Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 165324 |
|---|---|
| ensemblid | ENSG00000173960.14 |
| hgncid | 27265 |
| symbol | UBXN2A |
| name | UBX domain protein 2A |
| refseq_nuc | NM_181713.4 |
| refseq_prot | NP_859064.2 |
| ensembl_nuc | ENST00000309033.5 |
| ensembl_prot | ENSP00000312107.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 23940463 |
| end | 24004909 |
| strand | + |
| ver | v1.2 |
| region | chr2:23940463-24004909 |
| region5000 | chr2:23935463-24009909 |
| regionname0 | UBXN2A_chr2_23940463_24004909 |
| regionname5000 | UBXN2A_chr2_23935463_24009909 |
| 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 | 259 | 246 | 67 | 54 | 74 | 16 | 33 | 56 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0002 | 0/0 | 259 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0003 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0004 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0005 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| 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 | 1/1 | 780 | 246 | 67 | 54 | 74 | 16 | 33 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| c0002 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| c0003 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| c0004 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| c0005 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| 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 | 5242 | 61 | 10 | 13 | 24 | 4 | 10 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0002 | 1/1 | 5243 | 40 | 6 | 5 | 19 | 3 | 5 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0003 | 0/0 | 5244 | 17 | 2 | 6 | 5 | 0 | 4 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0004 | 0/0 | 5241 | 15 | 0 | 6 | 6 | 1 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0005 | 0/0 | 5243 | 14 | 13 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0006 | 0/0 | 5240 | 9 | 8 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0007 | 0/0 | 5242 | 9 | 9 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0008 | 0/0 | 5242 | 8 | 0 | 5 | 1 | 1 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0009 | 0/0 | 5241 | 8 | 2 | 2 | 2 | 1 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0010 | 0/0 | 5243 | 6 | 2 | 3 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0011 | 0/0 | 5242 | 6 | 0 | 2 | 0 | 2 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0012 | 0/0 | 5242 | 4 | 0 | 0 | 4 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0013 | 0/0 | 5242 | 4 | 1 | 1 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0014 | 0/0 | 5240 | 4 | 0 | 2 | 1 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0015 | 0/0 | 5243 | 3 | 2 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0016 | 0/0 | 5244 | 3 | 0 | 0 | 0 | 0 | 3 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0017 | 0/0 | 5243 | 3 | 0 | 1 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0018 | 0/0 | 5243 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0019 | 0/0 | 5242 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0020 | 0/0 | 5243 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0021 | 0/0 | 5245 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0022 | 0/0 | 5243 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0023 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0024 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0025 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0026 | 0/0 | 5244 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0027 | 0/0 | 5244 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0028 | 0/0 | 5242 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0029 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0030 | 0/0 | 5243 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0031 | 0/0 | 5241 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0032 | 0/0 | 5242 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0033 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0034 | 0/0 | 5242 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0035 | 0/0 | 5242 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0036 | 0/0 | 5242 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0037 | 0/0 | 5245 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0038 | 0/0 | 5244 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0039 | 0/0 | 5242 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0040 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0041 | 0/0 | 5243 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0042 | 0/0 | 5241 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0043 | 0/0 | 5241 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0044 | 0/0 | 5239 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0045 | 0/0 | 5240 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0046 | 0/0 | 5243 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0047 | 0/0 | 5244 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| t0048 | 0/0 | 5243 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| 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 | 1/1 | 780 | 246 | 67 | 54 | 74 | 16 | 33 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0002c0002 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0003c0004 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0004c0003 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0005c0005 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6021 | 60 | 9 | 13 | 24 | 4 | 10 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0002 | 1/1 | 6022 | 39 | 6 | 5 | 19 | 3 | 4 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0003 | 0/0 | 6023 | 17 | 2 | 6 | 5 | 0 | 4 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0004 | 0/0 | 6020 | 15 | 0 | 6 | 6 | 1 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0005 | 0/0 | 6022 | 14 | 13 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0006 | 0/0 | 6019 | 8 | 7 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0007 | 0/0 | 6021 | 9 | 9 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0008 | 0/0 | 6021 | 8 | 0 | 5 | 1 | 1 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0009 | 0/0 | 6020 | 8 | 2 | 2 | 2 | 1 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0010 | 0/0 | 6022 | 6 | 2 | 3 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0011 | 0/0 | 6021 | 6 | 0 | 2 | 0 | 2 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0012 | 0/0 | 6021 | 4 | 0 | 0 | 4 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0013 | 0/0 | 6021 | 4 | 1 | 1 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0014 | 0/0 | 6019 | 4 | 0 | 2 | 1 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0015 | 0/0 | 6022 | 3 | 2 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0016 | 0/0 | 6023 | 3 | 0 | 0 | 0 | 0 | 3 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0017 | 0/0 | 6022 | 3 | 0 | 1 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0018 | 0/0 | 6022 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0019 | 0/0 | 6021 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0020 | 0/0 | 6022 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0021 | 0/0 | 6024 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0022 | 0/0 | 6022 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0023 | 0/0 | 6022 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0024 | 0/0 | 6021 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0026 | 0/0 | 6023 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0027 | 0/0 | 6023 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0028 | 0/0 | 6021 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0029 | 0/0 | 6021 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0030 | 0/0 | 6022 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0031 | 0/0 | 6020 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0032 | 0/0 | 6021 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0033 | 0/0 | 6021 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0034 | 0/0 | 6021 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0035 | 0/0 | 6021 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0036 | 0/0 | 6021 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0037 | 0/0 | 6024 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0038 | 0/0 | 6023 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0039 | 0/0 | 6021 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0040 | 0/0 | 6022 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0041 | 0/0 | 6022 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0042 | 0/0 | 6020 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0043 | 0/0 | 6020 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0044 | 0/0 | 6018 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0045 | 0/0 | 6019 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0046 | 0/0 | 6022 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0047 | 0/0 | 6023 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0001c0001t0048 | 0/0 | 6022 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0002c0002t0002 | 0/0 | 6022 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0003c0004t0025 | 0/0 | 6022 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0004c0003t0001 | 0/0 | 6021 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| a0005c0005t0006 | 0/0 | 6019 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | copy fasta | chr2 | 23935463 | 24009909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0014g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0016g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0016g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0017g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0017g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0018g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0019g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0019g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0021g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0021g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0022g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0022g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0023g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0024g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0026g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0028g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0029g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0031g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0032g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0033g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0034g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0035g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0036g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0037g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0038g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0039g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0040g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0041g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0042g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0043g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0044g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0045g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0046g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0047g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0001c0001t0048g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0003c0004t0025g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0004c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| a0005c0005t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | GBR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0190 | EUR | GBR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00140 | hp2 | a0001 | c0001 | t0046 | g0184 | EUR | GBR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | FIN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0117 | EUR | FIN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00323 | hp2 | a0001 | c0001 | t0044 | g0181 | EUR | FIN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00735 | hp2 | a0001 | c0001 | t0011 | g0185 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0145 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0033 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01069 | hp2 | a0001 | c0001 | t0014 | g0189 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0142 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01070 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0192 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0113 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0186 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01109 | hp2 | a0001 | c0001 | t0034 | g0096 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01167 | hp1 | a0001 | c0001 | t0038 | g0013 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0137 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0241 | AMR | PUR | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0030 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0079 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0204 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01361 | hp1 | a0001 | c0001 | t0043 | g0215 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0217 | EUR | IBS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0183 | EUR | IBS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0144 | EUR | IBS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01517 | hp2 | a0001 | c0001 | t0011 | g0182 | EUR | IBS | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01891 | hp1 | a0001 | c0001 | t0039 | g0081 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0210 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01981 | hp1 | a0001 | c0001 | t0019 | g0077 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0170 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0115 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02129 | hp2 | a0001 | c0001 | t0014 | g0191 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02145 | hp1 | a0001 | c0001 | t0023 | g0080 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CDX | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02165 | hp2 | a0001 | c0001 | t0027 | g0232 | EAS | CDX | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02300 | hp1 | a0001 | c0001 | t0035 | g0038 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02572 | hp1 | a0001 | c0001 | t0037 | g0101 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0166 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02622 | hp2 | a0001 | c0001 | t0018 | g0017 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0001 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0098 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02723 | hp2 | a0001 | c0001 | t0021 | g0193 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0162 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0177 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0187 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0099 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0104 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03139 | hp1 | a0001 | c0001 | t0042 | g0200 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ESN | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03239 | hp2 | a0001 | c0001 | t0045 | g0180 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0016 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0097 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03490 | hp1 | a0001 | c0001 | t0016 | g0224 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03492 | hp2 | a0001 | c0001 | t0016 | g0223 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03654 | hp1 | a0001 | c0001 | t0010 | g0042 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0188 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03669 | hp2 | a0001 | c0001 | t0009 | g0076 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03688 | hp2 | a0001 | c0001 | t0048 | g0019 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03834 | hp1 | a0001 | c0001 | t0047 | g0230 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0195 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03942 | hp2 | a0001 | c0001 | t0029 | g0093 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0237 | SAS | BEB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04204 | hp2 | a0001 | c0001 | t0032 | g0156 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18522 | hp1 | a0001 | c0001 | t0020 | g0007 | AFR | YRI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0047 | AFR | YRI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18612 | hp2 | a0001 | c0001 | t0031 | g0134 | EAS | CHB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | YRI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18943 | hp1 | a0001 | c0001 | t0017 | g0123 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0052 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18952 | hp2 | a0001 | c0001 | t0028 | g0151 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18956 | hp2 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18963 | hp1 | a0001 | c0001 | t0012 | g0133 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18974 | hp1 | a0001 | c0001 | t0036 | g0141 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18980 | hp1 | a0001 | c0001 | t0017 | g0084 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18993 | hp1 | a0001 | c0001 | t0013 | g0056 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0078 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19000 | hp2 | a0001 | c0001 | t0009 | g0168 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0131 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19003 | hp2 | a0001 | c0001 | t0012 | g0175 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19006 | hp2 | a0001 | c0001 | t0030 | g0135 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19030 | hp2 | a0004 | c0003 | t0001 | g0108 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19043 | hp1 | a0001 | c0001 | t0041 | g0105 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19043 | hp2 | a0001 | c0001 | t0040 | g0021 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19057 | hp1 | a0001 | c0001 | t0022 | g0024 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19057 | hp2 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19079 | hp2 | a0001 | c0001 | t0022 | g0029 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | ASW | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20129 | hp2 | a0005 | c0005 | t0006 | g0212 | AFR | ASW | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0006 | EUR | TSI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | TSI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | GIH | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0075 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | CLM | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0242 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02486 | hp2 | a0001 | c0001 | t0024 | g0239 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02559 | hp1 | a0001 | c0001 | t0021 | g0214 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG02559 | hp2 | a0003 | c0004 | t0025 | g0243 | AFR | ACB | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0208 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| HG03471 | hp2 | a0001 | c0001 | t0033 | g0119 | AFR | MSL | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0207 | AFR | USA | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | USA | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | LWK | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0045 | REF | REF | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0039 | REF | REF | UBXN2A_chr2_23935463_24009909 | UBXN2A | chr2 | 23935463 | 24009909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:23958337
