C | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+11467C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147497 | ||||||
| chr5:177147583
|
G | GT | 4 | a0001c0001t0002g0149a0002c0002t0001g0090a0002c0002t0019g0081others(1): Show | 4 | HG01517.hp2 NA18970.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+11561dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177147583 | |||||
| chr5:177147675
|
C | T | 114 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(111): Show | 114 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.927+11645C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147675 | ||||||
| chr5:177147936
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+11906A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177147936 | ||||||
| chr5:177148119
|
GT | G | 81 | a0001c0001t0010g0264a0002c0002t0001g0028a0002c0002t0001g0030others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.927+12101delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177148119 | |||||
| chr5:177148134
|
T | G | 6 | a0001c0001t0006g0175a0001c0001t0006g0178a0001c0001t0006g0179others(3): Show | 6 | HG02145.hp1 HG02922.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+12104T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148134 | ||||||
| chr5:177148180
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+12150C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148180 | ||||||
| chr5:177148316
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+12286C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148316 | ||||||
| chr5:177148389
|
A | G | 1 | a0001c0011t0012g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.927+12359A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148389 | ||||||
| chr5:177148398
|
G | A | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+12368G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148398 | ||||||
| chr5:177148511
|
G | A | 4 | a0001c0001t0004g0223a0001c0004t0002g0226a0001c0004t0006g0224others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+12481G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148511 | ||||||
| chr5:177148573
|
C | T | 3 | a0002c0002t0001g0079a0002c0002t0001g0080a0002c0002t0001g0089 | 3 | HG02683.hp1 HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.927+12543C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148573 | ||||||
| chr5:177148629
|
TG | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+12602delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177148629 | |||||
| chr5:177148686
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+12656G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148686 | ||||||
| chr5:177148718
|
G | A | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.927+12688G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148718 | ||||||
| chr5:177148727
|
A | G | 1 | a0002c0002t0076g0035 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.927+12697A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148727 | ||||||
| chr5:177148765
|
C | G | 1 | a0001c0001t0013g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.927+12735C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148765 | ||||||
| chr5:177148797
|
A | G | 1 | a0001c0001t0036g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.927+12767A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148797 | ||||||
| chr5:177148806
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+12776G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177148806 | ||||||
| chr5:177149009
|
G | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12979G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149009 | ||||||
| chr5:177149010
|
G | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12980G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149010 | ||||||
| chr5:177149011
|
G | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12981G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149011 | ||||||
| chr5:177149012
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12982T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149012 | ||||||
| chr5:177149016
|
A | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12986A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149016 | ||||||
| chr5:177149021
|
G | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12991G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149021 | ||||||
| chr5:177149022
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12992T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149022 | ||||||
| chr5:177149023
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12993T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149023 | ||||||
| chr5:177149024
|
G | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12994G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149024 | ||||||
| chr5:177149025
|
G | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+12995G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149025 | ||||||
| chr5:177149032
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13002T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149032 | ||||||
| chr5:177149033
|
G | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13003G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149033 | ||||||
| chr5:177149034
|
G | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13004G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149034 | ||||||
| chr5:177149035
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13005T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149035 | ||||||
| chr5:177149037
|
T | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13007T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149037 | ||||||
| chr5:177149038
|
C | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13008C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149038 | ||||||
| chr5:177149039
|
G | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13009G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149039 | ||||||
| chr5:177149054
|
G | GTAACCCC others(11): Show |
1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13024_927+1302 others(22): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149054 | ||||||
| chr5:177149068
|
C | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13038C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149068 | ||||||
| chr5:177149069
|
T | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13039T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149069 | ||||||
| chr5:177149074
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13044T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149074 | ||||||
| chr5:177149097
|
G | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13067G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149097 | ||||||
| chr5:177149098
|
C | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13068C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149098 | ||||||
| chr5:177149099
|
A | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13069A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149099 | ||||||
| chr5:177149101
|
G | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13071G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149101 | ||||||
| chr5:177149102
|
A | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13072A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149102 | ||||||
| chr5:177149105
|
C | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13075C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149105 | ||||||
| chr5:177149106
|
A | T | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13076A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149106 | ||||||
| chr5:177149107
|
T | C | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13077T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149107 | ||||||
| chr5:177149114
|
T | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.927+13084T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149114 | ||||||
| chr5:177149135
|
A | G | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.927+13105A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149135 | ||||||
| chr5:177149161
|
G | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+13131G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149161 | ||||||
| chr5:177149224
|
G | GT | 19 | a0001c0005t0002g0007a0001c0005t0005g0008a0001c0009t0006g0222others(16): Show | 19 | HG01515.hp2 HG01517.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.927+13205dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177149224 | |||||
| chr5:177149247
|
T | C | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927+13217T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149247 | ||||||
| chr5:177149292
|
C | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+13262C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149292 | ||||||
| chr5:177149323
|
A | G | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.927+13293A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149323 | ||||||
| chr5:177149645
|
C | T | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.927+13615C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149645 | ||||||
| chr5:177149873
|
G | A | 1 | a0001c0001t0008g0239 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.927+13843G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149873 | ||||||
| chr5:177149873
|
G | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+13843G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149873 | ||||||
| chr5:177149889
|
C | G | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.927+13859C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149889 | ||||||
| chr5:177149950
|
T | C | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.927+13920T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177149950 | ||||||
| chr5:177150041
|
A | G | 1 | a0001c0001t0048g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.927+14011A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150041 | ||||||
| chr5:177150080
|
GT | G | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+14051delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150080 | ||||||
| chr5:177150164
|
C | T | 1 | a0017c0035t0025g0221 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.927+14134C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150164 | ||||||
| chr5:177150165
|
G | A | 1 | a0002c0002t0001g0042 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.927+14135G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150165 | ||||||
| chr5:177150214
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+14184A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150214 | ||||||
| chr5:177150274
|
C | T | 1 | a0001c0001t0034g0290 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.927+14244C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150274 | ||||||
| chr5:177150291
|
G | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+14261G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150291 | ||||||
| chr5:177150291
|
G | T | 1 | a0001c0005t0005g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.927+14261G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150291 | ||||||
| chr5:177150365
|
A | C | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+14335A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150365 | ||||||
| chr5:177150409
|
C | T | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+14379C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150409 | ||||||
| chr5:177150539
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14509T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150539 | ||||||
| chr5:177150542
|
T | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14512T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150542 | ||||||
| chr5:177150543
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14513T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150543 | ||||||
| chr5:177150545
|
C | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14515C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150545 | ||||||
| chr5:177150547
|
G | GATCCTCC others(62): Show |
2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14517_927+1451 others(73): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150547 | ||||||
| chr5:177150548
|
T | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+14518T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150548 | ||||||
| chr5:177150723
|
A | G | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+14693A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150723 | ||||||
| chr5:177150847
|
T | A | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+14817T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177150847 | ||||||
| chr5:177151025
|
TAA | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+14996_927+1499 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151025 | ||||||
| chr5:177151042
|
T | G | 2 | a0002c0002t0001g0043a0002c0002t0003g0044 | 2 | HG00733.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.927+15012T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151042 | ||||||
| chr5:177151071
|
G | A | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.927+15041G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151071 | ||||||
| chr5:177151481
|
C | T | 1 | a0002c0002t0003g0139 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.927+15451C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151481 | ||||||
| chr5:177151549
|
C | T | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+15519C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151549 | ||||||
| chr5:177151618
|
A | G | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+15588A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151618 | ||||||
| chr5:177151805
|
C | T | 1 | a0003c0006t0009g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.927+15775C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151805 | ||||||
| chr5:177151947
|
G | A | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.927+15917G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177151947 | ||||||
| chr5:177152120
|
A | G | 1 | a0016c0018t0004g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.927+16090A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152120 | ||||||
| chr5:177152309
|
TTGTG | T | 42 | a0002c0002t0001g0028a0002c0002t0001g0031a0002c0002t0001g0033others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.927+16289_927+1629 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152309 | |||||
| chr5:177152315
|
GTGTGTGT others(5): Show |
G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+16289_927+1630 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152315 | |||||
| chr5:177152319
|
G | A | 44 | a0002c0002t0001g0030a0002c0002t0001g0041a0002c0002t0001g0046others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.927+16289G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152319 | ||||||
| chr5:177152319
|
G | GTGTA | 4 | a0001c0001t0032g0155a0001c0004t0012g0259a0001c0004t0012g0263others(1): Show | 4 | HG00642.hp1 HG00642.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+16329_927+1633 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152319 | |||||
| chr5:177152319
|
GTGTA | G | 123 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(120): Show | 123 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.927+16329_927+1633 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152319 | |||||
| chr5:177152319
|
GTGTATGT others(5): Show |
G | 4 | a0001c0001t0033g0172a0004c0013t0001g0105a0004c0013t0020g0103others(1): Show | 4 | HG02129.hp2 HG02451.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+16321_927+1633 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152319 | |||||
| chr5:177152319
|
GTGTATGT others(9): Show |
G | 1 | a0001c0001t0005g0242 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.927+16317_927+1633 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152319 | |||||
| chr5:177152323
|
A | G | 1 | a0001c0001t0063g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.927+16293A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152323 | ||||||
| chr5:177152327
|
A | G | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+16297A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152327 | ||||||
| chr5:177152331
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+16301A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152331 | ||||||
| chr5:177152355
|
A | T | 2 | a0002c0002t0001g0077a0002c0002t0014g0029 | 2 | HG01109.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.927+16325A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152355 | ||||||
| chr5:177152476
|
C | CT | 10 | a0001c0001t0004g0274a0001c0001t0004g0286a0001c0001t0018g0238others(7): Show | 10 | HG00609.hp2 HG00673.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+16467dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152476 | |||||
| chr5:177152476
|
CT | C | 108 | a0001c0001t0002g0249a0001c0003t0002g0130a0001c0003t0002g0133others(105): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.927+16467delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177152476 | |||||
| chr5:177152532
|
C | T | 1 | a0002c0002t0076g0035 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.927+16502C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152532 | ||||||
| chr5:177152539
|
T | C | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.927+16509T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152539 | ||||||
| chr5:177152541
|
G | C | 2 | a0002c0002t0001g0033a0002c0002t0019g0086 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.927+16511G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152541 | ||||||
| chr5:177152566
|
G | T | 1 | a0002c0002t0003g0139 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.927+16536G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152566 | ||||||
| chr5:177152579
|
A | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+16549A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152579 | ||||||
| chr5:177152706
|
C | T | 1 | a0005c0007t0015g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.927+16676C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152706 | ||||||
| chr5:177152830
|
G | A | 1 | a0001c0003t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.927+16800G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152830 | ||||||
| chr5:177152910
|
T | G | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+16880T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177152910 | ||||||
| chr5:177153022
|
T | C | 1 | a0002c0002t0001g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.927+16992T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153022 | ||||||
| chr5:177153103
|
C | T | 1 | a0001c0001t0008g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+17073C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153103 | ||||||
| chr5:177153105
|
G | C | 1 | a0001c0003t0007g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+17075G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153105 | ||||||
| chr5:177153208
|
G | GTT | 20 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(17): Show | 20 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.927+17191_927+1719 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177153208 | |||||
| chr5:177153208
|
GT | G | 12 | a0001c0001t0004g0209a0001c0001t0072g0152a0001c0003t0002g0130others(9): Show | 12 | HG00280.hp2 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+17192delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177153208 | |||||
| chr5:177153222
|
T | A | 1 | a0001c0001t0023g0181 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.927+17192T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153222 | ||||||
| chr5:177153385
|
A | T | 1 | a0001c0001t0004g0196 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.927+17355A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153385 | ||||||
| chr5:177153566
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+17536G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153566 | ||||||
| chr5:177153598
|
G | A | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+17568G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153598 | ||||||
| chr5:177153769
|
C | T | 2 | a0003c0006t0009g0165a0003c0006t0009g0166 | 2 | HG00733.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.927+17739C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153769 | ||||||
| chr5:177153790
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.927+17760G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153790 | ||||||
| chr5:177153922
|
C | G | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+17892C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177153922 | ||||||
| chr5:177154000
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+17970G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154000 | ||||||
| chr5:177154084
|
A | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+18054A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154084 | ||||||
| chr5:177154253
|
A | G | 1 | a0001c0001t0005g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.927+18223A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154253 | ||||||
| chr5:177154318
|
T | G | 3 | a0001c0001t0004g0245a0001c0001t0008g0182a0001c0001t0008g0183 | 3 | HG01975.hp1 NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.927+18288T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154318 | ||||||
| chr5:177154365
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+18335C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154365 | ||||||
| chr5:177154425
|
C | T | 1 | a0003c0006t0009g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.927+18395C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154425 | ||||||
| chr5:177154469
|
A | G | 1 | a0001c0024t0002g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.927+18439A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154469 | ||||||
| chr5:177154551
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+18521C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154551 | ||||||
| chr5:177154738
|
C | G | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.927+18708C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154738 | ||||||
| chr5:177154856
|
C | T | 2 | a0001c0005t0006g0298a0001c0005t0058g0024 | 2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.927+18826C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177154856 | ||||||
| chr5:177154994
|
CA | C | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+18966delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177154994 | |||||
| chr5:177155095
|
A | G | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.927+19065A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155095 | ||||||
| chr5:177155116
|
G | A | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.927+19086G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155116 | ||||||
| chr5:177155278
|
C | T | 2 | a0008c0015t0002g0116a0008c0015t0002g0131 | 2 | HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.927+19248C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155278 | ||||||
| chr5:177155484
|
G | A | 1 | a0003c0006t0009g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.927+19454G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155484 | ||||||
| chr5:177155561
|
C | CT | 13 | a0001c0001t0005g0250a0001c0001t0018g0238a0001c0001t0036g0199others(10): Show | 13 | HG01109.hp1 HG01928.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+19552dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177155561 | |||||
| chr5:177155561
|
CT | C | 41 | a0001c0001t0002g0205a0001c0001t0002g0288a0001c0001t0008g0210others(38): Show | 41 | HG00323.hp1 HG00733.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.927+19552delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177155561 | |||||
| chr5:177155599
|
A | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+19569A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155599 | ||||||
| chr5:177155656
|
A | G | 1 | a0001c0003t0007g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.927+19626A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155656 | ||||||
| chr5:177155678
|
CTTAT | C | 3 | a0001c0001t0011g0157a0001c0001t0011g0236a0001c0001t0078g0237 | 3 | HG01884.hp1 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.927+19659_927+1966 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177155678 | |||||
| chr5:177155906
|
T | C | 2 | a0001c0001t0004g0245a0001c0001t0008g0182 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.927+19876T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155906 | ||||||
| chr5:177155997
|
G | A | 1 | a0001c0004t0012g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.927+19967G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177155997 | ||||||
| chr5:177156004
|
C | T | 1 | a0001c0003t0011g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+19974C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156004 | ||||||
| chr5:177156013
|
G | A | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.927+19983G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156013 | ||||||
| chr5:177156041
|
T | C | 1 | a0003c0031t0009g0154 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.927+20011T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156041 | ||||||
| chr5:177156070
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+20040A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156070 | ||||||
| chr5:177156174
|
A | AT | 86 | a0001c0001t0002g0293a0001c0001t0005g0242a0001c0001t0005g0250others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.927+20169dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177156174 | |||||
| chr5:177156174
|
A | ATT | 46 | a0001c0004t0002g0226a0001c0005t0002g0007a0001c0005t0002g0015others(43): Show | 46 | HG00423.hp1 HG01106.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.927+20168_927+2016 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177156174 | |||||
| chr5:177156174
|
A | ATTT | 7 | a0001c0005t0006g0023a0002c0002t0019g0074a0002c0002t0070g0097others(4): Show | 7 | HG00733.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+20167_927+2016 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177156174 | |||||
| chr5:177156174
|
AT | A | 63 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(60): Show | 63 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.927+20169delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177156174 | |||||
| chr5:177156189
|
T | C | 1 | a0001c0001t0075g0184 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.927+20159T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156189 | ||||||
| chr5:177156241
|
C | T | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+20211C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156241 | ||||||
| chr5:177156417
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+20387G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156417 | ||||||
| chr5:177156464
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.927+20434C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156464 | ||||||
| chr5:177156534
|
G | T | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.927+20504G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156534 | ||||||
| chr5:177156575
|
G | T | 1 | a0002c0002t0001g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+20545G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156575 | ||||||
| chr5:177156582
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.927+20552G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156582 | ||||||
| chr5:177156748
|
T | C | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+20718T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156748 | ||||||
| chr5:177156957
|
C | T | 2 | a0001c0005t0002g0007a0001c0005t0005g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.927+20927C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156957 | ||||||
| chr5:177156965
|
T | C | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.927+20935T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177156965 | ||||||
| chr5:177156970
|
C | CTAAA | 9 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(6): Show | 9 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+20962_927+2096 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177156970 | |||||
| chr5:177157381
|
T | TAAAA | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+21352_927+2135 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177157381 | |||||
| chr5:177157397
|
G | C | 1 | a0001c0001t0036g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.927+21367G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157397 | ||||||
| chr5:177157423
|
C | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.927+21393C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157423 | ||||||
| chr5:177157535
|
C | T | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+21505C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157535 | ||||||
| chr5:177157611
|
A | C | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.927+21581A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157611 | ||||||
| chr5:177157832
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.927+21802C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157832 | ||||||
| chr5:177157849
|
G | A | 23 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(20): Show | 23 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.927+21819G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157849 | ||||||
| chr5:177157858
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+21828T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157858 | ||||||
| chr5:177157969
|
T | C | 1 | a0001c0001t0044g0253 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.927+21939T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177157969 | ||||||
| chr5:177158116
|
C | T | 1 | a0001c0009t0006g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.927+22086C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158116 | ||||||
| chr5:177158237
|
A | ATTTC | 7 | a0001c0001t0004g0223a0001c0001t0004g0254a0001c0001t0010g0255others(4): Show | 7 | HG00280.hp1 HG01891.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+22271_927+2227 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
A | ATTTCTTT others(5): Show |
1 | a0014c0030t0064g0153 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.927+22263_927+2227 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
A | ATTTCTTT others(6): Show |
2 | a0002c0002t0001g0047a0002c0002t0001g0077 | 2 | HG04184.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.927+22210_927+2222 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
ATTTC | A | 15 | a0001c0001t0002g0203a0001c0001t0002g0205a0001c0001t0002g0288others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+22271_927+2227 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
ATTTCTTT others(1): Show |
A | 9 | a0001c0001t0002g0249a0001c0001t0012g0161a0001c0001t0012g0248others(6): Show | 9 | HG01496.hp1 HG01515.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+22267_927+2227 others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
ATTTCTTT others(5): Show |
A | 9 | a0001c0001t0002g0149a0001c0001t0002g0247a0001c0001t0004g0230others(6): Show | 9 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+22263_927+2227 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158237
|
ATTTCTTT others(9): Show |
A | 3 | a0001c0001t0054g0271a0001c0003t0049g0111a0001c0004t0012g0259 | 3 | HG00642.hp1 HG02015.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.927+22259_927+2227 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158237 | |||||
| chr5:177158241
|
C | A | 3 | a0001c0001t0004g0209a0003c0006t0009g0163a0004c0029t0065g0146 | 3 | HG00280.hp2 HG02015.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.927+22211C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158241 | ||||||
| chr5:177158241
|
C | CTTTCTTT others(2): Show |
7 | a0002c0002t0001g0078a0002c0002t0003g0048a0002c0002t0003g0139others(4): Show | 7 | HG00597.hp2 HG01123.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+22214_927+2222 others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158241 | |||||
| chr5:177158245
|
C | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22215C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158245 | ||||||
| chr5:177158245
|
C | CTTTCT | 9 | a0002c0002t0001g0041a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG00609.hp1 HG02027.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+22218_927+2222 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158245 | |||||
| chr5:177158249
|
C | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22219C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158249 | ||||||
| chr5:177158249
|
C | CT | 54 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(51): Show | 54 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.927+22222dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158249 | |||||
| chr5:177158250
|
TTTCTTTC others(4): Show |
T | 1 | a0002c0002t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+22223_927+2223 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158250 | |||||
| chr5:177158253
|
C | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22223C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158253 | ||||||
| chr5:177158257
|
C | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22227C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158257 | ||||||
| chr5:177158274
|
TTTCTTTC others(12): Show |
T | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.927+22247_927+2226 others(23): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158274 | |||||
| chr5:177158277
|
CTTTCTTT others(12): Show |
C | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.927+22248_927+2226 others(23): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158277 | ||||||
| chr5:177158277
|
CTTTCTTT others(18): Show |
C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22259_927+2228 others(29): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158277 | |||||
| chr5:177158278
|
TTTCTTTC others(8): Show |
T | 1 | a0015c0020t0008g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.927+22251_927+2226 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158278 | |||||
| chr5:177158281
|
C | CT | 3 | a0001c0001t0004g0281a0001c0003t0077g0108a0004c0013t0020g0103 | 3 | HG03486.hp2 NA18942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.927+22254dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158281 | |||||
| chr5:177158281
|
CTTTCTTT others(14): Show |
C | 2 | a0001c0001t0004g0196a0001c0001t0008g0174 | 2 | HG01081.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.927+22263_927+2228 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158281 | |||||
| chr5:177158282
|
TTTCTTTC others(4): Show |
T | 2 | a0001c0001t0013g0267a0013c0023t0013g0273 | 2 | HG00597.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.927+22255_927+2226 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158282 | |||||
| chr5:177158285
|
CTTTCTTT others(19): Show |
C | 1 | a0001c0001t0005g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.927+22267_927+2229 others(30): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158285 | |||||
| chr5:177158286
|
TTTCTTTC | T | 9 | a0001c0001t0004g0276a0001c0001t0006g0180a0001c0001t0008g0183others(6): Show | 9 | HG01192.hp2 HG01975.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+22259_927+2226 others(11): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158286 | |||||
| chr5:177158289
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0013g0177 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.927+22271_927+2228 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158289 | |||||
| chr5:177158290
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0008g0151 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.927+22274_927+2227 others(23): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158290 | |||||
| chr5:177158290
|
TTTC | T | 43 | a0001c0001t0008g0210a0001c0001t0010g0186a0001c0001t0010g0212others(40): Show | 43 | HG00408.hp2 HG00673.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.927+22263_927+2226 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158290 | |||||
| chr5:177158290
|
TTTCTTTC others(9): Show |
T | 1 | a0003c0006t0009g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.927+22263_927+2227 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158290 | |||||
| chr5:177158292
|
T | TTC | 4 | a0001c0005t0005g0017a0001c0005t0057g0020a0001c0024t0002g0009others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+22262_927+2226 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158292 | ||||||
| chr5:177158292
|
T | TTCTTTC | 6 | a0001c0001t0004g0281a0001c0001t0026g0201a0001c0001t0026g0246others(3): Show | 6 | HG02683.hp2 HG03490.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+22262_927+2226 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158292 | ||||||
| chr5:177158292
|
T | TTCTTTCT others(8): Show |
1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.927+22262_927+2226 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158292 | ||||||
| chr5:177158293
|
C | CT | 79 | a0001c0001t0004g0245a0001c0001t0004g0252a0001c0001t0004g0269others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.927+22266dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCT | 14 | a0001c0001t0004g0240a0001c0001t0005g0232a0001c0001t0010g0197others(11): Show | 14 | HG00408.hp1 HG01884.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.927+22266_927+2227 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(2): Show |
16 | a0001c0001t0004g0256a0001c0001t0004g0286a0001c0001t0008g0189others(13): Show | 16 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+22302_927+2231 others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(6): Show |
8 | a0001c0001t0008g0188a0001c0001t0011g0236a0001c0001t0017g0213others(5): Show | 8 | HG02145.hp2 HG02300.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+22274_927+2227 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(10): Show |
2 | a0001c0001t0008g0239a0001c0001t0018g0238 | 2 | HG02155.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.927+22274_927+2227 others(21): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(14): Show |
1 | a0001c0001t0004g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.927+22274_927+2227 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(7): Show |
1 | a0001c0005t0006g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.927+22266_927+2227 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(11): Show |
1 | a0001c0001t0045g0287 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.927+22293_927+2231 others(22): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(3): Show |
6 | a0001c0005t0005g0014a0001c0005t0005g0018a0001c0005t0038g0025others(3): Show | 6 | HG02451.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+22270_927+2227 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(7): Show |
1 | a0001c0009t0002g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+22270_927+2227 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTCTTT others(16): Show |
1 | a0001c0001t0048g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.927+22270_927+2227 others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTTCT | 9 | a0001c0005t0002g0015a0001c0005t0005g0016a0001c0005t0006g0019others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+22266_927+2226 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | CTTTTCTT others(3): Show |
6 | a0001c0001t0002g0292a0001c0001t0004g0202a0001c0001t0005g0241others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+22266_927+2226 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
C | T | 11 | a0001c0001t0004g0209a0001c0001t0004g0281a0001c0001t0026g0201others(8): Show | 11 | HG00280.hp2 HG02647.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+22263C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158293 | ||||||
| chr5:177158293
|
CTTTCTTT others(2): Show |
C | 3 | a0001c0001t0013g0279a0005c0007t0015g0003a0005c0007t0015g0006 | 3 | HG02818.hp2 NA18906.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.927+22302_927+2231 others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158293 | |||||
| chr5:177158293
|
CTTTCTTT others(14): Show |
C | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.927+22264_927+2228 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158293 | ||||||
| chr5:177158297
|
C | CT | 6 | a0001c0005t0002g0007a0001c0005t0005g0008a0003c0006t0009g0158others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+22270dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158297 | |||||
| chr5:177158297
|
C | CTTTCTTT others(6): Show |
2 | a0003c0006t0009g0160a0003c0006t0009g0166 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.927+22274_927+2227 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158297 | |||||
| chr5:177158297
|
CTTTCTTT others(7): Show |
C | 1 | a0001c0001t0005g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.927+22275_927+2228 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158297 | |||||
| chr5:177158303
|
T | TTCTTTCT others(3): Show |
1 | a0001c0004t0002g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.927+22274_927+2227 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158303 | |||||
