| geneid | 79815 |
|---|---|
| ensemblid | ENSG00000104361.10 |
| hgncid | 25854 |
| symbol | NIPAL2 |
| name | NIPA like domain containing 2 |
| refseq_nuc | NM_001321635.2 |
| refseq_prot | NP_001308564.1 |
| ensembl_nuc | ENST00000430223.7 |
| ensembl_prot | ENSP00000407087.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 98189826 |
| end | 98294235 |
| strand | - |
| ver | v1.2 |
| region | chr8:98189826-98294235 |
| region5000 | chr8:98184826-98299235 |
| regionname0 | NIPAL2_chr8_98189826_98294235 |
| regionname5000 | NIPAL2_chr8_98184826_98299235 |
| 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 | 383 | 305 | 81 | 66 | 111 | 13 | 32 | 82 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002 | 0/0 | 383 | 24 | 0 | 1 | 23 | 0 | 0 | 12 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0003 | 0/0 | 383 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0004 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| 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 | 1152 | 187 | 53 | 41 | 65 | 7 | 19 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0002 | 0/0 | 1152 | 111 | 21 | 25 | 46 | 6 | 13 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0003 | 0/0 | 1152 | 15 | 0 | 0 | 15 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0004 | 0/0 | 1152 | 9 | 0 | 1 | 8 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0005 | 0/0 | 1152 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0006 | 0/0 | 1152 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0007 | 0/0 | 1152 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| c0008 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| 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 | 3252 | 95 | 6 | 21 | 51 | 6 | 11 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0002 | 1/0 | 3251 | 75 | 19 | 12 | 39 | 2 | 2 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0003 | 0/0 | 3252 | 49 | 19 | 5 | 18 | 3 | 4 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0004 | 0/1 | 3251 | 45 | 10 | 14 | 10 | 3 | 7 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0005 | 0/0 | 3251 | 19 | 17 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0006 | 0/0 | 3251 | 11 | 1 | 4 | 1 | 0 | 5 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0007 | 0/0 | 3251 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0008 | 0/0 | 3247 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0009 | 0/0 | 3251 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0010 | 0/0 | 3251 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0011 | 0/0 | 3251 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0012 | 0/0 | 3251 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0013 | 0/0 | 3251 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0014 | 0/0 | 3252 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0015 | 0/0 | 3251 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0016 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0017 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0018 | 0/0 | 3251 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0019 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0020 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0021 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0022 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0023 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0024 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0025 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0026 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| t0027 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| 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 | 1152 | 187 | 53 | 41 | 65 | 7 | 19 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002 | 0/0 | 1152 | 111 | 21 | 25 | 46 | 6 | 13 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0005 | 0/0 | 1152 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0006 | 0/0 | 1152 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0003 | 0/0 | 1152 | 15 | 0 | 0 | 15 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0004 | 0/0 | 1152 | 9 | 0 | 1 | 8 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0003c0007 | 0/0 | 1152 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0004c0008 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4403 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0002 | 1/0 | 4402 | 61 | 17 | 11 | 29 | 1 | 2 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0003 | 0/0 | 4403 | 47 | 19 | 5 | 16 | 3 | 4 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0004 | 0/1 | 4402 | 44 | 9 | 14 | 10 | 3 | 7 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0006 | 0/0 | 4402 | 11 | 1 | 4 | 1 | 0 | 5 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0008 | 0/0 | 4398 | 4 | 2 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0009 | 0/0 | 4402 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0010 | 0/0 | 4402 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0011 | 0/0 | 4402 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0012 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0015 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0016 | 0/0 | 4402 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0017 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0019 | 0/0 | 4402 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0023 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0001t0026 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0001 | 0/0 | 4403 | 82 | 3 | 20 | 42 | 6 | 11 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0005 | 0/0 | 4402 | 17 | 15 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0007 | 0/0 | 4402 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0014 | 0/0 | 4403 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0020 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0021 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0022 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0024 | 0/0 | 4403 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0025 | 0/0 | 4403 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0002t0027 | 0/0 | 4403 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0005t0001 | 0/0 | 4403 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0005t0005 | 0/0 | 4402 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0001c0006t0002 | 0/0 | 4402 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0003t0002 | 0/0 | 4402 | 10 | 0 | 0 | 10 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0003t0003 | 0/0 | 4403 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0003t0013 | 0/0 | 4402 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0003t0018 | 0/0 | 4402 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0002c0004t0001 | 0/0 | 4403 | 9 | 0 | 1 | 8 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0003c0007t0002 | 0/0 | 4402 | 2 | 0 | 1 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| a0004c0008t0004 | 0/0 | 4402 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | copy fasta | chr8 | 98184826 | 98299235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0011g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0016g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0017g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0019g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0023g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0001t0026g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0014g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0014g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0020g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0022g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0024g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0025g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0002t0027g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0005t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0006t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0001c0006t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0003t0018g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0002c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0003c0007t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0003c0007t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| a0004c0008t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0007 | t0002 | g0231 | EUR | GBR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | GBR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0105 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0147 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0155 | EUR | FIN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00438 | hp2 | a0002 | c0004 | t0001 | g0269 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00609 | hp2 | a0002 | c0004 | t0001 | g0217 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00621 | hp1 | a0002 | c0003 | t0003 | g0271 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0132 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | CHS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0291 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00733 | hp2 | a0001 | c0001 | t0026 | g0145 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0292 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0135 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0134 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0138 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01099 | hp2 | a0001 | c0001 | t0019 | g0158 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01106 | hp2 | a0003 | c0007 | t0002 | g0064 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01175 | hp2 | a0001 | c0002 | t0027 | g0321 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0325 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01243 | hp2 | a0001 | c0002 | t0005 | g0084 | AMR | PUR | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0101 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01257 | hp2 | a0001 | c0002 | t0014 | g0056 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01258 | hp1 | a0001 | c0002 | t0014 | g0055 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0131 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0136 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01884 | hp1 | a0001 | c0002 | t0022 | g0313 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01975 | hp2 | a0002 | c0004 | t0001 | g0051 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02015 | hp2 | a0002 | c0004 | t0001 | g0287 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0295 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0017 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0191 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02080 | hp1 | a0002 | c0003 | t0002 | g0063 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0196 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02129 | hp2 | a0002 | c0003 | t0002 | g0162 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02132 | hp1 | a0002 | c0004 | t0001 | g0201 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0156 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CDX | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | PEL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02523 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0293 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0129 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0317 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0015 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02723 | hp2 | a0001 | c0002 | t0021 | g0086 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02818 | hp1 | a0001 | c0005 | t0005 | g0029 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0257 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0083 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0082 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0081 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0114 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02976 | hp1 | a0001 | c0006 | t0002 | g0117 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0304 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03017 | hp2 | a0001 | c0002 | t0025 | g0226 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0180 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03130 | hp1 | a0001 | c0006 | t0002 | g0020 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03209 | hp1 | a0001 | c0005 | t0005 | g0315 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0079 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0294 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0150 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03491 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03491 | hp2 | a0001 | c0002 | t0020 | g0309 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03516 | hp1 | a0004 | c0008 | t0004 | g0262 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03516 | hp2 | a0001 | c0001 | t0023 | g0286 | AFR | ESN | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0027 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0122 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03688 | hp2 | a0001 | c0001 | t0016 | g0190 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0318 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0144 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0228 | SAS | BEB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0281 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0008 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18612 | hp1 | a0002 | c0004 | t0001 | g0076 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18747 | hp1 | a0002 | c0003 | t0018 | g0212 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0307 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18941 | hp1 | a0002 | c0004 | t0001 | g0220 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18942 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18944 | hp2 | a0002 | c0004 | t0001 | g0248 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18960 | hp2 | a0002 | c0003 | t0013 | g0211 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18963 | hp1 | a0002 | c0003 | t0013 | g0207 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18966 | hp1 | a0001 | c0001 | t0015 | g0067 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18970 | hp2 | a0002 | c0003 | t0002 | g0189 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0245 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18980 | hp1 | a0002 | c0003 | t0003 | g0218 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18983 | hp2 | a0002 | c0003 | t0002 | g0219 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0187 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18997 | hp1 | a0001 | c0002 | t0007 | g0077 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | LWK | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19062 | hp1 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19063 | hp2 | a0001 | c0001 | t0015 | g0182 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19066 | hp2 | a0001 | c0002 | t0007 | g0274 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19082 | hp1 | a0001 | c0002 | t0007 | g0059 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19084 | hp1 | a0001 | c0002 | t0007 | g0241 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19088 | hp2 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19091 | hp2 | a0002 | c0004 | t0001 | g0297 | EAS | JPT | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0305 | AFR | ASW | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | ASW | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0320 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0251 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0232 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0204 | EUR | TSI | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02486 | hp1 | a0001 | c0002 | t0024 | g0303 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0030 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0306 | AFR | ACB | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0087 | AFR | USA | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0275 | REF | REF | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0208 | REF | REF | NIPAL2_chr8_98184826_98299235 | NIPAL2 | chr8 | 98184826 | 98299235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98205163
|
T | C | 1 | a0003 | 2 | HG00099.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.739A>G | p.Ile247Val | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/11 | 837/4402 | 739/1152 | 247/383 | chr8 | 98205163 | ||
| chr8:98222544
|
T | G | 1 | a0002 | 24 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(21): Show |
missense_variant | MODERATE | c.493A>C | p.Thr165Pro | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/11 | 591/4402 | 493/1152 | 165/383 | chr8 | 98222544 | ||
| chr8:98252527
|
G | T | 1 | a0004 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.312C>A | p.Asn104Lys | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/11 | 410/4402 | 312/1152 | 104/383 | chr8 | 98252527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98195962
|
A | C | 3 | a0001c0002a0001c0005a0002c0004 | 125 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
synonymous_variant | LOW | c.924T>G | p.Thr308Thr | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/11 | 1022/4402 | 924/1152 | 308/383 | chr8 | 98195962 | ||
| chr8:98254043
|
C | T | 2 | a0001c0005a0001c0006 | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
synonymous_variant | LOW | c.180G>A | p.Val60Val | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/11 | 278/4402 | 180/1152 | 60/383 | chr8 | 98254043 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98189921
|
A | G | 1 | a0002c0003t0018 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3057T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 3057 | chr8 | 98189921 | |||||
| chr8:98190029
|
C | T | 1 | a0001c0002t0027 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2949G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2949 | chr8 | 98190029 | |||||
| chr8:98190116
|
T | C | 1 | a0001c0001t0010 | 3 | HG02809.hp2 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2862A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2862 | chr8 | 98190116 | |||||
| chr8:98190132
|