|
A | G | 1 | a0005 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.23A>G | p.Lys8Arg | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/7 | 223/6022 | 23/780 | 8/259 | chr2 | 23958337 | ||
| chr2:23971350
|
G | A | 1 | a0002 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.116G>A | p.Ser39Asn | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/7 | 316/6022 | 116/780 | 39/259 | chr2 | 23971350 | ||
| chr2:23982982
|
C | T | 1 | a0003 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.374C>T | p.Ser125Phe | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/7 | 574/6022 | 374/780 | 125/259 | chr2 | 23982982 | ||
| chr2:23999706
|
C | G | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.619C>G | p.Gln207Glu | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 819/6022 | 619/780 | 207/259 | chr2 | 23999706 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:23940497
|
C | G | 1 | a0001c0001t0048 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-166C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/7 | 17818 | chr2 | 23940497 | |||||
| chr2:23940538
|
G | T | 1 | a0001c0001t0048 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/7 | 17777 | chr2 | 23940538 | |||||
| chr2:23940563
|
G | A | 2 | a0001c0001t0008a0001c0001t0023 | 9 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-100G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/7 | 17752 | chr2 | 23940563 | |||||
| chr2:23940581
|
C | T | 1 | a0001c0001t0047 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/7 | 17734 | chr2 | 23940581 | |||||
| chr2:24000064
|
C | G | 1 | a0001c0001t0022 | 2 | NA19057.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*197C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 197 | chr2 | 24000064 | |||||
| chr2:24000072
|
A | G | 5 | a0001c0001t0011a0001c0001t0014a0001c0001t0044others(2): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 205 | chr2 | 24000072 | |||||
| chr2:24000091
|
TAG | T | 2 | a0001c0001t0006a0005c0005t0006 | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*226_*227delGA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 226 | INFO_REALIGN_3_PRIME | chr2 | 24000091 | ||||
| chr2:24000159
|
G | A | 2 | a0001c0001t0005a0001c0001t0018 | 16 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*292G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 292 | chr2 | 24000159 | |||||
| chr2:24000216
|
G | A | 8 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(5): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*349G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 349 | chr2 | 24000216 | |||||
| chr2:24000332
|
A | G | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*465A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 465 | chr2 | 24000332 | |||||
| chr2:24000407
|
C | A | 1 | a0001c0001t0028 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*540C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 540 | chr2 | 24000407 | |||||
| chr2:24000413
|
G | A | 2 | a0001c0001t0024a0003c0004t0025 | 2 | HG02486.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*546G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 546 | chr2 | 24000413 | |||||
| chr2:24000492
|
A | G | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0021others(3): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*625A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 625 | chr2 | 24000492 | |||||
| chr2:24000585
|
C | T | 1 | a0001c0001t0016 | 3 | HG03490.hp1 HG03492.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*718C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 718 | chr2 | 24000585 | |||||
| chr2:24000586
|
G | A | 1 | a0001c0001t0010 | 6 | HG00738.hp2 HG01070.hp2 HG01123.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*719G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 719 | chr2 | 24000586 | |||||
| chr2:24000739
|
T | C | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*872T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 872 | chr2 | 24000739 | |||||
| chr2:24001085
|
G | A | 1 | a0001c0001t0042 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1218G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1218 | chr2 | 24001085 | |||||
| chr2:24001140
|
G | A | 1 | a0001c0001t0029 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1273G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1273 | chr2 | 24001140 | |||||
| chr2:24001176
|
C | G | 1 | a0001c0001t0042 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1309 | chr2 | 24001176 | |||||
| chr2:24001178
|
C | T | 2 | a0001c0001t0011a0001c0001t0046 | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1311C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1311 | chr2 | 24001178 | |||||
| chr2:24001190
|
A | G | 1 | a0003c0004t0025 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1323 | chr2 | 24001190 | |||||
| chr2:24001207
|
C | A | 1 | a0001c0001t0026 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1340 | chr2 | 24001207 | |||||
| chr2:24001209
|
C | G | 1 | a0001c0001t0020 | 2 | HG03209.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1342C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1342 | chr2 | 24001209 | |||||
| chr2:24001217
|
C | T | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1350C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1350 | chr2 | 24001217 | |||||
| chr2:24001358
|
G | A | 1 | a0001c0001t0021 | 2 | HG02559.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1491G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1491 | chr2 | 24001358 | |||||
| chr2:24001684
|
G | A | 1 | a0001c0001t0026 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1817G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1817 | chr2 | 24001684 | |||||
| chr2:24001713
|
A | G | 1 | a0001c0001t0019 | 2 | HG01981.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1846A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1846 | chr2 | 24001713 | |||||
| chr2:24001735
|
G | A | 3 | a0001c0001t0012a0001c0001t0030a0001c0001t0031 | 6 | NA18612.hp2 NA18956.hp2 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1868 | chr2 | 24001735 | |||||
| chr2:24001769
|
C | T | 1 | a0001c0001t0045 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1902C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1902 | chr2 | 24001769 | |||||
| chr2:24001852
|
G | A | 2 | a0001c0001t0006a0005c0005t0006 | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1985G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 1985 | chr2 | 24001852 | |||||
| chr2:24001908
|
C | G | 1 | a0001c0001t0021 | 2 | HG02559.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2041C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2041 | chr2 | 24001908 | |||||
| chr2:24001909
|
C | T | 1 | a0001c0001t0026 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2042C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2042 | chr2 | 24001909 | |||||
| chr2:24001959
|
CA | C | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0021others(3): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2104delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2104 | INFO_REALIGN_3_PRIME | chr2 | 24001959 | ||||
| chr2:24001983
|
A | G | 1 | a0001c0001t0018 | 2 | HG02622.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2116A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2116 | chr2 | 24001983 | |||||
| chr2:24002044
|
A | G | 1 | a0001c0001t0043 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2177 | chr2 | 24002044 | |||||
| chr2:24002203
|
G | A | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2336G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2336 | chr2 | 24002203 | |||||
| chr2:24002364
|
C | T | 2 | a0001c0001t0024a0003c0004t0025 | 2 | HG02486.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2497C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2497 | chr2 | 24002364 | |||||
| chr2:24002397
|
C | T | 1 | a0001c0001t0041 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2530C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2530 | chr2 | 24002397 | |||||
| chr2:24002416
|
C | CT | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2561dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2562 | INFO_REALIGN_3_PRIME | chr2 | 24002416 | ||||
| chr2:24002487
|
T | G | 1 | a0001c0001t0032 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2620T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2620 | chr2 | 24002487 | |||||
| chr2:24002498
|
C | T | 1 | a0001c0001t0040 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2631C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2631 | chr2 | 24002498 | |||||
| chr2:24002619
|
T | A | 2 | a0001c0001t0011a0001c0001t0046 | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2752T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2752 | chr2 | 24002619 | |||||
| chr2:24002751
|
T | C | 41 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(38): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2884T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2884 | chr2 | 24002751 | |||||
| chr2:24002797
|
A | G | 6 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(3): Show | 26 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2930A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2930 | chr2 | 24002797 | |||||
| chr2:24002817
|
C | T | 1 | a0001c0001t0039 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2950C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 2950 | chr2 | 24002817 | |||||
| chr2:24003018
|
T | G | 1 | a0001c0001t0033 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3151T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3151 | chr2 | 24003018 | |||||
| chr2:24003031
|
G | C | 6 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(3): Show | 26 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3164 | chr2 | 24003031 | |||||
| chr2:24003487
|
A | G | 1 | a0001c0001t0027 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3620A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3620 | chr2 | 24003487 | |||||
| chr2:24003722
|
AC | A | 1 | a0001c0001t0011 | 6 | HG00735.hp2 HG01106.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3857delC | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3857 | INFO_REALIGN_3_PRIME | chr2 | 24003722 | ||||
| chr2:24003723
|
CCA | C | 3 | a0001c0001t0017a0001c0001t0023a0001c0001t0030 | 5 | HG01243.hp1 HG02145.hp1 NA18943.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3857_*3858delCA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3857 | chr2 | 24003723 | |||||
| chr2:24003723
|
CCAA | C | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(15): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*3857_*3859delCAA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3857 | chr2 | 24003723 | |||||
| chr2:24003723
|
CCAAA | C | 7 | a0001c0001t0004a0001c0001t0009a0001c0001t0024others(4): Show | 28 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3857_*3860delCAAA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3857 | chr2 | 24003723 | |||||
| chr2:24003724
|
C | A | 1 | a0001c0001t0046 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3857C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3857 | chr2 | 24003724 | |||||
| chr2:24003724
|
CA | C | 2 | a0001c0001t0013a0001c0001t0038 | 5 | HG01167.hp1 HG01256.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3877delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3877 | INFO_REALIGN_3_PRIME | chr2 | 24003724 | ||||
| chr2:24003724
|
CAA | C | 6 | a0001c0001t0003a0001c0001t0016a0001c0001t0026others(3): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3876_*3877delAA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3876 | INFO_REALIGN_3_PRIME | chr2 | 24003724 | ||||
| chr2:24003724
|
CAAA | C | 2 | a0001c0001t0007a0001c0001t0015 | 12 | HG01243.hp2 HG02486.hp1 HG02615.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3875_*3877delAAA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 3875 | INFO_REALIGN_3_PRIME | chr2 | 24003724 | ||||
| chr2:24004037
|
G | A | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4170G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4170 | chr2 | 24004037 | |||||
| chr2:24004116
|
C | T | 3 | a0001c0001t0004a0001c0001t0042a0001c0001t0043 | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4249C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4249 | chr2 | 24004116 | |||||
| chr2:24004128
|
T | C | 1 | a0001c0001t0034 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4261T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4261 | chr2 | 24004128 | |||||
| chr2:24004131
|
A | G | 2 | a0001c0001t0007a0001c0001t0037 | 10 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4264A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4264 | chr2 | 24004131 | |||||
| chr2:24004237
|
C | CTG | 41 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(38): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*4370_*4371insTG | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4371 | chr2 | 24004237 | |||||
| chr2:24004255
|
A | G | 1 | a0001c0001t0036 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4388A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4388 | chr2 | 24004255 | |||||
| chr2:24004487
|
A | G | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(4): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4620A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4620 | chr2 | 24004487 | |||||
| chr2:24004580
|
G | A | 17 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(14): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4713G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4713 | chr2 | 24004580 | |||||
| chr2:24004603
|
G | A | 5 | a0001c0001t0011a0001c0001t0014a0001c0001t0044others(2): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4736G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4736 | chr2 | 24004603 | |||||
| chr2:24004610
|
T | C | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(27): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*4743T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4743 | chr2 | 24004610 | |||||
| chr2:24004759
|
TTC | T | 5 | a0001c0001t0011a0001c0001t0014a0001c0001t0044others(2): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4897_*4898delTC | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 7/7 | 4897 | INFO_REALIGN_3_PRIME | chr2 | 24004759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:23940661
|
G | A | 1 | a0001c0001t0003g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-15+13G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23940661 | ||||||
| chr2:23940717
|
G | A | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15+69G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23940717 | ||||||
| chr2:23940820
|
G | T | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-15+172G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23940820 | ||||||
| chr2:23940884
|
C | CT | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-15+236_-15+237ins others(1): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23940884 | ||||||
| chr2:23941121
|
T | A | 1 | a0001c0001t0009g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15+473T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941121 | ||||||
| chr2:23941259
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-15+611G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941259 | ||||||
| chr2:23941353
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-15+705A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941353 | ||||||
| chr2:23941367
|
T | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-15+719T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941367 | ||||||
| chr2:23941573
|
C | T | 1 | a0001c0001t0006g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+925C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941573 | ||||||
| chr2:23941637
|
T | A | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+989T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941637 | ||||||
| chr2:23941769
|
C | T | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+1121C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941769 | ||||||
| chr2:23941865
|
C | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-15+1217C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941865 | ||||||
| chr2:23941946
|
G | C | 2 | a0001c0001t0019g0077a0001c0001t0019g0078 | 2 | HG01981.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-15+1298G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23941946 | ||||||
| chr2:23942086
|
T | C | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+1438T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942086 | ||||||
| chr2:23942164
|
T | C | 2 | a0001c0001t0008g0079a0001c0001t0023g0080 | 2 | HG01256.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-15+1516T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942164 | ||||||
| chr2:23942268
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+1620C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942268 | ||||||
| chr2:23942365
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+1717A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942365 | ||||||
| chr2:23942402
|
A | G | 1 | a0001c0001t0010g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-15+1754A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942402 | ||||||
| chr2:23942419
|
C | CT | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0107others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-15+1793dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23942419 | |||||
| chr2:23942419
|
C | CTT | 26 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0171others(23): Show | 26 | HG00544.hp1 HG00735.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+1792_-15+1793d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23942419 | |||||
| chr2:23942419
|
C | CTTT | 10 | a0001c0001t0003g0005a0001c0001t0003g0236a0001c0001t0003g0238others(7): Show | 10 | HG00741.hp1 HG01243.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+1791_-15+1793d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23942419 | |||||
| chr2:23942633
|
G | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15+1985G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942633 | ||||||
| chr2:23942641
|
A | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+1993A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942641 | ||||||
| chr2:23942682
|
G | A | 1 | a0001c0001t0003g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+2034G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942682 | ||||||
| chr2:23942754
|
G | C | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+2106G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942754 | ||||||
| chr2:23942760
|
C | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15+2112C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942760 | ||||||
| chr2:23942921
|
C | T | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+2273C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23942921 | ||||||
| chr2:23942967
|
C | CT | 32 | a0001c0001t0002g0057a0001c0001t0004g0195a0001c0001t0004g0196others(29): Show | 32 | HG00733.hp1 HG01081.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-15+2333dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23942967 | |||||
| chr2:23943062
|
TCTC | T | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+2417_-15+2419d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23943062 | |||||
| chr2:23943131
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+2483A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943131 | ||||||
| chr2:23943177
|
G | A | 3 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0237 | 3 | HG03490.hp1 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-15+2529G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943177 | ||||||
| chr2:23943184
|
A | G | 1 | a0001c0001t0009g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15+2536A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943184 | ||||||
| chr2:23943351
|
G | A | 2 | a0001c0001t0004g0195a0001c0001t0043g0215 | 2 | HG01361.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+2703G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943351 | ||||||
| chr2:23943407
|
A | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+2759A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943407 | ||||||
| chr2:23943607
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-15+2959C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943607 | ||||||
| chr2:23943695
|
C | T | 1 | a0001c0001t0004g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-15+3047C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943695 | ||||||
| chr2:23943826
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-15+3178C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943826 | ||||||
| chr2:23943999
|
C | T | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+3351C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23943999 | ||||||
| chr2:23944022
|
T | C | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+3374T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944022 | ||||||
| chr2:23944250
|
A | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+3602A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944250 | ||||||
| chr2:23944397
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+3749A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944397 | ||||||
| chr2:23944398
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15+3750C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944398 | ||||||
| chr2:23944469
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+3821G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944469 | ||||||
| chr2:23944515
|
G | A | 55 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(52): Show | 55 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-15+3867G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944515 | ||||||
| chr2:23944547
|
T | A | 2 | a0001c0001t0003g0225a0001c0001t0003g0226 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-15+3899T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944547 | ||||||
| chr2:23944547
|
T | G | 25 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(22): Show | 25 | HG00741.hp1 HG01074.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-15+3899T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944547 | ||||||
| chr2:23944575
|
C | T | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+3927C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944575 | ||||||
| chr2:23944881
|
C | A | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-15+4233C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23944881 | ||||||
| chr2:23945079
|
A | T | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+4431A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945079 | ||||||
| chr2:23945318
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15+4670G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945318 | ||||||
| chr2:23945617
|
G | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0238 | 2 | HG00741.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-15+4969G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945617 | ||||||
| chr2:23945709
|
T | C | 1 | a0001c0001t0009g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-15+5061T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945709 | ||||||
| chr2:23945744
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-15+5096G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945744 | ||||||
| chr2:23945750
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+5102T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945750 | ||||||
| chr2:23945881
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-15+5233A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945881 | ||||||
| chr2:23945899
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15+5251C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23945899 | ||||||
| chr2:23946039
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15+5391C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23946039 | ||||||
| chr2:23946336
|
GT | G | 28 | a0001c0001t0002g0009a0001c0001t0003g0005a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-15+5700delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946336 | |||||
| chr2:23946486
|
A | AT | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-15+5847dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946486 | |||||
| chr2:23946601
|
A | G | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15+5953A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23946601 | ||||||
| chr2:23946655
|
C | T | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+6007C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23946655 | ||||||
| chr2:23946745
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+6097G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23946745 | ||||||
| chr2:23946839
|
A | G | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15+6191A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23946839 | ||||||
| chr2:23946840
|
TCAGA | T | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+6196_-15+6199d others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946840 | |||||
| chr2:23946887
|
A | AT | 15 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0198others(12): Show | 15 | HG01123.hp2 HG01255.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+6259dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946887 | |||||
| chr2:23946887
|
AT | A | 59 | a0001c0001t0001g0094a0001c0001t0002g0010a0001c0001t0003g0005others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15+6259delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946887 | |||||
| chr2:23946887
|
ATT | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-15+6258_-15+6259d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23946887 | |||||
| chr2:23947077
|
A | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+6429A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947077 | ||||||
| chr2:23947092
|
T | C | 1 | a0004c0003t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+6444T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947092 | ||||||
| chr2:23947193
|
G | A | 2 | a0001c0001t0024g0239a0003c0004t0025g0243 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-15+6545G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947193 | ||||||
| chr2:23947300
|
G | A | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+6652G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947300 | ||||||
| chr2:23947344
|
C | T | 55 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(52): Show | 55 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-15+6696C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947344 | ||||||
| chr2:23947490
|
T | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+6842T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947490 | ||||||
| chr2:23947567
|
T | C | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-15+6919T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947567 | ||||||
| chr2:23947652
|
G | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15+7004G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947652 | ||||||
| chr2:23947820
|
TG | T | 3 | a0001c0001t0006g0206a0001c0001t0006g0213a0005c0005t0006g0212 | 3 | HG02922.hp1 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+7175delG | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23947820 | |||||
| chr2:23947916
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15+7268G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947916 | ||||||
| chr2:23947964
|
C | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+7316C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947964 | ||||||
| chr2:23947964
|
C | T | 1 | a0001c0001t0005g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+7316C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947964 | ||||||
| chr2:23947981
|
A | G | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+7333A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23947981 | ||||||
| chr2:23948171
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0176 | 3 | NA18949.hp2 NA19002.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-15+7523C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948171 | ||||||
| chr2:23948254
|
C | CT | 44 | a0001c0001t0001g0158a0001c0001t0002g0055a0001c0001t0003g0005others(41): Show | 44 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-15+7622dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23948254 | |||||
| chr2:23948260
|
T | C | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15+7612T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948260 | ||||||
| chr2:23948312
|
G | A | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-15+7664G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948312 | ||||||
| chr2:23948334
|
A | G | 1 | a0001c0001t0005g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+7686A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948334 | ||||||
| chr2:23948495
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+7847T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948495 | ||||||
| chr2:23948639
|
A | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+7991A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948639 | ||||||
| chr2:23948819
|
G | A | 7 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(4): Show | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+8171G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948819 | ||||||
| chr2:23948891
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-15+8243A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948891 | ||||||
| chr2:23948936
|
C | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-15+8288C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948936 | ||||||
| chr2:23948945
|
C | CT | 5 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0002g0054others(2): Show | 5 | HG01168.hp2 HG02886.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+8314dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23948945 | |||||
| chr2:23948945
|
C | CTTT | 21 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(18): Show | 21 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15+8312_-15+8314d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23948945 | |||||
| chr2:23948945
|
CT | C | 8 | a0001c0001t0001g0109a0001c0001t0011g0182a0001c0001t0011g0183others(5): Show | 8 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+8314delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23948945 | |||||
| chr2:23948945
|
CTT | C | 16 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(13): Show | 16 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+8313_-15+8314d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23948945 | |||||
| chr2:23948963
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15+8315G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23948963 | ||||||
| chr2:23949002
|
G | A | 8 | a0001c0001t0014g0189a0001c0001t0014g0190a0001c0001t0014g0191others(5): Show | 8 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+8354G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949002 | ||||||
| chr2:23949116
|
C | CT | 30 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0167others(27): Show | 30 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+8485dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23949116 | |||||
| chr2:23949116
|
C | CTT | 19 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15+8484_-15+8485d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23949116 | |||||
| chr2:23949116
|
C | CTTT | 5 | a0001c0001t0004g0197a0001c0001t0004g0204a0001c0001t0004g0205others(2): Show | 5 | HG01081.hp2 HG01261.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+8483_-15+8485d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23949116 | |||||
| chr2:23949119
|
T | C | 1 | a0001c0001t0007g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-15+8471T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949119 | ||||||
| chr2:23949249
|
A | T | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15+8601A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949249 | ||||||
| chr2:23949323
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-15+8675G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949323 | ||||||
| chr2:23949442
|
A | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-15+8794A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949442 | ||||||
| chr2:23949579
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-14-8722A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949579 | ||||||
| chr2:23949598
|
G | T | 1 | a0001c0001t0014g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-14-8703G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949598 | ||||||
| chr2:23949666
|
G | A | 1 | a0001c0001t0005g0012 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-14-8635G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949666 | ||||||
| chr2:23949690
|
T | C | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-8611T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949690 | ||||||
| chr2:23949700
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14-8601C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949700 | ||||||
| chr2:23949840
|
A | G | 1 | a0001c0001t0006g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-8461A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949840 | ||||||
| chr2:23949874
|
C | CA | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-14-8414dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23949874 | |||||
| chr2:23949901
|
T | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-14-8400T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949901 | ||||||
| chr2:23949930
|
A | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-8371A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23949930 | ||||||
| chr2:23949999
|
CCCCCCA | C | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-8279_-14-8274d others(8): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23949999 | |||||
| chr2:23950000
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14-8301C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950000 | ||||||
| chr2:23950034
|
C | T | 1 | a0001c0001t0014g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-14-8267C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950034 | ||||||
| chr2:23950035
|
G | A | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-8266G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950035 | ||||||
| chr2:23950133
|
G | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-8168G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950133 | ||||||
| chr2:23950202
|
G | A | 1 | a0001c0001t0039g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-8099G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950202 | ||||||
| chr2:23950297
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-14-8004C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950297 | ||||||
| chr2:23950366
|
T | C | 1 | a0001c0001t0009g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-14-7935T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950366 | ||||||
| chr2:23950507
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-7794A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950507 | ||||||
| chr2:23950511
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-7790C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950511 | ||||||
| chr2:23950521
|
A | G | 1 | a0001c0001t0004g0196 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-14-7780A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950521 | ||||||
| chr2:23950547
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14-7754C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950547 | ||||||
| chr2:23950695
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-7606C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950695 | ||||||
| chr2:23950739
|
TTACGCCC others(2): Show |
T | 10 | a0001c0001t0005g0012a0001c0001t0005g0014a0001c0001t0005g0015others(7): Show | 10 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-7561_-14-7553d others(11): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950739 | ||||||
| chr2:23950793
|
C | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-7508C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23950793 | ||||||
| chr2:23951048
|
T | C | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-7253T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951048 | ||||||
| chr2:23951151
|
A | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-7150A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951151 | ||||||
| chr2:23951196
|
T | G | 8 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-7105T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951196 | ||||||
| chr2:23951291
|
T | G | 1 | a0001c0001t0013g0052 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-14-7010T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951291 | ||||||
| chr2:23951312
|
C | G | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-14-6989C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951312 | ||||||
| chr2:23951413
|
G | GAT | 13 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0066others(10): Show | 13 | HG01081.hp1 HG01081.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-6838_-14-6837d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