| chr5:177158314
|
T | C | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.927+22284T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158314 | ||||||
| chr5:177158324
|
CTTTCT | C | 4 | a0001c0001t0006g0175a0001c0001t0006g0179a0001c0001t0006g0180others(1): Show | 4 | HG02145.hp1 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+22302_927+2230 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158324 | |||||
| chr5:177158483
|
G | A | 3 | a0002c0002t0001g0050a0002c0002t0001g0085a0002c0002t0039g0040 | 3 | NA18985.hp1 NA19054.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.927+22453G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158483 | ||||||
| chr5:177158523
|
T | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+22493T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158523 | ||||||
| chr5:177158539
|
C | G | 1 | a0002c0002t0014g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+22509C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158539 | ||||||
| chr5:177158605
|
C | T | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.927+22575C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158605 | ||||||
| chr5:177158718
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+22688C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158718 | ||||||
| chr5:177158821
|
C | CAAAAAA | 8 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+22800_927+2280 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(3): Show |
6 | a0001c0003t0007g0113a0001c0003t0007g0127a0001c0003t0007g0128others(3): Show | 6 | HG00609.hp1 HG01167.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+22796_927+2280 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(4): Show |
92 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.927+22795_927+2280 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(5): Show |
28 | a0001c0003t0007g0124a0001c0003t0011g0135a0001c0003t0016g0114others(25): Show | 28 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.927+22794_927+2280 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(6): Show |
15 | a0001c0003t0027g0119a0001c0003t0027g0121a0001c0003t0050g0110others(12): Show | 15 | HG00733.hp1 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.927+22793_927+2280 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(7): Show |
4 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0028g0136others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+22792_927+2280 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(8): Show |
1 | a0003c0006t0009g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927+22805_927+2280 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(9): Show |
1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.927+22805_927+2280 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158821
|
C | CAAAAAAA others(10): Show |
1 | a0009c0012t0060g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+22805_927+2280 others(21): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158821 | |||||
| chr5:177158900
|
T | A | 1 | a0002c0002t0003g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+22870T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158900 | ||||||
| chr5:177158922
|
T | TTG | 33 | a0001c0001t0013g0270a0001c0005t0002g0007a0001c0005t0002g0015others(30): Show | 33 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.927+22908_927+2290 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158922 | |||||
| chr5:177158922
|
T | TTGTG | 5 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+22906_927+2290 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158922 | |||||
| chr5:177158922
|
TTGTGTG | T | 3 | a0001c0001t0004g0245a0001c0001t0008g0182a0001c0001t0008g0183 | 3 | HG01975.hp1 NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.927+22904_927+2290 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158922 | |||||
| chr5:177158927
|
T | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+22897T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158927 | ||||||
| chr5:177158938
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+22908G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177158938 | ||||||
| chr5:177158938
|
G | GTA | 113 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(110): Show | 113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.927+22915_927+2291 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158938 | |||||
| chr5:177158998
|
T | TTA | 8 | a0001c0001t0002g0203a0001c0001t0002g0293a0001c0005t0005g0016others(5): Show | 8 | HG01123.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+22994_927+2299 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATA | 3 | a0001c0001t0012g0161a0001c0005t0002g0007a0001c0005t0005g0008 | 3 | HG01515.hp2 HG01517.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.927+22990_927+2299 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(1): Show |
3 | a0007c0010t0002g0010a0007c0010t0002g0012a0007c0010t0011g0011 | 3 | HG02922.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+22988_927+2299 others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(3): Show |
2 | a0001c0005t0005g0017a0001c0024t0002g0009 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.927+22986_927+2299 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(5): Show |
1 | a0001c0005t0002g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927+22984_927+2299 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(7): Show |
1 | a0001c0014t0002g0027 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.927+22982_927+2299 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(9): Show |
1 | a0001c0014t0012g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+22980_927+2299 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(47): Show |
3 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0126 | 3 | HG02622.hp1 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.927+22987_927+2298 others(58): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(41): Show |
1 | a0001c0003t0007g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.927+22987_927+2298 others(52): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(45): Show |
1 | a0001c0003t0068g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.927+22987_927+2298 others(56): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(16): Show |
2 | a0001c0003t0028g0136a0001c0003t0051g0120 | 2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.927+22985_927+2298 others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(18): Show |
5 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(2): Show | 5 | HG02559.hp1 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+22985_927+2298 others(29): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(20): Show |
2 | a0001c0003t0027g0119a0001c0003t0050g0110 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.927+22985_927+2298 others(31): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(43): Show |
1 | a0001c0003t0011g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+22985_927+2298 others(54): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(43): Show |
1 | a0001c0003t0007g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+22985_927+2298 others(54): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
T | TTATATAT others(16): Show |
1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.927+22983_927+2298 others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
TTA | T | 113 | a0001c0001t0002g0249a0001c0001t0002g0292a0001c0001t0004g0187others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.927+22994_927+2299 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
TTATA | T | 11 | a0001c0001t0010g0212a0001c0001t0030g0280a0001c0033t0037g0262others(8): Show | 11 | HG02015.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+22992_927+2299 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
TTATATA | T | 3 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.927+22990_927+2299 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158998
|
TTATATAT others(3): Show |
T | 80 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(77): Show | 80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.927+22986_927+2299 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158998 | |||||
| chr5:177158999
|
T | TATATATA others(16): Show |
1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.927+22987_927+2298 others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158999 | |||||
| chr5:177158999
|
T | TATATATA others(14): Show |
2 | a0002c0002t0022g0087a0012c0032t0011g0109 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.927+22985_927+2298 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158999 | |||||
| chr5:177158999
|
T | TATATATA others(35): Show |
1 | a0008c0015t0002g0116 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.927+22983_927+2298 others(46): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177158999 | |||||
| chr5:177159001
|
T | TATATATA others(14): Show |
1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.927+22987_927+2298 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159001 | |||||
| chr5:177159001
|
T | TATATATA others(35): Show |
3 | a0001c0003t0007g0113a0001c0003t0007g0128a0001c0003t0007g0134 | 3 | HG01167.hp1 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.927+22987_927+2298 others(46): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159001 | |||||
| chr5:177159001
|
T | TATATATA others(33): Show |
1 | a0001c0003t0002g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.927+22985_927+2298 others(44): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159001 | |||||
| chr5:177159001
|
T | TATATATA others(10): Show |
1 | a0004c0026t0003g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+22983_927+2298 others(21): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159001 | |||||
| chr5:177159001
|
T | TATATATA others(33): Show |
2 | a0001c0003t0002g0130a0008c0015t0002g0131 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.927+22983_927+2298 others(44): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159001 | |||||
| chr5:177159007
|
T | TATATATA others(6): Show |
2 | a0001c0003t0007g0123a0001c0003t0007g0124 | 2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.927+22985_927+2298 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159007 | |||||
| chr5:177159007
|
TATATATA others(16): Show |
T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+23002_927+2302 others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159007 | |||||
| chr5:177159009
|
T | TATATATA others(6): Show |
1 | a0001c0003t0007g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+22987_927+2298 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159009 | |||||
| chr5:177159011
|
T | TATATGAA others(23): Show |
1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+22985_927+2298 others(34): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159011 | |||||
| chr5:177159015
|
TATATATA others(8): Show |
T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+22996_927+2301 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159015 | |||||
| chr5:177159023
|
TATGAATG | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02738.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+22996_927+2300 others(11): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159023 | |||||
| chr5:177159030
|
G | GAT | 15 | a0001c0001t0004g0240a0001c0001t0008g0170a0001c0001t0054g0271others(12): Show | 15 | HG00280.hp1 HG01109.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+23017_927+2301 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159030
|
G | GATAT | 3 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0128 | 3 | HG01167.hp1 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.927+23015_927+2301 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159030
|
G | GATATATA others(34): Show |
1 | a0001c0003t0007g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.927+23018_927+2301 others(45): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159030
|
G | GATATATA others(28): Show |
1 | a0001c0003t0007g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.927+23018_927+2301 others(39): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159030
|
G | GATATATA others(28): Show |
1 | a0001c0003t0007g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+23018_927+2301 others(39): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159030
|
GAT | G | 80 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(77): Show | 80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.927+23017_927+2301 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159030 | |||||
| chr5:177159034
|
T | C | 1 | a0001c0001t0017g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+23004T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159034 | ||||||
| chr5:177159036
|
T | TATATATA others(20): Show |
1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+23018_927+2301 others(31): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159036 | |||||
| chr5:177159150
|
C | G | 1 | a0001c0001t0008g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.927+23120C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159150 | ||||||
| chr5:177159183
|
C | T | 1 | a0001c0001t0013g0234 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.927+23153C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159183 | ||||||
| chr5:177159281
|
T | G | 7 | a0001c0001t0002g0203a0006c0008t0021g0142a0006c0008t0021g0143others(4): Show | 7 | HG01123.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+23251T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159281 | ||||||
| chr5:177159282
|
T | G | 1 | a0001c0004t0031g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+23252T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159282 | ||||||
| chr5:177159285
|
G | T | 3 | a0002c0002t0001g0079a0002c0002t0001g0089a0002c0002t0019g0074 | 3 | HG02683.hp1 HG03688.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.927+23255G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159285 | ||||||
| chr5:177159330
|
G | A | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.927+23300G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159330 | ||||||
| chr5:177159482
|
C | T | 1 | a0001c0005t0005g0016 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+23452C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159482 | ||||||
| chr5:177159512
|
G | C | 1 | a0001c0004t0012g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.927+23482G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159512 | ||||||
| chr5:177159580
|
G | A | 1 | a0001c0001t0006g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.927+23550G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159580 | ||||||
| chr5:177159593
|
A | AT | 17 | a0001c0001t0010g0212a0001c0001t0073g0251a0001c0004t0012g0162others(14): Show | 17 | HG00733.hp1 HG01123.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.927+23582dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159593 | |||||
| chr5:177159593
|
A | ATT | 6 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+23581_927+2358 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159593 | |||||
| chr5:177159593
|
AT | A | 19 | a0001c0001t0002g0205a0001c0001t0002g0249a0001c0001t0004g0269others(16): Show | 19 | HG00323.hp1 HG01074.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.927+23582delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177159593 | |||||
| chr5:177159625
|
C | T | 1 | a0002c0002t0003g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.927+23595C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159625 | ||||||
| chr5:177159659
|
G | A | 7 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+23629G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159659 | ||||||
| chr5:177159897
|
T | A | 210 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(207): Show | 210 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.927+23867T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159897 | ||||||
| chr5:177159899
|
T | A | 105 | a0001c0001t0004g0196a0001c0001t0004g0209a0001c0001t0004g0245others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.927+23869T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159899 | ||||||
| chr5:177159901
|
T | A | 12 | a0001c0001t0004g0245a0001c0001t0008g0182a0002c0002t0001g0033others(9): Show | 12 | HG02155.hp1 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.927+23871T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177159901 | ||||||
| chr5:177160022
|
T | G | 1 | a0001c0001t0059g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+23992T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160022 | ||||||
| chr5:177160110
|
T | C | 186 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0005g0147others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.927+24080T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160110 | ||||||
| chr5:177160186
|
C | T | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.927+24156C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160186 | ||||||
| chr5:177160374
|
C | T | 77 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(74): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.927+24344C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160374 | ||||||
| chr5:177160478
|
T | G | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.927+24448T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160478 | ||||||
| chr5:177160767
|
A | G | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.927+24737A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177160767 | ||||||
| chr5:177161239
|
G | A | 6 | a0001c0001t0006g0175a0001c0001t0006g0178a0001c0001t0006g0179others(3): Show | 6 | HG02145.hp1 HG02922.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+25209G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161239 | ||||||
| chr5:177161279
|
G | C | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.927+25249G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161279 | ||||||
| chr5:177161297
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+25267T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161297 | ||||||
| chr5:177161339
|
C | G | 1 | a0001c0001t0004g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+25309C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161339 | ||||||
| chr5:177161397
|
G | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+25367G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161397 | ||||||
| chr5:177161612
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+25582T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161612 | ||||||
| chr5:177161680
|
C | CT | 117 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(114): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.927+25665dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177161680 | |||||
| chr5:177161680
|
CT | C | 83 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(80): Show | 83 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.927+25665delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177161680 | |||||
| chr5:177161684
|
T | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+25654T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161684 | ||||||
| chr5:177161690
|
T | TG | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.927+25660_927+2566 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161690 | ||||||
| chr5:177161741
|
G | T | 1 | a0001c0011t0002g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.927+25711G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161741 | ||||||
| chr5:177161750
|
A | G | 2 | a0001c0001t0013g0279a0001c0001t0067g0278 | 2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.927+25720A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161750 | ||||||
| chr5:177161786
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+25756C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161786 | ||||||
| chr5:177161832
|
G | T | 4 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0127others(1): Show | 4 | HG01167.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+25802G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161832 | ||||||
| chr5:177161845
|
T | A | 8 | a0001c0001t0004g0252a0001c0001t0008g0210a0001c0001t0008g0239others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+25815T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161845 | ||||||
| chr5:177161897
|
T | C | 1 | a0001c0001t0017g0217 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.927+25867T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161897 | ||||||
| chr5:177161924
|
T | G | 1 | a0002c0002t0003g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.927+25894T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161924 | ||||||
| chr5:177161990
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+25960A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177161990 | ||||||
| chr5:177162020
|
G | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.927+25990G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162020 | ||||||
| chr5:177162056
|
G | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+26026G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162056 | ||||||
| chr5:177162296
|
T | C | 1 | a0002c0016t0040g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.927+26266T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162296 | ||||||
| chr5:177162297
|
TA | T | 13 | a0001c0001t0004g0281a0001c0001t0010g0208a0001c0001t0023g0181others(10): Show | 13 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+26282delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177162297 | |||||
| chr5:177162374
|
C | T | 2 | a0002c0002t0003g0037a0002c0002t0003g0138 | 2 | HG02071.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.927+26344C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162374 | ||||||
| chr5:177162392
|
A | AGTTT | 42 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0008g0170others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.927+26380_927+2638 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177162392 | |||||
| chr5:177162482
|
G | T | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.927+26452G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162482 | ||||||
| chr5:177162584
|
A | G | 179 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0005g0232others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.927+26554A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162584 | ||||||
| chr5:177162619
|
C | T | 1 | a0001c0001t0008g0151 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.927+26589C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162619 | ||||||
| chr5:177162625
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+26595G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162625 | ||||||
| chr5:177162645
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+26615G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177162645 | ||||||
| chr5:177162706
|
T | TCTTACTC others(4): Show |
1 | a0002c0016t0040g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.927+26677_927+2668 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177162706 | |||||
| chr5:177163023
|
G | GGTTGGTC | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.927+26994_927+2700 others(11): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177163023 | |||||
| chr5:177163142
|
C | CT | 79 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0024g0156others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.927+27130dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177163142 | |||||
| chr5:177163142
|
CT | C | 29 | a0001c0001t0002g0205a0001c0001t0004g0202a0001c0001t0010g0208others(26): Show | 29 | HG00323.hp1 HG02257.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.927+27130delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177163142 | |||||
| chr5:177163145
|
T | C | 1 | a0001c0001t0026g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.927+27115T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163145 | ||||||
| chr5:177163165
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.927+27135C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163165 | ||||||
| chr5:177163185
|
A | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.927+27155A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163185 | ||||||
| chr5:177163211
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+27181C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163211 | ||||||
| chr5:177163232
|
T | A | 1 | a0002c0002t0003g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.927+27202T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163232 | ||||||
| chr5:177163289
|
C | T | 1 | a0001c0003t0016g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.927+27259C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163289 | ||||||
| chr5:177163292
|
A | G | 1 | a0001c0001t0033g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.927+27262A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163292 | ||||||
| chr5:177163536
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.927+27506C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163536 | ||||||
| chr5:177163544
|
C | A | 1 | a0001c0005t0005g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.927+27514C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163544 | ||||||
| chr5:177163562
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+27532T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163562 | ||||||
| chr5:177163570
|
A | T | 4 | a0001c0001t0008g0170a0001c0004t0031g0169a0001c0004t0056g0261others(1): Show | 4 | HG00280.hp1 HG01255.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+27540A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163570 | ||||||
| chr5:177163967
|
A | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-27917A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177163967 | ||||||
| chr5:177164121
|
C | T | 1 | a0001c0005t0005g0016 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.928-27763C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164121 | ||||||
| chr5:177164149
|
C | CT | 246 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.928-27719dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177164149 | |||||
| chr5:177164149
|
C | CTT | 27 | a0001c0001t0066g0283a0001c0005t0002g0007a0001c0005t0002g0015others(24): Show | 27 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.928-27720_928-2771 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177164149 | |||||
| chr5:177164149
|
CT | C | 6 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-27719delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177164149 | |||||
| chr5:177164166
|
C | T | 1 | a0002c0002t0003g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.928-27718C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164166 | ||||||
| chr5:177164226
|
C | T | 2 | a0002c0002t0001g0033a0002c0002t0019g0086 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.928-27658C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164226 | ||||||
| chr5:177164366
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.928-27518A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164366 | ||||||
| chr5:177164392
|
G | T | 1 | a0001c0001t0005g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.928-27492G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164392 | ||||||
| chr5:177164409
|
G | A | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-27475G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164409 | ||||||
| chr5:177164444
|
A | G | 1 | a0017c0035t0025g0221 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.928-27440A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164444 | ||||||
| chr5:177164504
|
C | G | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-27380C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164504 | ||||||
| chr5:177164564
|
A | G | 9 | a0001c0005t0005g0014a0001c0005t0005g0016a0001c0005t0005g0018others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-27320A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164564 | ||||||
| chr5:177164611
|
A | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-27273A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164611 | ||||||
| chr5:177164680
|
G | A | 1 | a0001c0001t0059g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.928-27204G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164680 | ||||||
| chr5:177164872
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.928-27012G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164872 | ||||||
| chr5:177164902
|
C | A | 3 | a0001c0001t0004g0245a0001c0001t0008g0182a0001c0001t0008g0183 | 3 | HG01975.hp1 NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.928-26982C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164902 | ||||||
| chr5:177164903
|
G | A | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-26981G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177164903 | ||||||
| chr5:177165069
|
C | A | 1 | a0002c0002t0003g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.928-26815C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165069 | ||||||
| chr5:177165088
|
G | A | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.928-26796G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165088 | ||||||
| chr5:177165178
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-26706A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165178 | ||||||
| chr5:177165660
|
A | C | 1 | a0001c0001t0010g0211 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.928-26224A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165660 | ||||||
| chr5:177165683
|
C | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-26201C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165683 | ||||||
| chr5:177165723
|
C | G | 1 | a0001c0001t0048g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.928-26161C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165723 | ||||||
| chr5:177165802
|
G | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928-26082G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165802 | ||||||
| chr5:177165890
|
C | T | 1 | a0001c0003t0016g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.928-25994C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165890 | ||||||
| chr5:177165910
|
C | CT | 138 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(135): Show | 138 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.928-25957dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177165910 | |||||
| chr5:177165971
|
G | A | 7 | a0001c0001t0004g0281a0001c0001t0029g0284a0001c0001t0029g0285others(4): Show | 7 | HG02602.hp1 NA18942.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-25913G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177165971 | ||||||
| chr5:177166204
|
C | T | 1 | a0001c0001t0017g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-25680C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166204 | ||||||
| chr5:177166214
|
C | T | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0045g0287 | 3 | HG02572.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.928-25670C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166214 | ||||||
| chr5:177166215
|
C | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-25669C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166215 | ||||||
| chr5:177166227
|
C | G | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-25657C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166227 | ||||||
| chr5:177166288
|
C | G | 1 | a0001c0003t0007g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-25596C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166288 | ||||||
| chr5:177166540
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-25344G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166540 | ||||||
| chr5:177166544
|
G | GA | 6 | a0001c0001t0026g0246a0001c0003t0049g0111a0002c0016t0040g0069others(3): Show | 6 | HG00733.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.928-25327dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177166544 | |||||
| chr5:177166665
|
C | T | 2 | a0002c0002t0003g0002a0002c0002t0014g0073 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.928-25219C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166665 | ||||||
| chr5:177166743
|
C | CT | 13 | a0001c0003t0077g0108a0002c0002t0014g0039a0004c0029t0065g0146others(10): Show | 13 | HG01175.hp2 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.928-25124dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177166743 | |||||
| chr5:177166777
|
C | T | 1 | a0010c0025t0028g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.928-25107C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166777 | ||||||
| chr5:177166843
|
G | C | 79 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.928-25041G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166843 | ||||||
| chr5:177166888
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-24996C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177166888 | ||||||
| chr5:177167061
|
T | A | 2 | a0002c0002t0003g0002a0002c0002t0014g0073 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.928-24823T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167061 | ||||||
| chr5:177167391
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-24493C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167391 | ||||||
| chr5:177167392
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-24492A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167392 | ||||||
| chr5:177167395
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-24489C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167395 | ||||||
| chr5:177167396
|
T | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-24488T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167396 | ||||||
| chr5:177167485
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-24399A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167485 | ||||||
| chr5:177167504
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.928-24380C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167504 | ||||||
| chr5:177167523
|
A | G | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.928-24361A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167523 | ||||||
| chr5:177167543
|
A | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-24341A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167543 | ||||||
| chr5:177167545
|
A | T | 3 | a0004c0013t0020g0103a0009c0012t0060g0141a0009c0012t0061g0140 | 3 | HG02280.hp1 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-24339A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167545 | ||||||
| chr5:177167547
|
A | T | 10 | a0001c0001t0010g0208a0001c0001t0011g0236a0002c0002t0001g0060others(7): Show | 10 | HG02280.hp1 HG02647.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.928-24337A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167547 | ||||||
| chr5:177167549
|
T | A | 2 | a0001c0003t0002g0130a0012c0032t0011g0109 | 2 | HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.928-24335T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167549 | ||||||
| chr5:177167825
|
C | T | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.928-24059C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167825 | ||||||
| chr5:177167932
|
G | A | 2 | a0008c0015t0002g0116a0008c0015t0002g0131 | 2 | HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.928-23952G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177167932 | ||||||
| chr5:177168076
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-23808G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168076 | ||||||
| chr5:177168079
|
A | G | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.928-23805A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168079 | ||||||
| chr5:177168221
|
A | G | 2 | a0001c0009t0006g0168a0001c0009t0032g0258 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.928-23663A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168221 | ||||||
| chr5:177168409
|
G | A | 1 | a0001c0011t0012g0297 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.928-23475G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168409 | ||||||
| chr5:177168450
|
C | CT | 25 | a0001c0001t0004g0254a0001c0001t0005g0242a0001c0001t0024g0156others(22): Show | 25 | HG00609.hp2 HG01109.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.928-23417dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177168450 | |||||
| chr5:177168468
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.928-23416C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168468 | ||||||
| chr5:177168521
|
G | A | 114 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(111): Show | 114 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.928-23363G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168521 | ||||||
| chr5:177168611
|
C | T | 1 | a0003c0031t0009g0154 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.928-23273C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168611 | ||||||
| chr5:177168737
|
T | C | 1 | a0002c0002t0003g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.928-23147T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168737 | ||||||
| chr5:177168780
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.928-23104C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168780 | ||||||
| chr5:177168943
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-22941G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168943 | ||||||
| chr5:177168985
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-22899G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177168985 | ||||||
| chr5:177169037
|
G | A | 1 | a0001c0001t0004g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.928-22847G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169037 | ||||||
| chr5:177169403
|
C | T | 2 | a0001c0001t0004g0245a0001c0001t0008g0182 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.928-22481C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169403 | ||||||
| chr5:177169644
|
AG | A | 5 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-22239delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169644 | ||||||
| chr5:177169808
|
C | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-22076C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169808 | ||||||
| chr5:177169867
|
A | G | 1 | a0002c0002t0020g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.928-22017A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169867 | ||||||
| chr5:177169940
|
CAT | C | 79 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.928-21943_928-2194 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169940 | ||||||
| chr5:177169945
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-21939G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177169945 | ||||||
| chr5:177170062
|
C | T | 5 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-21822C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170062 | ||||||
| chr5:177170118
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-21766C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170118 | ||||||
| chr5:177170173
|
C | T | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-21711C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170173 | ||||||
| chr5:177170251
|
T | C | 280 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.928-21633T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170251 | ||||||
| chr5:177170290
|
T | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-21594T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170290 | ||||||
| chr5:177170362
|
T | G | 2 | a0001c0001t0010g0186a0001c0001t0033g0176 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.928-21522T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170362 | ||||||
| chr5:177170374
|
G | A | 1 | a0001c0001t0011g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.928-21510G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170374 | ||||||
| chr5:177170533
|
A | G | 2 | a0001c0005t0006g0019a0001c0005t0057g0020 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.928-21351A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170533 | ||||||
| chr5:177170558
|
G | T | 89 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.928-21326G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170558 | ||||||
| chr5:177170644
|
C | T | 7 | a0001c0001t0010g0186a0001c0001t0010g0197a0001c0001t0023g0181others(4): Show | 7 | HG02027.hp1 HG02129.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-21240C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170644 | ||||||
| chr5:177170660
|
T | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-21224T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170660 | ||||||
| chr5:177170684
|
C | T | 2 | a0003c0006t0009g0164a0003c0006t0009g0167 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.928-21200C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170684 | ||||||
| chr5:177170693
|
C | A | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.928-21191C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177170693 | ||||||
| chr5:177171017
|
TA | T | 6 | a0001c0001t0002g0149a0001c0001t0004g0254a0001c0001t0024g0195others(3): Show | 6 | HG01517.hp2 HG02698.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-20852delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177171017 | |||||