T | C | 1 | a0001c0001t0019 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2846A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2846 | chr8 | 98190132 | |||||
| chr8:98190237
|
G | A | 1 | a0001c0002t0014 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2741C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2741 | chr8 | 98190237 | |||||
| chr8:98190313
|
TTTTG | T | 1 | a0001c0001t0008 | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2661_*2664delCAAA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2661 | chr8 | 98190313 | |||||
| chr8:98190314
|
T | G | 2 | a0001c0001t0003a0002c0003t0003 | 49 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2664A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2664 | chr8 | 98190314 | |||||
| chr8:98190316
|
T | A | 1 | a0001c0002t0022 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2662A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2662 | chr8 | 98190316 | |||||
| chr8:98190359
|
G | A | 17 | a0001c0001t0001a0001c0001t0003a0001c0001t0023others(14): Show | 176 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2619 | chr8 | 98190359 | |||||
| chr8:98190362
|
G | A | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2616C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2616 | chr8 | 98190362 | |||||
| chr8:98190665
|
T | C | 1 | a0001c0001t0009 | 4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2313A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2313 | chr8 | 98190665 | |||||
| chr8:98190760
|
C | T | 1 | a0001c0002t0025 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2218G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 2218 | chr8 | 98190760 | |||||
| chr8:98191079
|
C | T | 1 | a0001c0002t0024 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1899 | chr8 | 98191079 | |||||
| chr8:98191156
|
G | A | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1822C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1822 | chr8 | 98191156 | |||||
| chr8:98191178
|
A | G | 1 | a0001c0001t0023 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1800 | chr8 | 98191178 | |||||
| chr8:98191280
|
C | T | 5 | a0001c0001t0004a0001c0001t0010a0001c0001t0016others(2): Show | 50 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1698G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1698 | chr8 | 98191280 | |||||
| chr8:98191330
|
C | T | 4 | a0001c0002t0005a0001c0002t0021a0001c0002t0022others(1): Show | 21 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1648G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1648 | chr8 | 98191330 | |||||
| chr8:98191481
|
G | GC | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0026others(10): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1496dupG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1496 | chr8 | 98191481 | |||||
| chr8:98191564
|
C | T | 1 | a0001c0001t0017 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1414 | chr8 | 98191564 | |||||
| chr8:98191700
|
C | T | 1 | a0001c0002t0021 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1278 | chr8 | 98191700 | |||||
| chr8:98191710
|
T | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0023others(15): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1268A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 1268 | chr8 | 98191710 | |||||
| chr8:98192160
|
C | T | 1 | a0001c0001t0016 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 818 | chr8 | 98192160 | |||||
| chr8:98192315
|
A | G | 1 | a0002c0003t0013 | 2 | NA18960.hp2 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*663T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 663 | chr8 | 98192315 | |||||
| chr8:98192490
|
C | T | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0023others(15): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 488 | chr8 | 98192490 | |||||
| chr8:98192495
|
T | G | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0026others(10): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*483A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 483 | chr8 | 98192495 | |||||
| chr8:98192538
|
T | A | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0026others(10): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*440A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 440 | chr8 | 98192538 | |||||
| chr8:98192543
|
GA | G | 1 | a0001c0002t0007 | 4 | NA18997.hp1 NA19066.hp2 NA19082.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 434 | chr8 | 98192543 | |||||
| chr8:98192652
|
C | T | 1 | a0001c0002t0020 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 326 | chr8 | 98192652 | |||||
| chr8:98192818
|
G | A | 1 | a0001c0001t0011 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*160C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 160 | chr8 | 98192818 | |||||
| chr8:98192883
|
T | C | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(19): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*95A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 95 | chr8 | 98192883 | |||||
| chr8:98192921
|
G | C | 1 | a0001c0001t0015 | 2 | NA18966.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 11/11 | 57 | chr8 | 98192921 | |||||
| chr8:98294139
|
A | G | 1 | a0001c0001t0012 | 2 | NA18942.hp1 NA18992.hp1 |
5_prime_UTR_variant | MODIFIER | c.-2T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/11 | 2 | chr8 | 98294139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:98193113
|
G | A | 4 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0111others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-23C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193113 | ||||||
| chr8:98193195
|
C | G | 3 | a0001c0002t0001g0195a0001c0002t0001g0199a0001c0002t0001g0200 | 3 | HG00558.hp1 NA18991.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1040-105G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193195 | ||||||
| chr8:98193201
|
G | A | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193201 | ||||||
| chr8:98193293
|
C | G | 1 | a0001c0001t0002g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1040-203G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193293 | ||||||
| chr8:98193384
|
C | T | 195 | a0001c0001t0001g0172a0001c0001t0003g0014a0001c0001t0003g0016others(192): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1040-294G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193384 | ||||||
| chr8:98193386
|
T | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1040-296A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193386 | ||||||
| chr8:98193616
|
C | T | 6 | a0001c0001t0002g0312a0001c0001t0002g0314a0001c0001t0002g0322others(3): Show | 6 | HG02976.hp1 HG03098.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040-526G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193616 | ||||||
| chr8:98193732
|
G | A | 3 | a0001c0001t0003g0109a0001c0001t0003g0179a0001c0001t0003g0290 | 3 | HG02572.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1040-642C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193732 | ||||||
| chr8:98193746
|
T | G | 128 | a0001c0001t0001g0172a0001c0001t0003g0014a0001c0001t0003g0016others(125): Show | 129 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1040-656A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193746 | ||||||
| chr8:98193802
|
C | CA | 117 | a0001c0001t0001g0172a0001c0001t0003g0024a0001c0001t0003g0025others(114): Show | 118 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1040-713dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193802 | ||||||
| chr8:98193802
|
CA | C | 38 | a0001c0001t0002g0111a0001c0001t0002g0164a0001c0001t0002g0166others(35): Show | 38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1040-713delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193802 | ||||||
| chr8:98193855
|
T | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1040-765A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98193855 | ||||||
| chr8:98194070
|
G | A | 103 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(100): Show | 104 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1039+658C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194070 | ||||||
| chr8:98194082
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1039+646T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194082 | ||||||
| chr8:98194112
|
GAGAGTGC others(3): Show |
G | 1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+606_1039+615d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194112 | ||||||
| chr8:98194125
|
G | A | 1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+603C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194125 | ||||||
| chr8:98194126
|
C | T | 1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1039+602G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194126 | ||||||
| chr8:98194140
|
A | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+588T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194140 | ||||||
| chr8:98194205
|
C | T | 1 | a0001c0001t0006g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1039+523G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194205 | ||||||
| chr8:98194233
|
G | A | 4 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324others(1): Show | 4 | HG02976.hp1 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+495C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194233 | ||||||
| chr8:98194359
|
G | C | 2 | a0002c0003t0002g0162a0002c0003t0002g0245 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1039+369C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194359 | ||||||
| chr8:98194646
|
T | C | 12 | a0001c0002t0001g0194a0001c0002t0001g0206a0001c0002t0001g0209others(9): Show | 12 | NA18953.hp2 NA18962.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039+82A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 10/10 | chr8 | 98194646 | ||||||
| chr8:98194874
|
G | A | 1 | a0001c0002t0001g0070 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.945-52C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194874 | ||||||
| chr8:98194889
|
G | A | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.945-67C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194889 | ||||||
| chr8:98194900
|
T | C | 3 | a0001c0002t0001g0003a0001c0002t0001g0127a0001c0002t0001g0128 | 4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-78A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194900 | ||||||
| chr8:98194978
|
A | G | 23 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(20): Show | 23 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.945-156T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98194978 | ||||||
| chr8:98195116
|
A | G | 13 | a0001c0001t0006g0002a0001c0001t0006g0131a0001c0001t0006g0133others(10): Show | 14 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.945-294T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195116 | ||||||
| chr8:98195150
|
A | G | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.945-328T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195150 | ||||||
| chr8:98195168
|
T | C | 1 | a0002c0004t0001g0076 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.945-346A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195168 | ||||||
| chr8:98195572
|
T | A | 1 | a0001c0002t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.944+370A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195572 | ||||||
| chr8:98195633
|
C | T | 4 | a0001c0001t0010g0012a0001c0001t0010g0013a0001c0001t0010g0180others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+309G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195633 | ||||||
| chr8:98195699
|
T | C | 1 | a0001c0002t0001g0022 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.944+243A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195699 | ||||||
| chr8:98195721
|
C | T | 124 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(121): Show | 125 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.944+221G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195721 | ||||||
| chr8:98195780
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944+162G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195780 | ||||||
| chr8:98195837
|
T | C | 171 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(168): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.944+105A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195837 | ||||||
| chr8:98195882
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+60C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195882 | ||||||
| chr8:98195892
|
C | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.944+50G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195892 | ||||||
| chr8:98195896
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.944+46T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195896 | ||||||
| chr8:98195914
|
A | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.944+28T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 9/10 | chr8 | 98195914 | ||||||
| chr8:98196016
|
G | T | 42 | a0001c0001t0001g0172a0001c0001t0004g0001a0001c0001t0004g0041others(39): Show | 44 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.881-11C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196016 | ||||||
| chr8:98196362
|
GC | G | 3 | a0001c0002t0001g0003a0001c0002t0001g0127a0001c0002t0001g0128 | 4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-358delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196362 | ||||||
| chr8:98196366
|
G | T | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.881-361C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196366 | ||||||
| chr8:98196466
|
G | T | 1 | a0001c0001t0006g0006 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.881-461C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196466 | ||||||
| chr8:98196630
|
T | G | 17 | a0001c0001t0006g0002a0001c0001t0006g0131a0001c0001t0006g0133others(14): Show | 18 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.881-625A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196630 | ||||||
| chr8:98196659
|
G | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.881-654C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196659 | ||||||
| chr8:98196793
|
G | A | 1 | a0001c0002t0005g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.881-788C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196793 | ||||||
| chr8:98196809
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.881-804C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196809 | ||||||
| chr8:98196834
|
G | A | 157 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(154): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.881-829C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196834 | ||||||
| chr8:98196858
|
A | G | 1 | a0001c0002t0005g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.881-853T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196858 | ||||||
| chr8:98196891
|
A | C | 3 | a0001c0001t0012g0004a0001c0001t0012g0005a0002c0003t0002g0066 | 3 | HG02523.hp1 NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.881-886T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196891 | ||||||
| chr8:98196976
|
C | A | 101 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.881-971G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98196976 | ||||||
| chr8:98197004
|
T | C | 2 | a0001c0002t0001g0308a0001c0002t0020g0309 | 2 | HG00738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.881-999A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197004 | ||||||
| chr8:98197020
|
C | T | 121 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(118): Show | 122 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.881-1015G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197020 | ||||||
| chr8:98197081
|
CT | C | 30 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.881-1077delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197081 | ||||||
| chr8:98197311
|
C | T | 3 | a0001c0001t0004g0041a0001c0001t0004g0050a0001c0001t0004g0053 | 3 | HG01975.hp1 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.881-1306G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197311 | ||||||
| chr8:98197437
|
T | C | 24 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(21): Show | 24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1432A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197437 | ||||||
| chr8:98197505
|
T | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.881-1500A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197505 | ||||||
| chr8:98197545
|
G | A | 24 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(21): Show | 24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1540C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197545 | ||||||
| chr8:98197580
|
C | T | 1 | a0001c0001t0006g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.881-1575G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197580 | ||||||
| chr8:98197735
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.881-1730T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197735 | ||||||
| chr8:98197751
|
T | C | 14 | a0001c0002t0005g0011a0001c0002t0005g0015a0001c0002t0005g0079others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.881-1746A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197751 | ||||||
| chr8:98197871
|
A | C | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0034others(1): Show | 4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-1866T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197871 | ||||||
| chr8:98197923
|
T | G | 24 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(21): Show | 24 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-1918A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197923 | ||||||
| chr8:98197947
|
C | T | 42 | a0001c0001t0001g0172a0001c0001t0004g0001a0001c0001t0004g0041others(39): Show | 44 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.881-1942G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98197947 | ||||||
| chr8:98198021
|
G | A | 1 | a0001c0001t0002g0173 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.881-2016C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198021 | ||||||
| chr8:98198146
|
AAAC | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0048a0001c0001t0004g0058others(3): Show | 8 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-2144_881-2142d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198146 | ||||||
| chr8:98198378
|