G | GATAT | 13 | a0001c0001t0002g0002a0001c0001t0002g0045a0001c0001t0002g0053others(10): Show | 14 | HG00544.hp2 HG01070.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-6840_-14-6837d others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
G | GATATAT | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0070 | 3 | HG00099.hp2 HG03540.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-14-6842_-14-6837d others(8): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
G | GATATATA others(1): Show |
4 | a0001c0001t0002g0010a0001c0001t0002g0050a0001c0001t0002g0071others(1): Show | 4 | HG01358.hp1 HG02970.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-6844_-14-6837d others(10): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
G | GATATATA others(3): Show |
4 | a0001c0001t0002g0055a0001c0001t0002g0057a0001c0001t0005g0018others(1): Show | 4 | HG01934.hp2 HG02723.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-6846_-14-6837d others(12): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
G | GATATATA others(7): Show |
1 | a0001c0001t0005g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14-6850_-14-6837d others(16): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GAT | G | 27 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0026others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-14-6838_-14-6837d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATAT | G | 16 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0060others(13): Show | 16 | HG00140.hp2 HG00735.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-6840_-14-6837d others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATAT | G | 6 | a0001c0001t0002g0020a0001c0001t0005g0074a0001c0001t0006g0213others(3): Show | 6 | HG02615.hp1 HG03453.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6842_-14-6837d others(8): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(1): Show |
G | 4 | a0001c0001t0011g0188a0001c0001t0014g0189a0001c0001t0014g0192others(1): Show | 4 | HG01069.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-6844_-14-6837d others(10): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(3): Show |
G | 28 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(25): Show | 28 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-6846_-14-6837d others(12): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(5): Show |
G | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-14-6848_-14-6837d others(14): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(7): Show |
G | 3 | a0001c0001t0007g0098a0001c0001t0020g0007a0001c0001t0020g0008 | 3 | HG02717.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-6850_-14-6837d others(16): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(9): Show |
G | 3 | a0001c0001t0004g0198a0001c0001t0006g0207a0001c0001t0043g0215 | 3 | HG01255.hp2 HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-6852_-14-6837d others(18): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(11): Show |
G | 3 | a0001c0001t0001g0092a0001c0001t0005g0245a0001c0001t0029g0093 | 3 | HG03942.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-14-6854_-14-6837d others(20): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(13): Show |
G | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0011g0182others(2): Show | 5 | HG01516.hp2 HG01517.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-6856_-14-6837d others(22): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(15): Show |
G | 5 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0001g0149others(2): Show | 5 | HG01074.hp2 HG02165.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-6858_-14-6837d others(24): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(17): Show |
G | 16 | a0001c0001t0001g0004a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 16 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-6860_-14-6837d others(26): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(19): Show |
G | 70 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-14-6862_-14-6837d others(28): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951413
|
GATATATA others(25): Show |
G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-14-6868_-14-6837d others(34): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951413 | |||||
| chr2:23951429
|
T | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14-6872T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951429 | ||||||
| chr2:23951435
|
T | G | 25 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-6866T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951435 | ||||||
| chr2:23951437
|
T | G | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-14-6864T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951437 | ||||||
| chr2:23951447
|
T | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14-6854T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951447 | ||||||
| chr2:23951450
|
A | G | 1 | a0001c0001t0011g0187 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14-6851A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951450 | ||||||
| chr2:23951452
|
A | C | 25 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.-14-6849A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951452 | ||||||
| chr2:23951529
|
T | C | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-6772T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951529 | ||||||
| chr2:23951613
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-14-6688A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951613 | ||||||
| chr2:23951616
|
A | C | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-6685A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951616 | ||||||
| chr2:23951746
|
T | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-14-6555T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951746 | ||||||
| chr2:23951774
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-14-6527G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23951774 | ||||||
| chr2:23951967
|
C | CT | 20 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0001g0176others(17): Show | 20 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-6317dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951967 | |||||
| chr2:23951967
|
CT | C | 16 | a0001c0001t0001g0109a0001c0001t0002g0022a0001c0001t0004g0197others(13): Show | 16 | HG01081.hp2 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.-14-6317delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23951967 | |||||
| chr2:23952044
|
G | A | 1 | a0001c0001t0004g0219 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-14-6257G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952044 | ||||||
| chr2:23952518
|
C | T | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-5783C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952518 | ||||||
| chr2:23952524
|
A | C | 2 | a0001c0001t0024g0239a0003c0004t0025g0243 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-14-5777A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952524 | ||||||
| chr2:23952537
|
C | T | 1 | a0001c0001t0044g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-14-5764C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952537 | ||||||
| chr2:23952654
|
AG | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-5645delG | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23952654 | |||||
| chr2:23952658
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-5643T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952658 | ||||||
| chr2:23952660
|
G | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-14-5641G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952660 | ||||||
| chr2:23952752
|
T | C | 1 | a0001c0001t0028g0151 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-14-5549T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952752 | ||||||
| chr2:23952827
|
C | T | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-14-5474C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23952827 | ||||||
| chr2:23952966
|
GT | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-14-5321delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23952966 | |||||
| chr2:23953005
|
A | G | 1 | a0001c0001t0014g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-14-5296A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953005 | ||||||
| chr2:23953044
|
A | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-14-5257A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953044 | ||||||
| chr2:23953293
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-5008T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953293 | ||||||
| chr2:23953434
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-14-4867C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953434 | ||||||
| chr2:23953504
|
C | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-4797C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953504 | ||||||
| chr2:23953564
|
C | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG01243.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-4737C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953564 | ||||||
| chr2:23953590
|
G | A | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-14-4711G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953590 | ||||||
| chr2:23953790
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-14-4511A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23953790 | ||||||
| chr2:23954411
|
A | G | 4 | a0001c0001t0020g0007a0001c0001t0020g0008a0001c0001t0024g0239others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-3890A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23954411 | ||||||
| chr2:23954471
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14-3830T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23954471 | ||||||
| chr2:23954733
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-3568G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23954733 | ||||||
| chr2:23954756
|
CT | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0112a0001c0001t0001g0153others(7): Show | 10 | HG00323.hp2 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-3528delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23954756 | |||||
| chr2:23954931
|
C | CT | 26 | a0001c0001t0001g0090a0001c0001t0001g0110a0001c0001t0001g0176others(23): Show | 26 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-3350dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23954931 | |||||
| chr2:23954931
|
C | CTT | 37 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(34): Show | 37 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-3351_-14-3350d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23954931 | |||||
| chr2:23954931
|
CTT | C | 6 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(3): Show | 6 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-3351_-14-3350d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23954931 | |||||
| chr2:23955025
|
C | T | 1 | a0001c0001t0036g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-14-3276C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955025 | ||||||
| chr2:23955183
|
G | A | 14 | a0001c0001t0002g0070a0001c0001t0011g0182a0001c0001t0011g0183others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-3118G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955183 | ||||||
| chr2:23955219
|
T | C | 1 | a0001c0001t0029g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-14-3082T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955219 | ||||||
| chr2:23955223
|
A | G | 29 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-14-3078A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955223 | ||||||
| chr2:23955284
|
G | A | 29 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-14-3017G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955284 | ||||||
| chr2:23955338
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-14-2963G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955338 | ||||||
| chr2:23955341
|
T | A | 29 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-14-2960T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955341 | ||||||
| chr2:23955709
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-2592G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955709 | ||||||
| chr2:23955814
|
C | T | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-2487C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955814 | ||||||
| chr2:23955926
|
G | A | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-14-2375G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23955926 | ||||||
| chr2:23956111
|
G | T | 2 | a0001c0001t0007g0103a0001c0001t0009g0104 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-2190G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956111 | ||||||
| chr2:23956177
|
T | TA | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-14-2111dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 23956177 | |||||
| chr2:23956414
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-14-1887G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956414 | ||||||
| chr2:23956558
|
G | A | 1 | a0001c0001t0006g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-1743G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956558 | ||||||
| chr2:23956608
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14-1693C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956608 | ||||||
| chr2:23956695
|
T | C | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-1606T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956695 | ||||||
| chr2:23956799
|
C | G | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-1502C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956799 | ||||||
| chr2:23956920
|
C | T | 1 | a0001c0001t0014g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-14-1381C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23956920 | ||||||
| chr2:23957011
|
A | G | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-14-1290A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957011 | ||||||
| chr2:23957052
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-14-1249A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957052 | ||||||
| chr2:23957208
|
T | A | 57 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(54): Show | 57 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-1093T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957208 | ||||||
| chr2:23957234
|
A | G | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-1067A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957234 | ||||||
| chr2:23957255
|
C | T | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-1046C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957255 | ||||||
| chr2:23957274
|
T | C | 57 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(54): Show | 57 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-1027T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957274 | ||||||
| chr2:23957294
|
A | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14-1007A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957294 | ||||||
| chr2:23957328
|
A | C | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-973A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957328 | ||||||
| chr2:23957519
|
G | C | 1 | a0001c0001t0020g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-782G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957519 | ||||||
| chr2:23957860
|
A | G | 1 | a0001c0001t0023g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-14-441A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957860 | ||||||
| chr2:23957906
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-14-395G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957906 | ||||||
| chr2:23957920
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0026g0006 | 2 | NA18979.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-14-381G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957920 | ||||||
| chr2:23957940
|
G | A | 1 | a0001c0001t0009g0113 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-14-361G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23957940 | ||||||
| chr2:23958054
|
T | C | 1 | a0001c0001t0009g0113 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-14-247T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23958054 | ||||||
| chr2:23958289
|
G | T | 57 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(54): Show | 57 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-12G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 1/6 | chr2 | 23958289 | ||||||
| chr2:23958383
|
G | C | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+28G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958383 | ||||||
| chr2:23958486
|
A | G | 1 | a0001c0001t0003g0236 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.41+131A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958486 | ||||||
| chr2:23958516
|
A | C | 6 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+161A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958516 | ||||||
| chr2:23958651
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.41+296C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958651 | ||||||
| chr2:23958702
|
G | A | 3 | a0001c0001t0005g0059a0001c0001t0005g0064a0001c0001t0005g0074 | 3 | HG02809.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.41+347G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958702 | ||||||
| chr2:23958713
|
C | T | 29 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.41+358C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958713 | ||||||
| chr2:23958786
|
A | G | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+431A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958786 | ||||||
| chr2:23958800
|
C | T | 57 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(54): Show | 57 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.41+445C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958800 | ||||||
| chr2:23958896
|
A | G | 1 | a0001c0001t0009g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.41+541A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958896 | ||||||
| chr2:23958975
|
G | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.41+620G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23958975 | ||||||
| chr2:23959155
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+800G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23959155 | ||||||
| chr2:23959289
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(105): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.41+934C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23959289 | ||||||
| chr2:23959446
|
C | T | 1 | a0001c0001t0044g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.41+1091C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23959446 | ||||||
| chr2:23959602
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.41+1247A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23959602 | ||||||
| chr2:23960040
|
C | G | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+1685C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960040 | ||||||