| chr5:177171039
|
C | T | 1 | a0001c0004t0012g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-20845C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171039 | ||||||
| chr5:177171177
|
T | C | 15 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-20707T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171177 | ||||||
| chr5:177171238
|
C | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-20646C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171238 | ||||||
| chr5:177171354
|
A | G | 1 | a0003c0006t0071g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.928-20530A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171354 | ||||||
| chr5:177171501
|
T | C | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.928-20383T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171501 | ||||||
| chr5:177171547
|
A | T | 20 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(17): Show | 20 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.928-20337A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171547 | ||||||
| chr5:177171566
|
A | G | 1 | a0003c0006t0009g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928-20318A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171566 | ||||||
| chr5:177171779
|
G | A | 2 | a0001c0003t0007g0132a0001c0003t0068g0137 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.928-20105G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171779 | ||||||
| chr5:177171954
|
T | C | 12 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-19930T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177171954 | ||||||
| chr5:177172105
|
C | G | 1 | a0001c0009t0006g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.928-19779C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177172105 | ||||||
| chr5:177172115
|
A | G | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.928-19769A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177172115 | ||||||
| chr5:177172301
|
A | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-19583A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177172301 | ||||||
| chr5:177172806
|
T | A | 2 | a0001c0003t0016g0114a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.928-19078T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177172806 | ||||||
| chr5:177172961
|
C | CA | 108 | a0001c0001t0004g0245a0001c0001t0010g0212a0001c0001t0029g0285others(105): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.928-18902dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177172961 | |||||
| chr5:177172961
|
C | CAA | 16 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0123others(13): Show | 16 | HG00099.hp2 HG00609.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.928-18903_928-1890 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177172961 | |||||
| chr5:177172961
|
CA | C | 17 | a0001c0001t0002g0149a0001c0001t0006g0175a0001c0001t0006g0178others(14): Show | 17 | HG00738.hp2 HG01257.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-18902delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177172961 | |||||
| chr5:177172982
|
AG | A | 3 | a0002c0002t0001g0079a0002c0002t0001g0080a0002c0002t0001g0089 | 3 | HG02683.hp1 HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.928-18901delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177172982 | ||||||
| chr5:177173022
|
G | A | 3 | a0001c0005t0005g0016a0001c0005t0005g0018a0001c0005t0006g0021 | 3 | HG02615.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.928-18862G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173022 | ||||||
| chr5:177173032
|
A | ACG | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-18851_928-1885 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173032 | |||||
| chr5:177173126
|
A | C | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-18758A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173126 | ||||||
| chr5:177173143
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-18741T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173143 | ||||||
| chr5:177173143
|
T | G | 9 | a0001c0001t0004g0269a0001c0001t0004g0274a0001c0001t0013g0267others(6): Show | 9 | HG01074.hp1 HG01192.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.928-18741T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173143 | ||||||
| chr5:177173291
|
CA | C | 153 | a0001c0001t0002g0205a0001c0001t0002g0292a0001c0001t0004g0187others(150): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.928-18573delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173291 | |||||
| chr5:177173291
|
CAA | C | 104 | a0001c0001t0006g0175a0001c0001t0006g0178a0001c0001t0006g0179others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.928-18574_928-1857 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173291 | |||||
| chr5:177173438
|
T | C | 1 | a0016c0018t0004g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.928-18446T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173438 | ||||||
| chr5:177173466
|
C | CT | 106 | a0001c0001t0002g0204a0001c0001t0002g0247a0001c0001t0002g0292others(103): Show | 106 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.928-18394dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173466 | |||||
| chr5:177173466
|
C | CTT | 28 | a0001c0001t0004g0240a0001c0001t0008g0151a0001c0001t0017g0213others(25): Show | 28 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.928-18395_928-1839 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173466 | |||||
| chr5:177173466
|
CT | C | 9 | a0001c0001t0002g0205a0001c0001t0024g0195a0001c0001t0045g0287others(6): Show | 9 | HG00323.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-18394delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177173466 | |||||
| chr5:177173495
|
C | T | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-18389C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173495 | ||||||
| chr5:177173499
|
G | T | 3 | a0001c0001t0008g0239a0001c0001t0013g0234a0001c0001t0059g0218 | 3 | HG00609.hp2 HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.928-18385G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173499 | ||||||
| chr5:177173536
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-18348C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173536 | ||||||
| chr5:177173566
|
T | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-18318T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173566 | ||||||
| chr5:177173719
|
G | A | 2 | a0002c0002t0001g0077a0002c0002t0014g0029 | 2 | HG01109.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.928-18165G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173719 | ||||||
| chr5:177173838
|
T | G | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-18046T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177173838 | ||||||
| chr5:177174030
|
C | T | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.928-17854C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174030 | ||||||
| chr5:177174086
|
G | A | 1 | a0002c0002t0022g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.928-17798G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174086 | ||||||
| chr5:177174105
|
G | A | 1 | a0008c0015t0002g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-17779G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174105 | ||||||
| chr5:177174142
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-17742G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174142 | ||||||
| chr5:177174198
|
T | C | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.928-17686T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174198 | ||||||
| chr5:177174200
|
A | G | 3 | a0001c0001t0008g0170a0001c0004t0031g0169a0001c0004t0056g0261 | 3 | HG00280.hp1 HG01255.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.928-17684A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174200 | ||||||
| chr5:177174285
|
C | T | 1 | a0003c0006t0009g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.928-17599C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174285 | ||||||
| chr5:177174410
|
G | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-17474G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174410 | ||||||
| chr5:177174495
|
G | A | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.928-17389G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174495 | ||||||
| chr5:177174558
|
T | C | 3 | a0001c0001t0011g0157a0001c0001t0011g0236a0001c0001t0078g0237 | 3 | HG01884.hp1 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.928-17326T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174558 | ||||||
| chr5:177174579
|
A | C | 1 | a0003c0006t0009g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.928-17305A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174579 | ||||||
| chr5:177174581
|
G | A | 1 | a0004c0017t0041g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.928-17303G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174581 | ||||||
| chr5:177174620
|
G | A | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.928-17264G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174620 | ||||||
| chr5:177174800
|
T | C | 1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.928-17084T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174800 | ||||||
| chr5:177174828
|
G | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-17056G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174828 | ||||||
| chr5:177174871
|
C | CT | 233 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0202others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.928-16993dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177174871 | |||||
| chr5:177174871
|
C | CTT | 35 | a0001c0001t0004g0196a0001c0001t0004g0245a0001c0001t0004g0286others(32): Show | 35 | HG00673.hp1 HG00733.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.928-16994_928-1699 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177174871 | |||||
| chr5:177174917
|
G | T | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.928-16967G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174917 | ||||||
| chr5:177174972
|
C | T | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.928-16912C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174972 | ||||||
| chr5:177174988
|
C | T | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.928-16896C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174988 | ||||||
| chr5:177174997
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-16887G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177174997 | ||||||
| chr5:177175072
|
C | T | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-16812C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175072 | ||||||
| chr5:177175081
|
C | T | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.928-16803C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175081 | ||||||
| chr5:177175115
|
C | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-16769C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175115 | ||||||
| chr5:177175118
|
G | T | 2 | a0001c0014t0002g0027a0001c0014t0012g0026 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.928-16766G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175118 | ||||||
| chr5:177175270
|
A | C | 1 | a0002c0002t0019g0074 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.928-16614A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175270 | ||||||
| chr5:177175476
|
A | T | 2 | a0001c0001t0004g0281a0002c0002t0001g0052 | 2 | NA18942.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.928-16408A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175476 | ||||||
| chr5:177175516
|
G | A | 2 | a0002c0002t0001g0033a0002c0002t0019g0086 | 2 | HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.928-16368G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175516 | ||||||
| chr5:177175879
|
CT | C | 8 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0024g0195others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-15991delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177175879 | |||||
| chr5:177175917
|
C | T | 1 | a0001c0003t0007g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-15967C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177175917 | ||||||
| chr5:177176119
|
A | G | 1 | a0001c0001t0017g0217 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.928-15765A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176119 | ||||||
| chr5:177176229
|
T | C | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-15655T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176229 | ||||||
| chr5:177176252
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.928-15632C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176252 | ||||||
| chr5:177176439
|
T | TC | 31 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(28): Show | 31 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.928-15444dupC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177176439 | |||||
| chr5:177176587
|
A | T | 43 | a0001c0001t0004g0187a0001c0001t0004g0202a0001c0001t0004g0209others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.928-15297A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176587 | ||||||
| chr5:177176592
|
C | T | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.928-15292C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176592 | ||||||
| chr5:177176668
|
A | G | 1 | a0009c0012t0060g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-15216A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176668 | ||||||
| chr5:177176725
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-15159C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176725 | ||||||
| chr5:177176889
|
C | A | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-14995C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177176889 | ||||||
| chr5:177177020
|
G | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-14864G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177177020 | ||||||
| chr5:177177424
|
C | T | 1 | a0001c0003t0007g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-14460C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177177424 | ||||||
| chr5:177177621
|
G | C | 1 | a0002c0002t0070g0097 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.928-14263G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177177621 | ||||||
| chr5:177177629
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928-14255G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177177629 | ||||||
| chr5:177177714
|
A | G | 1 | a0001c0001t0005g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.928-14170A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177177714 | ||||||
| chr5:177178052
|
G | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-13832G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178052 | ||||||
| chr5:177178272
|
G | A | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.928-13612G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178272 | ||||||
| chr5:177178319
|
C | T | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-13565C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178319 | ||||||
| chr5:177178334
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.928-13550C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178334 | ||||||
| chr5:177178483
|
G | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-13401G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178483 | ||||||
| chr5:177178722
|
G | A | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-13162G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178722 | ||||||
| chr5:177178896
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-12988A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178896 | ||||||
| chr5:177178931
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928-12953A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178931 | ||||||
| chr5:177178999
|
G | A | 1 | a0005c0007t0015g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.928-12885G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177178999 | ||||||
| chr5:177179014
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-12870A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179014 | ||||||
| chr5:177179025
|
A | G | 1 | a0001c0001t0048g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.928-12859A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179025 | ||||||
| chr5:177179051
|
T | A | 280 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.928-12833T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179051 | ||||||
| chr5:177179084
|
C | T | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.928-12800C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179084 | ||||||
| chr5:177179117
|
G | A | 1 | a0002c0002t0019g0074 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.928-12767G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179117 | ||||||
| chr5:177179282
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-12602C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179282 | ||||||
| chr5:177179304
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-12580C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179304 | ||||||
| chr5:177179390
|
T | G | 1 | a0001c0001t0004g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-12494T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179390 | ||||||
| chr5:177179830
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-12054G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179830 | ||||||
| chr5:177179928
|
A | T | 6 | a0001c0001t0006g0175a0001c0001t0006g0178a0001c0001t0006g0179others(3): Show | 6 | HG02145.hp1 HG02922.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-11956A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179928 | ||||||
| chr5:177179936
|
T | C | 1 | a0001c0009t0002g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.928-11948T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177179936 | ||||||
| chr5:177180003
|
C | T | 1 | a0003c0006t0009g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.928-11881C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180003 | ||||||
| chr5:177180054
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-11830A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180054 | ||||||
| chr5:177180101
|
A | AT | 8 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(5): Show | 8 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-11772dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177180101 | |||||
| chr5:177180101
|
A | T | 1 | a0001c0001t0004g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.928-11783A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180101 | ||||||
| chr5:177180105
|
T | A | 3 | a0001c0001t0004g0256a0001c0001t0010g0255a0002c0002t0003g0053 | 3 | NA18979.hp2 NA18985.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.928-11779T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180105 | ||||||
| chr5:177180180
|
C | T | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.928-11704C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180180 | ||||||
| chr5:177180241
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-11643C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180241 | ||||||
| chr5:177180381
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-11503C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180381 | ||||||
| chr5:177180414
|
G | A | 5 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-11470G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180414 | ||||||
| chr5:177180646
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-11238T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180646 | ||||||
| chr5:177180714
|
G | A | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.928-11170G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180714 | ||||||
| chr5:177180976
|
C | T | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-10908C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180976 | ||||||
| chr5:177180977
|
G | A | 11 | a0001c0005t0005g0014a0001c0005t0005g0016a0001c0005t0005g0018others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-10907G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180977 | ||||||
| chr5:177180987
|
G | A | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-10897G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177180987 | ||||||
| chr5:177181038
|
G | A | 2 | a0001c0003t0016g0114a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.928-10846G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181038 | ||||||
| chr5:177181042
|
C | CT | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0072g0152others(4): Show | 7 | HG02602.hp2 HG02818.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-10828dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181042 | |||||
| chr5:177181241
|
C | A | 1 | a0001c0003t0007g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.928-10643C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181241 | ||||||
| chr5:177181332
|
A | G | 6 | a0001c0001t0006g0175a0001c0001t0006g0178a0001c0001t0006g0179others(3): Show | 6 | HG02145.hp1 HG02922.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-10552A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181332 | ||||||
| chr5:177181355
|
C | T | 1 | a0004c0026t0003g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-10529C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181355 | ||||||
| chr5:177181422
|
T | G | 1 | a0002c0002t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.928-10462T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181422 | ||||||
| chr5:177181426
|
G | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-10458G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181426 | ||||||
| chr5:177181426
|
G | GT | 55 | a0002c0002t0001g0030a0002c0002t0001g0034a0002c0002t0001g0042others(52): Show | 55 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.928-10458_928-1045 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181426 | ||||||
| chr5:177181426
|
G | GTT | 22 | a0002c0002t0001g0028a0002c0002t0001g0031a0002c0002t0001g0033others(19): Show | 22 | HG00423.hp1 HG00673.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.928-10458_928-1045 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181426 | ||||||
| chr5:177181426
|
G | T | 4 | a0001c0001t0005g0147a0001c0001t0005g0148a0002c0002t0001g0077others(1): Show | 4 | HG01109.hp1 HG02818.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-10458G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181426 | ||||||
| chr5:177181427
|
G | GGTTTTTT others(4): Show |
1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.928-10457_928-1045 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181427 | ||||||
| chr5:177181427
|
G | GGTTTTTT others(5): Show |
1 | a0009c0012t0060g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.928-10457_928-1045 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181427 | ||||||
| chr5:177181427
|
G | GT | 47 | a0001c0001t0002g0204a0001c0001t0004g0202a0001c0001t0004g0230others(44): Show | 47 | HG00642.hp2 HG00733.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.928-10439dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181427 | |||||
| chr5:177181427
|
G | GTT | 32 | a0001c0001t0066g0283a0001c0003t0002g0133a0001c0003t0007g0112others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.928-10440_928-1043 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181427 | |||||
| chr5:177181427
|
G | GTTGTTTT others(3): Show |
1 | a0006c0008t0021g0145 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.928-10455_928-1045 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181427 | |||||
| chr5:177181427
|
G | GTTT | 7 | a0001c0003t0002g0130a0001c0003t0007g0132a0001c0003t0011g0135others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-10441_928-1043 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181427 | |||||
| chr5:177181427
|
G | GTTTTTTT others(3): Show |
2 | a0005c0007t0015g0005a0005c0007t0015g0006 | 2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-10448_928-1043 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177181427 | |||||
| chr5:177181427
|
G | T | 79 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.928-10457G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181427 | ||||||
| chr5:177181428
|
T | TG | 4 | a0001c0001t0010g0212a0001c0001t0010g0255a0001c0001t0033g0176others(1): Show | 4 | NA18947.hp2 NA18967.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-10456_928-1045 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181428 | ||||||
| chr5:177181429
|
T | G | 19 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(16): Show | 19 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.928-10455T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181429 | ||||||
| chr5:177181509
|
T | G | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0009t0002g0257others(4): Show | 7 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-10375T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181509 | ||||||
| chr5:177181878
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928-10006C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181878 | ||||||
| chr5:177181890
|
C | T | 1 | a0001c0003t0011g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.928-9994C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181890 | ||||||
| chr5:177181979
|
T | C | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.928-9905T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181979 | ||||||
| chr5:177181995
|
A | G | 2 | a0001c0004t0002g0229a0001c0004t0012g0162 | 2 | HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.928-9889A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177181995 | ||||||
| chr5:177182020
|
C | T | 2 | a0004c0013t0001g0105a0004c0026t0003g0104 | 2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.928-9864C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182020 | ||||||
| chr5:177182025
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-9859G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182025 | ||||||
| chr5:177182089
|
T | C | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.928-9795T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182089 | ||||||
| chr5:177182150
|
TC | T | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.928-9733delC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182150 | ||||||
| chr5:177182151
|
C | CA | 8 | a0001c0001t0004g0252a0001c0001t0010g0264a0001c0009t0002g0257others(5): Show | 8 | HG01175.hp1 HG02071.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-9717dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177182151 | |||||
| chr5:177182151
|
CA | C | 118 | a0001c0001t0018g0238a0001c0001t0045g0287a0001c0003t0002g0133others(115): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.928-9717delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177182151 | |||||
| chr5:177182232
|
G | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-9652G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182232 | ||||||
| chr5:177182593
|
T | C | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.928-9291T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182593 | ||||||
| chr5:177182620
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-9264C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182620 | ||||||
| chr5:177182698
|
G | A | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928-9186G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182698 | ||||||
| chr5:177182880
|
C | T | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.928-9004C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177182880 | ||||||
| chr5:177183011
|
G | A | 275 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(272): Show | 275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.928-8873G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183011 | ||||||
| chr5:177183096
|
T | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-8788T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183096 | ||||||
| chr5:177183386
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.928-8498C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183386 | ||||||
| chr5:177183475
|
T | C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-8409T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183475 | ||||||
| chr5:177183535
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-8349G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183535 | ||||||
| chr5:177183634
|
A | T | 1 | a0001c0001t0026g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.928-8250A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183634 | ||||||
| chr5:177183770
|
C | T | 1 | a0003c0006t0071g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.928-8114C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183770 | ||||||
| chr5:177183798
|
C | G | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.928-8086C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183798 | ||||||
| chr5:177183917
|
A | G | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-7967A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177183917 | ||||||
| chr5:177184334
|
T | C | 1 | a0001c0003t0051g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.928-7550T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184334 | ||||||
| chr5:177184439
|
T | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-7445T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184439 | ||||||
| chr5:177184569
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-7315C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184569 | ||||||
| chr5:177184585
|
G | T | 1 | a0001c0001t0011g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.928-7299G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184585 | ||||||
| chr5:177184715
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-7169G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184715 | ||||||
| chr5:177184770
|
G | A | 1 | a0002c0002t0022g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.928-7114G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184770 | ||||||
| chr5:177184774
|
G | A | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928-7110G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184774 | ||||||
| chr5:177184946
|
A | G | 1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.928-6938A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184946 | ||||||
| chr5:177184997
|
G | C | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-6887G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177184997 | ||||||
| chr5:177185190
|
G | C | 1 | a0001c0004t0012g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.928-6694G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185190 | ||||||
| chr5:177185222
|
C | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-6662C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185222 | ||||||
| chr5:177185294
|
C | CCTGT | 8 | a0002c0002t0001g0030a0002c0002t0001g0041a0002c0002t0003g0048others(5): Show | 8 | HG00423.hp1 HG02148.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-6587_928-6584d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185294 | |||||
| chr5:177185471
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-6413G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185471 | ||||||
| chr5:177185530
|
G | A | 2 | a0001c0005t0002g0007a0001c0005t0005g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928-6354G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185530 | ||||||
| chr5:177185664
|
TTA | T | 8 | a0001c0001t0004g0202a0001c0003t0007g0123a0001c0003t0011g0135others(5): Show | 8 | HG02257.hp2 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-6207_928-6206d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185664 | |||||
| chr5:177185689
|
GT | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-6189delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185689 | |||||
| chr5:177185711
|
CATTATAT | C | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-6156_928-6150d others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185711 | |||||
| chr5:177185730
|
T | TATATATT others(16): Show |
1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.928-6137_928-6115d others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185730 | |||||
| chr5:177185746
|
T | A | 79 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.928-6138T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185746 | ||||||
| chr5:177185767
|
AT | A | 7 | a0002c0002t0001g0031a0002c0002t0003g0045a0002c0002t0003g0051others(4): Show | 7 | HG01069.hp1 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-6114delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185767 | |||||
| chr5:177185777
|
T | G | 1 | a0001c0001t0010g0212 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.928-6107T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185777 | ||||||
| chr5:177185789
|
TTA | T | 5 | a0001c0001t0004g0230a0001c0001t0005g0232a0001c0004t0002g0229others(2): Show | 5 | HG00099.hp1 HG01192.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-6078_928-6077d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185789 | |||||
| chr5:177185795
|
A | ATATATAT others(3): Show |
4 | a0001c0003t0002g0130a0001c0003t0077g0108a0008c0015t0002g0116others(1): Show | 4 | HG02809.hp1 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-6080_928-6079i others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185795 | |||||
| chr5:177185795
|
A | ATATATAT others(1): Show |
124 | a0001c0001t0004g0245a0001c0001t0008g0182a0001c0001t0008g0183others(121): Show | 124 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.928-6082_928-6081i others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185795 | |||||
| chr5:177185795
|
A | ATATATT | 111 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.928-6084_928-6083i others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185795 | |||||
| chr5:177185795
|
A | ATATT | 27 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(24): Show | 27 | HG00423.hp2 HG02027.hp1 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.928-6086_928-6085i others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185795 | |||||
| chr5:177185795
|
A | T | 1 | a0002c0016t0040g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.928-6089A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185795 | ||||||
| chr5:177185802
|
T | C | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.928-6082T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185802 | ||||||
| chr5:177185803
|
A | T | 2 | a0001c0005t0002g0007a0001c0005t0005g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928-6081A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185803 | ||||||
| chr5:177185808
|
A | T | 3 | a0001c0005t0002g0007a0001c0005t0005g0008a0004c0029t0065g0146 | 3 | HG01515.hp2 HG01517.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.928-6076A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185808 | ||||||
| chr5:177185810
|
T | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-6074T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185810 | ||||||
| chr5:177185811
|
T | A | 3 | a0001c0005t0002g0007a0001c0005t0005g0008a0004c0029t0065g0146 | 3 | HG01515.hp2 HG01517.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.928-6073T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185811 | ||||||
| chr5:177185821
|
AAT | A | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.928-6057_928-6056d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185821 | |||||
| chr5:177185830
|
G | A | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.928-6054G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185830 | ||||||
| chr5:177185837
|
A | T | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.928-6047A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185837 | ||||||
| chr5:177185839
|
ATT | A | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-6043_928-6042d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185839 | |||||
| chr5:177185841
|
T | A | 5 | a0001c0003t0002g0130a0001c0003t0077g0108a0008c0015t0002g0116others(2): Show | 5 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-6043T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185841 | ||||||
| chr5:177185858
|
A | T | 2 | a0001c0003t0007g0122a0001c0003t0007g0126 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.928-6026A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185858 | ||||||
| chr5:177185880
|
A | ATATATAA others(15): Show |
4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-5995_928-5974d others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185880 | |||||
| chr5:177185910
|
T | TTATATAT others(15): Show |
1 | a0001c0005t0058g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.928-5971_928-5950d others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185910 | |||||
| chr5:177185920
|
T | TTA | 111 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(108): Show | 111 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.928-5955_928-5954d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185920 | |||||
| chr5:177185957
|
AT | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-5924delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177185957 | |||||
| chr5:177185979
|
T | C | 12 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-5905T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177185979 | ||||||
| chr5:177186004
|
TTATATTA | T | 3 | a0002c0002t0003g0044a0009c0012t0060g0141a0009c0012t0061g0140 | 3 | HG00733.hp2 HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-5859_928-5853d others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186004 | |||||
| chr5:177186004
|
TTATATTA others(7): Show |
T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-5866_928-5853d others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186004 | |||||
| chr5:177186008
|
A | G | 1 | a0001c0001t0026g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.928-5876A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186008 | ||||||
| chr5:177186029
|
AT | A | 14 | a0001c0001t0017g0213a0003c0006t0009g0013a0003c0006t0009g0158others(11): Show | 14 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.928-5849delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186029 | |||||
| chr5:177186031
|
T | A | 1 | a0002c0016t0040g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.928-5853T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186031 | ||||||
| chr5:177186034
|
T | A | 1 | a0001c0001t0004g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928-5850T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186034 | ||||||
| chr5:177186037
|
TATATATA | T | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-5834_928-5828d others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186037 | |||||
| chr5:177186055
|
T | C | 89 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.928-5829T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186055 | ||||||
| chr5:177186058
|
C | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-5826C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186058 | ||||||
| chr5:177186058
|
CATATA | C | 17 | a0001c0001t0004g0254a0001c0003t0002g0133a0001c0003t0007g0112others(14): Show | 17 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-5820_928-5816d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186058 | |||||
| chr5:177186058
|
CATATAAT others(14): Show |
C | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-5820_928-5800d others(23): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186058 | |||||
| chr5:177186080
|
ATATAT | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-5798_928-5794d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177186080 | |||||
| chr5:177186100
|
A | T | 29 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(26): Show | 29 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.928-5784A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186100 | ||||||
| chr5:177186228
|
C | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-5656C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186228 | ||||||
| chr5:177186274
|
T | C | 3 | a0001c0001t0008g0170a0001c0004t0031g0169a0001c0004t0056g0261 | 3 | HG00280.hp1 HG01255.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.928-5610T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186274 | ||||||
| chr5:177186332
|
T | A | 1 | a0001c0001t0005g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-5552T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186332 | ||||||
| chr5:177186449
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-5435G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186449 | ||||||
| chr5:177186504
|
T | A | 3 | a0001c0001t0004g0187a0001c0001t0004g0254a0001c0001t0004g0256 | 3 | NA18985.hp2 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.928-5380T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186504 | ||||||
| chr5:177186542
|
G | A | 1 | a0001c0004t0056g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.928-5342G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186542 | ||||||
| chr5:177186876
|
C | T | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.928-5008C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177186876 | ||||||
| chr5:177187082
|
G | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-4802G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187082 | ||||||