T | C | 179 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(176): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.881-2373A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198378 | ||||||
| chr8:98198572
|
G | C | 125 | a0001c0001t0026g0145a0001c0002t0001g0003a0001c0002t0001g0019others(122): Show | 126 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.881-2567C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198572 | ||||||
| chr8:98198843
|
C | T | 1 | a0001c0001t0003g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.881-2838G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98198843 | ||||||
| chr8:98199071
|
C | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.881-3066G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199071 | ||||||
| chr8:98199175
|
C | T | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.881-3170G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199175 | ||||||
| chr8:98199203
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0004g0276 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.881-3198C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199203 | ||||||
| chr8:98199460
|
T | C | 196 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(193): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.881-3455A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199460 | ||||||
| chr8:98199484
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.881-3479G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199484 | ||||||
| chr8:98199863
|
T | G | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+3245A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199863 | ||||||
| chr8:98199978
|
A | G | 182 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(179): Show | 183 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.880+3130T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98199978 | ||||||
| chr8:98200568
|
T | C | 131 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(128): Show | 132 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.880+2540A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200568 | ||||||
| chr8:98200576
|
A | G | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880+2532T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200576 | ||||||
| chr8:98200644
|
G | A | 30 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.880+2464C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200644 | ||||||
| chr8:98200732
|
C | A | 3 | a0001c0001t0010g0012a0001c0001t0010g0013a0001c0001t0010g0180 | 3 | HG02809.hp2 HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.880+2376G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200732 | ||||||
| chr8:98200735
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0276 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.880+2373G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98200735 | ||||||
| chr8:98201020
|
G | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.880+2088C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201020 | ||||||
| chr8:98201160
|
G | T | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1948C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201160 | ||||||
| chr8:98201170
|
G | A | 1 | a0001c0001t0004g0319 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.880+1938C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201170 | ||||||
| chr8:98201241
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.880+1867G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201241 | ||||||
| chr8:98201414
|
C | T | 5 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0034others(2): Show | 5 | HG01243.hp1 HG02155.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+1694G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201414 | ||||||
| chr8:98201415
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+1693C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201415 | ||||||
| chr8:98201722
|
T | C | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880+1386A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201722 | ||||||
| chr8:98201744
|
T | C | 14 | a0001c0002t0005g0011a0001c0002t0005g0015a0001c0002t0005g0079others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.880+1364A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201744 | ||||||
| chr8:98201801
|
T | G | 1 | a0001c0001t0006g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.880+1307A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98201801 | ||||||
| chr8:98202020
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1088T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202020 | ||||||
| chr8:98202028
|
C | A | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880+1080G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202028 | ||||||
| chr8:98202238
|
C | G | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+870G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202238 | ||||||
| chr8:98202251
|
T | C | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+857A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202251 | ||||||
| chr8:98202252
|
T | C | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.880+856A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202252 | ||||||
| chr8:98202315
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.880+793T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202315 | ||||||
| chr8:98202323
|
C | G | 1 | a0001c0001t0004g0282 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.880+785G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202323 | ||||||
| chr8:98202481
|
C | T | 30 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.880+627G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202481 | ||||||
| chr8:98202515
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880+593A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202515 | ||||||
| chr8:98202531
|
C | A | 1 | a0001c0001t0004g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880+577G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202531 | ||||||
| chr8:98202591
|
G | A | 2 | a0001c0001t0008g0307a0001c0001t0008g0317 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.880+517C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202591 | ||||||
| chr8:98202842
|
A | G | 4 | a0002c0003t0002g0073a0002c0003t0002g0187a0002c0003t0002g0189others(1): Show | 4 | NA18970.hp2 NA18983.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+266T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202842 | ||||||
| chr8:98202874
|
A | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(16): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.880+234T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 8/10 | chr8 | 98202874 | ||||||
| chr8:98203228
|
CTTTAGGA others(4): Show |
C | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.792-43_792-33delTG others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203228 | ||||||
| chr8:98203283
|
T | C | 2 | a0001c0001t0015g0067a0001c0001t0015g0182 | 2 | NA18966.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.792-87A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203283 | ||||||
| chr8:98203338
|
G | A | 1 | a0001c0002t0001g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.792-142C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203338 | ||||||
| chr8:98203383
|
C | T | 17 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(14): Show | 17 | HG01109.hp1 HG02145.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.792-187G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203383 | ||||||
| chr8:98203570
|
T | C | 1 | a0001c0001t0006g0191 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.792-374A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203570 | ||||||
| chr8:98203576
|
G | A | 6 | a0001c0001t0002g0139a0001c0001t0002g0160a0001c0001t0002g0283others(3): Show | 6 | HG00099.hp1 HG00323.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.792-380C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203576 | ||||||
| chr8:98203695
|
T | C | 4 | a0001c0002t0005g0257a0001c0002t0005g0294a0001c0002t0005g0295others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-499A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203695 | ||||||
| chr8:98203831
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.792-635G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203831 | ||||||
| chr8:98203846
|
C | CTG | 93 | a0001c0001t0002g0094a0001c0001t0003g0123a0001c0001t0023g0286others(90): Show | 94 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.792-652_792-651dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTG | 30 | a0001c0002t0001g0022a0001c0002t0001g0078a0001c0002t0001g0080others(27): Show | 30 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.792-654_792-651dup others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTG | 26 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0141others(23): Show | 26 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.792-656_792-651dup others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0003g0028a0001c0001t0009g0031a0001c0001t0009g0034others(1): Show | 4 | HG02155.hp2 NA19062.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-660_792-651dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTGT others(5): Show |
8 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.792-662_792-651dup others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTGT others(9): Show |
4 | a0001c0001t0003g0179a0001c0001t0003g0188a0001c0001t0003g0311others(1): Show | 4 | HG02145.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-666_792-651dup others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTGT others(11): Show |
8 | a0001c0001t0003g0014a0001c0001t0003g0038a0001c0001t0003g0039others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.792-668_792-651dup others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
C | CTGTGTGT others(13): Show |
3 | a0001c0001t0003g0016a0001c0001t0003g0109a0001c0001t0003g0120 | 3 | HG02451.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.792-670_792-651dup others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98203846
|
CTG | C | 14 | a0001c0001t0002g0110a0001c0001t0004g0018a0001c0001t0004g0281others(11): Show | 15 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.792-652_792-651del others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98203846 | ||||||
| chr8:98204042
|
G | T | 15 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.792-846C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204042 | ||||||
| chr8:98204315
|
C | G | 15 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.791+796G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204315 | ||||||
| chr8:98204523
|
G | A | 3 | a0001c0001t0004g0202a0001c0001t0004g0266a0001c0001t0004g0267 | 3 | HG00558.hp2 NA18948.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.791+588C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204523 | ||||||
| chr8:98204569
|
T | A | 19 | a0001c0002t0001g0003a0001c0002t0001g0060a0001c0002t0001g0070others(16): Show | 20 | HG00408.hp1 HG00609.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.791+542A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204569 | ||||||
| chr8:98204890
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.791+221G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204890 | ||||||
| chr8:98204891
|
G | A | 12 | a0001c0002t0005g0011a0001c0002t0005g0015a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.791+220C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 7/10 | chr8 | 98204891 | ||||||
| chr8:98205424
|
G | A | 8 | a0001c0002t0001g0049a0001c0002t0001g0054a0001c0002t0001g0061others(5): Show | 8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-178C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205424 | ||||||
| chr8:98205435
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.656-189G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205435 | ||||||
| chr8:98205478
|
G | GT | 25 | a0001c0001t0002g0243a0001c0001t0003g0014a0001c0001t0003g0016others(22): Show | 25 | HG01074.hp1 HG01109.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.656-233dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205478 | ||||||
| chr8:98205478
|
G | T | 100 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.656-232C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205478 | ||||||
| chr8:98205480
|
T | G | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-234A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205480 | ||||||
| chr8:98205490
|
T | A | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-244A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205490 | ||||||
| chr8:98205582
|
A | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0048a0001c0001t0004g0281others(1): Show | 6 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-336T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205582 | ||||||
| chr8:98205661
|
T | G | 1 | a0001c0001t0004g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.656-415A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205661 | ||||||
| chr8:98205677
|
T | A | 148 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(145): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.656-431A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205677 | ||||||
| chr8:98205941
|
A | G | 1 | a0001c0001t0004g0319 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-695T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98205941 | ||||||
| chr8:98206048
|
G | A | 2 | a0001c0001t0003g0188a0001c0001t0003g0311 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.656-802C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206048 | ||||||
| chr8:98206214
|
G | A | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-968C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206214 | ||||||
| chr8:98206316
|
G | GTA | 14 | a0001c0001t0003g0098a0001c0001t0003g0141a0001c0001t0003g0142others(11): Show | 14 | HG00544.hp1 HG00673.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-1072_656-1071d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | ||||||
| chr8:98206316
|
G | GTGTATA | 27 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(24): Show | 27 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-1071_656-1070i others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | ||||||
| chr8:98206316
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0006g0006a0001c0001t0006g0008 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.656-1071_656-1070i others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | ||||||
| chr8:98206316
|
G | GTGTATAT others(5): Show |
13 | a0001c0001t0004g0018a0001c0001t0004g0115a0001c0001t0004g0116others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.656-1071_656-1070i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | ||||||
| chr8:98206316
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0006g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.656-1071_656-1070i others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206316 | ||||||
| chr8:98206326
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-1081_656-1080i others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206326 | ||||||
| chr8:98206326
|
A | G | 21 | a0001c0001t0004g0018a0001c0001t0004g0115a0001c0001t0004g0116others(18): Show | 22 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.656-1080T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206326 | ||||||
| chr8:98206354
|
A | AAT | 22 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0001t0004g0115others(19): Show | 23 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.656-1110_656-1109d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206354 | ||||||
| chr8:98206513
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.656-1267C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206513 | ||||||
| chr8:98206561
|
C | T | 121 | a0001c0001t0004g0001a0001c0001t0004g0048a0001c0001t0004g0281others(118): Show | 124 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.656-1315G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206561 | ||||||
| chr8:98206705
|
G | A | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.656-1459C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206705 | ||||||
| chr8:98206718
|
G | T | 201 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(198): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.656-1472C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206718 | ||||||
| chr8:98206726
|
C | T | 29 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.656-1480G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206726 | ||||||
| chr8:98206763
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.656-1517G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206763 | ||||||
| chr8:98206776
|
C | CA | 27 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(24): Show | 27 | HG01074.hp1 HG01109.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-1531dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206776 | ||||||
| chr8:98206776
|
CA | C | 119 | a0001c0001t0002g0095a0001c0001t0002g0110a0001c0001t0003g0300others(116): Show | 120 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.656-1531delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206776 | ||||||
| chr8:98206849
|
C | T | 10 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(7): Show | 10 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-1603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206849 | ||||||
| chr8:98206851
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-1605G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98206851 | ||||||
| chr8:98207191
|
G | A | 1 | a0001c0001t0004g0159 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.656-1945C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207191 | ||||||
| chr8:98207193
|
C | T | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0034others(1): Show | 4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-1947G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207193 | ||||||
| chr8:98207268
|
TTC | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0124a0001c0001t0002g0125 | 3 | NA18747.hp2 NA18953.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.656-2024_656-2023d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207268 | ||||||
| chr8:98207316
|
G | A | 4 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2070C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207316 | ||||||