| chr2:23960335
|
T | C | 6 | a0001c0001t0014g0189a0001c0001t0014g0190a0001c0001t0014g0191others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+1980T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960335 | ||||||
| chr2:23960534
|
A | G | 6 | a0001c0001t0012g0131a0001c0001t0012g0132a0001c0001t0012g0133others(3): Show | 6 | NA18612.hp2 NA18956.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+2179A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960534 | ||||||
| chr2:23960659
|
A | C | 3 | a0001c0001t0020g0007a0001c0001t0020g0008a0003c0004t0025g0243 | 3 | HG02559.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.41+2304A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960659 | ||||||
| chr2:23960737
|
A | G | 1 | a0001c0001t0003g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.41+2382A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960737 | ||||||
| chr2:23960761
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.41+2406T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960761 | ||||||
| chr2:23960905
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41+2550G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960905 | ||||||
| chr2:23960935
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.41+2580G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960935 | ||||||
| chr2:23960979
|
T | C | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.41+2624T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23960979 | ||||||
| chr2:23961092
|
T | TTTTTTG | 57 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(54): Show | 57 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.41+2749_41+2754dup others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961092 | |||||
| chr2:23961141
|
GC | G | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG01243.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+2787delC | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961141 | ||||||
| chr2:23961257
|
G | GGCTAATT others(447): Show |
1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.41+3208_41+3209ins others(454): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961257 | |||||
| chr2:23961376
|
G | A | 7 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(4): Show | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+3021G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961376 | ||||||
| chr2:23961393
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.41+3038G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961393 | ||||||
| chr2:23961421
|
T | C | 1 | a0001c0001t0004g0199 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.41+3066T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961421 | ||||||
| chr2:23961473
|
A | G | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.41+3118A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961473 | ||||||
| chr2:23961496
|
T | C | 2 | a0001c0001t0002g0053a0001c0001t0013g0052 | 2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.41+3141T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961496 | ||||||
| chr2:23961539
|
C | CT | 14 | a0001c0001t0001g0083a0001c0001t0002g0010a0001c0001t0002g0023others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.41+3208dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961539 | |||||
| chr2:23961539
|
C | CTT | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.41+3207_41+3208dup others(2): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961539 | |||||
| chr2:23961539
|
C | CTTT | 25 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0109others(22): Show | 25 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.41+3206_41+3208dup others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961539 | |||||
| chr2:23961539
|
CT | C | 34 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0197others(31): Show | 34 | HG01081.hp2 HG01123.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.41+3208delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23961539 | |||||
| chr2:23961563
|
T | TTG | 22 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(19): Show | 22 | HG01074.hp1 HG01257.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+3208_41+3209ins others(2): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961563 | ||||||
| chr2:23961563
|
T | TTTG | 6 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0234others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+3208_41+3209ins others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961563 | ||||||
| chr2:23961750
|
G | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.41+3395G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961750 | ||||||
| chr2:23961795
|
C | G | 6 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+3440C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961795 | ||||||
| chr2:23961806
|
A | G | 29 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.41+3451A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961806 | ||||||
| chr2:23961817
|
A | G | 1 | a0001c0001t0004g0203 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.41+3462A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961817 | ||||||
| chr2:23961840
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.41+3485C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961840 | ||||||
| chr2:23961854
|
T | C | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+3499T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23961854 | ||||||
| chr2:23962227
|
C | T | 16 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(13): Show | 16 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+3872C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962227 | ||||||
| chr2:23962399
|
C | G | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.41+4044C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962399 | ||||||
| chr2:23962605
|
C | CTTT | 26 | a0001c0001t0003g0005a0001c0001t0003g0221a0001c0001t0003g0222others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.41+4265_41+4267dup others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23962605 | |||||
| chr2:23962605
|
CT | C | 5 | a0001c0001t0002g0025a0001c0001t0008g0162a0001c0001t0010g0043others(2): Show | 5 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.41+4267delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23962605 | |||||
| chr2:23962651
|
G | C | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.41+4296G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962651 | ||||||
| chr2:23962655
|
G | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+4300G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962655 | ||||||
| chr2:23962690
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0045 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.41+4335C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962690 | ||||||
| chr2:23962754
|
T | C | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+4399T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962754 | ||||||
| chr2:23962890
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+4535A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962890 | ||||||
| chr2:23962940
|
G | T | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+4585G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23962940 | ||||||
| chr2:23963070
|
C | A | 1 | a0001c0001t0020g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.41+4715C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963070 | ||||||
| chr2:23963101
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.41+4746A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963101 | ||||||
| chr2:23963128
|
A | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.41+4773A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963128 | ||||||
| chr2:23963141
|
A | G | 55 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(52): Show | 55 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.41+4786A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963141 | ||||||
| chr2:23963413
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+5058G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963413 | ||||||
| chr2:23963468
|
T | A | 6 | a0001c0001t0008g0115a0001c0001t0008g0142a0001c0001t0008g0143others(3): Show | 6 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+5113T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963468 | ||||||
| chr2:23963471
|
C | CA | 68 | a0001c0001t0001g0169a0001c0001t0002g0025a0001c0001t0002g0026others(65): Show | 68 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.41+5131dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23963471 | |||||
| chr2:23963491
|
A | G | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+5136A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963491 | ||||||
| chr2:23963497
|
G | A | 1 | a0001c0001t0048g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.41+5142G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963497 | ||||||
| chr2:23963517
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.41+5162A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963517 | ||||||
| chr2:23963735
|
G | A | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.41+5380G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963735 | ||||||
| chr2:23963825
|
A | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.41+5470A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963825 | ||||||
| chr2:23963931
|
C | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.41+5576C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23963931 | ||||||
| chr2:23964134
|
C | CA | 17 | a0001c0001t0002g0073a0001c0001t0004g0199a0001c0001t0004g0219others(14): Show | 17 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.41+5795dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23964134 | |||||
| chr2:23964134
|
CA | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.41+5795delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23964134 | |||||
| chr2:23964173
|
A | C | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+5818A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964173 | ||||||
| chr2:23964214
|
TC | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+5861delC | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23964214 | |||||
| chr2:23964215
|
C | CT | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+5860_41+5861ins others(1): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964215 | ||||||
| chr2:23964216
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.41+5861C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964216 | ||||||
| chr2:23964241
|
G | T | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.41+5886G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964241 | ||||||
| chr2:23964287
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+5932C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964287 | ||||||
| chr2:23964288
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+5933A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964288 | ||||||
| chr2:23964304
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.41+5949A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964304 | ||||||
| chr2:23964320
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+5965C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964320 | ||||||
| chr2:23964372
|
G | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0089others(3): Show | 6 | HG01167.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+6017G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964372 | ||||||
| chr2:23964401
|
G | A | 1 | a0001c0001t0032g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.41+6046G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964401 | ||||||
| chr2:23964418
|
C | G | 1 | a0001c0001t0008g0170 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.41+6063C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964418 | ||||||
| chr2:23964776
|
A | C | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.41+6421A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964776 | ||||||
| chr2:23964870
|
G | A | 1 | a0001c0001t0003g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42-6406G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964870 | ||||||
| chr2:23964907
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.42-6369G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23964907 | ||||||
| chr2:23965144
|
G | A | 1 | a0001c0001t0014g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42-6132G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965144 | ||||||
| chr2:23965258
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.42-6018G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965258 | ||||||
| chr2:23965316
|
A | G | 3 | a0001c0001t0018g0016a0001c0001t0018g0017a0001c0001t0038g0013 | 3 | HG01167.hp1 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.42-5960A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965316 | ||||||
| chr2:23965324
|
C | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-5952C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965324 | ||||||
| chr2:23965574
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.42-5702G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965574 | ||||||
| chr2:23965786
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-5490C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965786 | ||||||
| chr2:23965897
|
A | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.42-5379A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965897 | ||||||
| chr2:23965984
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.42-5292A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965984 | ||||||
| chr2:23965993
|
G | A | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-5283G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23965993 | ||||||
| chr2:23966014
|
C | G | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.42-5262C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966014 | ||||||
| chr2:23966052
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-5224A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966052 | ||||||
| chr2:23966202
|
G | A | 2 | a0001c0001t0008g0142a0001c0001t0008g0143 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.42-5074G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966202 | ||||||
| chr2:23966338
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.42-4938G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966338 | ||||||
| chr2:23966378
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-4898G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966378 | ||||||
| chr2:23966424
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-4852C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966424 | ||||||
| chr2:23966456
|
C | CT | 13 | a0001c0001t0001g0140a0001c0001t0003g0225a0001c0001t0003g0236others(10): Show | 13 | HG00735.hp1 HG01255.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-4806dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23966456 | |||||
| chr2:23966491
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0027 | 3 | HG00280.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.42-4785T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966491 | ||||||
| chr2:23966514
|
G | A | 1 | a0001c0001t0004g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.42-4762G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966514 | ||||||
| chr2:23966515
|
T | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.42-4761T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966515 | ||||||
| chr2:23966577
|
C | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-4699C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966577 | ||||||
| chr2:23966598
|
G | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.42-4678G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966598 | ||||||
| chr2:23966601
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.42-4675C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966601 | ||||||
| chr2:23966639
|
G | C | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.42-4637G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966639 | ||||||
| chr2:23966658
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0007g0164 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.42-4618A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966658 | ||||||
| chr2:23966666
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.42-4610T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966666 | ||||||
| chr2:23966667
|
G | C | 2 | a0001c0001t0011g0185a0001c0001t0046g0184 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.42-4609G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966667 | ||||||
| chr2:23966681
|
G | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-4595G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966681 | ||||||
| chr2:23966683
|
C | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-4593C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966683 | ||||||
| chr2:23966686
|
T | C | 4 | a0001c0001t0002g0040a0001c0001t0016g0223a0001c0001t0016g0224others(1): Show | 4 | HG03490.hp1 HG03492.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-4590T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966686 | ||||||
| chr2:23966698
|
A | G | 3 | a0001c0001t0016g0223a0001c0001t0016g0224a0001c0001t0016g0237 | 3 | HG03490.hp1 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.42-4578A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966698 | ||||||
| chr2:23966750
|
CT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.42-4504delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23966750 | |||||
| chr2:23966750
|
CTT | C | 48 | a0001c0001t0001g0114a0001c0001t0001g0154a0001c0001t0003g0005others(45): Show | 48 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.42-4505_42-4504del others(2): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23966750 | |||||
| chr2:23966750
|
CTTT | C | 12 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(9): Show | 12 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-4506_42-4504del others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23966750 | |||||
| chr2:23966876
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.42-4400G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966876 | ||||||
| chr2:23966887
|
A | G | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.42-4389A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966887 | ||||||
| chr2:23966895
|
C | T | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.42-4381C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966895 | ||||||
| chr2:23966924
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.42-4352A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23966924 | ||||||
| chr2:23967171
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.42-4105C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967171 | ||||||
| chr2:23967183
|
G | A | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.42-4093G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967183 | ||||||
| chr2:23967241
|