| chr5:177187100
|
CT | C | 253 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(250): Show | 253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.928-4762delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177187100 | |||||
| chr5:177187100
|
CTT | C | 11 | a0001c0001t0002g0249a0001c0001t0008g0183a0001c0001t0024g0195others(8): Show | 11 | HG01074.hp2 HG01256.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-4763_928-4762d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177187100 | |||||
| chr5:177187112
|
T | C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-4772T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187112 | ||||||
| chr5:177187305
|
A | G | 1 | a0001c0001t0043g0291 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.928-4579A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187305 | ||||||
| chr5:177187311
|
G | T | 1 | a0001c0001t0011g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.928-4573G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187311 | ||||||
| chr5:177187402
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-4482G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187402 | ||||||
| chr5:177187528
|
G | A | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.928-4356G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187528 | ||||||
| chr5:177187578
|
G | A | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.928-4306G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187578 | ||||||
| chr5:177187674
|
G | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-4210G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187674 | ||||||
| chr5:177187698
|
TTCTG | T | 3 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0033t0037g0262 | 3 | HG02145.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.928-4180_928-4177d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177187698 | |||||
| chr5:177187823
|
C | T | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0009t0002g0257others(4): Show | 7 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-4061C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187823 | ||||||
| chr5:177187914
|
A | G | 15 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-3970A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177187914 | ||||||
| chr5:177188045
|
A | G | 1 | a0004c0026t0003g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-3839A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188045 | ||||||
| chr5:177188082
|
A | G | 2 | a0003c0006t0009g0164a0003c0006t0009g0167 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.928-3802A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188082 | ||||||
| chr5:177188372
|
G | A | 1 | a0002c0002t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.928-3512G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188372 | ||||||
| chr5:177188409
|
C | T | 1 | a0001c0001t0005g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-3475C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188409 | ||||||
| chr5:177188485
|
A | G | 2 | a0001c0001t0018g0191a0001c0001t0018g0192 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.928-3399A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188485 | ||||||
| chr5:177188509
|
A | AT | 95 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(92): Show | 95 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.928-3373dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177188509 | |||||
| chr5:177188560
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-3324T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188560 | ||||||
| chr5:177188639
|
G | T | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-3245G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188639 | ||||||
| chr5:177188737
|
G | A | 114 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(111): Show | 114 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.928-3147G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188737 | ||||||
| chr5:177188844
|
T | A | 6 | a0001c0001t0002g0288a0001c0001t0005g0207a0001c0003t0007g0134others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-3040T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188844 | ||||||
| chr5:177188844
|
TA | T | 12 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(9): Show | 12 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.928-3030delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177188844 | |||||
| chr5:177188845
|
A | T | 2 | a0001c0011t0012g0297a0002c0002t0039g0040 | 2 | HG04228.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.928-3039A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188845 | ||||||
| chr5:177188893
|
C | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.928-2991C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177188893 | ||||||
| chr5:177189005
|
T | C | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.928-2879T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189005 | ||||||
| chr5:177189064
|
A | C | 8 | a0001c0001t0004g0252a0001c0001t0008g0210a0001c0001t0008g0239others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-2820A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189064 | ||||||
| chr5:177189113
|
T | C | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.928-2771T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189113 | ||||||
| chr5:177189459
|
A | G | 15 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-2425A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189459 | ||||||
| chr5:177189523
|
T | C | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-2361T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189523 | ||||||
| chr5:177189567
|
T | C | 17 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-2317T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189567 | ||||||
| chr5:177189789
|
C | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.928-2095C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177189789 | ||||||
| chr5:177190009
|
G | C | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.928-1875G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190009 | ||||||
| chr5:177190105
|
C | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-1779C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190105 | ||||||
| chr5:177190340
|
C | T | 1 | a0015c0020t0008g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.928-1544C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190340 | ||||||
| chr5:177190421
|
C | T | 2 | a0003c0006t0009g0164a0003c0006t0009g0167 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.928-1463C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190421 | ||||||
| chr5:177190458
|
T | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-1426T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190458 | ||||||
| chr5:177190582
|
G | A | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.928-1302G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190582 | ||||||
| chr5:177190673
|
G | GT | 9 | a0001c0001t0004g0256a0001c0001t0010g0197a0001c0001t0073g0251others(6): Show | 9 | HG00597.hp1 HG01109.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-1199dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177190673 | |||||
| chr5:177190756
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-1128G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190756 | ||||||
| chr5:177190825
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-1059A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190825 | ||||||
| chr5:177190826
|
T | C | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-1058T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190826 | ||||||
| chr5:177190831
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-1053A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190831 | ||||||
| chr5:177190841
|
T | TTG | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-1042_928-1041i others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177190841 | |||||
| chr5:177190965
|
CCTTTTTT others(8): Show |
C | 1 | a0001c0009t0032g0258 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-905_928-891del others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177190965 | |||||
| chr5:177190966
|
C | CTT | 76 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0033others(73): Show | 76 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.928-905_928-904dup others(2): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177190966 | |||||
| chr5:177190966
|
C | CTTT | 7 | a0002c0002t0001g0028a0002c0002t0001g0056a0002c0002t0001g0077others(4): Show | 7 | HG01109.hp1 HG01928.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-906_928-904dup others(3): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177190966 | |||||
| chr5:177190980
|
T | TTTC | 27 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(24): Show | 27 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.928-904_928-903ins others(3): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190980 | ||||||
| chr5:177190980
|
TC | T | 5 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-903delC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190980 | ||||||
| chr5:177190981
|
C | T | 33 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(30): Show | 33 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.928-903C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190981 | ||||||
| chr5:177190982
|
T | C | 1 | a0005c0007t0015g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.928-902T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190982 | ||||||
| chr5:177190983
|
T | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-901T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177190983 | ||||||
| chr5:177191018
|
T | C | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.928-866T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191018 | ||||||
| chr5:177191226
|
T | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-658T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191226 | ||||||
| chr5:177191237
|
T | G | 2 | a0002c0002t0001g0028a0002c0034t0047g0093 | 2 | NA19000.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.928-647T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191237 | ||||||
| chr5:177191256
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.928-628C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191256 | ||||||
| chr5:177191306
|
GTATT | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-575_928-572del others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr5 | 177191306 | |||||
| chr5:177191454
|
T | C | 16 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(13): Show | 16 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.928-430T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191454 | ||||||
| chr5:177191492
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.928-392A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 2/22 | chr5 | 177191492 | ||||||
| chr5:177192132
|
G | A | 1 | a0014c0030t0064g0153 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1063+113G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192132 | ||||||
| chr5:177192210
|
T | G | 7 | a0001c0003t0077g0108a0006c0008t0021g0142a0006c0008t0021g0143others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+191T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192210 | ||||||
| chr5:177192346
|
G | C | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1063+327G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192346 | ||||||
| chr5:177192386
|
T | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063+367T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192386 | ||||||
| chr5:177192391
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1063+372T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192391 | ||||||
| chr5:177192401
|
T | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1063+382T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192401 | ||||||
| chr5:177192452
|
A | T | 1 | a0014c0030t0064g0153 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1063+433A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192452 | ||||||
| chr5:177192468
|
C | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1063+449C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192468 | ||||||
| chr5:177192553
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1063+534C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192553 | ||||||
| chr5:177192585
|
G | A | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0009t0002g0257others(4): Show | 7 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+566G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192585 | ||||||
| chr5:177192681
|
C | G | 1 | a0001c0001t0010g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1063+662C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192681 | ||||||
| chr5:177192732
|
T | C | 1 | a0005c0007t0015g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1063+713T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192732 | ||||||
| chr5:177192734
|
T | G | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1063+715T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192734 | ||||||
| chr5:177192735
|
T | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1063+716T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192735 | ||||||
| chr5:177192903
|
C | T | 1 | a0001c0001t0034g0235 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1063+884C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177192903 | ||||||
| chr5:177193183
|
C | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1063+1164C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193183 | ||||||
| chr5:177193200
|
G | T | 1 | a0001c0004t0002g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1063+1181G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193200 | ||||||
| chr5:177193207
|
C | T | 2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1063+1188C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193207 | ||||||
| chr5:177193209
|
C | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1063+1190C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193209 | ||||||
| chr5:177193211
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1063+1192G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193211 | ||||||
| chr5:177193535
|
C | G | 1 | a0001c0001t0008g0239 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1063+1516C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193535 | ||||||
| chr5:177193602
|
T | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1063+1583T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193602 | ||||||
| chr5:177193612
|
G | A | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1063+1593G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177193612 | ||||||
| chr5:177194074
|
G | C | 84 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1063+2055G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194074 | ||||||
| chr5:177194141
|
T | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+2122T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194141 | ||||||
| chr5:177194147
|
C | T | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1063+2128C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194147 | ||||||
| chr5:177194298
|
T | G | 1 | a0001c0003t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1063+2279T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194298 | ||||||
| chr5:177194329
|
G | A | 1 | a0002c0002t0022g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1063+2310G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194329 | ||||||
| chr5:177194384
|
T | G | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063+2365T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194384 | ||||||
| chr5:177194441
|
C | CT | 17 | a0001c0001t0004g0252a0001c0001t0012g0248a0001c0003t0016g0117others(14): Show | 17 | HG01175.hp1 HG02015.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1063+2439dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194441 | |||||
| chr5:177194579
|
C | CT | 7 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238others(4): Show | 7 | HG02055.hp1 HG02071.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063+2583dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194579 | |||||
| chr5:177194579
|
CT | C | 36 | a0001c0001t0002g0249a0001c0001t0002g0288a0001c0001t0006g0175others(33): Show | 36 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1063+2583delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194579 | |||||
| chr5:177194600
|
T | A | 1 | a0006c0008t0062g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1063+2581T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194600 | ||||||
| chr5:177194600
|
T | TA | 3 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145 | 3 | HG02630.hp1 HG02886.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1063+2581_1063+258 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194600 | ||||||
| chr5:177194601
|
T | A | 6 | a0003c0006t0009g0158a0006c0008t0021g0142a0006c0008t0021g0143others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063+2582T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194601 | ||||||
| chr5:177194601
|
T | TA | 7 | a0001c0003t0007g0132a0004c0029t0065g0146a0005c0007t0015g0003others(4): Show | 7 | HG02109.hp2 HG02738.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1063+2582_1063+258 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194601 | ||||||
| chr5:177194602
|
T | A | 128 | a0001c0003t0002g0130a0001c0003t0007g0128a0001c0003t0007g0132others(125): Show | 128 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1063+2583T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194602 | ||||||
| chr5:177194602
|
T | TA | 26 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(23): Show | 26 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1063+2588dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194602 | |||||
| chr5:177194694
|
C | CT | 80 | a0001c0001t0004g0252a0001c0001t0004g0274a0001c0001t0004g0286others(77): Show | 80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1063+2700dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194694 | |||||
| chr5:177194694
|
C | CTT | 15 | a0001c0003t0007g0123a0001c0003t0007g0124a0001c0003t0007g0125others(12): Show | 15 | HG01069.hp1 HG01109.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1063+2699_1063+270 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194694 | |||||
| chr5:177194694
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0012g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1063+2689_1063+270 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177194694 | |||||
| chr5:177194771
|
G | A | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+2752G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194771 | ||||||
| chr5:177194783
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1063+2764G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194783 | ||||||
| chr5:177194929
|
C | T | 1 | a0001c0001t0004g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1063+2910C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177194929 | ||||||
| chr5:177195078
|
G | C | 5 | a0004c0029t0065g0146a0006c0008t0021g0142a0006c0008t0021g0143others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+3059G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195078 | ||||||
| chr5:177195453
|
G | GTC | 22 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(19): Show | 22 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1063+3451_1063+345 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177195453 | |||||
| chr5:177195529
|
G | A | 2 | a0002c0002t0001g0056a0002c0002t0003g0055 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1063+3510G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195529 | ||||||
| chr5:177195598
|
G | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+3579G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195598 | ||||||
| chr5:177195622
|
T | A | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1063+3603T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195622 | ||||||
| chr5:177195623
|
A | T | 23 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(20): Show | 23 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.1063+3604A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195623 | ||||||
| chr5:177195702
|
C | G | 1 | a0001c0009t0002g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1063+3683C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195702 | ||||||
| chr5:177195720
|
C | T | 12 | a0001c0009t0002g0257a0004c0029t0065g0146a0005c0007t0015g0003others(9): Show | 12 | HG02071.hp2 HG02280.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1063+3701C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195720 | ||||||
| chr5:177195740
|
G | A | 1 | a0001c0001t0004g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1063+3721G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177195740 | ||||||
| chr5:177196297
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1063+4278C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196297 | ||||||
| chr5:177196528
|
G | A | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1063+4509G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196528 | ||||||
| chr5:177196600
|
C | A | 2 | a0002c0002t0003g0037a0002c0002t0003g0138 | 2 | HG02071.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1063+4581C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196600 | ||||||
| chr5:177196910
|
C | T | 1 | a0001c0001t0004g0281 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1063+4891C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196910 | ||||||
| chr5:177196934
|
T | C | 1 | a0001c0001t0004g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1063+4915T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196934 | ||||||
| chr5:177196946
|
C | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+4927C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196946 | ||||||
| chr5:177196990
|
G | A | 5 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+4971G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196990 | ||||||
| chr5:177196990
|
G | T | 1 | a0009c0012t0060g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1063+4971G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177196990 | ||||||
| chr5:177197114
|
C | A | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1063+5095C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177197114 | ||||||
| chr5:177197127
|
G | A | 1 | a0002c0002t0001g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1063+5108G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177197127 | ||||||
| chr5:177197370
|
C | G | 3 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1063+5351C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177197370 | ||||||
| chr5:177197615
|
C | G | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+5596C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177197615 | ||||||
| chr5:177197733
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1063+5714G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177197733 | ||||||
| chr5:177197924
|
CAG | C | 3 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0121 | 3 | HG02559.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1063+5909_1063+591 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177197924 | |||||
| chr5:177198048
|
C | T | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1063+6029C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198048 | ||||||
| chr5:177198274
|
C | G | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-5846C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198274 | ||||||
| chr5:177198527
|
A | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1064-5593A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198527 | ||||||
| chr5:177198639
|
G | A | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1064-5481G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198639 | ||||||
| chr5:177198809
|
A | G | 1 | a0002c0002t0003g0139 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1064-5311A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198809 | ||||||
| chr5:177198925
|
C | A | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1064-5195C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177198925 | ||||||
| chr5:177199023
|
T | C | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1064-5097T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199023 | ||||||
| chr5:177199051
|
G | A | 15 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1064-5069G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199051 | ||||||
| chr5:177199192
|
C | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-4928C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199192 | ||||||
| chr5:177199228
|
G | A | 2 | a0001c0005t0006g0019a0001c0005t0057g0020 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1064-4892G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199228 | ||||||
| chr5:177199440
|
A | G | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1064-4680A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199440 | ||||||
| chr5:177199482
|
A | C | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064-4638A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199482 | ||||||
| chr5:177199550
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1064-4570G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199550 | ||||||
| chr5:177199579
|
A | ATTTTC | 11 | a0001c0001t0004g0269a0001c0001t0004g0274a0001c0001t0013g0267others(8): Show | 11 | HG01074.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064-4511_1064-450 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(8): Show |
5 | a0003c0006t0009g0160a0003c0006t0009g0163a0003c0006t0009g0165others(2): Show | 5 | HG00733.hp1 HG02015.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-4521_1064-450 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(13): Show |
7 | a0001c0005t0002g0015a0001c0005t0005g0017a0001c0005t0006g0298others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1064-4526_1064-450 others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(18): Show |
5 | a0001c0005t0005g0014a0001c0005t0006g0019a0001c0005t0006g0022others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-4531_1064-450 others(29): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(23): Show |
3 | a0001c0005t0006g0023a0001c0014t0012g0026a0003c0006t0009g0013 | 3 | HG02486.hp2 HG03139.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1064-4536_1064-450 others(34): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(28): Show |
7 | a0001c0005t0002g0007a0001c0005t0005g0008a0001c0005t0005g0016others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1064-4507_1064-450 others(39): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
A | ATTTTCTT others(33): Show |
2 | a0001c0005t0006g0021a0007c0010t0011g0011 | 2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1064-4507_1064-450 others(44): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
ATTTTC | A | 12 | a0002c0002t0070g0097a0004c0029t0065g0146a0005c0007t0015g0003others(9): Show | 12 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064-4511_1064-450 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199579
|
ATTTTCTT others(3): Show |
A | 4 | a0001c0001t0004g0187a0001c0001t0004g0256a0001c0001t0008g0193others(1): Show | 4 | HG03225.hp1 NA18964.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-4516_1064-450 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177199579 | |||||
| chr5:177199614
|
T | C | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.1064-4506T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199614 | ||||||
| chr5:177199663
|
G | A | 1 | a0001c0001t0008g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1064-4457G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199663 | ||||||
| chr5:177199745
|
A | G | 11 | a0004c0029t0065g0146a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064-4375A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199745 | ||||||
| chr5:177199864
|
G | A | 11 | a0001c0005t0005g0014a0001c0005t0005g0016a0001c0005t0005g0018others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064-4256G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199864 | ||||||
| chr5:177199890
|
C | T | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1064-4230C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199890 | ||||||
| chr5:177199925
|
A | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1064-4195A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177199925 | ||||||
| chr5:177200160
|
AG | A | 6 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064-3959delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200160 | ||||||
| chr5:177200164
|
C | T | 1 | a0002c0002t0003g0055 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1064-3956C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200164 | ||||||
| chr5:177200309
|
A | G | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1064-3811A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200309 | ||||||
| chr5:177200630
|
A | G | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1064-3490A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200630 | ||||||
| chr5:177200709
|
A | G | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1064-3411A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200709 | ||||||
| chr5:177200879
|
A | G | 1 | a0002c0002t0079g0032 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064-3241A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177200879 | ||||||
| chr5:177200899
|
A | AT | 8 | a0001c0001t0012g0161a0001c0003t0002g0133a0001c0003t0007g0113others(5): Show | 8 | HG01167.hp1 HG02280.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1064-3208dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177200899 | |||||
| chr5:177200899
|
AT | A | 6 | a0001c0005t0006g0298a0001c0005t0058g0024a0006c0008t0021g0142others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1064-3208delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177200899 | |||||
| chr5:177201016
|
T | C | 1 | a0002c0002t0001g0042 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1064-3104T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201016 | ||||||
| chr5:177201036
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1064-3084C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201036 | ||||||
| chr5:177201061
|
A | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-3059A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201061 | ||||||
| chr5:177201213
|
T | C | 2 | a0001c0014t0002g0027a0001c0014t0012g0026 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1064-2907T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201213 | ||||||
| chr5:177201392
|
C | T | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1064-2728C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201392 | ||||||
| chr5:177201460
|
T | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-2660T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201460 | ||||||
| chr5:177201483
|
G | T | 1 | a0001c0001t0012g0248 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1064-2637G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201483 | ||||||
| chr5:177201547
|
A | G | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1064-2573A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201547 | ||||||
| chr5:177201740
|
G | A | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1064-2380G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177201740 | ||||||
| chr5:177202065
|
G | A | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1064-2055G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202065 | ||||||
| chr5:177202093
|
G | C | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1064-2027G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202093 | ||||||
| chr5:177202170
|
GA | G | 156 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(153): Show | 156 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1064-1936delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177202170 | |||||
| chr5:177202225
|
G | C | 1 | a0001c0001t0059g0218 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1064-1895G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202225 | ||||||
| chr5:177202295
|
A | G | 85 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1064-1825A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202295 | ||||||
| chr5:177202337
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064-1783C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202337 | ||||||
| chr5:177202545
|
G | A | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1064-1575G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177202545 | ||||||
| chr5:177203176
|
T | G | 2 | a0001c0005t0002g0015a0001c0005t0005g0017 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1064-944T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203176 | ||||||
| chr5:177203361
|
A | T | 1 | a0001c0004t0002g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1064-759A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203361 | ||||||
| chr5:177203553
|
C | T | 1 | a0001c0001t0018g0191 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1064-567C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203553 | ||||||
| chr5:177203588
|
A | C | 1 | a0002c0002t0001g0079 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1064-532A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203588 | ||||||
| chr5:177203634
|
C | T | 1 | a0001c0001t0005g0295 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1064-486C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203634 | ||||||
| chr5:177203721
|
G | GT | 89 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1064-390dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | 177203721 | |||||
| chr5:177203722
|
T | G | 1 | a0001c0009t0006g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1064-398T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203722 | ||||||
| chr5:177203926
|
T | C | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1064-194T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203926 | ||||||
| chr5:177203983
|
T | C | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1064-137T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177203983 | ||||||
| chr5:177204026
|
C | T | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1064-94C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 3/22 | chr5 | 177204026 | ||||||
| chr5:177204374
|
G | C | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1236+82G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204374 | ||||||
| chr5:177204393
|
T | G | 1 | a0001c0001t0078g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1236+101T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204393 | ||||||
| chr5:177204786
|
G | T | 92 | a0001c0003t0002g0130a0001c0003t0016g0114a0001c0003t0016g0117others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1236+494G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204786 | ||||||
| chr5:177204787
|
T | G | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1236+495T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204787 | ||||||
| chr5:177204867
|
A | T | 1 | a0003c0006t0009g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1236+575A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204867 | ||||||
| chr5:177204981
|
C | T | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1236+689C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177204981 | ||||||
| chr5:177205013
|
A | T | 1 | a0002c0002t0001g0095 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1236+721A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205013 | ||||||
| chr5:177205106
|
G | A | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1236+814G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205106 | ||||||
| chr5:177205304
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1012G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205304 | ||||||
| chr5:177205551
|
A | G | 1 | a0001c0004t0002g0272 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1236+1259A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205551 | ||||||
| chr5:177205553
|
T | A | 1 | a0001c0001t0025g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1236+1261T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205553 | ||||||
| chr5:177205730
|
A | G | 4 | a0001c0001t0004g0276a0001c0004t0002g0272a0013c0023t0013g0273others(1): Show | 4 | HG00597.hp1 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1438A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205730 | ||||||
| chr5:177205768
|
AAAT | A | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.1236+1483_1236+148 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177205768 | |||||
| chr5:177205907
|
A | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1236+1615A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205907 | ||||||
| chr5:177205908
|
T | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1616T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177205908 | ||||||
| chr5:177206055
|
A | C | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1236+1763A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206055 | ||||||
| chr5:177206392
|
G | A | 89 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1236+2100G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206392 | ||||||
| chr5:177206492
|
G | A | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1236+2200G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206492 | ||||||
| chr5:177206702
|
G | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1236+2410G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206702 | ||||||
| chr5:177206748
|
C | T | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1236+2456C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206748 | ||||||
| chr5:177206790
|
C | T | 1 | a0003c0006t0009g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1236+2498C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206790 | ||||||
| chr5:177206857
|
TA | T | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1236+2578delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177206857 | |||||
| chr5:177206868
|
A | AT | 12 | a0001c0005t0006g0021a0003c0006t0009g0013a0003c0006t0009g0158others(9): Show | 12 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+2576_1236+257 others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206868 | ||||||
| chr5:177206914
|
G | T | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0045g0287 | 3 | HG02572.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1236+2622G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177206914 | ||||||
| chr5:177207089
|
A | G | 1 | a0001c0001t0005g0148 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1237-2547A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207089 | ||||||
| chr5:177207151
|
G | A | 85 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1237-2485G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207151 | ||||||
| chr5:177207179
|
C | T | 1 | a0014c0030t0064g0153 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1237-2457C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207179 | ||||||
| chr5:177207188
|
C | T | 17 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1237-2448C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207188 | ||||||
| chr5:177207213
|
G | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-2423G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207213 | ||||||
| chr5:177207216
|
A | G | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-2420A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207216 | ||||||
| chr5:177207243
|
C | T | 1 | a0001c0001t0023g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1237-2393C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207243 | ||||||
| chr5:177207256
|
G | A | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-2380G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207256 | ||||||
| chr5:177207373
|
C | T | 5 | a0002c0002t0001g0034a0002c0002t0001g0077a0002c0002t0003g0038others(2): Show | 5 | HG00099.hp2 HG00323.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-2263C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207373 | ||||||
| chr5:177207442
|
C | A | 115 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(112): Show | 115 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1237-2194C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207442 | ||||||
| chr5:177207593
|
A | AT | 55 | a0001c0001t0002g0249a0001c0001t0004g0230a0001c0001t0004g0240others(52): Show | 55 | HG00733.hp1 HG01071.hp2 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.1237-2014dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATT | 19 | a0001c0001t0002g0292a0001c0001t0010g0186a0001c0001t0010g0212others(16): Show | 19 | HG00423.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1237-2015_1237-201 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTT | 51 | a0001c0001t0010g0197a0001c0001t0010g0208a0002c0002t0001g0031others(48): Show | 51 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1237-2016_1237-201 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTATTT others(13): Show |