| chr8:98207477
|
T | C | 17 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0015others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-2231A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207477 | ||||||
| chr8:98207479
|
C | T | 27 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(24): Show | 27 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-2233G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207479 | ||||||
| chr8:98207594
|
T | TA | 7 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0111others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-2349dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207594 | ||||||
| chr8:98207749
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.656-2503C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207749 | ||||||
| chr8:98207809
|
A | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-2563T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207809 | ||||||
| chr8:98207962
|
G | T | 1 | a0001c0002t0001g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.656-2716C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207962 | ||||||
| chr8:98207979
|
A | G | 1 | a0001c0001t0004g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.656-2733T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207979 | ||||||
| chr8:98207981
|
G | A | 1 | a0001c0001t0004g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.656-2735C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98207981 | ||||||
| chr8:98208057
|
A | T | 1 | a0001c0001t0002g0279 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.656-2811T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208057 | ||||||
| chr8:98208172
|
G | T | 146 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(143): Show | 147 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.656-2926C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208172 | ||||||
| chr8:98208196
|
T | C | 1 | a0001c0001t0006g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-2950A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208196 | ||||||
| chr8:98208288
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.656-3042G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208288 | ||||||
| chr8:98208313
|
T | C | 190 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(187): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.656-3067A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208313 | ||||||
| chr8:98208416
|
C | A | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.656-3170G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208416 | ||||||
| chr8:98208540
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.656-3294C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208540 | ||||||
| chr8:98208920
|
C | T | 9 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(6): Show | 9 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+3485G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208920 | ||||||
| chr8:98208942
|
A | G | 1 | a0002c0004t0001g0248 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.655+3463T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98208942 | ||||||
| chr8:98209100
|
T | C | 1 | a0001c0002t0001g0070 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.655+3305A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209100 | ||||||
| chr8:98209192
|
A | G | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.655+3213T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209192 | ||||||
| chr8:98209401
|
G | A | 10 | a0001c0001t0003g0118a0001c0001t0008g0291a0001c0001t0008g0292others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.655+3004C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209401 | ||||||
| chr8:98209418
|
G | A | 36 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2987C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209418 | ||||||
| chr8:98209427
|
G | A | 36 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2978C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209427 | ||||||
| chr8:98209445
|
C | CA | 26 | a0001c0001t0001g0172a0001c0001t0002g0095a0001c0001t0002g0103others(23): Show | 26 | HG00438.hp1 HG01192.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+2959dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAA | 8 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.655+2956_655+2959d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAAAA | 13 | a0001c0001t0003g0118a0001c0002t0001g0093a0001c0002t0005g0011others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+2954_655+2959d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAAAAA | 89 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(86): Show | 90 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.655+2953_655+2959d others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAAAAA others(1): Show |
34 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0028others(31): Show | 34 | HG00280.hp1 HG00438.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.655+2952_655+2959d others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0003g0026a0001c0001t0003g0311a0001c0001t0006g0006others(3): Show | 6 | HG02698.hp2 HG03471.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+2951_655+2959d others(11): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+2937_655+2959d others(25): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209445
|
CA | C | 34 | a0001c0001t0002g0139a0001c0001t0003g0098a0001c0001t0003g0121others(31): Show | 35 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.655+2959delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209445 | ||||||
| chr8:98209457
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.655+2948T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209457 | ||||||
| chr8:98209488
|
C | T | 18 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(15): Show | 18 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.655+2917G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209488 | ||||||
| chr8:98209512
|
G | A | 37 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(34): Show | 38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.655+2893C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209512 | ||||||
| chr8:98209557
|
G | A | 3 | a0001c0002t0001g0250a0001c0002t0024g0303a0001c0005t0001g0027 | 3 | HG02486.hp1 HG03579.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.655+2848C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209557 | ||||||
| chr8:98209582
|
T | C | 151 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(148): Show | 152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.655+2823A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209582 | ||||||
| chr8:98209622
|
C | G | 141 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(138): Show | 142 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.655+2783G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209622 | ||||||
| chr8:98209675
|
A | AT | 16 | a0001c0001t0002g0110a0001c0001t0002g0279a0001c0001t0002g0301others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+2729dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98209675 | ||||||
| chr8:98210048
|
T | C | 37 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(34): Show | 38 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.655+2357A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210048 | ||||||
| chr8:98210231
|
G | T | 1 | a0001c0002t0005g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.655+2174C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210231 | ||||||
| chr8:98210267
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+2138C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210267 | ||||||
| chr8:98210275
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.655+2130G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210275 | ||||||
| chr8:98210310
|
ATAAT | A | 36 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(33): Show | 37 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.655+2091_655+2094d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210310 | ||||||
| chr8:98210928
|
C | T | 126 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(123): Show | 127 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.655+1477G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98210928 | ||||||
| chr8:98211049
|
G | A | 2 | a0001c0001t0004g0284a0001c0001t0023g0286 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+1356C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211049 | ||||||
| chr8:98211138
|
A | G | 1 | a0001c0006t0002g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.655+1267T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211138 | ||||||
| chr8:98211530
|
G | A | 289 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.655+875C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211530 | ||||||
| chr8:98211561
|
G | T | 117 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0022others(114): Show | 118 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.655+844C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211561 | ||||||
| chr8:98211711
|
T | TGA | 8 | a0001c0001t0003g0014a0001c0001t0003g0042a0001c0001t0003g0099others(5): Show | 8 | HG02630.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.655+692_655+693dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211711 | ||||||
| chr8:98211732
|
A | G | 142 | a0001c0001t0003g0016a0001c0001t0003g0024a0001c0001t0003g0025others(139): Show | 143 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.655+673T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211732 | ||||||
| chr8:98211733
|
A | AAAGT | 10 | a0001c0001t0003g0016a0001c0001t0003g0038a0001c0001t0003g0039others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGT | 57 | a0001c0001t0003g0109a0001c0001t0003g0118a0001c0001t0003g0290others(54): Show | 57 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(1): Show |
29 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(26): Show | 30 | HG00438.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(3): Show |
20 | a0001c0001t0004g0284a0001c0001t0009g0031a0001c0001t0009g0032others(17): Show | 20 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(5): Show |
12 | a0001c0002t0001g0070a0001c0002t0001g0090a0001c0002t0001g0093others(9): Show | 12 | HG00408.hp1 HG02015.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(7): Show |
2 | a0001c0001t0023g0286a0001c0002t0024g0303 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+671_655+672ins others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(9): Show |
5 | a0001c0002t0005g0017a0001c0002t0005g0079a0001c0002t0005g0304others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AAAGTGTG others(11): Show |
1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.655+671_655+672ins others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGAAAGTG others(3): Show |
6 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(3): Show | 6 | HG02683.hp2 HG02698.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+671_655+672ins others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGT | 3 | a0001c0001t0002g0243a0001c0001t0002g0301a0001c0001t0006g0138 | 3 | HG01074.hp1 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.655+670_655+671dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGT | 29 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(26): Show | 29 | HG00323.hp1 HG00609.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.655+668_655+671dup others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGTGT | 14 | a0001c0001t0002g0113a0001c0001t0002g0170a0001c0001t0002g0177others(11): Show | 14 | HG00099.hp1 HG00621.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+666_655+671dup others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGTGTG others(1): Show |
28 | a0001c0001t0002g0102a0001c0001t0002g0106a0001c0001t0002g0108others(25): Show | 31 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+664_655+671dup others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGTGTG others(3): Show |
48 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0111others(45): Show | 48 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.655+662_655+671dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGTGTG others(5): Show |
13 | a0001c0001t0004g0050a0001c0001t0004g0115a0001c0001t0004g0116others(10): Show | 13 | HG00438.hp1 HG01255.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+660_655+671dup others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211733
|
A | AGTGTGTG others(7): Show |
1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+658_655+671dup others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211733 | ||||||
| chr8:98211787
|
A | C | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.655+618T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211787 | ||||||
| chr8:98211929
|
T | C | 1 | a0001c0006t0002g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.655+476A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98211929 | ||||||
| chr8:98212153
|
A | C | 1 | a0001c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.655+252T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212153 | ||||||
| chr8:98212281
|
T | C | 2 | a0001c0001t0006g0007a0001c0001t0006g0009 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.655+124A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212281 | ||||||
| chr8:98212304
|
A | G | 2 | a0001c0002t0014g0055a0001c0002t0014g0056 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.655+101T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212304 | ||||||
| chr8:98212306
|
C | A | 140 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(137): Show | 141 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.655+99G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 6/10 | chr8 | 98212306 | ||||||
| chr8:98212708
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.559-207A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212708 | ||||||
| chr8:98212795
|
C | T | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.559-294G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212795 | ||||||
| chr8:98212851
|
C | A | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.559-350G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212851 | ||||||
| chr8:98212852
|
C | A | 4 | a0001c0002t0001g0119a0001c0002t0001g0136a0001c0002t0001g0137others(1): Show | 4 | HG01358.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-351G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212852 | ||||||
| chr8:98212955
|
A | G | 3 | a0001c0001t0003g0118a0001c0001t0004g0284a0001c0001t0023g0286 | 3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-454T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212955 | ||||||
| chr8:98212992
|
C | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0284a0001c0001t0023g0286 | 3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-491G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98212992 | ||||||
| chr8:98213109
|
T | C | 138 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(135): Show | 139 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.559-608A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213109 | ||||||
| chr8:98213118
|
C | A | 3 | a0001c0001t0003g0118a0001c0001t0004g0284a0001c0001t0023g0286 | 3 | HG02965.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.559-617G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213118 | ||||||
| chr8:98213126
|
G | C | 7 | a0001c0001t0003g0118a0001c0001t0004g0284a0001c0001t0006g0006others(4): Show | 7 | HG02698.hp2 HG02965.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.559-625C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213126 | ||||||
| chr8:98213442
|
T | A | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.559-941A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213442 | ||||||
| chr8:98213620
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.559-1119G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213620 | ||||||
| chr8:98213757
|
C | T | 12 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(9): Show | 12 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.559-1256G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98213757 | ||||||
| chr8:98214167
|
CTT | C | 140 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(137): Show | 141 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.559-1668_559-1667d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214167 | ||||||
| chr8:98214167
|
CTTT | C | 10 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0109others(7): Show | 10 | HG02451.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.559-1669_559-1667d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214167 | ||||||
| chr8:98214209
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.559-1708C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214209 | ||||||
| chr8:98214283
|
A | C | 151 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(148): Show | 152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.559-1782T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214283 | ||||||
| chr8:98214291
|
G | A | 105 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(102): Show | 106 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.559-1790C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214291 | ||||||
| chr8:98214337
|
T | C | 4 | a0001c0001t0003g0123a0001c0001t0003g0175a0001c0001t0003g0235others(1): Show | 4 | HG00609.hp1 HG00735.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-1836A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214337 | ||||||
| chr8:98214382
|
T | G | 122 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(119): Show | 123 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.559-1881A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214382 | ||||||
| chr8:98214428
|
T | G | 41 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.559-1927A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214428 | ||||||
| chr8:98214490
|
A | G | 151 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(148): Show | 152 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.559-1989T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214490 | ||||||
| chr8:98214513
|
A | G | 1 | a0001c0002t0001g0069 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.559-2012T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214513 | ||||||