T | C | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.42-4035T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967241 | ||||||
| chr2:23967252
|
A | C | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-4024A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967252 | ||||||
| chr2:23967320
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.42-3956G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967320 | ||||||
| chr2:23967393
|
A | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.42-3883A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967393 | ||||||
| chr2:23967490
|
A | G | 6 | a0001c0001t0004g0194a0001c0001t0004g0199a0001c0001t0004g0201others(3): Show | 6 | NA18949.hp1 NA18963.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3786A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967490 | ||||||
| chr2:23967762
|
G | A | 2 | a0001c0001t0009g0113a0001c0001t0009g0117 | 2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.42-3514G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23967762 | ||||||
| chr2:23968169
|
C | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.42-3107C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968169 | ||||||
| chr2:23968445
|
G | A | 1 | a0001c0001t0044g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.42-2831G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968445 | ||||||
| chr2:23968447
|
C | G | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.42-2829C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968447 | ||||||
| chr2:23968452
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.42-2824G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968452 | ||||||
| chr2:23968459
|
G | C | 1 | a0001c0001t0048g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.42-2817G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968459 | ||||||
| chr2:23968569
|
AG | A | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.42-2705delG | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23968569 | |||||
| chr2:23968622
|
G | A | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.42-2654G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968622 | ||||||
| chr2:23968648
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.42-2628G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968648 | ||||||
| chr2:23968675
|
G | GA | 19 | a0001c0001t0001g0095a0001c0001t0001g0118a0001c0001t0001g0148others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-2587dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23968675 | |||||
| chr2:23968675
|
GA | G | 7 | a0001c0001t0003g0231a0001c0001t0003g0233a0001c0001t0003g0234others(4): Show | 7 | HG02080.hp2 HG02129.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-2587delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23968675 | |||||
| chr2:23968786
|
G | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-2490G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968786 | ||||||
| chr2:23968852
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.42-2424C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968852 | ||||||
| chr2:23968894
|
C | CT | 20 | a0001c0001t0001g0088a0001c0001t0001g0139a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp1 HG01261.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.42-2365dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23968894 | |||||
| chr2:23968894
|
CT | C | 26 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.42-2365delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23968894 | |||||
| chr2:23968933
|
G | A | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.42-2343G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968933 | ||||||
| chr2:23968962
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.42-2314G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968962 | ||||||
| chr2:23968995
|
C | T | 1 | a0001c0001t0039g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.42-2281C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23968995 | ||||||
| chr2:23969039
|
C | T | 1 | a0001c0001t0034g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42-2237C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969039 | ||||||
| chr2:23969336
|
C | A | 1 | a0001c0001t0033g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42-1940C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969336 | ||||||
| chr2:23969627
|
C | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.42-1649C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969627 | ||||||
| chr2:23969640
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-1636C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969640 | ||||||
| chr2:23969702
|
G | A | 1 | a0001c0001t0007g0102 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.42-1574G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969702 | ||||||
| chr2:23969909
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.42-1367T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969909 | ||||||
| chr2:23969931
|
A | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.42-1345A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23969931 | ||||||
| chr2:23970082
|
A | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-1194A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970082 | ||||||
| chr2:23970196
|
A | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-1080A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970196 | ||||||
| chr2:23970329
|
T | G | 1 | a0001c0001t0042g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.42-947T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970329 | ||||||
| chr2:23970451
|
CT | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0053a0001c0001t0002g0057others(3): Show | 6 | HG01081.hp1 NA18952.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-823delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 23970451 | |||||
| chr2:23970539
|
T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.42-737T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970539 | ||||||
| chr2:23970759
|
G | A | 2 | a0001c0001t0012g0131a0001c0001t0031g0134 | 2 | NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.42-517G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970759 | ||||||
| chr2:23970953
|
C | T | 1 | a0001c0001t0004g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.42-323C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23970953 | ||||||
| chr2:23971077
|
G | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.42-199G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23971077 | ||||||
| chr2:23971180
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.42-96G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23971180 | ||||||
| chr2:23971180
|
G | T | 1 | a0001c0001t0042g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.42-96G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23971180 | ||||||
| chr2:23971196
|
A | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0015 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.42-80A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23971196 | ||||||
| chr2:23971238
|
A | G | 1 | a0001c0001t0002g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.42-38A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 2/6 | chr2 | 23971238 | ||||||
| chr2:23971444
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.180+30C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971444 | ||||||
| chr2:23971466
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+52G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971466 | ||||||
| chr2:23971520
|
T | C | 1 | a0001c0001t0044g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.180+106T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971520 | ||||||
| chr2:23971620
|
G | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+206G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971620 | ||||||
| chr2:23971679
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+265G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971679 | ||||||
| chr2:23971711
|
A | G | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.180+297A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971711 | ||||||
| chr2:23971738
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+324C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971738 | ||||||
| chr2:23971800
|
T | C | 1 | a0001c0001t0004g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.180+386T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971800 | ||||||
| chr2:23971806
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0136a0001c0001t0009g0003 | 3 | HG00741.hp2 HG01257.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.180+392C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23971806 | ||||||
| chr2:23972009
|
G | T | 1 | a0001c0001t0006g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180+595G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972009 | ||||||
| chr2:23972098
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.180+684G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972098 | ||||||
| chr2:23972194
|
G | A | 36 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(33): Show | 36 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.180+780G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972194 | ||||||
| chr2:23972562
|
G | A | 1 | a0001c0001t0013g0030 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.180+1148G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972562 | ||||||
| chr2:23972686
|
G | A | 1 | a0001c0001t0005g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.180+1272G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972686 | ||||||
| chr2:23972835
|
A | T | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.180+1421A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972835 | ||||||
| chr2:23972839
|
T | A | 10 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0121others(7): Show | 10 | HG01361.hp2 HG01934.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+1425T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23972839 | ||||||
| chr2:23973059
|
A | G | 1 | a0001c0001t0003g0240 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.180+1645A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973059 | ||||||
| chr2:23973079
|
G | C | 2 | a0001c0001t0012g0131a0001c0001t0031g0134 | 2 | NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.180+1665G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973079 | ||||||
| chr2:23973165
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.180+1751G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973165 | ||||||
| chr2:23973282
|
G | T | 1 | a0001c0001t0010g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.180+1868G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973282 | ||||||
| chr2:23973298
|
C | T | 2 | a0001c0001t0003g0220a0001c0001t0003g0238 | 2 | HG00741.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.180+1884C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973298 | ||||||
| chr2:23973310
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.180+1896C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973310 | ||||||
| chr2:23973320
|
G | A | 1 | a0001c0001t0004g0201 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.180+1906G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973320 | ||||||
| chr2:23973370
|
G | A | 2 | a0001c0001t0011g0185a0001c0001t0046g0184 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.180+1956G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973370 | ||||||
| chr2:23973402
|
G | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.180+1988G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973402 | ||||||
| chr2:23973470
|
C | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.180+2056C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973470 | ||||||
| chr2:23973574
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.180+2160G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973574 | ||||||
| chr2:23973639
|
C | CT | 30 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.180+2238dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 23973639 | |||||
| chr2:23973920
|
G | A | 1 | a0001c0001t0017g0123 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.180+2506G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23973920 | ||||||
| chr2:23974016
|
A | AT | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.180+2618dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 23974016 | |||||
| chr2:23974016
|
A | ATTT | 23 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0225others(20): Show | 23 | HG00735.hp1 HG01243.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.180+2616_180+2618d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 23974016 | |||||
| chr2:23974029
|
T | TC | 7 | a0001c0001t0001g0163a0001c0001t0012g0131a0001c0001t0012g0132others(4): Show | 7 | NA18612.hp2 NA18956.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+2615_180+2616i others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974029 | ||||||
| chr2:23974061
|
C | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(103): Show | 106 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.180+2647C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974061 | ||||||
| chr2:23974078
|
G | A | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+2664G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974078 | ||||||
| chr2:23974355
|
T | G | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.181-2614T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974355 | ||||||
| chr2:23974384
|
C | T | 28 | a0001c0001t0001g0136a0001c0001t0003g0005a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.181-2585C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974384 | ||||||
| chr2:23974502
|
C | T | 1 | a0001c0001t0009g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.181-2467C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974502 | ||||||
| chr2:23974532
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.181-2437G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974532 | ||||||
| chr2:23974595
|
C | T | 4 | a0001c0001t0010g0033a0001c0001t0010g0042a0001c0001t0010g0043others(1): Show | 4 | HG00738.hp2 HG01070.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2374C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974595 | ||||||
| chr2:23974598
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.181-2371G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974598 | ||||||
| chr2:23974625
|
C | T | 1 | a0001c0001t0004g0217 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.181-2344C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974625 | ||||||
| chr2:23974677
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0153a0001c0001t0029g0093 | 3 | HG01074.hp2 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.181-2292T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974677 | ||||||
| chr2:23974945
|
C | T | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181-2024C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23974945 | ||||||
| chr2:23975112
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0045 | 2 | HG03710.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.181-1857G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975112 | ||||||
| chr2:23975172
|
A | G | 1 | a0001c0001t0014g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.181-1797A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975172 | ||||||
| chr2:23975182
|
G | A | 6 | a0001c0001t0014g0189a0001c0001t0014g0190a0001c0001t0014g0191others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1787G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975182 | ||||||
| chr2:23975352
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.181-1617G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975352 | ||||||
| chr2:23975472
|
A | C | 24 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.181-1497A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975472 | ||||||
| chr2:23975502
|
A | C | 1 | a0001c0001t0018g0016 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.181-1467A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975502 | ||||||
| chr2:23975506
|
G | A | 55 | a0001c0001t0003g0005a0001c0001t0003g0220a0001c0001t0003g0221others(52): Show | 55 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.181-1463G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975506 | ||||||
| chr2:23975602
|
A | C | 1 | a0001c0001t0002g0062 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.181-1367A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975602 | ||||||
| chr2:23975688
|
GAGTGC | G | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.181-1276_181-1272d others(7): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 23975688 | |||||
| chr2:23975702
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-1267G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975702 | ||||||
| chr2:23975998
|
A | G | 1 | a0001c0001t0010g0033 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.181-971A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23975998 | ||||||
| chr2:23976137
|
T | A | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.181-832T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976137 | ||||||
| chr2:23976173
|
A | G | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-796A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976173 | ||||||
| chr2:23976181
|
A | T | 1 | a0001c0001t0003g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-788A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976181 | ||||||
| chr2:23976232
|
C | T | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.181-737C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976232 | ||||||
| chr2:23976302
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.181-667G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976302 | ||||||
| chr2:23976389
|
T | C | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.181-580T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976389 | ||||||
| chr2:23976442
|
G | A | 1 | a0001c0001t0020g0007 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.181-527G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976442 | ||||||
| chr2:23976508
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.181-461C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976508 | ||||||
| chr2:23976674
|
C | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181-295C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976674 | ||||||
| chr2:23976676
|
C | T | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.181-293C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976676 | ||||||
| chr2:23976742
|
A | G | 2 | a0001c0001t0022g0024a0001c0001t0022g0029 | 2 | NA19057.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.181-227A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976742 | ||||||
| chr2:23976755
|
A | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.181-214A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976755 | ||||||
| chr2:23976778
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0009g0004 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.181-191G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976778 | ||||||