1 | a0001c0003t0007g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1237-2040_1237-203 others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTT | 25 | a0001c0003t0002g0130a0001c0003t0052g0129a0002c0002t0001g0030others(22): Show | 25 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237-2017_1237-201 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTT | 12 | a0001c0003t0007g0128a0001c0003t0049g0111a0002c0002t0001g0028others(9): Show | 12 | HG01167.hp1 HG02027.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1237-2018_1237-201 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(3): Show |
3 | a0001c0003t0016g0117a0001c0003t0028g0136a0001c0003t0050g0110 | 3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1237-2023_1237-201 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(6): Show |
2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1237-2026_1237-201 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(7): Show |
2 | a0001c0003t0016g0114a0005c0007t0015g0003 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1237-2027_1237-201 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(9): Show |
1 | a0001c0003t0007g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1237-2029_1237-201 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(11): Show |
1 | a0001c0003t0068g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1237-2031_1237-201 others(22): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(12): Show |
1 | a0001c0003t0007g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1237-2032_1237-201 others(23): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(13): Show |
2 | a0001c0003t0007g0134a0001c0003t0077g0108 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1237-2033_1237-201 others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(14): Show |
1 | a0001c0003t0007g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1237-2034_1237-201 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(18): Show |
1 | a0001c0003t0007g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1237-2038_1237-201 others(29): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207593
|
A | ATTTTTTT others(19): Show |
1 | a0001c0003t0002g0133 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1237-2039_1237-201 others(30): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207593 | |||||
| chr5:177207768
|
G | A | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1237-1868G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207768 | ||||||
| chr5:177207779
|
G | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-1857G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207779 | ||||||
| chr5:177207905
|
AGTGTGTG others(5): Show |
A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1237-1725_1237-171 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207905 | |||||
| chr5:177207911
|
TGTGTGTG others(5): Show |
T | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1237-1713_1237-170 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177207911 | |||||
| chr5:177207982
|
T | C | 1 | a0001c0001t0017g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1237-1654T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177207982 | ||||||
| chr5:177208406
|
A | G | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1237-1230A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177208406 | ||||||
| chr5:177208650
|
C | G | 5 | a0001c0001t0005g0241a0001c0003t0002g0130a0008c0015t0002g0116others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-986C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177208650 | ||||||
| chr5:177208908
|
G | T | 2 | a0001c0014t0002g0027a0001c0014t0012g0026 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1237-728G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177208908 | ||||||
| chr5:177208939
|
G | A | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1237-697G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177208939 | ||||||
| chr5:177209350
|
A | G | 1 | a0001c0003t0007g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1237-286A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177209350 | ||||||
| chr5:177209390
|
G | A | 32 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(29): Show | 32 | HG00733.hp1 HG01515.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.1237-246G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177209390 | ||||||
| chr5:177209454
|
G | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1237-182G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | chr5 | 177209454 | ||||||
| chr5:177209528
|
C | CA | 14 | a0001c0001t0005g0250a0001c0001t0013g0270a0001c0001t0032g0155others(11): Show | 14 | HG00597.hp1 HG00642.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1237-92dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177209528 | |||||
| chr5:177209544
|
AG | A | 113 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(110): Show | 113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1237-90delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177209544 | |||||
| chr5:177209548
|
A | AT | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1237-87dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | 177209548 | |||||
| chr5:177212216
|
T | TA | 92 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.3796+34dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212216 | |||||
| chr5:177212303
|
C | G | 290 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(287): Show | 290 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.3796+108C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212303 | ||||||
| chr5:177212324
|
A | G | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3796+129A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212324 | ||||||
| chr5:177212445
|
ATCTT | A | 5 | a0002c0002t0001g0033a0002c0002t0001g0050a0002c0002t0001g0085others(2): Show | 5 | HG01256.hp1 HG02155.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.3796+258_3796+261d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212445 | |||||
| chr5:177212458
|
ACTTTCTC others(7): Show |
A | 6 | a0001c0005t0002g0007a0001c0005t0005g0008a0001c0024t0002g0009others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3796+282_3796+295d others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212458 | |||||
| chr5:177212473
|
CTTTCTCT others(8): Show |
C | 15 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3796+282_3796+296d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212473 | |||||
| chr5:177212487
|
C | CT | 112 | a0001c0003t0002g0130a0001c0003t0016g0114a0001c0003t0016g0117others(109): Show | 112 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3796+306dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212487 | |||||
| chr5:177212487
|
C | CTT | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3796+305_3796+306d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212487 | |||||
| chr5:177212487
|
C | T | 2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3796+292C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212487 | ||||||
| chr5:177212487
|
CT | C | 16 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(13): Show | 16 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3796+306delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177212487 | |||||
| chr5:177212562
|
C | G | 1 | a0002c0002t0003g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3796+367C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212562 | ||||||
| chr5:177212791
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3796+596C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212791 | ||||||
| chr5:177212838
|
C | T | 1 | a0001c0001t0004g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3796+643C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177212838 | ||||||
| chr5:177213002
|
C | T | 4 | a0001c0001t0004g0223a0001c0004t0002g0226a0001c0004t0006g0224others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.3796+807C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213002 | ||||||
| chr5:177213003
|
G | A | 5 | a0001c0001t0017g0294a0006c0008t0021g0142a0006c0008t0021g0143others(2): Show | 5 | HG01496.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3796+808G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213003 | ||||||
| chr5:177213161
|
A | G | 2 | a0001c0009t0006g0168a0001c0009t0032g0258 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3796+966A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213161 | ||||||
| chr5:177213250
|
C | T | 1 | a0001c0001t0004g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3796+1055C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213250 | ||||||
| chr5:177213339
|
T | C | 81 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.3796+1144T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213339 | ||||||
| chr5:177213542
|
A | C | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+1347A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213542 | ||||||
| chr5:177213558
|
C | T | 1 | a0001c0001t0012g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3796+1363C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213558 | ||||||
| chr5:177213613
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+1418G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213613 | ||||||
| chr5:177213660
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3796+1465C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213660 | ||||||
| chr5:177213678
|
G | A | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3796+1483G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213678 | ||||||
| chr5:177213681
|
A | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+1486A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213681 | ||||||
| chr5:177213717
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3796+1522C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213717 | ||||||
| chr5:177213741
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3796+1546G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213741 | ||||||
| chr5:177213843
|
A | G | 297 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.3796+1648A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213843 | ||||||
| chr5:177213872
|
T | G | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3796+1677T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177213872 | ||||||
| chr5:177213978
|
G | GT | 9 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0066g0283others(6): Show | 9 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3796+1793dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177213978 | |||||
| chr5:177214040
|
C | T | 1 | a0002c0002t0020g0001 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3796+1845C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214040 | ||||||
| chr5:177214134
|
C | G | 1 | a0002c0002t0001g0052 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3796+1939C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214134 | ||||||
| chr5:177214224
|
C | T | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+2029C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214224 | ||||||
| chr5:177214238
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3796+2043A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214238 | ||||||
| chr5:177214305
|
G | A | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+2110G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214305 | ||||||
| chr5:177214366
|
A | T | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3796+2171A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214366 | ||||||
| chr5:177214433
|
A | G | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.3796+2238A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214433 | ||||||
| chr5:177214667
|
CCTTTT | C | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3796+2473_3796+247 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214667 | ||||||
| chr5:177214668
|
C | CT | 8 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3796+2490dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177214668 | |||||
| chr5:177214668
|
CT | C | 220 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(217): Show | 220 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.3796+2490delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177214668 | |||||
| chr5:177214728
|
C | T | 11 | a0002c0027t0001g0099a0005c0007t0015g0003a0005c0007t0015g0004others(8): Show | 11 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.3796+2533C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214728 | ||||||
| chr5:177214791
|
G | A | 1 | a0001c0001t0025g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3796+2596G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214791 | ||||||
| chr5:177214838
|
T | C | 1 | a0003c0006t0071g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3796+2643T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214838 | ||||||
| chr5:177214962
|
A | C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3796+2767A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177214962 | ||||||
| chr5:177215180
|
A | AT | 33 | a0001c0001t0002g0292a0001c0001t0023g0181a0001c0003t0002g0130others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.3796+3001dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177215180 | |||||
| chr5:177215445
|
GGATTACA others(22): Show |
G | 1 | a0001c0001t0066g0283 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3796+3254_3796+328 others(33): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177215445 | |||||
| chr5:177215564
|
G | A | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+3369G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177215564 | ||||||
| chr5:177215744
|
C | T | 2 | a0001c0005t0006g0019a0001c0005t0057g0020 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3796+3549C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177215744 | ||||||
| chr5:177215782
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+3587C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177215782 | ||||||
| chr5:177216035
|
G | GT | 6 | a0001c0005t0002g0007a0001c0005t0005g0008a0001c0024t0002g0009others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3796+3847dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177216035 | |||||
| chr5:177216150
|
A | G | 118 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(115): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.3796+3955A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177216150 | ||||||
| chr5:177216168
|
C | T | 2 | a0001c0014t0002g0027a0001c0014t0012g0026 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3796+3973C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177216168 | ||||||
| chr5:177216425
|
A | C | 1 | a0002c0002t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3796+4230A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177216425 | ||||||
| chr5:177216670
|
G | GT | 38 | a0001c0001t0004g0276a0001c0001t0013g0267a0001c0003t0002g0133others(35): Show | 38 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.3796+4494dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177216670 | |||||
| chr5:177216670
|
GT | G | 7 | a0001c0001t0004g0274a0001c0001t0078g0237a0001c0003t0049g0111others(4): Show | 7 | HG00099.hp1 HG01069.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.3796+4494delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177216670 | |||||
| chr5:177216911
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3796+4716A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177216911 | ||||||
| chr5:177216948
|
GT | G | 17 | a0001c0001t0026g0201a0001c0004t0035g0233a0003c0006t0009g0013others(14): Show | 17 | HG00733.hp1 HG01167.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.3796+4767delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177216948 | |||||
| chr5:177216948
|
GTT | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3796+4766_3796+476 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177216948 | |||||
| chr5:177216953
|
T | G | 85 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3796+4758T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177216953 | ||||||
| chr5:177217080
|
A | G | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3796+4885A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217080 | ||||||
| chr5:177217174
|
G | A | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.3796+4979G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217174 | ||||||
| chr5:177217347
|
A | G | 1 | a0001c0001t0008g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3796+5152A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217347 | ||||||
| chr5:177217373
|
C | T | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3796+5178C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217373 | ||||||
| chr5:177217572
|
A | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3796+5377A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217572 | ||||||
| chr5:177217651
|
G | A | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+5456G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217651 | ||||||
| chr5:177217666
|
C | CT | 42 | a0001c0001t0018g0192a0001c0001t0029g0285a0001c0003t0002g0130others(39): Show | 42 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.3796+5489dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177217666 | |||||
| chr5:177217691
|
G | T | 1 | a0001c0004t0012g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3796+5496G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217691 | ||||||
| chr5:177217692
|
A | T | 1 | a0001c0004t0012g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3796+5497A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217692 | ||||||
| chr5:177217736
|
C | A | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.3796+5541C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217736 | ||||||
| chr5:177217769
|
G | A | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3796+5574G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177217769 | ||||||
| chr5:177218011
|
C | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3796+5816C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218011 | ||||||
| chr5:177218238
|
A | G | 1 | a0001c0003t0007g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3796+6043A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218238 | ||||||
| chr5:177218434
|
C | A | 275 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(272): Show | 275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.3796+6239C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218434 | ||||||
| chr5:177218524
|
A | G | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3796+6329A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218524 | ||||||
| chr5:177218526
|
C | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3796+6331C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218526 | ||||||
| chr5:177218527
|
G | A | 1 | a0015c0020t0008g0275 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3796+6332G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218527 | ||||||
| chr5:177218574
|
T | G | 1 | a0001c0005t0006g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3796+6379T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218574 | ||||||
| chr5:177218598
|
C | T | 5 | a0001c0001t0004g0196a0001c0001t0008g0174a0001c0001t0013g0177others(2): Show | 5 | HG01081.hp2 HG01106.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.3796+6403C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218598 | ||||||
| chr5:177218676
|
T | G | 1 | a0002c0002t0003g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3796+6481T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218676 | ||||||
| chr5:177218712
|
C | A | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3796+6517C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218712 | ||||||
| chr5:177218738
|
T | G | 13 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3796+6543T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218738 | ||||||
| chr5:177218802
|
C | T | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3796+6607C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218802 | ||||||
| chr5:177218973
|
G | A | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3796+6778G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177218973 | ||||||
| chr5:177219082
|
T | C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3796+6887T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219082 | ||||||
| chr5:177219097
|
A | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3796+6902A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219097 | ||||||
| chr5:177219127
|
A | G | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3796+6932A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219127 | ||||||
| chr5:177219218
|
G | A | 3 | a0001c0001t0011g0157a0001c0001t0011g0236a0001c0001t0078g0237 | 3 | HG01884.hp1 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3796+7023G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219218 | ||||||
| chr5:177219586
|
G | T | 6 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3796+7391G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219586 | ||||||
| chr5:177219700
|
T | C | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.3796+7505T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219700 | ||||||
| chr5:177219702
|
C | T | 2 | a0001c0014t0002g0027a0001c0014t0012g0026 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3796+7507C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219702 | ||||||
| chr5:177219974
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3796+7779C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177219974 | ||||||
| chr5:177220069
|
T | C | 2 | a0002c0002t0001g0041a0002c0002t0003g0048 | 2 | NA18944.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3796+7874T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220069 | ||||||
| chr5:177220081
|
C | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+7886C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220081 | ||||||
| chr5:177220088
|
T | C | 1 | a0001c0022t0011g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3796+7893T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220088 | ||||||
| chr5:177220173
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+7978C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220173 | ||||||
| chr5:177220232
|
C | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3796+8037C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220232 | ||||||
| chr5:177220408
|
T | G | 2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3796+8213T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220408 | ||||||
| chr5:177220563
|
C | CT | 93 | a0001c0001t0002g0292a0001c0001t0004g0202a0001c0001t0004g0230others(90): Show | 93 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.3796+8392dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177220563 | |||||
| chr5:177220563
|
C | CTT | 12 | a0002c0002t0001g0041a0002c0002t0001g0082a0002c0002t0001g0085others(9): Show | 12 | HG00597.hp2 HG02027.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.3796+8391_3796+839 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177220563 | |||||
| chr5:177220563
|
CT | C | 15 | a0001c0001t0004g0252a0001c0001t0004g0274a0001c0003t0007g0112others(12): Show | 15 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.3796+8392delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177220563 | |||||
| chr5:177220563
|
CTT | C | 8 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3796+8391_3796+839 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177220563 | |||||
| chr5:177220641
|
C | G | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3796+8446C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220641 | ||||||
| chr5:177220781
|
C | T | 8 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0163others(5): Show | 8 | HG02015.hp1 HG02109.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.3796+8586C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177220781 | ||||||
| chr5:177221003
|
A | G | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3796+8808A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221003 | ||||||
| chr5:177221016
|
A | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3796+8821A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221016 | ||||||
| chr5:177221126
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3796+8931G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221126 | ||||||
| chr5:177221135
|
A | G | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3796+8940A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221135 | ||||||
| chr5:177221216
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+9021T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221216 | ||||||
| chr5:177221274
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3796+9079G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221274 | ||||||
| chr5:177221301
|
G | GT | 27 | a0001c0001t0013g0279a0001c0001t0067g0278a0001c0003t0002g0133others(24): Show | 27 | HG01106.hp2 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.3796+9117dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177221301 | |||||
| chr5:177221309
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+9114T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221309 | ||||||
| chr5:177221388
|
G | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+9193G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221388 | ||||||
| chr5:177221399
|
A | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+9204A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221399 | ||||||
| chr5:177221408
|
C | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0085a0002c0002t0039g0040 | 3 | NA18985.hp1 NA19054.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3796+9213C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221408 | ||||||
| chr5:177221452
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+9257T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221452 | ||||||
| chr5:177221495
|
G | A | 5 | a0001c0001t0012g0161a0006c0008t0021g0142a0006c0008t0021g0143others(2): Show | 5 | HG02630.hp1 HG02738.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3796+9300G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221495 | ||||||
| chr5:177221623
|
A | G | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3796+9428A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221623 | ||||||
| chr5:177221654
|
A | G | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3796+9459A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221654 | ||||||
| chr5:177221670
|
C | T | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3796+9475C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221670 | ||||||
| chr5:177221675
|
C | T | 1 | a0001c0001t0008g0188 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3796+9480C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221675 | ||||||
| chr5:177221849
|
G | A | 23 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(20): Show | 23 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.3796+9654G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221849 | ||||||
| chr5:177221962
|
A | G | 1 | a0001c0001t0011g0157 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3796+9767A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177221962 | ||||||
| chr5:177222155
|
G | T | 1 | a0001c0003t0007g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3796+9960G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222155 | ||||||
| chr5:177222273
|
C | T | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3796+10078C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222273 | ||||||
| chr5:177222282
|
C | T | 6 | a0001c0001t0004g0281a0001c0001t0029g0284a0001c0001t0029g0285others(3): Show | 6 | NA18942.hp1 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.3796+10087C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222282 | ||||||
| chr5:177222316
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3796+10121G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222316 | ||||||
| chr5:177222319
|
G | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+10124G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222319 | ||||||
| chr5:177222351
|
T | C | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+10156T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222351 | ||||||
| chr5:177222626
|
A | G | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3796+10431A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222626 | ||||||
| chr5:177222684
|
G | T | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3796+10489G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222684 | ||||||
| chr5:177222773
|
C | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3796+10578C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177222773 | ||||||
| chr5:177223002
|
A | G | 1 | a0002c0002t0001g0052 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3796+10807A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223002 | ||||||
| chr5:177223051
|
C | T | 1 | a0001c0003t0007g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3796+10856C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223051 | ||||||
| chr5:177223087
|
T | C | 7 | a0001c0003t0049g0111a0005c0007t0015g0003a0005c0007t0015g0004others(4): Show | 7 | HG02280.hp1 HG02738.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3796+10892T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223087 | ||||||
| chr5:177223339
|
G | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3796+11144G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223339 | ||||||
| chr5:177223488
|
A | G | 275 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(272): Show | 275 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.3796+11293A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223488 | ||||||
| chr5:177223516
|
T | A | 3 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.3796+11321T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223516 | ||||||
| chr5:177223923
|
T | A | 6 | a0001c0005t0002g0007a0001c0005t0005g0008a0001c0024t0002g0009others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3796+11728T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223923 | ||||||
| chr5:177223970
|
G | T | 115 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(112): Show | 115 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.3796+11775G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177223970 | ||||||
| chr5:177224022
|
GTTACAGT others(17): Show |
G | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3797-11772_3797-11 others(30): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177224022 | |||||
| chr5:177224082
|
T | C | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3797-11739T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224082 | ||||||
| chr5:177224220
|
A | G | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3797-11601A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224220 | ||||||
| chr5:177224240
|
G | A | 297 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.3797-11581G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224240 | ||||||
| chr5:177224318
|
T | G | 4 | a0001c0024t0002g0009a0007c0010t0002g0010a0007c0010t0002g0012others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-11503T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224318 | ||||||
| chr5:177224671
|
G | T | 1 | a0001c0003t0007g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3797-11150G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224671 | ||||||
| chr5:177224672
|
C | T | 1 | a0001c0003t0007g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3797-11149C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224672 | ||||||
| chr5:177224806
|
T | A | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3797-11015T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224806 | ||||||
| chr5:177224894
|
G | T | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-10927G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177224894 | ||||||
| chr5:177225071
|
A | G | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3797-10750A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177225071 | ||||||
| chr5:177225170
|
G | A | 4 | a0001c0005t0002g0015a0001c0005t0005g0017a0001c0014t0002g0027others(1): Show | 4 | HG02717.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3797-10651G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177225170 | ||||||
| chr5:177225170
|
G | C | 1 | a0001c0001t0008g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3797-10651G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177225170 | ||||||
| chr5:177225229
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-10592G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177225229 | ||||||
| chr5:177225373
|
T | G | 1 | a0001c0001t0010g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3797-10448T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177225373 | ||||||
| chr5:177226052
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3797-9769C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226052 | ||||||
| chr5:177226053
|
G | A | 8 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0163others(5): Show | 8 | HG02015.hp1 HG02109.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797-9768G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226053 | ||||||
| chr5:177226223
|
T | C | 4 | a0001c0001t0029g0284a0001c0001t0029g0285a0001c0001t0030g0282others(1): Show | 4 | NA18969.hp1 NA18991.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.3797-9598T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226223 | ||||||
| chr5:177226444
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3797-9377G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226444 | ||||||
| chr5:177226467
|
G | A | 1 | a0016c0018t0004g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3797-9354G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226467 | ||||||
| chr5:177226472
|
A | G | 1 | a0001c0001t0078g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3797-9349A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226472 | ||||||
| chr5:177226515
|
T | C | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3797-9306T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226515 | ||||||
| chr5:177226519
|
G | A | 155 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(152): Show | 155 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3797-9302G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226519 | ||||||
| chr5:177226820
|
A | T | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-9001A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177226820 | ||||||
| chr5:177227054
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3797-8767C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227054 | ||||||
| chr5:177227141
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-8680A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227141 | ||||||
| chr5:177227223
|
G | C | 1 | a0001c0003t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3797-8598G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227223 | ||||||
| chr5:177227412
|
T | G | 1 | a0001c0009t0002g0257 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3797-8409T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227412 | ||||||
| chr5:177227478
|
A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0045g0287 | 3 | HG02572.hp2 HG02630.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3797-8343A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227478 | ||||||
| chr5:177227576
|
A | G | 1 | a0001c0001t0008g0183 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3797-8245A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227576 | ||||||
| chr5:177227590
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-8231G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227590 | ||||||
| chr5:177227694
|
G | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-8127G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227694 | ||||||
| chr5:177227896
|
C | T | 3 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3797-7925C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177227896 | ||||||
| chr5:177227946
|
CA | C | 16 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0050others(13): Show | 16 | HG00408.hp2 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.3797-7861delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177227946 | |||||
| chr5:177228077
|
G | A | 2 | a0002c0002t0001g0043a0002c0002t0003g0044 | 2 | HG00733.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3797-7744G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228077 | ||||||
| chr5:177228236
|
T | G | 115 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(112): Show | 115 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.3797-7585T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228236 | ||||||
| chr5:177228265
|
C | CT | 6 | a0001c0001t0008g0183a0001c0001t0036g0199a0001c0003t0002g0130others(3): Show | 6 | HG00423.hp1 HG01975.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3797-7542dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177228265 | |||||
| chr5:177228344
|
T | C | 125 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(122): Show | 125 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.3797-7477T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228344 | ||||||
| chr5:177228357
|
C | T | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3797-7464C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228357 | ||||||
| chr5:177228405
|
C | T | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3797-7416C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228405 | ||||||
| chr5:177228496
|
C | T | 2 | a0003c0031t0009g0154a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3797-7325C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228496 | ||||||
| chr5:177228525
|
A | G | 3 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.3797-7296A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228525 | ||||||
| chr5:177228824
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-6997T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228824 | ||||||
| chr5:177228848
|
T | A | 1 | a0001c0001t0010g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3797-6973T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228848 | ||||||
| chr5:177228928
|
A | G | 85 | a0002c0002t0001g0028a0002c0002t0001g0030a0002c0002t0001g0031others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.3797-6893A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228928 | ||||||
| chr5:177228984
|
G | C | 9 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(6): Show | 9 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3797-6837G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177228984 | ||||||
| chr5:177229082
|
TA | T | 8 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797-6728delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177229082 | |||||
| chr5:177229212
|
T | A | 1 | a0002c0002t0003g0055 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3797-6609T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229212 | ||||||
| chr5:177229262
|
C | G | 1 | a0001c0001t0034g0235 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3797-6559C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229262 | ||||||
| chr5:177229316
|
T | G | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.3797-6505T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229316 | ||||||
| chr5:177229330
|
T | A | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3797-6491T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229330 | ||||||
| chr5:177229394
|
T | C | 2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3797-6427T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229394 | ||||||
| chr5:177229532
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-6289C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229532 | ||||||
| chr5:177229578
|
C | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3797-6243C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229578 | ||||||
| chr5:177229822
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3797-5999C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177229822 | ||||||
| chr5:177230283
|
T | C | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3797-5538T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230283 | ||||||
| chr5:177230288
|
G | T | 157 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.3797-5533G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230288 | ||||||
| chr5:177230427
|
A | G | 2 | a0001c0003t0007g0122a0001c0003t0007g0126 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3797-5394A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230427 | ||||||
| chr5:177230551
|
C | A | 1 | a0002c0002t0019g0081 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3797-5270C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230551 | ||||||
| chr5:177230552
|
G | A | 3 | a0001c0001t0023g0181a0001c0001t0023g0200a0001c0001t0075g0184 | 3 | HG02523.hp1 NA18941.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.3797-5269G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230552 | ||||||
| chr5:177230621
|
T | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3797-5200T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230621 | ||||||
| chr5:177230778
|
G | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-5043G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230778 | ||||||
| chr5:177230822
|
G | A | 5 | a0001c0001t0024g0156a0001c0001t0024g0195a0001c0001t0024g0243others(2): Show | 5 | HG00423.hp2 NA18946.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.3797-4999G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177230822 | ||||||
| chr5:177231065
|
A | T | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.3797-4756A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231065 | ||||||
| chr5:177231133
|
T | C | 3 | a0001c0004t0002g0220a0001c0004t0002g0231a0004c0017t0041g0260 | 3 | HG02698.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3797-4688T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231133 | ||||||
| chr5:177231233
|
G | A | 17 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.3797-4588G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231233 | ||||||
| chr5:177231576
|
C | T | 1 | a0001c0001t0026g0201 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3797-4245C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231576 | ||||||
| chr5:177231665
|
C | A | 2 | a0002c0016t0003g0068a0002c0016t0040g0069 | 2 | HG02165.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.3797-4156C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231665 | ||||||
| chr5:177231743
|
C | A | 1 | a0016c0018t0004g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3797-4078C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177231743 | ||||||
| chr5:177232059
|
G | C | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3797-3762G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232059 | ||||||
| chr5:177232410
|
G | T | 1 | a0001c0001t0008g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3797-3411G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232410 | ||||||
| chr5:177232453
|
C | G | 1 | a0005c0007t0015g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3797-3368C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232453 | ||||||
| chr5:177232569
|
G | A | 276 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(273): Show | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.3797-3252G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232569 | ||||||
| chr5:177232590
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-3231C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232590 | ||||||
| chr5:177232918
|
A | G | 1 | a0001c0001t0023g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3797-2903A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232918 | ||||||
| chr5:177232937
|
G | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3797-2884G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177232937 | ||||||
| chr5:177233331
|
A | G | 1 | a0002c0002t0022g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3797-2490A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177233331 | ||||||
| chr5:177233392
|
A | T | 1 | a0002c0002t0022g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3797-2429A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177233392 | ||||||
| chr5:177233512
|
A | G | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3797-2309A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177233512 | ||||||
| chr5:177233537
|
A | AT | 160 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.3797-2264dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177233537 | |||||
| chr5:177233537
|
A | ATT | 31 | a0001c0001t0012g0161a0001c0001t0013g0270a0001c0001t0078g0237others(28): Show | 31 | HG00733.hp1 HG01069.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.3797-2265_3797-226 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177233537 | |||||
| chr5:177233537
|
A | ATTT | 96 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(93): Show | 96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.3797-2266_3797-226 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177233537 | |||||
| chr5:177233537
|
A | ATTTT | 9 | a0001c0003t0077g0108a0002c0002t0001g0028a0002c0002t0001g0033others(6): Show | 9 | HG01175.hp2 HG02027.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.3797-2267_3797-226 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177233537 | |||||
| chr5:177233598
|
C | T | 1 | a0017c0035t0025g0221 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3797-2223C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177233598 | ||||||
| chr5:177233650
|
C | T | 2 | a0001c0001t0004g0245a0001c0001t0008g0182 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3797-2171C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177233650 | ||||||
| chr5:177234217
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3797-1604C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234217 | ||||||
| chr5:177234246
|
A | C | 5 | a0001c0001t0024g0156a0001c0001t0024g0195a0001c0001t0024g0243others(2): Show | 5 | HG00423.hp2 NA18946.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.3797-1575A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234246 | ||||||
| chr5:177234271
|
C | A | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3797-1550C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234271 | ||||||
| chr5:177234409
|
T | A | 1 | a0001c0001t0010g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3797-1412T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234409 | ||||||
| chr5:177234474
|
T | C | 1 | a0001c0001t0017g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3797-1347T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234474 | ||||||
| chr5:177234543
|
G | A | 20 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(17): Show | 20 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3797-1278G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234543 | ||||||
| chr5:177234623
|
G | T | 6 | a0001c0001t0004g0281a0001c0001t0029g0284a0001c0001t0029g0285others(3): Show | 6 | NA18942.hp1 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.3797-1198G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234623 | ||||||
| chr5:177234628
|
A | T | 6 | a0001c0001t0004g0281a0001c0001t0029g0284a0001c0001t0029g0285others(3): Show | 6 | NA18942.hp1 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.3797-1193A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234628 | ||||||
| chr5:177234693
|
G | A | 2 | a0001c0005t0006g0019a0001c0005t0057g0020 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3797-1128G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234693 | ||||||
| chr5:177234780
|
G | GACTTTAG others(7): Show |
4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-1039_3797-102 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177234780 | |||||
| chr5:177234807
|
T | C | 222 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(219): Show | 222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.3797-1014T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234807 | ||||||
| chr5:177234826
|
T | C | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3797-995T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234826 | ||||||
| chr5:177234893
|
A | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-928A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234893 | ||||||
| chr5:177234897
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3797-924G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234897 | ||||||
| chr5:177234932
|
TAGATGGA others(7): Show |
T | 2 | a0001c0005t0002g0007a0001c0005t0005g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3797-886_3797-873d others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | 177234932 | |||||
| chr5:177234952
|
G | A | 1 | a0001c0001t0010g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3797-869G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234952 | ||||||
| chr5:177234968
|
T | G | 1 | a0001c0005t0006g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3797-853T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234968 | ||||||
| chr5:177234997
|
G | T | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3797-824G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177234997 | ||||||
| chr5:177235238
|
T | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3797-583T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235238 | ||||||
| chr5:177235292
|
G | A | 214 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(211): Show | 214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.3797-529G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235292 | ||||||
| chr5:177235416
|
A | G | 1 | a0001c0001t0023g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3797-405A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235416 | ||||||
| chr5:177235538
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3797-283T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235538 | ||||||
| chr5:177235573
|
T | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3797-248T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235573 | ||||||
| chr5:177235578
|
A | T | 1 | a0001c0001t0005g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3797-243A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235578 | ||||||
| chr5:177235755
|
C | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3797-66C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 5/22 | chr5 | 177235755 | ||||||
| chr5:177236033
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3921+88A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236033 | ||||||
| chr5:177236364
|
T | A | 1 | a0001c0001t0004g0254 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3921+419T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236364 | ||||||
| chr5:177236414
|
A | G | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.3921+469A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236414 | ||||||
| chr5:177236488
|
T | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3921+543T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236488 | ||||||
| chr5:177236520
|
A | T | 1 | a0001c0001t0025g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3921+575A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236520 | ||||||
| chr5:177236807
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3921+862T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177236807 | ||||||
| chr5:177237290
|
T | C | 1 | a0016c0018t0004g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3922-947T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237290 | ||||||
| chr5:177237496
|
A | AT | 22 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0005g0232others(19): Show | 22 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.3922-741_3922-740i others(3): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237496 | ||||||
| chr5:177237496
|
A | T | 1 | a0002c0002t0014g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3922-741A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237496 | ||||||
| chr5:177237511
|
T | C | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.3922-726T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237511 | ||||||
| chr5:177237524
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3922-713A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237524 | ||||||
| chr5:177237531
|
C | CT | 29 | a0001c0001t0004g0252a0001c0001t0004g0276a0001c0001t0012g0161others(26): Show | 29 | HG00280.hp1 HG00597.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.3922-687dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 177237531 | |||||
| chr5:177237531
|
C | CTT | 26 | a0001c0003t0007g0123a0001c0003t0011g0135a0001c0003t0016g0114others(23): Show | 26 | HG00733.hp1 HG00733.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.3922-688_3922-687d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 177237531 | |||||
| chr5:177237531
|
CT | C | 6 | a0001c0001t0026g0201a0001c0001t0033g0176a0001c0003t0077g0108others(3): Show | 6 | HG02273.hp1 HG02602.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3922-687delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 177237531 | |||||
| chr5:177237572
|
G | T | 1 | a0001c0001t0012g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3922-665G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237572 | ||||||
| chr5:177237627
|
T | A | 1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3922-610T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237627 | ||||||
| chr5:177237637
|
A | G | 1 | a0001c0001t0054g0271 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3922-600A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237637 | ||||||
| chr5:177237723
|
C | A | 1 | a0001c0003t0007g0126 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3922-514C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237723 | ||||||
| chr5:177237780
|
G | T | 6 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3922-457G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177237780 | ||||||
| chr5:177238048
|
T | C | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3922-189T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | chr5 | 177238048 | ||||||
| chr5:177238078
|
CT | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3922-157delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr5 | 177238078 | |||||
| chr5:177238602
|
A | G | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4192+95A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177238602 | ||||||
| chr5:177238701
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4192+194A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177238701 | ||||||
| chr5:177238761
|
C | T | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4192+254C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177238761 | ||||||
| chr5:177238878
|
G | A | 140 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.4192+371G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177238878 | ||||||
| chr5:177238985
|
A | AT | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4192+480dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr5 | 177238985 | |||||
| chr5:177239169
|
C | T | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4193-587C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177239169 | ||||||
| chr5:177239264
|
T | C | 3 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4193-492T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177239264 | ||||||
| chr5:177239486
|
C | T | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4193-270C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 7/22 | chr5 | 177239486 | ||||||
| chr5:177239875
|
T | C | 1 | a0002c0016t0003g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4302+10T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177239875 | ||||||
| chr5:177240117
|
G | C | 2 | a0001c0003t0016g0114a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4302+252G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240117 | ||||||
| chr5:177240202
|
ACT | A | 3 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.4302+341_4302+342d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177240202 | |||||
| chr5:177240207
|
C | A | 1 | a0001c0001t0074g0215 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4302+342C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240207 | ||||||
| chr5:177240326
|
C | A | 161 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.4302+461C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240326 | ||||||
| chr5:177240540
|
C | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4302+675C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240540 | ||||||
| chr5:177240569
|
T | C | 4 | a0001c0024t0002g0009a0007c0010t0002g0010a0007c0010t0002g0012others(1): Show | 4 | HG02647.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4302+704T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240569 | ||||||
| chr5:177240628
|
G | A | 1 | a0001c0001t0067g0278 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4302+763G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240628 | ||||||
| chr5:177240640
|
G | A | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4302+775G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240640 | ||||||
| chr5:177240662
|
G | A | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0009t0002g0257others(4): Show | 7 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4302+797G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240662 | ||||||
| chr5:177240742
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4302+877C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240742 | ||||||
| chr5:177240877
|
A | G | 13 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.4302+1012A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240877 | ||||||
| chr5:177240951
|
C | T | 1 | a0001c0005t0057g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4302+1086C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240951 | ||||||
| chr5:177240975
|
C | T | 5 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0127others(2): Show | 5 | HG01167.hp1 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4302+1110C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177240975 | ||||||
| chr5:177241088
|
G | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4302+1223G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241088 | ||||||
| chr5:177241149
|
GT | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4302+1288delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177241149 | |||||
| chr5:177241154
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4302+1289G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241154 | ||||||
| chr5:177241342
|
C | CA | 11 | a0001c0001t0002g0249a0001c0001t0008g0239a0001c0001t0066g0283others(8): Show | 11 | HG00597.hp1 HG00597.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.4302+1491dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177241342 | |||||
| chr5:177241499
|
T | A | 3 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.4302+1634T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241499 | ||||||
| chr5:177241508
|
C | CA | 6 | a0002c0002t0001g0089a0005c0007t0015g0006a0006c0008t0021g0142others(3): Show | 6 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4302+1654dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177241508 | |||||
| chr5:177241584
|
A | G | 1 | a0002c0002t0022g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4302+1719A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241584 | ||||||
| chr5:177241623
|
T | C | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4302+1758T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241623 | ||||||
| chr5:177241729
|
G | C | 1 | a0001c0001t0004g0269 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4302+1864G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241729 | ||||||
| chr5:177241795
|
T | C | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4302+1930T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241795 | ||||||
| chr5:177241818
|
C | T | 3 | a0002c0002t0001g0034a0002c0002t0003g0038a0002c0002t0020g0001 | 3 | HG00099.hp2 HG00323.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.4302+1953C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241818 | ||||||
| chr5:177241854
|
C | G | 1 | a0001c0001t0030g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4302+1989C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241854 | ||||||
| chr5:177241923
|
G | A | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.4302+2058G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177241923 | ||||||
| chr5:177242029
|
A | G | 21 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0008g0170others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.4302+2164A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242029 | ||||||
| chr5:177242228
|
TA | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4303-1964delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242228 | |||||
| chr5:177242472
|
T | G | 2 | a0001c0004t0002g0227a0001c0004t0011g0219 | 2 | HG00099.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.4303-1723T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242472 | ||||||
| chr5:177242486
|
T | C | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.4303-1709T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242486 | ||||||
| chr5:177242505
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4303-1690A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242505 | ||||||
| chr5:177242514
|
A | ATTAT | 27 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(24): Show | 27 | HG00423.hp2 HG00609.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.4303-1654_4303-165 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242514 | |||||
| chr5:177242514
|
A | ATTATTTA others(1): Show |
23 | a0001c0001t0005g0232a0001c0001t0005g0241a0001c0001t0005g0242others(20): Show | 23 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.4303-1658_4303-165 others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242514 | |||||
| chr5:177242514
|
A | ATTATTTA others(5): Show |
80 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.4303-1662_4303-165 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242514 | |||||
| chr5:177242514
|
A | ATTATTTA others(9): Show |
49 | a0001c0001t0004g0209a0001c0001t0004g0240a0001c0001t0004g0245others(46): Show | 49 | HG00280.hp2 HG00673.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.4303-1666_4303-165 others(20): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242514 | |||||
| chr5:177242514
|
A | ATTATTTA others(13): Show |
7 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0001t0044g0253others(4): Show | 7 | HG00609.hp2 HG02145.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.4303-1670_4303-165 others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177242514 | |||||
| chr5:177242584
|
A | G | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4303-1611A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242584 | ||||||
| chr5:177242780
|
C | T | 1 | a0001c0001t0013g0270 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4303-1415C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242780 | ||||||
| chr5:177242790
|
A | G | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.4303-1405A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177242790 | ||||||
| chr5:177243194
|
C | CT | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4303-998dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | 177243194 | |||||
| chr5:177243198
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4303-997C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177243198 | ||||||
| chr5:177243223
|
C | T | 2 | a0001c0001t0072g0152a0001c0001t0073g0251 | 2 | NA18967.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.4303-972C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177243223 | ||||||
| chr5:177243956
|
G | A | 1 | a0003c0006t0009g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4303-239G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177243956 | ||||||
| chr5:177244039
|
T | C | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4303-156T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 8/22 | chr5 | 177244039 | ||||||
| chr5:177244590
|
C | T | 2 | a0001c0003t0016g0114a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4378+320C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177244590 | ||||||
| chr5:177245025
|
G | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4378+755G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245025 | ||||||
| chr5:177245549
|
C | T | 1 | a0001c0005t0005g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4379-1129C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245549 | ||||||
| chr5:177245632
|
C | CT | 30 | a0001c0001t0004g0196a0001c0001t0013g0177a0001c0001t0013g0279others(27): Show | 30 | HG00733.hp1 HG01106.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.4379-1030dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr5 | 177245632 | |||||
| chr5:177245973
|
TA | T | 208 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(205): Show | 208 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.4379-704delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245973 | ||||||
| chr5:177245974
|
A | T | 4 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104others(1): Show | 4 | HG02451.hp1 HG06807.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4379-704A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245974 | ||||||
| chr5:177245976
|
T | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4379-702T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245976 | ||||||
| chr5:177245977
|
T | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4379-701T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245977 | ||||||
| chr5:177245978
|
T | A | 191 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(188): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.4379-700T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177245978 | ||||||
| chr5:177246067
|
T | A | 161 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.4379-611T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177246067 | ||||||
| chr5:177246278
|
T | C | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.4379-400T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 9/22 | chr5 | 177246278 | ||||||
| chr5:177246895
|
A | G | 6 | a0001c0001t0004g0269a0001c0001t0013g0267a0001c0001t0013g0270others(3): Show | 6 | HG01074.hp1 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.4497+99A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177246895 | ||||||
| chr5:177247124
|
T | TA | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4497+329dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr5 | 177247124 | |||||
| chr5:177247195
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4497+399C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177247195 | ||||||
| chr5:177247253
|
A | G | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4497+457A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177247253 | ||||||
| chr5:177247565
|
T | TA | 35 | a0001c0001t0012g0161a0001c0003t0007g0112a0001c0003t0007g0113others(32): Show | 35 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.4498-597dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr5 | 177247565 | |||||
| chr5:177247565
|
TA | T | 6 | a0001c0001t0004g0274a0001c0001t0008g0193a0001c0001t0011g0157others(3): Show | 6 | HG02015.hp2 HG02055.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4498-597delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr5 | 177247565 | |||||
| chr5:177247566
|
A | T | 2 | a0001c0005t0002g0007a0001c0005t0005g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4498-615A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177247566 | ||||||
| chr5:177247587
|
G | A | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.4498-594G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177247587 | ||||||
| chr5:177247643
|
A | G | 1 | a0001c0001t0004g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4498-538A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 10/22 | chr5 | 177247643 | ||||||
| chr5:177248422
|
A | G | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4641+98A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177248422 | ||||||
| chr5:177248530
|
G | C | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4641+206G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177248530 | ||||||
| chr5:177249008
|
G | A | 1 | a0001c0004t0035g0233 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4641+684G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249008 | ||||||
| chr5:177249009
|
G | A | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.4641+685G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249009 | ||||||
| chr5:177249302
|
C | G | 15 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(12): Show | 15 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4641+978C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249302 | ||||||
| chr5:177249322
|
T | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4641+998T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249322 | ||||||
| chr5:177249350
|
T | C | 182 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.4641+1026T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249350 | ||||||
| chr5:177249456
|
A | T | 12 | a0001c0003t0068g0137a0002c0002t0001g0033a0002c0002t0001g0077others(9): Show | 12 | HG01069.hp1 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.4641+1132A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249456 | ||||||
| chr5:177249460
|
T | A | 159 | a0001c0001t0002g0149a0001c0001t0002g0204a0001c0001t0002g0247others(156): Show | 159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4641+1136T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249460 | ||||||
| chr5:177249462
|
T | A | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4641+1138T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249462 | ||||||
| chr5:177249464
|
T | A | 9 | a0001c0001t0004g0245a0001c0001t0008g0182a0001c0001t0045g0287others(6): Show | 9 | HG01515.hp2 HG01517.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.4641+1140T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249464 | ||||||
| chr5:177249489
|
C | T | 11 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0050others(8): Show | 11 | HG00408.hp2 HG01256.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.4641+1165C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249489 | ||||||
| chr5:177249568
|
GCCATTCT others(14): Show |
G | 5 | a0001c0001t0024g0156a0001c0001t0024g0195a0001c0001t0024g0243others(2): Show | 5 | HG00423.hp2 NA18946.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.4641+1267_4641+128 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | 177249568 | |||||
| chr5:177249586
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4641+1262C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249586 | ||||||
| chr5:177249688
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4641+1364C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249688 | ||||||
| chr5:177249896
|
G | A | 2 | a0001c0004t0012g0259a0001c0004t0012g0263 | 2 | HG00642.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.4641+1572G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177249896 | ||||||
| chr5:177250077
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4642-1653A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177250077 | ||||||
| chr5:177250380
|
G | C | 1 | a0002c0002t0069g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4642-1350G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177250380 | ||||||
| chr5:177250384
|
C | T | 3 | a0002c0002t0003g0045a0002c0002t0003g0051a0002c0002t0003g0083 | 3 | HG01069.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.4642-1346C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177250384 | ||||||
| chr5:177250562
|
G | GT | 29 | a0001c0003t0007g0134a0001c0003t0077g0108a0001c0004t0002g0227others(26): Show | 29 | HG00738.hp1 HG01515.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.4642-1153dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | 177250562 | |||||
| chr5:177250562
|
GT | G | 6 | a0001c0001t0008g0239a0001c0001t0013g0234a0001c0001t0059g0218others(3): Show | 6 | HG00609.hp2 HG01257.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.4642-1153delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | 177250562 | |||||
| chr5:177250562
|
GTT | G | 19 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(16): Show | 19 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.4642-1154_4642-115 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | 177250562 | |||||
| chr5:177250706
|
T | G | 3 | a0001c0004t0002g0220a0001c0004t0002g0231a0004c0017t0041g0260 | 3 | HG02698.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4642-1024T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177250706 | ||||||
| chr5:177250798
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4642-932C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177250798 | ||||||
| chr5:177251005
|
C | T | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4642-725C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177251005 | ||||||
| chr5:177251189
|
C | CA | 52 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(49): Show | 52 | HG00733.hp1 HG01109.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.4642-526dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | 177251189 | |||||
| chr5:177251234
|
C | T | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.4642-496C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177251234 | ||||||
| chr5:177251276
|
G | A | 1 | a0001c0001t0008g0239 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4642-454G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177251276 | ||||||
| chr5:177251363
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4642-367G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 11/22 | chr5 | 177251363 | ||||||
| chr5:177251943
|
G | A | 13 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.4765+90G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177251943 | ||||||
| chr5:177252052
|
C | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4765+199C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252052 | ||||||
| chr5:177252232
|
G | A | 4 | a0002c0002t0001g0050a0002c0002t0001g0085a0002c0002t0039g0040others(1): Show | 4 | HG01256.hp1 NA18985.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.4765+379G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252232 | ||||||
| chr5:177252310
|
A | G | 7 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0124others(4): Show | 7 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4765+457A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252310 | ||||||
| chr5:177252388
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4765+535G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252388 | ||||||
| chr5:177252406
|
G | A | 89 | a0001c0001t0004g0187a0001c0001t0004g0196a0001c0001t0004g0202others(86): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.4765+553G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252406 | ||||||
| chr5:177252536
|
G | GTT | 8 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0122others(5): Show | 8 | HG01167.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.4765+684_4765+685d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252536 | |||||
| chr5:177252536
|
G | GTTT | 3 | a0001c0003t0007g0126a0001c0003t0007g0134a0001c0003t0068g0137 | 3 | HG01109.hp2 HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4765+685_4765+686i others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252536 | |||||
| chr5:177252539
|
C | CT | 26 | a0001c0005t0005g0008a0001c0005t0005g0014a0001c0005t0005g0017others(23): Show | 26 | HG01175.hp2 HG01256.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.4765+716dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
C | CTT | 8 | a0001c0005t0002g0007a0001c0005t0005g0016a0001c0005t0005g0018others(5): Show | 8 | HG01515.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.4765+715_4765+716d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
C | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.4765+686C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252539 | ||||||
| chr5:177252539
|
CT | C | 46 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(43): Show | 46 | HG00323.hp1 HG00423.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.4765+716delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTT | C | 76 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(73): Show | 76 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.4765+715_4765+716d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTT | C | 30 | a0001c0001t0004g0209a0001c0001t0004g0223a0001c0001t0004g0230others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.4765+714_4765+716d others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTTTT | C | 10 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(7): Show | 10 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.4765+712_4765+716d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTTTTTT others(3): Show |
C | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4765+707_4765+716d others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTTTTTT others(4): Show |
C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4765+706_4765+716d others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTTTTTT others(5): Show |
C | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4765+705_4765+716d others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252539
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0010g0255 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4765+702_4765+716d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177252539 | |||||
| chr5:177252547
|
T | C | 2 | a0001c0001t0023g0150a0001c0001t0073g0251 | 2 | NA18967.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.4765+694T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252547 | ||||||
| chr5:177252548
|
T | C | 1 | a0001c0001t0072g0152 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4765+695T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252548 | ||||||
| chr5:177252649
|
T | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4765+796T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252649 | ||||||
| chr5:177252694
|
A | G | 186 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.4765+841A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252694 | ||||||
| chr5:177252796
|
C | CT | 28 | a0001c0005t0002g0015a0001c0005t0005g0014a0001c0005t0005g0016others(25): Show | 28 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.4765+943_4765+944i others(3): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252796 | ||||||
| chr5:177252796
|
C | CTT | 14 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(11): Show | 14 | HG01109.hp2 HG01167.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.4765+943_4765+944i others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252796 | ||||||
| chr5:177252796
|
C | CTTTT | 9 | a0003c0006t0009g0013a0003c0006t0009g0160a0003c0006t0009g0163others(6): Show | 9 | HG00733.hp1 HG02015.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.4765+943_4765+944i others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252796 | ||||||
| chr5:177252797
|
C | T | 212 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.4765+944C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177252797 | ||||||
| chr5:177253112
|
T | C | 1 | a0001c0001t0006g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4765+1259T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253112 | ||||||
| chr5:177253268
|
C | A | 17 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(14): Show | 17 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.4765+1415C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253268 | ||||||
| chr5:177253390
|
T | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4765+1537T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253390 | ||||||
| chr5:177253424
|
T | C | 1 | a0002c0002t0001g0030 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4765+1571T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253424 | ||||||
| chr5:177253492
|
G | C | 1 | a0001c0001t0004g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4765+1639G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253492 | ||||||
| chr5:177253672
|
G | A | 1 | a0001c0001t0063g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4765+1819G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253672 | ||||||
| chr5:177253867
|
G | C | 1 | a0008c0015t0002g0116 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4765+2014G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177253867 | ||||||
| chr5:177254024
|
G | A | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4765+2171G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254024 | ||||||
| chr5:177254033
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4765+2180C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254033 | ||||||
| chr5:177254348
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4765+2495G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254348 | ||||||
| chr5:177254392
|
G | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4765+2539G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254392 | ||||||
| chr5:177254448
|
G | A | 7 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0009t0002g0257others(4): Show | 7 | HG02071.hp2 HG02602.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4766-2503G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254448 | ||||||
| chr5:177254463
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4766-2488G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254463 | ||||||
| chr5:177254589
|
G | A | 1 | a0005c0007t0015g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4766-2362G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254589 | ||||||
| chr5:177254647
|
G | C | 15 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(12): Show | 15 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4766-2304G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254647 | ||||||
| chr5:177254705
|