| chr8:98214545
|
C | T | 1 | a0002c0003t0003g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.559-2044G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214545 | ||||||
| chr8:98214554
|
A | AT | 6 | a0001c0001t0002g0324a0001c0001t0003g0316a0001c0001t0010g0012others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-2054dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214554 | ||||||
| chr8:98214563
|
C | CT | 41 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(38): Show | 42 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.559-2063dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214563 | ||||||
| chr8:98214593
|
C | T | 150 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0024others(147): Show | 151 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.559-2092G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214593 | ||||||
| chr8:98214841
|
T | C | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.559-2340A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214841 | ||||||
| chr8:98214929
|
T | C | 39 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.559-2428A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98214929 | ||||||
| chr8:98215039
|
C | T | 39 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(36): Show | 40 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.559-2538G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215039 | ||||||
| chr8:98215061
|
C | T | 4 | a0002c0003t0002g0063a0002c0003t0002g0162a0002c0003t0002g0196others(1): Show | 4 | HG02080.hp1 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-2560G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215061 | ||||||
| chr8:98215062
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.559-2561C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215062 | ||||||
| chr8:98215121
|
G | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-2620C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215121 | ||||||
| chr8:98215503
|
C | T | 1 | a0001c0002t0001g0268 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.559-3002G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215503 | ||||||
| chr8:98215714
|
C | T | 1 | a0002c0003t0013g0211 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.559-3213G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215714 | ||||||
| chr8:98215995
|
G | A | 2 | a0001c0001t0003g0289a0001c0001t0003g0300 | 2 | NA18997.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.559-3494C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98215995 | ||||||
| chr8:98216245
|
A | G | 230 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.559-3744T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216245 | ||||||
| chr8:98216344
|
G | A | 2 | a0001c0001t0003g0290a0001c0002t0024g0303 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.559-3843C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216344 | ||||||
| chr8:98216356
|
C | T | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.559-3855G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216356 | ||||||
| chr8:98216526
|
G | C | 1 | a0001c0002t0001g0318 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.559-4025C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216526 | ||||||
| chr8:98216563
|
T | C | 58 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0312others(55): Show | 60 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.559-4062A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216563 | ||||||
| chr8:98216660
|
A | AT | 27 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.559-4160dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216660 | ||||||
| chr8:98216760
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.559-4259C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98216760 | ||||||
| chr8:98217080
|
C | T | 10 | a0001c0002t0001g0049a0001c0002t0001g0054a0001c0002t0001g0061others(7): Show | 10 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.559-4579G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217080 | ||||||
| chr8:98217339
|
G | T | 162 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.559-4838C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217339 | ||||||
| chr8:98217340
|
CA | C | 162 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.559-4840delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217340 | ||||||
| chr8:98217344
|
A | T | 162 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.559-4843T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217344 | ||||||
| chr8:98217346
|
T | TGTGA | 162 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.559-4846_559-4845i others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217346 | ||||||
| chr8:98217347
|
A | G | 162 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.559-4846T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217347 | ||||||
| chr8:98217646
|
T | C | 3 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0034 | 3 | NA19062.hp1 NA19064.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.558+4833A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217646 | ||||||
| chr8:98217903
|
T | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0048a0001c0001t0004g0058others(3): Show | 8 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+4576A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217903 | ||||||
| chr8:98217945
|
C | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.558+4534G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217945 | ||||||
| chr8:98217959
|
C | T | 13 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(10): Show | 14 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+4520G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217959 | ||||||
| chr8:98217988
|
G | C | 2 | a0001c0001t0004g0169a0001c0001t0004g0230 | 2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.558+4491C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98217988 | ||||||
| chr8:98218256
|
G | A | 1 | a0001c0001t0004g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.558+4223C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218256 | ||||||
| chr8:98218341
|
A | C | 2 | a0001c0002t0001g0089a0001c0002t0001g0273 | 2 | HG02300.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.558+4138T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218341 | ||||||
| chr8:98218368
|
G | A | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+4111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218368 | ||||||
| chr8:98218502
|
C | G | 291 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(288): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.558+3977G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218502 | ||||||
| chr8:98218556
|
G | T | 13 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+3923C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218556 | ||||||
| chr8:98218584
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3895C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218584 | ||||||
| chr8:98218594
|
A | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3885T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218594 | ||||||
| chr8:98218667
|
C | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.558+3812G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218667 | ||||||
| chr8:98218694
|
G | A | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+3785C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218694 | ||||||
| chr8:98218723
|
A | C | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+3756T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218723 | ||||||
| chr8:98218731
|
A | G | 28 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+3748T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218731 | ||||||
| chr8:98218750
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.558+3729G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218750 | ||||||
| chr8:98218755
|
G | A | 102 | a0001c0001t0002g0091a0001c0001t0002g0124a0001c0001t0002g0125others(99): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.558+3724C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218755 | ||||||
| chr8:98218789
|
G | T | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+3690C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218789 | ||||||
| chr8:98218926
|
G | C | 1 | a0001c0002t0001g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.558+3553C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98218926 | ||||||
| chr8:98219084
|
T | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+3395A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219084 | ||||||
| chr8:98219484
|
C | T | 1 | a0001c0002t0001g0298 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.558+2995G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219484 | ||||||
| chr8:98219598
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.558+2881C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219598 | ||||||
| chr8:98219609
|
C | T | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+2870G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219609 | ||||||
| chr8:98219788
|
A | C | 1 | a0001c0001t0026g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.558+2691T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219788 | ||||||
| chr8:98219798
|
C | T | 3 | a0001c0002t0001g0003a0001c0002t0001g0127a0001c0002t0001g0128 | 4 | HG01515.hp2 HG01517.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+2681G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219798 | ||||||
| chr8:98219799
|
C | T | 14 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+2680G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219799 | ||||||
| chr8:98219825
|
G | A | 1 | a0001c0002t0007g0059 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.558+2654C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219825 | ||||||
| chr8:98219983
|
G | A | 3 | a0001c0001t0002g0161a0001c0001t0002g0233a0001c0001t0002g0243 | 3 | HG00741.hp1 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.558+2496C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98219983 | ||||||
| chr8:98220041
|
A | AT | 6 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.558+2437dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220041 | ||||||
| chr8:98220041
|
AT | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0110a0001c0001t0002g0314others(6): Show | 9 | HG00558.hp1 HG01069.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+2437delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220041 | ||||||
| chr8:98220055
|
A | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+2424T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220055 | ||||||
| chr8:98220188
|
A | G | 2 | a0001c0001t0003g0290a0001c0002t0024g0303 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.558+2291T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220188 | ||||||
| chr8:98220408
|
A | AT | 54 | a0001c0001t0002g0177a0001c0001t0002g0301a0001c0001t0002g0314others(51): Show | 55 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.558+2070dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220408 | ||||||
| chr8:98220408
|
A | ATT | 9 | a0001c0001t0002g0170a0001c0001t0003g0174a0001c0001t0003g0290others(6): Show | 9 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+2069_558+2070d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220408 | ||||||
| chr8:98220624
|
G | T | 4 | a0001c0002t0001g0078a0001c0002t0001g0223a0001c0002t0001g0278others(1): Show | 4 | HG03017.hp2 NA18978.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1855C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220624 | ||||||
| chr8:98220660
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.558+1819A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220660 | ||||||
| chr8:98220727
|
C | T | 1 | a0002c0004t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.558+1752G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220727 | ||||||
| chr8:98220728
|
G | A | 14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+1751C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220728 | ||||||
| chr8:98220848
|
A | C | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1631T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220848 | ||||||
| chr8:98220853
|
G | A | 33 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.558+1626C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220853 | ||||||
| chr8:98220868
|
C | T | 14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+1611G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220868 | ||||||
| chr8:98220889
|
C | G | 2 | a0001c0001t0002g0312a0001c0001t0002g0314 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.558+1590G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220889 | ||||||
| chr8:98220930
|
ACACCTTC others(12): Show |
A | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.558+1530_558+1548d others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220930 | ||||||
| chr8:98220964
|
C | CT | 50 | a0001c0001t0002g0094a0001c0001t0002g0106a0001c0001t0002g0108others(47): Show | 50 | HG00544.hp2 HG00597.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.558+1514dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
C | CTT | 10 | a0001c0001t0002g0091a0001c0001t0003g0025a0001c0001t0003g0028others(7): Show | 10 | HG01433.hp1 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+1513_558+1514d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CT | C | 26 | a0001c0001t0002g0139a0001c0001t0002g0160a0001c0001t0003g0181others(23): Show | 26 | HG00323.hp1 HG00738.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.558+1514delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTT | C | 16 | a0001c0001t0002g0283a0001c0002t0001g0022a0001c0002t0001g0069others(13): Show | 16 | HG00099.hp1 HG01243.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.558+1513_558+1514d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTT | C | 6 | a0001c0001t0003g0290a0001c0002t0001g0080a0001c0002t0005g0257others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.558+1512_558+1514d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTT | C | 7 | a0001c0001t0004g0101a0001c0001t0004g0169a0001c0001t0004g0178others(4): Show | 7 | HG00673.hp2 HG01167.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.558+1511_558+1514d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTT | C | 67 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0170others(64): Show | 70 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.558+1510_558+1514d others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1505_558+1514d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0003g0014others(3): Show | 6 | HG01167.hp2 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+1504_558+1514d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(5): Show | 8 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.558+1501_558+1514d others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.558+1499_558+1514d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98220964
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.558+1496_558+1514d others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98220964 | ||||||
| chr8:98221201
|
C | A | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+1278G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221201 | ||||||
| chr8:98221252
|
G | A | 155 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.558+1227C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221252 | ||||||
| chr8:98221255
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0019g0158 | 2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.558+1224G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221255 | ||||||
| chr8:98221274
|
C | G | 2 | a0001c0001t0004g0115a0001c0001t0004g0116 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.558+1205G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221274 | ||||||
| chr8:98221292
|
T | G | 2 | a0001c0001t0004g0115a0001c0001t0004g0116 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.558+1187A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221292 | ||||||
| chr8:98221343
|
G | A | 4 | a0001c0001t0009g0031a0001c0001t0009g0032a0001c0001t0009g0034others(1): Show | 4 | HG02155.hp2 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1136C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221343 | ||||||
| chr8:98221363
|
C | CT | 114 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(111): Show | 116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.558+1115dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221363 | ||||||
| chr8:98221474
|
G | T | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.558+1005C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221474 | ||||||
| chr8:98221529
|
G | T | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+950C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221529 | ||||||
| chr8:98221554
|
A | T | 14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+925T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221554 | ||||||
| chr8:98221575
|
T | C | 13 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.558+904A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221575 | ||||||
| chr8:98221580
|
T | C | 2 | a0001c0002t0001g0022a0001c0002t0001g0153 | 2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.558+899A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221580 | ||||||
| chr8:98221585
|
G | A | 28 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+894C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221585 | ||||||
| chr8:98221793
|
C | A | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558+686G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221793 | ||||||
| chr8:98221857
|
G | A | 54 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0314others(51): Show | 56 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.558+622C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221857 | ||||||
| chr8:98221876
|
C | T | 28 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(25): Show | 28 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98221876 | ||||||
| chr8:98222234
|
C | T | 1 | a0001c0002t0001g0003 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.558+245G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98222234 | ||||||
| chr8:98222253
|
G | C | 55 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.558+226C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 5/10 | chr8 | 98222253 | ||||||