| chr2:23976812
|
C | T | 3 | a0001c0001t0005g0059a0001c0001t0005g0064a0001c0001t0005g0074 | 3 | HG02809.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181-157C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976812 | ||||||
| chr2:23976841
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-128G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 3/6 | chr2 | 23976841 | ||||||
| chr2:23977327
|
C | A | 1 | a0001c0001t0008g0144 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.287+252C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977327 | ||||||
| chr2:23977346
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.287+271G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977346 | ||||||
| chr2:23977348
|
C | CG | 13 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0124others(10): Show | 13 | HG01934.hp1 HG02135.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.287+280dupG | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23977348 | |||||
| chr2:23977361
|
G | T | 1 | a0001c0001t0017g0084 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.287+286G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977361 | ||||||
| chr2:23977499
|
G | A | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287+424G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977499 | ||||||
| chr2:23977801
|
A | G | 1 | a0001c0001t0005g0245 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287+726A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977801 | ||||||
| chr2:23977808
|
GA | G | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.287+735delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23977808 | |||||
| chr2:23977850
|
G | A | 11 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.287+775G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977850 | ||||||
| chr2:23977917
|
C | T | 13 | a0001c0001t0003g0005a0001c0001t0003g0222a0001c0001t0003g0225others(10): Show | 13 | HG00735.hp1 HG01433.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+842C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23977917 | ||||||
| chr2:23978460
|
G | A | 1 | a0001c0001t0004g0198 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.287+1385G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978460 | ||||||
| chr2:23978528
|
C | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.287+1453C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978528 | ||||||
| chr2:23978528
|
C | G | 11 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.287+1453C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978528 | ||||||
| chr2:23978729
|
G | T | 56 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(53): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.287+1654G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978729 | ||||||
| chr2:23978746
|
G | A | 1 | a0001c0001t0017g0123 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.287+1671G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978746 | ||||||
| chr2:23978790
|
C | T | 1 | a0001c0001t0010g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.287+1715C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978790 | ||||||
| chr2:23978825
|
C | G | 56 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(53): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.287+1750C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978825 | ||||||
| chr2:23978831
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.287+1756A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978831 | ||||||
| chr2:23978832
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.287+1757C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978832 | ||||||
| chr2:23978845
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.287+1770C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23978845 | ||||||
| chr2:23978962
|
C | CA | 27 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.287+1900dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23978962 | |||||
| chr2:23978962
|
CA | C | 30 | a0001c0001t0001g0107a0001c0001t0004g0194a0001c0001t0004g0195others(27): Show | 30 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.287+1900delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23978962 | |||||
| chr2:23979413
|
G | C | 2 | a0001c0001t0007g0164a0001c0001t0037g0101 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.287+2338G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23979413 | ||||||
| chr2:23979642
|
C | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0110others(66): Show | 69 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.287+2567C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23979642 | ||||||
| chr2:23979684
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.287+2609T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23979684 | ||||||
| chr2:23979810
|
A | G | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.287+2735A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23979810 | ||||||
| chr2:23979949
|
T | C | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.287+2874T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23979949 | ||||||
| chr2:23980328
|
T | C | 9 | a0001c0001t0008g0079a0001c0001t0008g0115a0001c0001t0008g0142others(6): Show | 9 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.288-2568T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23980328 | ||||||
| chr2:23980696
|
C | T | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.288-2200C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23980696 | ||||||
| chr2:23980872
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.288-2024C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23980872 | ||||||
| chr2:23980942
|
G | A | 2 | a0001c0001t0020g0007a0001c0001t0020g0008 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.288-1954G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23980942 | ||||||
| chr2:23981024
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.288-1872G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981024 | ||||||
| chr2:23981184
|
G | A | 2 | a0001c0001t0018g0016a0001c0001t0018g0017 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.288-1712G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981184 | ||||||
| chr2:23981273
|
T | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(244): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.288-1623T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981273 | ||||||
| chr2:23981278
|
C | G | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.288-1618C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981278 | ||||||
| chr2:23981303
|
C | CA | 16 | a0001c0001t0001g0118a0001c0001t0001g0147a0001c0001t0002g0034others(13): Show | 16 | HG00544.hp2 HG00642.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.288-1574dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981303 | |||||
| chr2:23981303
|
C | CAA | 25 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.288-1575_288-1574d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981303 | |||||
| chr2:23981303
|
CA | C | 36 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0020others(33): Show | 37 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.288-1574delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981303 | |||||
| chr2:23981355
|
A | G | 1 | a0001c0001t0008g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.288-1541A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981355 | ||||||
| chr2:23981370
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.288-1526T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981370 | ||||||
| chr2:23981476
|
T | TA | 51 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0025others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.288-1389dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
T | TAA | 15 | a0001c0001t0002g0009a0001c0001t0002g0022a0001c0001t0002g0032others(12): Show | 15 | HG02027.hp1 HG02486.hp1 HG03209.hp1 others(12): Show |
intron_variant | MODIFIER | c.288-1390_288-1389d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TA | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.288-1389delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TAA | T | 13 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0006g0206others(10): Show | 13 | HG00140.hp2 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.288-1390_288-1389d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TAAA | T | 19 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0100others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.288-1391_288-1389d others(5): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TAAAAAA | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-1394_288-1389d others(8): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0002g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.288-1400_288-1389d others(14): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981476
|
TAAAAAAA others(7): Show |
T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.288-1402_288-1389d others(16): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981476 | |||||
| chr2:23981508
|
T | A | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.288-1388T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981508 | ||||||
| chr2:23981590
|
A | AATTTG | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0176 | 3 | NA18949.hp2 NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.288-1305_288-1301d others(7): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23981590 | |||||
| chr2:23981616
|
G | A | 4 | a0001c0001t0005g0058a0001c0001t0013g0030a0001c0001t0019g0077others(1): Show | 4 | HG01256.hp1 HG01981.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-1280G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981616 | ||||||
| chr2:23981773
|
C | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.288-1123C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23981773 | ||||||
| chr2:23982204
|
C | CA | 38 | a0001c0001t0002g0050a0001c0001t0003g0005a0001c0001t0003g0044others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.288-679dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 23982204 | |||||
| chr2:23982284
|
G | A | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.288-612G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982284 | ||||||
| chr2:23982315
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.288-581C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982315 | ||||||
| chr2:23982323
|
T | C | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.288-573T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982323 | ||||||
| chr2:23982414
|
C | T | 1 | a0001c0001t0013g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.288-482C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982414 | ||||||
| chr2:23982491
|
G | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.288-405G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982491 | ||||||
| chr2:23982492
|
T | G | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.288-404T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982492 | ||||||
| chr2:23982559
|
T | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.288-337T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982559 | ||||||
| chr2:23982828
|
T | C | 1 | a0001c0001t0034g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.288-68T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982828 | ||||||
| chr2:23982859
|
T | C | 1 | a0005c0005t0006g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.288-37T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 4/6 | chr2 | 23982859 | ||||||
| chr2:23983229
|
G | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425+196G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983229 | ||||||
| chr2:23983443
|
A | G | 55 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(52): Show | 55 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.425+410A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983443 | ||||||
| chr2:23983448
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.425+415G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983448 | ||||||
| chr2:23983780
|
A | G | 7 | a0001c0001t0004g0194a0001c0001t0004g0199a0001c0001t0004g0201others(4): Show | 7 | HG04228.hp1 NA18949.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.425+747A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983780 | ||||||
| chr2:23983876
|
A | G | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.426-797A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983876 | ||||||
| chr2:23983892
|
T | A | 1 | a0001c0001t0042g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.426-781T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983892 | ||||||
| chr2:23983949
|
T | G | 1 | a0001c0001t0002g0037 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.426-724T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23983949 | ||||||
| chr2:23984041
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0013g0052 | 2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.426-632G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 5/6 | chr2 | 23984041 | ||||||
| chr2:23985046
|
A | G | 2 | a0001c0001t0003g0240a0001c0001t0027g0232 | 2 | HG02080.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.584+215A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985046 | ||||||
| chr2:23985068
|
C | CT | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+248dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23985068 | |||||
| chr2:23985088
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.584+257T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985088 | ||||||
| chr2:23985144
|
C | T | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+313C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985144 | ||||||
| chr2:23985259
|
A | T | 15 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(12): Show | 15 | HG00738.hp2 HG01070.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.584+428A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985259 | ||||||
| chr2:23985351
|
T | C | 56 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(53): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.584+520T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985351 | ||||||
| chr2:23985497
|
C | T | 4 | a0001c0001t0014g0189a0001c0001t0014g0190a0001c0001t0014g0192others(1): Show | 4 | HG00140.hp1 HG01069.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+666C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985497 | ||||||
| chr2:23985602
|
G | GT | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.584+786dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23985602 | |||||
| chr2:23985602
|
G | GTT | 13 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(10): Show | 13 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+785_584+786dup others(2): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23985602 | |||||
| chr2:23985602
|
G | GTTT | 25 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0221others(22): Show | 25 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.584+784_584+786dup others(3): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23985602 | |||||
| chr2:23985662
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0109a0001c0001t0009g0004 | 3 | HG02818.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.584+831C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985662 | ||||||
| chr2:23985685
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0136a0001c0001t0009g0003 | 3 | HG00741.hp2 HG01257.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.584+854A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985685 | ||||||
| chr2:23985718
|
A | G | 1 | a0001c0001t0034g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.584+887A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985718 | ||||||
| chr2:23985876
|
G | A | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+1045G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985876 | ||||||
| chr2:23985919
|
G | T | 1 | a0001c0001t0048g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.584+1088G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23985919 | ||||||
| chr2:23986031
|
G | A | 1 | a0001c0001t0009g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.584+1200G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986031 | ||||||
| chr2:23986078
|
A | G | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+1247A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986078 | ||||||
| chr2:23986135
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.584+1304T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986135 | ||||||
| chr2:23986176
|
G | A | 1 | a0001c0001t0007g0166 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.584+1345G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986176 | ||||||
| chr2:23986478
|
T | C | 56 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(53): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.584+1647T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986478 | ||||||
| chr2:23986608
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.584+1777A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986608 | ||||||
| chr2:23986633
|
C | T | 1 | a0001c0001t0014g0191 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.584+1802C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986633 | ||||||
| chr2:23986650
|
C | G | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.584+1819C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23986650 | ||||||
| chr2:23986918
|
C | CT | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+2095dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23986918 | |||||
| chr2:23987029
|
G | T | 1 | a0001c0001t0007g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.584+2198G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987029 | ||||||
| chr2:23987098
|
G | GA | 25 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.584+2278dupA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23987098 | |||||
| chr2:23987181
|
AT | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+2358delT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23987181 | |||||
| chr2:23987206
|
GATAA | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.584+2380_584+2383d others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23987206 | |||||
| chr2:23987405
|
G | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0053a0001c0001t0002g0057others(3): Show | 6 | HG01081.hp1 NA18952.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+2574G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987405 | ||||||
| chr2:23987463
|
T | C | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+2632T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987463 | ||||||
| chr2:23987560
|
C | T | 1 | a0001c0001t0004g0197 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.584+2729C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987560 | ||||||
| chr2:23987635
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.584+2804G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987635 | ||||||