A | G | 1 | a0002c0002t0069g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4766-2246A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254705 | ||||||
| chr5:177254796
|
TA | T | 216 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.4766-2152delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177254796 | |||||
| chr5:177254867
|
G | T | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4766-2084G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254867 | ||||||
| chr5:177254995
|
G | C | 1 | a0003c0006t0009g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4766-1956G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177254995 | ||||||
| chr5:177255150
|
T | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4766-1801T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255150 | ||||||
| chr5:177255304
|
C | CA | 11 | a0001c0001t0034g0290a0003c0006t0009g0013a0003c0006t0009g0158others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4766-1633dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177255304 | |||||
| chr5:177255589
|
T | G | 119 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.4766-1362T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255589 | ||||||
| chr5:177255700
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4766-1251A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255700 | ||||||
| chr5:177255733
|
C | T | 119 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.4766-1218C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255733 | ||||||
| chr5:177255811
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4766-1140C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255811 | ||||||
| chr5:177255883
|
T | C | 7 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4766-1068T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177255883 | ||||||
| chr5:177256095
|
T | C | 1 | a0001c0001t0004g0274 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.4766-856T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256095 | ||||||
| chr5:177256112
|
T | C | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4766-839T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256112 | ||||||
| chr5:177256165
|
G | C | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4766-786G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256165 | ||||||
| chr5:177256199
|
G | A | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4766-752G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256199 | ||||||
| chr5:177256203
|
G | A | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4766-748G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256203 | ||||||
| chr5:177256233
|
T | C | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4766-718T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256233 | ||||||
| chr5:177256275
|
C | CT | 8 | a0001c0003t0052g0129a0002c0002t0001g0028a0002c0002t0001g0057others(5): Show | 8 | HG00597.hp2 HG01175.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.4766-651dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177256275 | |||||
| chr5:177256275
|
CT | C | 29 | a0001c0001t0012g0161a0001c0001t0024g0156a0001c0001t0055g0214others(26): Show | 29 | HG00423.hp1 HG02145.hp2 HG02148.hp2 others(26): Show |
intron_variant | MODIFIER | c.4766-651delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177256275 | |||||
| chr5:177256275
|
CTT | C | 68 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(65): Show | 68 | HG00323.hp1 HG00423.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.4766-652_4766-651d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177256275 | |||||
| chr5:177256275
|
CTTT | C | 109 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0004g0196others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.4766-653_4766-651d others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | 177256275 | |||||
| chr5:177256358
|
A | G | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4766-593A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256358 | ||||||
| chr5:177256755
|
C | T | 10 | a0001c0003t0016g0114a0001c0003t0016g0117a0001c0003t0016g0118others(7): Show | 10 | HG02559.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.4766-196C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256755 | ||||||
| chr5:177256793
|
A | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4766-158A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 12/22 | chr5 | 177256793 | ||||||
| chr5:177257181
|
T | C | 2 | a0001c0001t0010g0186a0001c0001t0033g0176 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.4966+30T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257181 | ||||||
| chr5:177257217
|
C | CT | 23 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0197others(20): Show | 23 | HG00423.hp2 HG02027.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.4966+72dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257217 | |||||
| chr5:177257224
|
C | CTTT | 6 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(3): Show | 6 | HG02280.hp1 HG02738.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4966+74_4966+76dup others(3): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257224 | |||||
| chr5:177257224
|
C | CTTTT | 8 | a0003c0006t0009g0013a0003c0006t0009g0163a0003c0006t0009g0167others(5): Show | 8 | HG02015.hp1 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.4966+76_4966+77ins others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257224 | |||||
| chr5:177257224
|
C | CTTTTT | 5 | a0003c0006t0009g0158a0003c0006t0009g0164a0003c0006t0009g0165others(2): Show | 5 | HG00733.hp1 HG02630.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4966+76_4966+77ins others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257224 | |||||
| chr5:177257228
|
C | CT | 22 | a0001c0001t0004g0252a0001c0001t0004g0274a0001c0001t0008g0210others(19): Show | 22 | HG00408.hp1 HG00408.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.4966+96dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257228 | |||||
| chr5:177257228
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4966+77C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257228 | ||||||
| chr5:177257228
|
CT | C | 31 | a0001c0001t0010g0208a0001c0001t0029g0284a0001c0001t0034g0290others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.4966+96delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257228 | |||||
| chr5:177257232
|
T | C | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4966+81T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257232 | ||||||
| chr5:177257311
|
A | G | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4966+160A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257311 | ||||||
| chr5:177257453
|
G | A | 2 | a0001c0001t0002g0288a0001c0001t0005g0207 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.4966+302G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257453 | ||||||
| chr5:177257695
|
C | T | 1 | a0002c0002t0076g0035 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4966+544C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257695 | ||||||
| chr5:177257817
|
T | A | 1 | a0001c0009t0006g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4966+666T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257817 | ||||||
| chr5:177257817
|
T | TTTTTA | 130 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.4966+691_4966+695d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257817 | |||||
| chr5:177257817
|
T | TTTTTATT others(3): Show |
1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4966+686_4966+695d others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257817 | |||||
| chr5:177257821
|
T | A | 5 | a0001c0003t0049g0111a0006c0008t0021g0142a0006c0008t0021g0143others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4966+670T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257821 | ||||||
| chr5:177257832
|
AT | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4966+685delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257832 | |||||
| chr5:177257832
|
ATTTTATT others(8): Show |
A | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4966+686_4966+700d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257832 | |||||
| chr5:177257836
|
T | A | 17 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(14): Show | 17 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4966+685T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257836 | ||||||
| chr5:177257837
|
A | T | 18 | a0001c0003t0002g0130a0003c0006t0009g0013a0003c0006t0009g0158others(15): Show | 18 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.4966+686A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257837 | ||||||
| chr5:177257840
|
T | A | 17 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(14): Show | 17 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4966+689T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257840 | ||||||
| chr5:177257841
|
T | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.4966+690T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257841 | ||||||
| chr5:177257842
|
A | ATTTTT | 8 | a0001c0001t0004g0252a0001c0001t0008g0210a0001c0001t0008g0239others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.4966+696_4966+700d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257842 | |||||
| chr5:177257842
|
A | T | 25 | a0001c0003t0002g0130a0003c0006t0009g0013a0003c0006t0009g0158others(22): Show | 25 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.4966+691A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257842 | ||||||
| chr5:177257900
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4966+749G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257900 | ||||||
| chr5:177257904
|
G | T | 183 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(180): Show | 183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.4966+753G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177257904 | ||||||
| chr5:177257973
|
C | CT | 136 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(133): Show | 136 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.4966+846dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257973 | |||||
| chr5:177257973
|
C | CTT | 38 | a0001c0001t0002g0292a0001c0001t0004g0187a0001c0001t0005g0148others(35): Show | 38 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.4966+845_4966+846d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257973 | |||||
| chr5:177257973
|
C | CTTTT | 14 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0008g0170others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.4966+843_4966+846d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257973 | |||||
| chr5:177257973
|
C | CTTTTT | 13 | a0001c0004t0002g0220a0001c0004t0002g0226a0001c0004t0002g0227others(10): Show | 13 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.4966+842_4966+846d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257973 | |||||
| chr5:177257973
|
CTTTTTTT others(5): Show |
C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4966+835_4966+846d others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177257973 | |||||
| chr5:177258200
|
G | T | 1 | a0001c0001t0025g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4966+1049G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258200 | ||||||
| chr5:177258201
|
A | T | 1 | a0001c0001t0025g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4966+1050A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258201 | ||||||
| chr5:177258401
|
C | T | 1 | a0002c0002t0003g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4966+1250C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258401 | ||||||
| chr5:177258510
|
G | A | 3 | a0003c0006t0009g0160a0003c0006t0009g0165a0003c0006t0009g0166 | 3 | HG00733.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.4966+1359G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258510 | ||||||
| chr5:177258516
|
T | TTTG | 3 | a0001c0001t0006g0179a0001c0001t0006g0180a0001c0033t0037g0262 | 3 | HG02145.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4966+1380_4966+138 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177258516 | |||||
| chr5:177258522
|
GTTGTTGT others(3): Show |
G | 1 | a0002c0002t0070g0097 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4966+1384_4966+139 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177258522 | |||||
| chr5:177258532
|
T | G | 1 | a0001c0001t0010g0208 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4966+1381T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258532 | ||||||
| chr5:177258541
|
G | GT | 13 | a0002c0002t0014g0073a0002c0002t0069g0107a0003c0006t0009g0013others(10): Show | 13 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.4966+1401dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | 177258541 | |||||
| chr5:177258541
|
G | T | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4966+1390G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258541 | ||||||
| chr5:177258683
|
A | G | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4967-1306A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177258683 | ||||||
| chr5:177259032
|
G | A | 3 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131 | 3 | HG02809.hp1 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4967-957G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259032 | ||||||
| chr5:177259115
|
T | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4967-874T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259115 | ||||||
| chr5:177259156
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4967-833C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259156 | ||||||
| chr5:177259801
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4967-188G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259801 | ||||||
| chr5:177259814
|
G | T | 10 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(7): Show | 10 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.4967-175G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259814 | ||||||
| chr5:177259829
|
T | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4967-160T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 13/22 | chr5 | 177259829 | ||||||
| chr5:177260252
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5146+84T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260252 | ||||||
| chr5:177260339
|
C | CT | 79 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.5146+196dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177260339 | |||||
| chr5:177260339
|
C | CTT | 8 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0011g0157others(5): Show | 8 | HG02055.hp2 HG02738.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.5146+195_5146+196d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177260339 | |||||
| chr5:177260339
|
CT | C | 19 | a0001c0001t0008g0188a0001c0005t0002g0015a0001c0005t0005g0014others(16): Show | 19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5146+196delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177260339 | |||||
| chr5:177260339
|
CTTTTTT | C | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.5146+191_5146+196d others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177260339 | |||||
| chr5:177260410
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5146+242A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260410 | ||||||
| chr5:177260411
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5146+243A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260411 | ||||||
| chr5:177260447
|
A | G | 1 | a0003c0006t0071g0159 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5146+279A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260447 | ||||||
| chr5:177260480
|
G | C | 1 | a0001c0011t0002g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5146+312G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260480 | ||||||
| chr5:177260595
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5146+427G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260595 | ||||||
| chr5:177260800
|
C | T | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.5146+632C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260800 | ||||||
| chr5:177260973
|
G | A | 1 | a0001c0004t0056g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5146+805G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177260973 | ||||||
| chr5:177261171
|
G | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5146+1003G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177261171 | ||||||
| chr5:177261236
|
A | AT | 12 | a0001c0003t0077g0108a0002c0002t0001g0028a0002c0002t0001g0031others(9): Show | 12 | HG00597.hp2 HG01109.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.5146+1092dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177261236 | |||||
| chr5:177261236
|
AT | A | 179 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(176): Show | 179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.5146+1092delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177261236 | |||||
| chr5:177261236
|
ATTTTTTT others(2): Show |
A | 20 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(17): Show | 20 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.5146+1084_5146+109 others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177261236 | |||||
| chr5:177261299
|
CT | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5146+1133delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177261299 | |||||
| chr5:177261781
|
C | G | 2 | a0002c0002t0014g0071a0002c0002t0014g0072 | 2 | NA18981.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.5146+1613C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177261781 | ||||||
| chr5:177261816
|
G | C | 1 | a0001c0003t0007g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5146+1648G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177261816 | ||||||
| chr5:177261935
|
G | A | 1 | a0001c0004t0012g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5146+1767G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177261935 | ||||||
| chr5:177262165
|
C | A | 112 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.5146+1997C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262165 | ||||||
| chr5:177262180
|
T | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5146+2012T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262180 | ||||||
| chr5:177262372
|
TG | T | 210 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.5146+2208delG | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177262372 | |||||
| chr5:177262605
|
G | A | 1 | a0002c0002t0003g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5146+2437G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262605 | ||||||
| chr5:177262693
|
A | G | 4 | a0001c0001t0004g0276a0001c0004t0002g0272a0013c0023t0013g0273others(1): Show | 4 | HG00597.hp1 HG02004.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.5146+2525A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262693 | ||||||
| chr5:177262700
|
G | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5146+2532G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262700 | ||||||
| chr5:177262746
|
G | A | 2 | a0002c0002t0001g0079a0002c0002t0001g0089 | 2 | HG02683.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.5146+2578G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262746 | ||||||
| chr5:177262894
|
G | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.5146+2726G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177262894 | ||||||
| chr5:177263009
|
CT | C | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.5146+2845delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177263009 | |||||
| chr5:177263177
|
T | C | 2 | a0002c0002t0001g0078a0002c0002t0014g0039 | 2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.5146+3009T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263177 | ||||||
| chr5:177263311
|
T | A | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5146+3143T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263311 | ||||||
| chr5:177263334
|
C | CAAAGACT others(10): Show |
1 | a0001c0005t0006g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5146+3167_5146+318 others(21): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177263334 | |||||
| chr5:177263345
|
G | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5146+3177G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263345 | ||||||
| chr5:177263399
|
A | G | 2 | a0001c0001t0010g0212a0001c0001t0010g0216 | 2 | NA18947.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.5146+3231A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263399 | ||||||
| chr5:177263432
|
T | C | 1 | a0001c0001t0011g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.5146+3264T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263432 | ||||||
| chr5:177263899
|
A | G | 2 | a0001c0001t0004g0240a0001c0001t0008g0151 | 2 | NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.5147-3663A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263899 | ||||||
| chr5:177263924
|
A | G | 1 | a0001c0001t0013g0234 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5147-3638A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177263924 | ||||||
| chr5:177264028
|
A | AT | 20 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0005t0006g0298others(17): Show | 20 | HG00408.hp2 HG00597.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.5147-3508dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATT | 17 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(14): Show | 17 | HG01515.hp2 HG01517.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.5147-3509_5147-350 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTT | 8 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0121others(5): Show | 8 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5147-3511_5147-350 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTT | 9 | a0001c0003t0002g0130a0001c0003t0027g0119a0001c0003t0028g0136others(6): Show | 9 | HG02572.hp1 HG02602.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.5147-3512_5147-350 others(9): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(1): Show |
7 | a0001c0001t0005g0295a0001c0001t0008g0174a0001c0001t0008g0183others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.5147-3515_5147-350 others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(2): Show |
28 | a0001c0001t0002g0293a0001c0001t0004g0187a0001c0001t0004g0196others(25): Show | 28 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.5147-3516_5147-350 others(13): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(3): Show |
30 | a0001c0001t0004g0202a0001c0001t0004g0209a0001c0001t0004g0269others(27): Show | 30 | HG00280.hp2 HG00408.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.5147-3517_5147-350 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(4): Show |
18 | a0001c0001t0004g0245a0001c0001t0004g0252a0001c0001t0004g0254others(15): Show | 18 | HG00423.hp2 HG00738.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.5147-3518_5147-350 others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0063g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5147-3519_5147-350 others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0002g0149a0016c0018t0004g0194 | 2 | HG01517.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.5147-3520_5147-350 others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0002g0288a0001c0001t0005g0207 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.5147-3521_5147-350 others(18): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(8): Show |
2 | a0001c0003t0049g0111a0004c0013t0001g0105 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.5147-3522_5147-350 others(19): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0002g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5147-3527_5147-350 others(24): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0012g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5147-3528_5147-350 others(25): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0002g0247 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5147-3532_5147-350 others(29): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0002g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5147-3508_5147-350 others(31): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(22): Show |
2 | a0001c0001t0002g0292a0001c0001t0011g0173 | 2 | HG01256.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.5147-3508_5147-350 others(33): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
A | ATTTTTTT others(30): Show |
1 | a0001c0001t0005g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5147-3508_5147-350 others(41): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
AT | A | 8 | a0001c0001t0033g0172a0001c0001t0055g0214a0002c0002t0001g0031others(5): Show | 8 | HG00323.hp2 HG01975.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.5147-3508delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
ATTT | A | 15 | a0001c0001t0012g0248a0001c0001t0078g0237a0003c0006t0009g0013others(12): Show | 15 | HG00733.hp1 HG01884.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.5147-3510_5147-350 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
ATTTT | A | 21 | a0001c0001t0004g0223a0001c0001t0004g0230a0001c0001t0008g0170others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.5147-3511_5147-350 others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
ATTTTTT | A | 13 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.5147-3513_5147-350 others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264028
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244 | 3 | HG02300.hp1 HG02683.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.5147-3517_5147-350 others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177264028 | |||||
| chr5:177264278
|
T | G | 155 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(152): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.5147-3284T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264278 | ||||||
| chr5:177264286
|
G | A | 2 | a0002c0002t0003g0038a0002c0002t0020g0001 | 2 | HG00099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.5147-3276G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264286 | ||||||
| chr5:177264483
|
C | T | 23 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(20): Show | 23 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.5147-3079C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264483 | ||||||
| chr5:177264510
|
A | G | 1 | a0002c0002t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5147-3052A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264510 | ||||||
| chr5:177264594
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5147-2968A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264594 | ||||||
| chr5:177264617
|
C | T | 1 | a0001c0003t0016g0114 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5147-2945C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264617 | ||||||
| chr5:177264693
|
A | C | 1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5147-2869A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264693 | ||||||
| chr5:177264745
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5147-2817A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264745 | ||||||
| chr5:177264747
|
C | T | 1 | a0002c0002t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5147-2815C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264747 | ||||||
| chr5:177264770
|
C | T | 2 | a0002c0002t0001g0094a0002c0002t0003g0088 | 2 | HG00673.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.5147-2792C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264770 | ||||||
| chr5:177264849
|
C | T | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.5147-2713C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177264849 | ||||||
| chr5:177265152
|
C | G | 1 | a0002c0002t0001g0042 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5147-2410C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265152 | ||||||
| chr5:177265277
|
T | TA | 12 | a0001c0001t0010g0208a0005c0007t0015g0003a0005c0007t0015g0004others(9): Show | 12 | HG02280.hp1 HG02630.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.5147-2274dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177265277 | |||||
| chr5:177265277
|
T | TAA | 10 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(7): Show | 10 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.5147-2275_5147-227 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr5 | 177265277 | |||||
| chr5:177265506
|
G | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5147-2056G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265506 | ||||||
| chr5:177265580
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5147-1982C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265580 | ||||||
| chr5:177265662
|
C | T | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5147-1900C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265662 | ||||||
| chr5:177265687
|
G | A | 1 | a0001c0001t0018g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5147-1875G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265687 | ||||||
| chr5:177265974
|
C | G | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5147-1588C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177265974 | ||||||
| chr5:177266015
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5147-1547C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266015 | ||||||
| chr5:177266053
|
G | T | 1 | a0002c0002t0001g0052 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.5147-1509G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266053 | ||||||
| chr5:177266079
|
C | G | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5147-1483C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266079 | ||||||
| chr5:177266574
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5147-988C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266574 | ||||||
| chr5:177266575
|
T | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5147-987T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266575 | ||||||
| chr5:177266640
|
A | G | 1 | a0002c0002t0069g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.5147-922A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266640 | ||||||
| chr5:177266676
|
G | A | 1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5147-886G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266676 | ||||||
| chr5:177266834
|
C | T | 180 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.5147-728C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266834 | ||||||
| chr5:177266887
|
G | A | 210 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.5147-675G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177266887 | ||||||
| chr5:177267106
|
C | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147-456C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177267106 | ||||||
| chr5:177267268
|
T | C | 16 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(13): Show | 16 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.5147-294T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177267268 | ||||||
| chr5:177267480
|
T | A | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5147-82T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177267480 | ||||||
| chr5:177267513
|
A | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147-49A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 14/22 | chr5 | 177267513 | ||||||
| chr5:177267831
|
T | G | 9 | a0001c0005t0005g0014a0001c0005t0005g0016a0001c0005t0005g0018others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.5303+113T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177267831 | ||||||
| chr5:177267835
|
CTCT | C | 4 | a0001c0001t0029g0285a0001c0001t0030g0282a0001c0001t0066g0283others(1): Show | 4 | HG02572.hp1 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.5303+125_5303+127d others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 177267835 | |||||
| chr5:177267953
|
GT | G | 201 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.5303+252delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr5 | 177267953 | |||||
| chr5:177268041
|
G | A | 1 | a0001c0001t0075g0184 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5303+323G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268041 | ||||||
| chr5:177268065
|
C | T | 1 | a0001c0004t0002g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5303+347C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268065 | ||||||
| chr5:177268424
|
A | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5303+706A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268424 | ||||||
| chr5:177268440
|
G | A | 3 | a0001c0001t0018g0191a0001c0001t0018g0192a0001c0001t0018g0238 | 3 | HG02717.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.5303+722G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268440 | ||||||
| chr5:177268777
|
A | G | 2 | a0001c0005t0002g0015a0001c0005t0005g0017 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5304-825A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268777 | ||||||
| chr5:177268833
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5304-769C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268833 | ||||||
| chr5:177268969
|
T | C | 4 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0127others(1): Show | 4 | HG01167.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5304-633T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177268969 | ||||||
| chr5:177269044
|
G | A | 1 | a0001c0003t0011g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5304-558G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269044 | ||||||
| chr5:177269089
|
G | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5304-513G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269089 | ||||||
| chr5:177269393
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5304-209G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269393 | ||||||
| chr5:177269412
|
T | G | 1 | a0001c0001t0002g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5304-190T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269412 | ||||||
| chr5:177269419
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5304-183A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269419 | ||||||
| chr5:177269573
|
G | T | 1 | a0002c0002t0069g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.5304-29G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 15/22 | chr5 | 177269573 | ||||||
| chr5:177270154
|
A | AGTCTT | 142 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(139): Show | 142 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.5509+379_5509+383d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177270154 | |||||
| chr5:177270154
|
A | AGTCTTGT others(3): Show |
54 | a0001c0001t0004g0187a0001c0001t0004g0223a0001c0001t0004g0230others(51): Show | 54 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.5509+374_5509+383d others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177270154 | |||||
| chr5:177270154
|
A | AGTCTTGT others(8): Show |
3 | a0001c0011t0002g0228a0004c0013t0001g0105a0004c0026t0003g0104 | 3 | HG02451.hp1 HG03654.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5509+369_5509+383d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177270154 | |||||
| chr5:177270320
|
T | C | 2 | a0002c0002t0001g0046a0002c0002t0001g0060 | 2 | NA18942.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.5509+513T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177270320 | ||||||
| chr5:177270651
|
T | C | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5509+844T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177270651 | ||||||
| chr5:177270843
|
C | T | 134 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(131): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.5509+1036C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177270843 | ||||||
| chr5:177270990
|
G | A | 1 | a0002c0002t0003g0002 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5509+1183G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177270990 | ||||||
| chr5:177272134
|
G | A | 1 | a0018c0019t0002g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5510-1538G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272134 | ||||||
| chr5:177272230
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5510-1442A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272230 | ||||||
| chr5:177272267
|
T | C | 212 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.5510-1405T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272267 | ||||||
| chr5:177272372
|
ACT | A | 3 | a0002c0002t0001g0094a0002c0002t0001g0098a0002c0002t0003g0088 | 3 | HG00673.hp2 NA18943.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.5510-1297_5510-129 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177272372 | |||||
| chr5:177272753
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5510-919C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272753 | ||||||
| chr5:177272810
|
A | G | 182 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.5510-862A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272810 | ||||||
| chr5:177272859
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5510-813A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177272859 | ||||||
| chr5:177273022
|
C | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5510-650C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177273022 | ||||||
| chr5:177273127
|
C | A | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5510-545C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177273127 | ||||||
| chr5:177273251
|
GGAA | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5510-414_5510-412d others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177273251 | |||||
| chr5:177273312
|
T | TA | 173 | a0001c0001t0004g0223a0001c0001t0006g0178a0001c0001t0006g0179others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.5510-339dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177273312 | |||||
| chr5:177273312
|
T | TAA | 108 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.5510-340_5510-339d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | 177273312 | |||||
| chr5:177273370
|
A | G | 1 | a0002c0002t0019g0086 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5510-302A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177273370 | ||||||
| chr5:177273525
|
G | A | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5510-147G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177273525 | ||||||
| chr5:177273560
|
G | A | 4 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0127others(1): Show | 4 | HG01167.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5510-112G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 16/22 | chr5 | 177273560 | ||||||
| chr5:177273831
|
A | G | 1 | a0003c0006t0009g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5622+47A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177273831 | ||||||
| chr5:177273884
|
G | A | 140 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.5622+100G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177273884 | ||||||
| chr5:177273971
|
C | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5622+187C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177273971 | ||||||
| chr5:177273976
|
C | T | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5622+192C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177273976 | ||||||
| chr5:177273980
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5622+196C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177273980 | ||||||
| chr5:177274149
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5622+365G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274149 | ||||||
| chr5:177274394
|
G | A | 5 | a0001c0001t0004g0196a0001c0001t0008g0174a0001c0001t0013g0177others(2): Show | 5 | HG01081.hp2 HG01106.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.5622+610G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274394 | ||||||
| chr5:177274523
|
A | G | 1 | a0004c0026t0003g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5622+739A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274523 | ||||||
| chr5:177274542
|
A | G | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5622+758A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274542 | ||||||
| chr5:177274697
|
T | TTG | 34 | a0001c0001t0002g0205a0001c0001t0002g0292a0001c0001t0005g0148others(31): Show | 34 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.5622+943_5622+944d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274697
|
T | TTGTG | 3 | a0001c0004t0035g0233a0002c0002t0022g0087a0003c0006t0009g0164 | 3 | HG01167.hp2 HG03516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5622+941_5622+944d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274697
|
T | TTGTGTG | 9 | a0001c0001t0005g0147a0001c0005t0005g0014a0001c0005t0005g0018others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.5622+939_5622+944d others(8): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274697
|
T | TTGTGTGT others(1): Show |
13 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(10): Show | 13 | HG01515.hp2 HG01517.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.5622+937_5622+944d others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274697
|
TTG | T | 7 | a0001c0001t0018g0191a0001c0004t0002g0226a0002c0002t0001g0090others(4): Show | 7 | HG01106.hp1 HG02074.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5622+943_5622+944d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274697