| chr8:98222613
|
T | C | 2 | a0001c0001t0012g0004a0001c0001t0012g0005 | 2 | NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.437-13A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222613 | ||||||
| chr8:98222658
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.437-58G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222658 | ||||||
| chr8:98222659
|
G | A | 1 | a0002c0003t0013g0207 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.437-59C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222659 | ||||||
| chr8:98222704
|
C | T | 13 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-104G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222704 | ||||||
| chr8:98222825
|
C | T | 55 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0314others(52): Show | 57 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.437-225G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222825 | ||||||
| chr8:98222849
|
A | G | 248 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.437-249T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222849 | ||||||
| chr8:98222951
|
G | A | 14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-351C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222951 | ||||||
| chr8:98222961
|
T | G | 4 | a0001c0002t0005g0079a0001c0002t0005g0304a0001c0002t0005g0305others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-361A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98222961 | ||||||
| chr8:98223073
|
T | C | 3 | a0001c0002t0001g0326a0001c0002t0001g0327a0001c0002t0001g0328 | 3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.437-473A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223073 | ||||||
| chr8:98223219
|
T | A | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-619A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223219 | ||||||
| chr8:98223490
|
AAACTTGC others(3): Show |
A | 1 | a0001c0001t0002g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.437-900_437-891del others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223490 | ||||||
| chr8:98223600
|
A | G | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1000T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223600 | ||||||
| chr8:98223682
|
A | T | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.437-1082T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223682 | ||||||
| chr8:98223688
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.437-1088G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223688 | ||||||
| chr8:98223720
|
C | T | 210 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.437-1120G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223720 | ||||||
| chr8:98223753
|
C | A | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-1153G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98223753 | ||||||
| chr8:98224071
|
T | C | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1471A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224071 | ||||||
| chr8:98224139
|
A | G | 3 | a0001c0005t0001g0030a0001c0005t0001g0035a0001c0005t0005g0029 | 3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.437-1539T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224139 | ||||||
| chr8:98224341
|
T | G | 2 | a0001c0001t0008g0307a0001c0001t0008g0317 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.437-1741A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224341 | ||||||
| chr8:98224373
|
T | A | 57 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0312others(54): Show | 59 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.437-1773A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224373 | ||||||
| chr8:98224392
|
T | G | 1 | a0001c0001t0002g0285 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.437-1792A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224392 | ||||||
| chr8:98224461
|
A | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1861T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224461 | ||||||
| chr8:98224489
|
A | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1889T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224489 | ||||||
| chr8:98224572
|
A | C | 2 | a0001c0001t0002g0102a0001c0001t0002g0285 | 2 | HG01167.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.437-1972T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224572 | ||||||
| chr8:98224616
|
G | A | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-2016C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224616 | ||||||
| chr8:98224671
|
A | G | 249 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.437-2071T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224671 | ||||||
| chr8:98224755
|
C | CT | 6 | a0001c0001t0003g0174a0001c0001t0003g0290a0001c0001t0004g0281others(3): Show | 6 | HG02486.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-2156dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | ||||||
| chr8:98224755
|
C | CTT | 145 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(142): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.437-2157_437-2156d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | ||||||
| chr8:98224755
|
C | CTTT | 23 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(20): Show | 24 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.437-2158_437-2156d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | ||||||
| chr8:98224755
|
CTTTTTTT | C | 16 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.437-2162_437-2156d others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224755 | ||||||
| chr8:98224760
|
T | C | 13 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-2160A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224760 | ||||||
| chr8:98224911
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.437-2311G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98224911 | ||||||
| chr8:98225018
|
A | C | 198 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(195): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.437-2418T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225018 | ||||||
| chr8:98225037
|
G | T | 198 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(195): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.437-2437C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225037 | ||||||
| chr8:98225185
|
A | G | 3 | a0001c0001t0002g0161a0001c0001t0002g0233a0001c0001t0002g0243 | 3 | HG00741.hp1 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.437-2585T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225185 | ||||||
| chr8:98225414
|
G | T | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-2814C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225414 | ||||||
| chr8:98225462
|
G | A | 2 | a0001c0001t0003g0290a0001c0002t0024g0303 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.437-2862C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225462 | ||||||
| chr8:98225586
|
A | G | 1 | a0001c0002t0005g0011 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437-2986T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225586 | ||||||
| chr8:98225675
|
G | GT | 240 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.437-3076_437-3075i others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225675 | ||||||
| chr8:98225699
|
G | A | 168 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.437-3099C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225699 | ||||||
| chr8:98225785
|
T | C | 232 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.437-3185A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225785 | ||||||
| chr8:98225888
|
G | A | 1 | a0001c0001t0016g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.437-3288C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225888 | ||||||
| chr8:98225922
|
T | A | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-3322A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225922 | ||||||
| chr8:98225979
|
A | G | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-3379T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98225979 | ||||||
| chr8:98226151
|
G | A | 1 | a0001c0002t0001g0318 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.437-3551C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226151 | ||||||
| chr8:98226219
|
G | A | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.437-3619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226219 | ||||||
| chr8:98226240
|
G | A | 10 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0081others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3640C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226240 | ||||||
| chr8:98226285
|
T | C | 14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(11): Show | 15 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-3685A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226285 | ||||||
| chr8:98226303
|
G | A | 10 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0081others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3703C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226303 | ||||||
| chr8:98226328
|
G | A | 3 | a0001c0002t0005g0257a0001c0002t0005g0294a0001c0002t0005g0295 | 3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-3728C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226328 | ||||||
| chr8:98226329
|
C | G | 3 | a0001c0002t0005g0257a0001c0002t0005g0294a0001c0002t0005g0295 | 3 | HG02055.hp1 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-3729G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226329 | ||||||
| chr8:98226450
|
A | G | 109 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(106): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.437-3850T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226450 | ||||||
| chr8:98226495
|
T | C | 1 | a0001c0001t0015g0182 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.437-3895A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226495 | ||||||
| chr8:98226552
|
G | T | 10 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0081others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3952C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226552 | ||||||
| chr8:98226582
|
C | T | 1 | a0001c0002t0001g0310 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437-3982G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226582 | ||||||
| chr8:98226624
|
G | C | 1 | a0001c0001t0004g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.437-4024C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226624 | ||||||
| chr8:98226625
|
T | C | 27 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.437-4025A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226625 | ||||||
| chr8:98226873
|
T | C | 289 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.437-4273A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226873 | ||||||
| chr8:98226978
|
A | C | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4378T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98226978 | ||||||
| chr8:98227334
|
T | C | 8 | a0001c0002t0001g0089a0001c0002t0001g0092a0001c0002t0001g0149others(5): Show | 8 | HG00597.hp2 HG02300.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-4734A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227334 | ||||||
| chr8:98227365
|
CACCTGAA others(6): Show |
C | 1 | a0001c0002t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-4778_437-4766d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227365 | ||||||
| chr8:98227377
|
A | G | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4777T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227377 | ||||||
| chr8:98227390
|
T | C | 1 | a0001c0002t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-4790A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227390 | ||||||
| chr8:98227466
|
G | A | 100 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.437-4866C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227466 | ||||||
| chr8:98227523
|
G | A | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.437-4923C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227523 | ||||||
| chr8:98227537
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.437-4937C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227537 | ||||||
| chr8:98227604
|
A | C | 1 | a0001c0002t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-5004T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227604 | ||||||
| chr8:98227605
|
T | A | 1 | a0001c0002t0001g0214 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437-5005A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227605 | ||||||
| chr8:98227735
|
C | T | 157 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.437-5135G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227735 | ||||||
| chr8:98227852
|
A | G | 1 | a0001c0001t0006g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.437-5252T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227852 | ||||||
| chr8:98227865
|
A | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5265T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227865 | ||||||
| chr8:98227932
|
C | T | 4 | a0001c0002t0001g0090a0001c0002t0001g0244a0001c0002t0001g0263others(1): Show | 4 | HG00408.hp1 HG02015.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5332G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98227932 | ||||||
| chr8:98228006
|
G | C | 195 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.437-5406C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228006 | ||||||
| chr8:98228052
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.437-5452G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228052 | ||||||
| chr8:98228381
|
G | A | 191 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(188): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.437-5781C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228381 | ||||||
| chr8:98228486
|
A | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-5886T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228486 | ||||||
| chr8:98228655
|
G | GATCCATC others(9): Show |
24 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(21): Show | 25 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-6071_437-6056d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228655 | ||||||
| chr8:98228807
|
C | A | 1 | a0001c0001t0006g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.437-6207G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228807 | ||||||
| chr8:98228835
|
G | A | 57 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0314others(54): Show | 59 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.437-6235C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98228835 | ||||||
| chr8:98229507
|
G | A | 1 | a0001c0001t0003g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.436+6648C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229507 | ||||||
| chr8:98229510
|
C | T | 27 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.436+6645G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229510 | ||||||
| chr8:98229580
|
G | A | 2 | a0001c0001t0003g0118a0001c0002t0005g0015 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436+6575C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229580 | ||||||
| chr8:98229718
|
G | A | 5 | a0001c0001t0003g0290a0001c0002t0005g0257a0001c0002t0005g0294others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+6437C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229718 | ||||||
| chr8:98229844
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+6311T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229844 | ||||||
| chr8:98229934
|
T | C | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+6221A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98229934 | ||||||
| chr8:98230169
|
C | T | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436+5986G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230169 | ||||||
| chr8:98230171
|
G | A | 10 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0081others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+5984C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230171 | ||||||
| chr8:98230442
|
T | C | 17 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(14): Show | 18 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+5713A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230442 | ||||||
| chr8:98230643
|
G | A | 3 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0111 | 3 | HG02109.hp1 HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.436+5512C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230643 | ||||||
| chr8:98230687
|
T | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+5468A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230687 | ||||||
| chr8:98230950
|
G | A | 160 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.436+5205C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230950 | ||||||
| chr8:98230951
|
G | A | 1 | a0001c0001t0011g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.436+5204C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98230951 | ||||||
| chr8:98231350
|
T | C | 1 | a0001c0001t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436+4805A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231350 | ||||||
| chr8:98231457
|
C | G | 4 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+4698G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231457 | ||||||
| chr8:98231654
|
A | T | 1 | a0001c0001t0002g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.436+4501T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231654 | ||||||
| chr8:98231689
|
A | AAT | 162 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(159): Show | 163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.436+4465_436+4466i others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231689 | ||||||
| chr8:98231952
|
T | C | 3 | a0001c0001t0004g0018a0001c0001t0004g0115a0001c0001t0004g0116 | 3 | HG02109.hp2 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.436+4203A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231952 | ||||||
| chr8:98231996
|
G | A | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436+4159C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231996 | ||||||
| chr8:98231997
|
CT | C | 29 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.436+4157delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98231997 | ||||||
| chr8:98232004
|