| chr2:23987676
|
G | A | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+2845G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987676 | ||||||
| chr2:23987732
|
C | T | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.584+2901C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987732 | ||||||
| chr2:23987777
|
CA | C | 30 | a0001c0001t0001g0088a0001c0001t0001g0124a0001c0001t0001g0152others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.584+2960delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23987777 | |||||
| chr2:23987777
|
CAA | C | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.584+2959_584+2960d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23987777 | |||||
| chr2:23987892
|
G | A | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.584+3061G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987892 | ||||||
| chr2:23987992
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.584+3161G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987992 | ||||||
| chr2:23987994
|
A | G | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+3163A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23987994 | ||||||
| chr2:23988122
|
CA | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.584+3308delA | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23988122 | |||||
| chr2:23988222
|
T | A | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+3391T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988222 | ||||||
| chr2:23988325
|
G | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG01243.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+3494G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988325 | ||||||
| chr2:23988476
|
G | C | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+3645G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988476 | ||||||
| chr2:23988624
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.584+3793G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988624 | ||||||
| chr2:23988680
|
T | C | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+3849T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988680 | ||||||
| chr2:23988744
|
AGATT | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.584+3930_584+3933d others(6): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23988744 | |||||
| chr2:23988780
|
T | C | 13 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.584+3949T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988780 | ||||||
| chr2:23988945
|
A | G | 1 | a0001c0001t0009g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.584+4114A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988945 | ||||||
| chr2:23988949
|
T | C | 1 | a0001c0001t0026g0006 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.584+4118T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23988949 | ||||||
| chr2:23989002
|
G | T | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | NA18986.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.584+4171G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989002 | ||||||
| chr2:23989076
|
C | G | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+4245C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989076 | ||||||
| chr2:23989246
|
ATG | A | 6 | a0001c0001t0003g0227a0001c0001t0007g0103a0001c0001t0009g0104others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+4433_584+4434d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23989246 | |||||
| chr2:23989306
|
C | CT | 52 | a0001c0001t0001g0138a0001c0001t0002g0036a0001c0001t0003g0005others(49): Show | 52 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.584+4490dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23989306 | |||||
| chr2:23989306
|
C | CTT | 10 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(7): Show | 10 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.584+4489_584+4490d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23989306 | |||||
| chr2:23989530
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.584+4699G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989530 | ||||||
| chr2:23989601
|
A | T | 2 | a0001c0001t0009g0113a0001c0001t0009g0117 | 2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.584+4770A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989601 | ||||||
| chr2:23989690
|
C | G | 1 | a0001c0001t0005g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.584+4859C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989690 | ||||||
| chr2:23989732
|
A | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.584+4901A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989732 | ||||||
| chr2:23989764
|
G | A | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+4933G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989764 | ||||||
| chr2:23989819
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.584+4988C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23989819 | ||||||
| chr2:23990493
|
G | A | 1 | a0001c0001t0024g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.584+5662G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990493 | ||||||
| chr2:23990510
|
A | G | 10 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(7): Show | 10 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.584+5679A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990510 | ||||||
| chr2:23990533
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.584+5702G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990533 | ||||||
| chr2:23990538
|
G | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+5707G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990538 | ||||||
| chr2:23990699
|
A | C | 4 | a0001c0001t0020g0007a0001c0001t0020g0008a0001c0001t0021g0193others(1): Show | 4 | HG02559.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.584+5868A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990699 | ||||||
| chr2:23990835
|
A | G | 3 | a0001c0001t0004g0197a0001c0001t0004g0198a0001c0001t0004g0204 | 3 | HG01081.hp2 HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.584+6004A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990835 | ||||||
| chr2:23990884
|
G | A | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+6053G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990884 | ||||||
| chr2:23990906
|
T | C | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+6075T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990906 | ||||||
| chr2:23990923
|
A | C | 1 | a0001c0001t0002g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.584+6092A>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23990923 | ||||||
| chr2:23991406
|
T | TAC | 30 | a0001c0001t0001g0157a0001c0001t0004g0194a0001c0001t0004g0195others(27): Show | 30 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.584+6599_584+6600d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991406 | |||||
| chr2:23991406
|
T | TACACACA others(3): Show |
8 | a0001c0001t0003g0221a0001c0001t0003g0227a0001c0001t0003g0229others(5): Show | 8 | HG01243.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+6591_584+6600d others(12): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991406 | |||||
| chr2:23991406
|
T | TACACACA others(5): Show |
13 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0222others(10): Show | 13 | HG01168.hp1 HG02080.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.584+6589_584+6600d others(14): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991406 | |||||
| chr2:23991406
|
T | TACACACA others(7): Show |
6 | a0001c0001t0003g0220a0001c0001t0003g0225a0001c0001t0003g0226others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+6587_584+6600d others(16): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991406 | |||||
| chr2:23991406
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0006g0244 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.584+6589_584+6600d others(14): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991406 | |||||
| chr2:23991430
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+6599C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991430 | ||||||
| chr2:23991434
|
T | C | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+6603T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991434 | ||||||
| chr2:23991436
|
C | CAT | 28 | a0001c0001t0001g0095a0001c0001t0003g0005a0001c0001t0003g0044others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+6616_584+6617d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23991436 | |||||
| chr2:23991436
|
C | T | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.584+6605C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991436 | ||||||
| chr2:23991503
|
C | T | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+6672C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991503 | ||||||
| chr2:23991645
|
G | T | 3 | a0001c0001t0003g0231a0001c0001t0003g0233a0001c0001t0003g0234 | 3 | HG02129.hp1 NA18986.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.584+6814G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991645 | ||||||
| chr2:23991705
|
C | T | 8 | a0001c0001t0007g0097a0001c0001t0007g0098a0001c0001t0007g0099others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.584+6874C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23991705 | ||||||
| chr2:23992096
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0176 | 3 | NA18949.hp2 NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.584+7265C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23992096 | ||||||
| chr2:23992525
|
G | T | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(172): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.585-7147G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23992525 | ||||||
| chr2:23992763
|
T | C | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.585-6909T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23992763 | ||||||
| chr2:23992835
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.585-6837A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23992835 | ||||||
| chr2:23993112
|
T | A | 2 | a0001c0001t0024g0239a0003c0004t0025g0243 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.585-6560T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23993112 | ||||||
| chr2:23993301
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.585-6371A>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23993301 | ||||||
| chr2:23993352
|
T | C | 2 | a0001c0001t0011g0185a0001c0001t0046g0184 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.585-6320T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23993352 | ||||||
| chr2:23993588
|
A | G | 3 | a0001c0001t0015g0177a0001c0001t0015g0241a0001c0001t0015g0242 | 3 | HG01243.hp2 HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.585-6084A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23993588 | ||||||
| chr2:23993682
|
A | G | 1 | a0001c0001t0020g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.585-5990A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23993682 | ||||||
| chr2:23993691
|
A | AT | 26 | a0001c0001t0001g0152a0001c0001t0003g0005a0001c0001t0003g0044others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.585-5967dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23993691 | |||||
| chr2:23993711
|
CAG | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.585-5958_585-5957d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23993711 | |||||
| chr2:23994065
|
A | G | 3 | a0001c0001t0004g0196a0001c0001t0004g0202a0001c0001t0004g0205 | 3 | HG00733.hp1 HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.585-5607A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23994065 | ||||||
| chr2:23994139
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0179 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.585-5533C>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23994139 | ||||||
| chr2:23994471
|
T | C | 7 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(4): Show | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.585-5201T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23994471 | ||||||
| chr2:23995225
|
T | C | 2 | a0001c0001t0005g0012a0001c0001t0005g0015 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.585-4447T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995225 | ||||||
| chr2:23995229
|
T | C | 66 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(63): Show | 66 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.585-4443T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995229 | ||||||
| chr2:23995380
|
C | T | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.585-4292C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995380 | ||||||
| chr2:23995462
|
C | T | 1 | a0001c0001t0005g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.585-4210C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995462 | ||||||
| chr2:23995463
|
G | A | 1 | a0003c0004t0025g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.585-4209G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995463 | ||||||
| chr2:23995466
|
C | T | 1 | a0001c0001t0021g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.585-4206C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995466 | ||||||
| chr2:23995562
|
G | A | 1 | a0001c0001t0013g0052 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.585-4110G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995562 | ||||||
| chr2:23995586
|
G | A | 9 | a0001c0001t0006g0206a0001c0001t0006g0207a0001c0001t0006g0208others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.585-4086G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995586 | ||||||
| chr2:23995630
|
T | C | 1 | a0001c0001t0002g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.585-4042T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995630 | ||||||
| chr2:23995661
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.585-4011C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995661 | ||||||
| chr2:23995710
|
G | A | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.585-3962G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995710 | ||||||
| chr2:23995774
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.585-3898G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995774 | ||||||
| chr2:23995914
|
G | T | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585-3758G>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995914 | ||||||
| chr2:23995916
|
G | A | 2 | a0001c0001t0021g0193a0001c0001t0021g0214 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.585-3756G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23995916 | ||||||
| chr2:23996039
|
C | T | 17 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(14): Show | 17 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.585-3633C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23996039 | ||||||
| chr2:23996065
|
A | AT | 36 | a0001c0001t0001g0124a0001c0001t0001g0130a0001c0001t0001g0154others(33): Show | 36 | HG00544.hp2 HG00733.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.585-3588dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23996065 | |||||
| chr2:23996065
|
A | ATT | 24 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.585-3589_585-3588d others(4): Show |
UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23996065 | |||||
| chr2:23996546
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.585-3126G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23996546 | ||||||
| chr2:23996550
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0048 | 2 | HG00099.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.585-3122C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23996550 | ||||||
| chr2:23996670
|
T | C | 1 | a0001c0001t0038g0013 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.585-3002T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23996670 | ||||||
| chr2:23996774
|
C | CT | 11 | a0001c0001t0001g0138a0001c0001t0006g0206a0001c0001t0006g0207others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.585-2882dupT | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 23996774 | |||||
| chr2:23996993
|
A | G | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 28 | HG00733.hp1 HG01081.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.585-2679A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23996993 | ||||||
| chr2:23997271
|
A | G | 25 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.585-2401A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23997271 | ||||||
| chr2:23997482
|
T | C | 56 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(53): Show | 56 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.585-2190T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23997482 | ||||||
| chr2:23997528
|
T | G | 1 | a0001c0001t0037g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.585-2144T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23997528 | ||||||
| chr2:23998005
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.585-1667T>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998005 | ||||||
| chr2:23998091
|
C | T | 6 | a0001c0001t0014g0189a0001c0001t0014g0190a0001c0001t0014g0191others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-1581C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998091 | ||||||
| chr2:23998447
|
C | T | 25 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(22): Show | 25 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.585-1225C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998447 | ||||||
| chr2:23998605
|
A | G | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.585-1067A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998605 | ||||||
| chr2:23998688
|
T | G | 1 | a0001c0001t0041g0105 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.585-984T>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998688 | ||||||
| chr2:23998779
|
G | C | 1 | a0001c0001t0042g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.585-893G>C | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998779 | ||||||
| chr2:23998785
|
G | A | 7 | a0001c0001t0011g0182a0001c0001t0011g0183a0001c0001t0011g0185others(4): Show | 7 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.585-887G>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998785 | ||||||
| chr2:23998824
|
C | G | 28 | a0001c0001t0003g0005a0001c0001t0003g0044a0001c0001t0003g0220others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.585-848C>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23998824 | ||||||
| chr2:23999312
|
T | A | 2 | a0001c0001t0006g0213a0005c0005t0006g0212 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.585-360T>A | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23999312 | ||||||
| chr2:23999367
|
A | G | 3 | a0001c0001t0018g0016a0001c0001t0018g0017a0001c0001t0038g0013 | 3 | HG01167.hp1 HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.585-305A>G | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23999367 | ||||||
| chr2:23999409
|
C | T | 1 | a0001c0001t0038g0013 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.585-263C>T | UBXN2A | ENSG00000173960.14 | transcript | ENST00000309033.5 | protein_coding | 6/6 | chr2 | 23999409 |