|
TTGTGTGT others(1): Show |
T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5622+937_5622+944d others(10): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177274697 | |||||
| chr5:177274849
|
G | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5622+1065G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274849 | ||||||
| chr5:177274859
|
G | A | 2 | a0005c0007t0015g0004a0005c0007t0015g0005 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5622+1075G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274859 | ||||||
| chr5:177274980
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5622+1196C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177274980 | ||||||
| chr5:177275051
|
G | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5622+1267G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275051 | ||||||
| chr5:177275095
|
G | A | 1 | a0001c0005t0002g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5622+1311G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275095 | ||||||
| chr5:177275212
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5622+1428T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275212 | ||||||
| chr5:177275336
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5622+1552C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275336 | ||||||
| chr5:177275363
|
G | A | 1 | a0001c0001t0036g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5622+1579G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275363 | ||||||
| chr5:177275435
|
C | CT | 127 | a0001c0001t0002g0249a0001c0001t0004g0196a0001c0001t0004g0202others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.5622+1677dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177275435 | |||||
| chr5:177275435
|
C | CTT | 38 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.5622+1676_5622+167 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177275435 | |||||
| chr5:177275435
|
C | CTTT | 16 | a0001c0001t0012g0161a0001c0001t0026g0246a0001c0005t0002g0015others(13): Show | 16 | HG02451.hp2 HG02486.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.5622+1675_5622+167 others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177275435 | |||||
| chr5:177275435
|
CT | C | 13 | a0002c0002t0076g0035a0003c0006t0009g0013a0003c0006t0009g0158others(10): Show | 13 | HG00733.hp1 HG01256.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.5622+1677delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177275435 | |||||
| chr5:177275745
|
T | C | 140 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.5622+1961T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275745 | ||||||
| chr5:177275832
|
G | T | 212 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(209): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.5622+2048G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275832 | ||||||
| chr5:177275851
|
A | G | 1 | a0003c0006t0009g0163 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5622+2067A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177275851 | ||||||
| chr5:177276019
|
G | A | 2 | a0002c0002t0003g0100a0002c0002t0003g0106 | 2 | NA18949.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.5622+2235G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276019 | ||||||
| chr5:177276031
|
C | T | 1 | a0002c0002t0003g0002 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5622+2247C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276031 | ||||||
| chr5:177276086
|
C | T | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5622+2302C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276086 | ||||||
| chr5:177276577
|
C | T | 2 | a0001c0001t0008g0188a0001c0001t0008g0189 | 2 | HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.5622+2793C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276577 | ||||||
| chr5:177276583
|
C | T | 1 | a0002c0002t0014g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5622+2799C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276583 | ||||||
| chr5:177276603
|
G | A | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5622+2819G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276603 | ||||||
| chr5:177276650
|
C | A | 1 | a0001c0001t0006g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5622+2866C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276650 | ||||||
| chr5:177276990
|
C | A | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.5622+3206C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177276990 | ||||||
| chr5:177277024
|
A | G | 1 | a0001c0004t0012g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5622+3240A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277024 | ||||||
| chr5:177277128
|
AT | A | 25 | a0001c0001t0011g0173a0001c0001t0017g0294a0001c0001t0023g0181others(22): Show | 25 | HG00733.hp1 HG01256.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.5622+3361delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177277128 | |||||
| chr5:177277299
|
T | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5623-3266T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277299 | ||||||
| chr5:177277378
|
A | G | 1 | a0002c0002t0003g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5623-3187A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277378 | ||||||
| chr5:177277456
|
G | A | 182 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.5623-3109G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277456 | ||||||
| chr5:177277473
|
T | G | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.5623-3092T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277473 | ||||||
| chr5:177277488
|
C | T | 1 | a0001c0001t0075g0184 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5623-3077C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277488 | ||||||
| chr5:177277624
|
G | A | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5623-2941G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277624 | ||||||
| chr5:177277662
|
T | A | 140 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.5623-2903T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277662 | ||||||
| chr5:177277677
|
G | A | 1 | a0002c0002t0003g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5623-2888G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277677 | ||||||
| chr5:177277715
|
GA | G | 22 | a0001c0004t0006g0225a0003c0006t0009g0013a0003c0006t0009g0158others(19): Show | 22 | HG00733.hp1 HG01069.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.5623-2839delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177277715 | |||||
| chr5:177277795
|
T | C | 1 | a0002c0034t0047g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5623-2770T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277795 | ||||||
| chr5:177277868
|
G | T | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5623-2697G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277868 | ||||||
| chr5:177277996
|
G | A | 3 | a0001c0001t0004g0187a0001c0001t0004g0254a0001c0001t0004g0256 | 3 | NA18985.hp2 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.5623-2569G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177277996 | ||||||
| chr5:177278243
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5623-2322A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278243 | ||||||
| chr5:177278674
|
G | A | 1 | a0002c0002t0022g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.5623-1891G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278674 | ||||||
| chr5:177278770
|
A | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5623-1795A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278770 | ||||||
| chr5:177278864
|
C | G | 1 | a0001c0004t0002g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5623-1701C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278864 | ||||||
| chr5:177278865
|
A | T | 1 | a0002c0002t0003g0106 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5623-1700A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278865 | ||||||
| chr5:177278873
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5623-1692A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278873 | ||||||
| chr5:177278974
|
A | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5623-1591A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177278974 | ||||||
| chr5:177279042
|
C | T | 1 | a0001c0022t0011g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5623-1523C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279042 | ||||||
| chr5:177279131
|
G | T | 2 | a0001c0003t0007g0132a0001c0003t0068g0137 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.5623-1434G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279131 | ||||||
| chr5:177279203
|
C | T | 1 | a0001c0001t0004g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.5623-1362C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279203 | ||||||
| chr5:177279238
|
T | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5623-1327T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279238 | ||||||
| chr5:177279370
|
T | C | 1 | a0001c0005t0005g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5623-1195T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279370 | ||||||
| chr5:177279413
|
G | A | 2 | a0003c0006t0009g0164a0003c0006t0009g0167 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.5623-1152G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279413 | ||||||
| chr5:177279597
|
A | C | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5623-968A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279597 | ||||||
| chr5:177279609
|
A | ATT | 9 | a0001c0003t0007g0112a0001c0003t0007g0123a0001c0003t0007g0124others(6): Show | 9 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.5623-956_5623-955i others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279609 | ||||||
| chr5:177279609
|
A | ATTT | 4 | a0001c0003t0002g0133a0001c0003t0007g0113a0001c0003t0007g0128others(1): Show | 4 | HG01167.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.5623-956_5623-955i others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279609 | ||||||
| chr5:177279610
|
A | AT | 62 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.5623-927dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
A | ATT | 76 | a0001c0001t0002g0293a0001c0001t0004g0187a0001c0001t0004g0196others(73): Show | 76 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.5623-928_5623-927d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
A | ATTT | 26 | a0001c0001t0004g0202a0001c0001t0004g0252a0001c0001t0005g0241others(23): Show | 26 | HG00423.hp2 HG01175.hp1 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.5623-929_5623-927d others(5): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
A | ATTTT | 11 | a0001c0001t0059g0218a0001c0005t0002g0015a0001c0005t0005g0016others(8): Show | 11 | HG00609.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.5623-930_5623-927d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
A | ATTTTT | 9 | a0001c0001t0002g0292a0001c0005t0005g0014a0001c0005t0006g0022others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.5623-931_5623-927d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
A | T | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.5623-955A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279610 | ||||||
| chr5:177279610
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5623-938_5623-927d others(14): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
ATTTTTTT others(6): Show |
A | 20 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(17): Show | 20 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.5623-939_5623-927d others(15): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279610
|
ATTTTTTT others(7): Show |
A | 1 | a0005c0007t0015g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5623-940_5623-927d others(16): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279610 | |||||
| chr5:177279624
|
T | A | 20 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(17): Show | 20 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.5623-941T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279624 | ||||||
| chr5:177279625
|
T | A | 1 | a0005c0007t0015g0004 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5623-940T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279625 | ||||||
| chr5:177279644
|
G | A | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5623-921G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279644 | ||||||
| chr5:177279652
|
G | A | 1 | a0001c0001t0017g0213 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5623-913G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279652 | ||||||
| chr5:177279683
|
C | T | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5623-882C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279683 | ||||||
| chr5:177279798
|
G | T | 216 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.5623-767G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279798 | ||||||
| chr5:177279949
|
T | A | 1 | a0003c0006t0009g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5623-616T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177279949 | ||||||
| chr5:177279961
|
A | ATATTT | 41 | a0001c0001t0013g0234a0001c0001t0017g0213a0001c0001t0018g0191others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.5623-552_5623-548d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
A | ATATTTTA others(3): Show |
9 | a0001c0001t0018g0192a0001c0001t0024g0156a0001c0001t0045g0287others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.5623-557_5623-548d others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
A | ATATTTTA others(8): Show |
2 | a0001c0003t0002g0130a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5623-562_5623-548d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
ATATTT | A | 23 | a0001c0001t0004g0223a0001c0001t0005g0147a0001c0001t0005g0148others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.5623-552_5623-548d others(7): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
ATATTTTA others(3): Show |
A | 19 | a0001c0001t0002g0149a0001c0001t0005g0207a0001c0004t0011g0219others(16): Show | 19 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.5623-557_5623-548d others(12): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
ATATTTTA others(8): Show |
A | 18 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0205others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.5623-562_5623-548d others(17): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
ATATTTTA others(13): Show |
A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5623-567_5623-548d others(22): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177279961
|
ATATTTTA others(18): Show |
A | 19 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(16): Show | 19 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.5623-572_5623-548d others(27): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | 177279961 | |||||
| chr5:177280014
|
T | A | 1 | a0001c0004t0006g0224 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.5623-551T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177280014 | ||||||
| chr5:177280038
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.5623-527C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177280038 | ||||||
| chr5:177280543
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5623-22G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 17/22 | chr5 | 177280543 | ||||||
| chr5:177280869
|
T | G | 1 | a0002c0027t0001g0099 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5892+35T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177280869 | ||||||
| chr5:177280995
|
G | A | 1 | a0001c0009t0032g0258 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5892+161G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177280995 | ||||||
| chr5:177281333
|
C | CT | 173 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(170): Show | 173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.5892+513dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr5 | 177281333 | |||||
| chr5:177281333
|
C | CTT | 15 | a0001c0001t0044g0253a0001c0003t0007g0134a0001c0003t0016g0114others(12): Show | 15 | HG02559.hp1 HG02572.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.5892+512_5892+513d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr5 | 177281333 | |||||
| chr5:177281347
|
TAATA | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5892+516_5892+519d others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr5 | 177281347 | |||||
| chr5:177281352
|
A | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5892+518A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281352 | ||||||
| chr5:177281403
|
G | A | 1 | a0002c0002t0003g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5892+569G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281403 | ||||||
| chr5:177281412
|
T | C | 1 | a0001c0001t0004g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5892+578T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281412 | ||||||
| chr5:177281522
|
A | G | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5892+688A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281522 | ||||||
| chr5:177281692
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5893-773G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281692 | ||||||
| chr5:177281717
|
A | G | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5893-748A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281717 | ||||||
| chr5:177281883
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.5893-582G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177281883 | ||||||
| chr5:177282118
|
C | T | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.5893-347C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177282118 | ||||||
| chr5:177282148
|
G | C | 5 | a0001c0009t0002g0257a0001c0009t0006g0168a0001c0009t0006g0222others(2): Show | 5 | HG02071.hp2 HG02602.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.5893-317G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177282148 | ||||||
| chr5:177282332
|
G | A | 3 | a0001c0001t0004g0202a0001c0001t0004g0209a0001c0001t0048g0198 | 3 | HG00280.hp2 HG00738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.5893-133G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177282332 | ||||||
| chr5:177282395
|
A | T | 1 | a0002c0002t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5893-70A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 18/22 | chr5 | 177282395 | ||||||
| chr5:177282901
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6009+320G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177282901 | ||||||
| chr5:177282960
|
T | A | 2 | a0001c0003t0007g0123a0001c0003t0011g0135 | 2 | HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6009+379T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177282960 | ||||||
| chr5:177282961
|
A | T | 8 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0124others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.6009+380A>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177282961 | ||||||
| chr5:177283005
|
G | A | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.6009+424G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283005 | ||||||
| chr5:177283064
|
C | G | 216 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.6009+483C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283064 | ||||||
| chr5:177283079
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6009+498A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283079 | ||||||
| chr5:177283110
|
C | T | 30 | a0001c0003t0002g0130a0001c0003t0002g0133a0001c0003t0007g0112others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.6009+529C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283110 | ||||||
| chr5:177283114
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.6009+533C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283114 | ||||||
| chr5:177283206
|
G | A | 2 | a0001c0001t0018g0191a0001c0001t0018g0192 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.6010-581G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283206 | ||||||
| chr5:177283337
|
A | C | 1 | a0002c0002t0022g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6010-450A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283337 | ||||||
| chr5:177283340
|
TC | T | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.6010-445delC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | 177283340 | |||||
| chr5:177283546
|
C | G | 213 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(210): Show | 213 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.6010-241C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283546 | ||||||
| chr5:177283546
|
C | T | 3 | a0001c0001t0004g0202a0001c0001t0004g0209a0001c0001t0048g0198 | 3 | HG00280.hp2 HG00738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.6010-241C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283546 | ||||||
| chr5:177283625
|
T | G | 4 | a0001c0003t0002g0130a0008c0015t0002g0116a0008c0015t0002g0131others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.6010-162T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283625 | ||||||
| chr5:177283683
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6010-104G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283683 | ||||||
| chr5:177283726
|
A | C | 1 | a0001c0001t0005g0241 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6010-61A>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 19/22 | chr5 | 177283726 | ||||||
| chr5:177284003
|
G | T | 1 | a0001c0004t0012g0259 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.6151+75G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284003 | ||||||
| chr5:177284065
|
G | A | 5 | a0002c0002t0022g0087a0006c0008t0021g0142a0006c0008t0021g0143others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6151+137G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284065 | ||||||
| chr5:177284149
|
A | G | 1 | a0001c0003t0077g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6151+221A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284149 | ||||||
| chr5:177284215
|
A | G | 6 | a0001c0003t0016g0117a0001c0003t0016g0118a0001c0003t0027g0119others(3): Show | 6 | HG02559.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.6151+287A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284215 | ||||||
| chr5:177284237
|
C | T | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6151+309C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284237 | ||||||
| chr5:177284455
|
G | GT | 9 | a0001c0001t0004g0240a0001c0001t0012g0248a0001c0001t0029g0285others(6): Show | 9 | HG02135.hp1 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.6151+537dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177284455 | |||||
| chr5:177284616
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6151+688G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284616 | ||||||
| chr5:177284651
|
A | G | 3 | a0001c0005t0005g0016a0001c0005t0005g0018a0001c0005t0006g0021 | 3 | HG02615.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6151+723A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284651 | ||||||
| chr5:177284818
|
C | T | 1 | a0003c0006t0009g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6151+890C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284818 | ||||||
| chr5:177284881
|
C | T | 11 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(8): Show | 11 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.6151+953C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177284881 | ||||||
| chr5:177285228
|
C | T | 1 | a0009c0012t0061g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6151+1300C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285228 | ||||||
| chr5:177285297
|
T | C | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6151+1369T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285297 | ||||||
| chr5:177285345
|
C | T | 2 | a0001c0003t0016g0114a0010c0025t0028g0115 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.6151+1417C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285345 | ||||||
| chr5:177285415
|
T | C | 2 | a0001c0005t0006g0019a0001c0005t0057g0020 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6151+1487T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285415 | ||||||
| chr5:177285421
|
G | A | 1 | a0003c0006t0009g0164 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6151+1493G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285421 | ||||||
| chr5:177285481
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6151+1553G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285481 | ||||||
| chr5:177285519
|
G | A | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.6151+1591G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285519 | ||||||
| chr5:177285523
|
C | T | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6151+1595C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285523 | ||||||
| chr5:177285559
|
A | G | 1 | a0001c0001t0034g0290 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6151+1631A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285559 | ||||||
| chr5:177285563
|
C | CA | 141 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.6151+1659dupA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177285563 | |||||
| chr5:177285563
|
C | CAA | 25 | a0001c0001t0005g0242a0001c0001t0006g0179a0001c0001t0010g0212others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.6151+1658_6151+165 others(6): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177285563 | |||||
| chr5:177285563
|
CA | C | 17 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(14): Show | 17 | HG00323.hp2 HG01256.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.6151+1659delA | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177285563 | |||||
| chr5:177285563
|
CAAAAAAA | C | 20 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0163others(17): Show | 20 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.6151+1653_6151+165 others(11): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177285563 | |||||
| chr5:177285619
|
C | CAAGAAAG others(315): Show |
1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6151+1711_6151+171 others(326): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177285619 | |||||
| chr5:177285641
|
A | G | 1 | a0002c0002t0001g0042 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.6151+1713A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177285641 | ||||||
| chr5:177286061
|
A | G | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6151+2133A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286061 | ||||||
| chr5:177286157
|
C | A | 1 | a0002c0002t0003g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6151+2229C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286157 | ||||||
| chr5:177286292
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6151+2364A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286292 | ||||||
| chr5:177286304
|
C | T | 1 | a0001c0001t0010g0186 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6151+2376C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286304 | ||||||
| chr5:177286335
|
A | G | 2 | a0003c0006t0009g0164a0003c0006t0009g0167 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.6151+2407A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286335 | ||||||
| chr5:177286366
|
C | T | 1 | a0001c0001t0023g0150 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6151+2438C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286366 | ||||||
| chr5:177286465
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6152-2354A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286465 | ||||||
| chr5:177286497
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6152-2322C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286497 | ||||||
| chr5:177286574
|
C | A | 1 | a0002c0002t0022g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6152-2245C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286574 | ||||||
| chr5:177286633
|
T | G | 3 | a0001c0001t0023g0150a0001c0001t0072g0152a0001c0001t0073g0251 | 3 | NA18967.hp1 NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.6152-2186T>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286633 | ||||||
| chr5:177286854
|
G | T | 1 | a0002c0002t0001g0034 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6152-1965G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286854 | ||||||
| chr5:177286935
|
A | G | 1 | a0001c0024t0002g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6152-1884A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177286935 | ||||||
| chr5:177287231
|
G | A | 1 | a0001c0001t0004g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6152-1588G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287231 | ||||||
| chr5:177287366
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6152-1453C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287366 | ||||||
| chr5:177287465
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6152-1354G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287465 | ||||||
| chr5:177287568
|
G | A | 216 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.6152-1251G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287568 | ||||||
| chr5:177287630
|
C | T | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6152-1189C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287630 | ||||||
| chr5:177287737
|
G | A | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6152-1082G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287737 | ||||||
| chr5:177287837
|
G | A | 1 | a0002c0002t0001g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.6152-982G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287837 | ||||||
| chr5:177287931
|
C | G | 140 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.6152-888C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287931 | ||||||
| chr5:177287942
|
T | C | 216 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(213): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.6152-877T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287942 | ||||||
| chr5:177287984
|
T | A | 3 | a0004c0013t0001g0105a0004c0013t0020g0103a0004c0026t0003g0104 | 3 | HG02451.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.6152-835T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177287984 | ||||||
| chr5:177288110
|
T | C | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.6152-709T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | chr5 | 177288110 | ||||||
| chr5:177288172
|
AAG | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6152-641_6152-640d others(4): Show |
NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | 177288172 | |||||
| chr5:177289158
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6258+233A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289158 | ||||||
| chr5:177289181
|
C | T | 1 | a0001c0003t0049g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6258+256C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289181 | ||||||
| chr5:177289347
|
A | G | 4 | a0001c0001t0011g0157a0001c0001t0011g0236a0001c0001t0078g0237others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.6258+422A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289347 | ||||||
| chr5:177289527
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6258+602G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289527 | ||||||
| chr5:177289658
|
C | T | 4 | a0006c0008t0021g0142a0006c0008t0021g0143a0006c0008t0021g0145others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.6258+733C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289658 | ||||||
| chr5:177289834
|
G | GT | 26 | a0001c0003t0007g0112a0001c0003t0007g0122a0001c0003t0007g0124others(23): Show | 26 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.6258+920dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr5 | 177289834 | |||||
| chr5:177289834
|
GT | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6258+920delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr5 | 177289834 | |||||
| chr5:177289866
|
T | A | 1 | a0002c0002t0042g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6258+941T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289866 | ||||||
| chr5:177289883
|
A | G | 1 | a0002c0002t0042g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6258+958A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289883 | ||||||
| chr5:177289891
|
A | G | 1 | a0002c0002t0003g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6258+966A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289891 | ||||||
| chr5:177289963
|
A | G | 1 | a0002c0002t0001g0061 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6258+1038A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289963 | ||||||
| chr5:177289976
|
C | T | 130 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(127): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.6258+1051C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289976 | ||||||
| chr5:177289984
|
T | C | 1 | a0001c0004t0012g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6258+1059T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177289984 | ||||||
| chr5:177290035
|
A | G | 3 | a0002c0002t0001g0056a0002c0002t0003g0055a0008c0015t0002g0116 | 3 | HG01928.hp2 HG01975.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.6258+1110A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290035 | ||||||
| chr5:177290042
|
T | A | 1 | a0001c0001t0008g0193 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.6258+1117T>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290042 | ||||||
| chr5:177290045
|
G | C | 1 | a0002c0002t0001g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.6258+1120G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290045 | ||||||
| chr5:177290079
|
T | C | 2 | a0002c0016t0003g0068a0002c0016t0040g0069 | 2 | HG02165.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.6258+1154T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290079 | ||||||
| chr5:177290080
|
A | G | 2 | a0002c0016t0003g0068a0002c0016t0040g0069 | 2 | HG02165.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.6258+1155A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290080 | ||||||
| chr5:177290095
|
T | C | 1 | a0002c0002t0020g0049 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.6258+1170T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290095 | ||||||
| chr5:177290117
|
T | C | 18 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.6258+1192T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290117 | ||||||
| chr5:177290118
|
G | A | 18 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.6258+1193G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290118 | ||||||
| chr5:177290119
|
T | C | 18 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.6258+1194T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290119 | ||||||
| chr5:177290173
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.6258+1248C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290173 | ||||||
| chr5:177290408
|
A | AT | 84 | a0001c0001t0004g0187a0001c0001t0004g0202a0001c0001t0004g0209others(81): Show | 84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.6258+1500dupT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr5 | 177290408 | |||||
| chr5:177290408
|
AT | A | 35 | a0001c0003t0007g0122a0001c0003t0016g0114a0001c0003t0016g0117others(32): Show | 35 | HG00733.hp1 HG01070.hp2 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.6258+1500delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr5 | 177290408 | |||||
| chr5:177290431
|
G | A | 1 | a0001c0003t0052g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6258+1506G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290431 | ||||||
| chr5:177290638
|
A | AC | 21 | a0001c0005t0002g0007a0001c0005t0002g0015a0001c0005t0005g0008others(18): Show | 21 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.6259-1314dupC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr5 | 177290638 | |||||
| chr5:177290771
|
A | G | 3 | a0001c0005t0005g0014a0001c0005t0006g0022a0001c0005t0038g0025 | 3 | HG02451.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.6259-1183A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290771 | ||||||
| chr5:177290905
|
T | C | 1 | a0004c0013t0001g0105 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6259-1049T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290905 | ||||||
| chr5:177290970
|
G | C | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6259-984G>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177290970 | ||||||
| chr5:177291302
|
A | G | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6259-652A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291302 | ||||||
| chr5:177291309
|
T | C | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6259-645T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291309 | ||||||
| chr5:177291360
|
A | G | 162 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(159): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.6259-594A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291360 | ||||||
| chr5:177291481
|
C | T | 1 | a0001c0001t0005g0242 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6259-473C>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291481 | ||||||
| chr5:177291718
|
T | C | 2 | a0005c0007t0015g0003a0005c0007t0015g0006 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6259-236T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291718 | ||||||
| chr5:177291895
|
G | A | 3 | a0001c0003t0028g0136a0004c0013t0001g0105a0004c0026t0003g0104 | 3 | HG02451.hp1 HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6259-59G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 21/22 | chr5 | 177291895 | ||||||
| chr5:177292191
|
G | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6463+33G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292191 | ||||||
| chr5:177292338
|
T | C | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6463+180T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292338 | ||||||
| chr5:177292354
|
G | A | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6463+196G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292354 | ||||||
| chr5:177292500
|
G | T | 17 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(14): Show | 17 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.6463+342G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292500 | ||||||
| chr5:177292535
|
C | G | 15 | a0001c0003t0002g0133a0001c0003t0007g0112a0001c0003t0007g0113others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.6463+377C>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292535 | ||||||
| chr5:177292758
|
C | A | 1 | a0004c0029t0065g0146 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6463+600C>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177292758 | ||||||
| chr5:177293121
|
G | A | 4 | a0005c0007t0015g0003a0005c0007t0015g0004a0005c0007t0015g0005others(1): Show | 4 | HG02818.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6464-711G>A | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293121 | ||||||
| chr5:177293387
|
T | C | 1 | a0002c0002t0001g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.6464-445T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293387 | ||||||
| chr5:177293480
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6464-352A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293480 | ||||||
| chr5:177293502
|
T | C | 1 | a0012c0032t0011g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6464-330T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293502 | ||||||
| chr5:177293512
|
A | G | 21 | a0003c0006t0009g0013a0003c0006t0009g0158a0003c0006t0009g0160others(18): Show | 21 | HG00733.hp1 HG02015.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.6464-320A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293512 | ||||||
| chr5:177293534
|
G | GC | 114 | a0001c0001t0002g0149a0001c0001t0002g0292a0001c0001t0004g0202others(111): Show | 114 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.6464-290dupC | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | 177293534 | |||||
| chr5:177293542
|
CT | C | 11 | a0001c0001t0026g0201a0001c0001t0026g0246a0001c0001t0046g0244others(8): Show | 11 | HG02300.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.6464-289delT | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293542 | ||||||
| chr5:177293543
|
T | C | 7 | a0001c0003t0050g0110a0001c0003t0051g0120a0006c0008t0021g0142others(4): Show | 7 | HG02630.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.6464-289T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293543 | ||||||
| chr5:177293671
|
A | G | 2 | a0009c0012t0060g0141a0009c0012t0061g0140 | 2 | HG02280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.6464-161A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293671 | ||||||
| chr5:177293765
|
A | G | 112 | a0001c0001t0002g0149a0001c0001t0002g0203a0001c0001t0002g0204others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.6464-67A>G | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293765 | ||||||
| chr5:177293824
|
G | T | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.6464-8G>T | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293824 | ||||||
| chr5:177293827
|
T | C | 1 | a0004c0013t0020g0103 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.6464-5T>C | NSD1 | ENSG00000165671.22 | transcript | ENST00000439151.7 | protein_coding | 22/22 | chr5 | 177293827 |