T | A | 6 | a0001c0001t0002g0125a0001c0001t0003g0290a0001c0002t0005g0017others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+4151A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232004 | ||||||
| chr8:98232011
|
T | A | 234 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.436+4144A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232011 | ||||||
| chr8:98232016
|
T | G | 206 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.436+4139A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232016 | ||||||
| chr8:98232057
|
C | T | 3 | a0001c0002t0005g0017a0001c0005t0001g0027a0001c0005t0005g0315 | 3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+4098G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232057 | ||||||
| chr8:98232058
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.436+4097C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232058 | ||||||
| chr8:98232138
|
C | T | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.436+4017G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232138 | ||||||
| chr8:98232139
|
G | T | 3 | a0001c0002t0005g0017a0001c0005t0001g0027a0001c0005t0005g0315 | 3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+4016C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232139 | ||||||
| chr8:98232171
|
G | A | 3 | a0001c0002t0005g0017a0001c0005t0001g0027a0001c0005t0005g0315 | 3 | HG02055.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.436+3984C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232171 | ||||||
| chr8:98232275
|
C | T | 9 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0081others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3880G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232275 | ||||||
| chr8:98232308
|
T | C | 12 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3847A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232308 | ||||||
| chr8:98232556
|
T | C | 2 | a0001c0002t0005g0257a0001c0002t0005g0295 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.436+3599A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232556 | ||||||
| chr8:98232747
|
T | TA | 59 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0312others(56): Show | 61 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.436+3407dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232747 | ||||||
| chr8:98232780
|
T | C | 108 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(105): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.436+3375A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232780 | ||||||
| chr8:98232833
|
T | C | 186 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(183): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.436+3322A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98232833 | ||||||
| chr8:98233033
|
G | A | 11 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(8): Show | 11 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.436+3122C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233033 | ||||||
| chr8:98233058
|
G | A | 12 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3097C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233058 | ||||||
| chr8:98233059
|
A | G | 12 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3096T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233059 | ||||||
| chr8:98233082
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+3073C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233082 | ||||||
| chr8:98233115
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+3040C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233115 | ||||||
| chr8:98233214
|
C | T | 2 | a0002c0003t0002g0162a0002c0003t0002g0245 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.436+2941G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233214 | ||||||
| chr8:98233215
|
G | A | 12 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+2940C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233215 | ||||||
| chr8:98233262
|
GA | G | 6 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+2892delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233262 | ||||||
| chr8:98233263
|
A | T | 2 | a0001c0001t0002g0312a0001c0001t0002g0314 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.436+2892T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233263 | ||||||
| chr8:98233340
|
A | ATG | 138 | a0001c0001t0002g0091a0001c0001t0002g0100a0001c0001t0002g0139others(135): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.436+2813_436+2814d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | ||||||
| chr8:98233340
|
A | ATGTG | 7 | a0001c0002t0001g0019a0001c0002t0001g0088a0001c0002t0001g0150others(4): Show | 7 | HG01099.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+2811_436+2814d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | ||||||
| chr8:98233340
|
ATG | A | 73 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0110others(70): Show | 75 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.436+2813_436+2814d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233340 | ||||||
| chr8:98233445
|
G | A | 5 | a0001c0001t0004g0247a0002c0003t0002g0066a0002c0004t0001g0217others(2): Show | 5 | HG00438.hp1 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2710C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233445 | ||||||
| chr8:98233636
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.436+2519T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233636 | ||||||
| chr8:98233838
|
T | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2317A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233838 | ||||||
| chr8:98233882
|
C | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+2273G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233882 | ||||||
| chr8:98233934
|
A | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+2221T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98233934 | ||||||
| chr8:98234020
|
TC | T | 27 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.436+2134delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234020 | ||||||
| chr8:98234037
|
T | C | 5 | a0001c0001t0003g0290a0001c0002t0005g0114a0001c0002t0005g0257others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2118A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234037 | ||||||
| chr8:98234039
|
G | A | 2 | a0001c0001t0003g0290a0001c0002t0024g0303 | 2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.436+2116C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234039 | ||||||
| chr8:98234219
|
C | T | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1936G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234219 | ||||||
| chr8:98234308
|
C | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.436+1847G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234308 | ||||||
| chr8:98234526
|
T | A | 6 | a0001c0002t0005g0017a0001c0002t0005g0079a0001c0002t0005g0304others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+1629A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234526 | ||||||
| chr8:98234546
|
G | C | 59 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0314others(56): Show | 61 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.436+1609C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234546 | ||||||
| chr8:98234587
|
G | T | 1 | a0001c0002t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.436+1568C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234587 | ||||||
| chr8:98234623
|
C | T | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1532G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234623 | ||||||
| chr8:98234670
|
C | T | 17 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(14): Show | 17 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.436+1485G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234670 | ||||||
| chr8:98234713
|
AT | A | 52 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.436+1441delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234713 | ||||||
| chr8:98234713
|
ATT | A | 178 | a0001c0001t0001g0172a0001c0001t0002g0091a0001c0001t0002g0110others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.436+1440_436+1441d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234713 | ||||||
| chr8:98234771
|
C | T | 1 | a0001c0001t0003g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+1384G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234771 | ||||||
| chr8:98234795
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1360C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234795 | ||||||
| chr8:98234825
|
T | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1330A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98234825 | ||||||
| chr8:98235022
|
C | G | 33 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.436+1133G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235022 | ||||||
| chr8:98235176
|
C | T | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.436+979G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235176 | ||||||
| chr8:98235239
|
T | C | 59 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0312others(56): Show | 61 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.436+916A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235239 | ||||||
| chr8:98235260
|
T | C | 1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.436+895A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235260 | ||||||
| chr8:98235498
|
A | T | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+657T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235498 | ||||||
| chr8:98235537
|
C | T | 6 | a0001c0002t0005g0082a0001c0002t0005g0083a0001c0002t0005g0084others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+618G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235537 | ||||||
| chr8:98235538
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.436+617C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235538 | ||||||
| chr8:98235641
|
ATAT | A | 22 | a0001c0001t0004g0247a0002c0003t0002g0063a0002c0003t0002g0066others(19): Show | 22 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.436+511_436+513del others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235641 | ||||||
| chr8:98235669
|
A | G | 12 | a0001c0002t0001g0069a0001c0002t0005g0011a0001c0002t0005g0079others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+486T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235669 | ||||||
| chr8:98235718
|
T | C | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+437A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235718 | ||||||
| chr8:98235735
|
C | A | 1 | a0001c0001t0004g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.436+420G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235735 | ||||||
| chr8:98235987
|
C | T | 33 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.436+168G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235987 | ||||||
| chr8:98235995
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+160C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98235995 | ||||||
| chr8:98236113
|
A | T | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436+42T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 4/10 | chr8 | 98236113 | ||||||
| chr8:98236354
|
T | C | 1 | a0001c0002t0005g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377-140A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236354 | ||||||
| chr8:98236478
|
A | T | 13 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(10): Show | 13 | HG01243.hp2 HG02559.hp2 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-264T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236478 | ||||||
| chr8:98236563
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.377-349C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236563 | ||||||
| chr8:98236851
|
C | CA | 64 | a0001c0001t0001g0172a0001c0001t0002g0033a0001c0001t0002g0110others(61): Show | 66 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.377-638dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
C | CAA | 16 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(13): Show | 17 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.377-639_377-638dup others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
C | CAAAAAAA | 20 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0141others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.377-644_377-638dup others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0003g0123a0001c0001t0003g0148a0001c0001t0003g0152others(4): Show | 7 | HG00609.hp1 HG02074.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-645_377-638dup others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0006g0006a0001c0001t0006g0008 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.377-647_377-638dup others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
CA | C | 90 | a0001c0001t0002g0091a0001c0001t0002g0160a0001c0001t0002g0283others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.377-638delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
CAA | C | 6 | a0001c0001t0002g0139a0001c0001t0003g0038a0001c0002t0001g0043others(3): Show | 6 | HG00323.hp1 HG01070.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-639_377-638del others(2): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98236851
|
CAAAAAAA others(2): Show |
C | 19 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(16): Show | 19 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.377-646_377-638del others(9): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98236851 | ||||||
| chr8:98237060
|
C | T | 1 | a0001c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.377-846G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237060 | ||||||
| chr8:98237093
|
C | T | 106 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(103): Show | 107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.377-879G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237093 | ||||||
| chr8:98237131
|
A | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-917T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237131 | ||||||
| chr8:98237137
|
T | C | 8 | a0001c0002t0001g0049a0001c0002t0001g0054a0001c0002t0001g0061others(5): Show | 8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-923A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237137 | ||||||
| chr8:98237173
|
G | A | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-959C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237173 | ||||||
| chr8:98237209
|
A | G | 8 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-995T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237209 | ||||||
| chr8:98237216
|
T | TA | 20 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(17): Show | 20 | HG00733.hp1 HG00738.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.377-1003dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237216 | ||||||
| chr8:98237222
|
T | G | 37 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(34): Show | 37 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.377-1008A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237222 | ||||||
| chr8:98237253
|
T | C | 2 | a0001c0002t0005g0017a0001c0005t0005g0315 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.377-1039A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237253 | ||||||
| chr8:98237287
|
A | G | 17 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.377-1073T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237287 | ||||||
| chr8:98237474
|
C | A | 17 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(14): Show | 17 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.377-1260G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237474 | ||||||
| chr8:98237512
|
C | T | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1298G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237512 | ||||||
| chr8:98237576
|
C | T | 2 | a0002c0003t0002g0187a0002c0003t0002g0189 | 2 | NA18970.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.377-1362G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237576 | ||||||
| chr8:98237629
|
T | G | 1 | a0001c0001t0002g0259 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.377-1415A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237629 | ||||||
| chr8:98237630
|
G | A | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1416C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237630 | ||||||
| chr8:98237892
|
G | A | 27 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(24): Show | 27 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.377-1678C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237892 | ||||||
| chr8:98237949
|
C | T | 1 | a0001c0001t0004g0299 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.377-1735G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98237949 | ||||||
| chr8:98238016
|
A | G | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1802T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238016 | ||||||
| chr8:98238492
|
G | A | 1 | a0002c0003t0002g0066 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.377-2278C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238492 | ||||||
| chr8:98238608
|
C | CT | 37 | a0001c0001t0002g0085a0001c0001t0002g0259a0001c0001t0002g0280others(34): Show | 37 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.377-2395dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238608 | ||||||
| chr8:98238616
|
T | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.377-2402A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238616 | ||||||
| chr8:98238621
|
T | C | 31 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(28): Show | 31 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.377-2407A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238621 | ||||||
| chr8:98238622
|
C | T | 34 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(31): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.377-2408G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238622 | ||||||
| chr8:98238676
|
C | T | 61 | a0001c0001t0001g0172a0001c0001t0002g0110a0001c0001t0002g0312others(58): Show | 63 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.377-2462G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238676 | ||||||
| chr8:98238726
|
T | C | 2 | a0002c0003t0002g0162a0002c0003t0002g0245 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.377-2512A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238726 | ||||||
| chr8:98238873
|
C | T | 1 | a0002c0004t0001g0248 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.377-2659G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238873 | ||||||
| chr8:98238903
|
G | A | 1 | a0001c0002t0001g0223 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.377-2689C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238903 | ||||||
| chr8:98238904
|
G | A | 1 | a0001c0001t0026g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.377-2690C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238904 | ||||||
| chr8:98238937
|
G | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-2723C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98238937 | ||||||
| chr8:98239130
|
G | A | 12 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(9): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-2916C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239130 | ||||||
| chr8:98239215
|
T | C | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.377-3001A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239215 | ||||||
| chr8:98239316
|
C | T | 1 | a0001c0002t0005g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.377-3102G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239316 | ||||||
| chr8:98239761
|
C | T | 8 | a0001c0002t0001g0049a0001c0002t0001g0054a0001c0002t0001g0061others(5): Show | 8 | HG01109.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-3547G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239761 | ||||||
| chr8:98239777
|
A | G | 1 | a0002c0003t0002g0219 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.377-3563T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239777 | ||||||
| chr8:98239887
|
G | A | 243 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.377-3673C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98239887 | ||||||
| chr8:98240109
|
A | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-3895T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240109 | ||||||
| chr8:98240144
|
T | C | 1 | a0002c0003t0002g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.377-3930A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240144 | ||||||
| chr8:98240217
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.377-4003A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240217 | ||||||
| chr8:98240272
|
A | G | 1 | a0002c0004t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.377-4058T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240272 | ||||||
| chr8:98240334
|
T | C | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-4120A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240334 | ||||||
| chr8:98240619
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.377-4405G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240619 | ||||||
| chr8:98240638
|
T | C | 3 | a0001c0005t0001g0030a0001c0005t0001g0035a0001c0005t0005g0029 | 3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.377-4424A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240638 | ||||||
| chr8:98240864
|
G | A | 100 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.377-4650C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240864 | ||||||
| chr8:98240883
|
C | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-4669G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240883 | ||||||
| chr8:98240898
|
G | A | 8 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-4684C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98240898 | ||||||
| chr8:98241139
|
A | T | 22 | a0001c0001t0002g0085a0001c0001t0003g0014a0001c0001t0003g0016others(19): Show | 22 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.377-4925T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241139 | ||||||
| chr8:98241411
|
C | T | 242 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.377-5197G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241411 | ||||||
| chr8:98241649
|
G | A | 242 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.377-5435C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241649 | ||||||
| chr8:98241781
|
G | C | 242 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.377-5567C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241781 | ||||||
| chr8:98241817
|
C | T | 242 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.377-5603G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241817 | ||||||
| chr8:98241831
|
CT | C | 50 | a0001c0001t0001g0172a0001c0001t0003g0316a0001c0001t0004g0001others(47): Show | 52 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.377-5618delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241831 | ||||||
| chr8:98241835
|
C | T | 1 | a0001c0001t0004g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-5621G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241835 | ||||||
| chr8:98241847
|
C | T | 1 | a0001c0006t0002g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.377-5633G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241847 | ||||||
| chr8:98241904
|
C | T | 8 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-5690G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98241904 | ||||||
| chr8:98242037
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.377-5823C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242037 | ||||||
| chr8:98242093
|
G | C | 241 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(238): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.377-5879C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242093 | ||||||
| chr8:98242264
|
C | G | 4 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(1): Show | 4 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-6050G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242264 | ||||||
| chr8:98242300
|
C | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-6086G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242300 | ||||||
| chr8:98242315
|
G | T | 240 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(237): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.377-6101C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242315 | ||||||
| chr8:98242402
|
G | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-6188C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242402 | ||||||
| chr8:98242488
|
A | ATTT | 25 | a0001c0001t0003g0098a0001c0001t0003g0121a0001c0001t0003g0123others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.377-6277_377-6275d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(4): Show |
1 | a0001c0002t0001g0327 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.377-6275_377-6274i others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(5): Show |
1 | a0001c0002t0001g0224 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.377-6275_377-6274i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(5): Show |
50 | a0001c0001t0002g0091a0001c0001t0002g0139a0001c0001t0002g0160others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(6): Show |
37 | a0001c0001t0004g0144a0001c0001t0004g0165a0001c0002t0001g0003others(34): Show | 38 | HG00408.hp1 HG00558.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(7): Show |
8 | a0001c0001t0004g0247a0001c0002t0001g0060a0001c0002t0001g0061others(5): Show | 8 | HG00438.hp1 HG01109.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-6275_377-6274i others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTG others(8): Show |
1 | a0002c0004t0001g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.377-6275_377-6274i others(17): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(2): Show |
7 | a0001c0001t0002g0177a0001c0001t0008g0307a0001c0001t0008g0317others(4): Show | 7 | HG01255.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.377-6283_377-6275d others(11): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(3): Show |
9 | a0001c0001t0002g0170a0001c0001t0002g0301a0001c0001t0006g0002others(6): Show | 10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.377-6284_377-6275d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(4): Show |
16 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0003g0038others(13): Show | 16 | HG01346.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-6285_377-6275d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0003g0120a0001c0002t0007g0241a0001c0006t0002g0020 | 3 | HG02818.hp2 HG03130.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.377-6286_377-6275d others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(6): Show |
2 | a0001c0002t0007g0059a0001c0002t0007g0274 | 2 | NA19066.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.377-6287_377-6275d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(7): Show |
6 | a0001c0001t0002g0085a0001c0001t0003g0025a0001c0001t0003g0026others(3): Show | 6 | HG02280.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-6288_377-6275d others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0003g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-6290_377-6275d others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242488
|
AT | A | 54 | a0001c0001t0001g0172a0001c0001t0002g0065a0001c0001t0002g0110others(51): Show | 56 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.377-6275delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242488 | ||||||
| chr8:98242489
|
T | TTTTTTGT others(7): Show |
1 | a0001c0002t0022g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.377-6276_377-6275i others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242489 | ||||||
| chr8:98242494
|
T | TGTTTTTT others(5): Show |
1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.377-6281_377-6280i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242494 | ||||||
| chr8:98242585
|
G | A | 238 | a0001c0001t0001g0172a0001c0001t0002g0085a0001c0001t0002g0091others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.377-6371C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242585 | ||||||
| chr8:98242635
|
A | G | 33 | a0001c0001t0002g0139a0001c0001t0002g0160a0001c0001t0002g0283others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.377-6421T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242635 | ||||||
| chr8:98242652
|
A | G | 22 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(19): Show | 23 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.377-6438T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242652 | ||||||
| chr8:98242779
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.377-6565G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242779 | ||||||
| chr8:98242780
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6566C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242780 | ||||||
| chr8:98242839
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6625A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242839 | ||||||
| chr8:98242857
|
A | G | 1 | a0001c0002t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.377-6643T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242857 | ||||||
| chr8:98242942
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.377-6728T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98242942 | ||||||
| chr8:98243197
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.377-6983G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243197 | ||||||
| chr8:98243318
|
G | A | 2 | a0001c0001t0003g0289a0002c0004t0001g0076 | 2 | NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.377-7104C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243318 | ||||||
| chr8:98243486
|
G | A | 21 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0002g0323others(18): Show | 21 | HG00558.hp2 HG00673.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.377-7272C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243486 | ||||||
| chr8:98243550
|
G | A | 7 | a0001c0001t0003g0016a0001c0001t0003g0316a0001c0001t0010g0012others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.377-7336C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243550 | ||||||
| chr8:98243691
|
T | C | 14 | a0001c0001t0002g0110a0001c0001t0003g0038a0001c0001t0003g0039others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.377-7477A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243691 | ||||||
| chr8:98243772
|
A | G | 5 | a0001c0001t0003g0290a0001c0002t0005g0015a0001c0002t0024g0303others(2): Show | 5 | HG02486.hp1 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-7558T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243772 | ||||||
| chr8:98243793
|
AC | A | 74 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(71): Show | 77 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.377-7580delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243793 | ||||||
| chr8:98243870
|
T | A | 2 | a0001c0002t0001g0318a0001c0002t0001g0320 | 2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.377-7656A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243870 | ||||||
| chr8:98243893
|
A | T | 1 | a0001c0002t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.377-7679T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243893 | ||||||
| chr8:98243926
|
T | G | 10 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(7): Show | 10 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.377-7712A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98243926 | ||||||
| chr8:98244081
|
A | G | 3 | a0001c0001t0003g0290a0001c0002t0024g0303a0004c0008t0004g0262 | 3 | HG02486.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.377-7867T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244081 | ||||||
| chr8:98244202
|
C | CA | 66 | a0001c0001t0002g0037a0001c0001t0002g0139a0001c0001t0002g0160others(63): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.377-7989dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244202 | ||||||
| chr8:98244266
|
C | CGGTGGGC others(33): Show |
2 | a0001c0001t0004g0115a0001c0001t0004g0116 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.377-8092_377-8053d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244266 | ||||||
| chr8:98244266
|
C | CGGTGGGC others(73): Show |
2 | a0001c0002t0005g0015a0001c0005t0001g0027 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.377-8053_377-8052i others(82): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244266 | ||||||
| chr8:98244267
|
G | T | 8 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0002t0005g0082others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-8053C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244267 | ||||||
| chr8:98244285
|
A | AGGTAGTC others(33): Show |
1 | a0001c0001t0016g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.377-8111_377-8072d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | ||||||
| chr8:98244285
|
AGGTAGTC others(33): Show |
A | 9 | a0001c0001t0002g0285a0001c0001t0003g0118a0001c0001t0004g0284others(6): Show | 9 | HG02004.hp1 HG02155.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-8111_377-8072d others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | ||||||
| chr8:98244285
|
AGGTAGTC others(73): Show |
A | 184 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0002g0046others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.376+8098_377-8072d others(82): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244285 | ||||||
| chr8:98244287
|
G | GTAGTCTG others(33): Show |
66 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(63): Show | 69 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.377-8074_377-8073i others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244287 | ||||||
| chr8:98244325
|
G | A | 70 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(67): Show | 73 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.377-8111C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244325 | ||||||
| chr8:98244327
|
G | A | 2 | a0001c0002t0005g0015a0001c0005t0001g0027 | 2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.377-8113C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244327 | ||||||
| chr8:98244365
|
G | A | 71 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0036others(68): Show | 74 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.376+8098C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244365 | ||||||
| chr8:98244405
|
G | C | 16 | a0001c0001t0002g0110a0001c0001t0003g0038a0001c0001t0003g0039others(13): Show | 16 | HG00733.hp1 HG00738.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.376+8058C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244405 | ||||||
| chr8:98244500
|
T | C | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.376+7963A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244500 | ||||||
| chr8:98244572
|
C | CGCTGTGG others(14): Show |
59 | a0001c0001t0002g0037a0001c0001t0002g0139a0001c0001t0002g0160others(56): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.376+7870_376+7890d others(23): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244572 | ||||||
| chr8:98244572
|
CGCTGTGG others(14): Show |
C | 96 | a0001c0001t0002g0033a0001c0001t0002g0046a0001c0001t0002g0047others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.376+7870_376+7890d others(23): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244572 | ||||||
| chr8:98244579
|
G | A | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7884C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244579 | ||||||
| chr8:98244581
|
G | A | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7882C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244581 | ||||||
| chr8:98244582
|
ATG | A | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7879_376+7880d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244582 | ||||||
| chr8:98244585
|
A | G | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7878T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244585 | ||||||
| chr8:98244587
|
A | G | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7876T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244587 | ||||||
| chr8:98244593
|
G | C | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7870C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244593 | ||||||
| chr8:98244635
|
T | C | 5 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0301others(2): Show | 5 | HG01123.hp2 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+7828A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244635 | ||||||
| chr8:98244645
|
G | A | 2 | a0001c0002t0005g0257a0001c0002t0005g0295 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.376+7818C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244645 | ||||||
| chr8:98244870
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.376+7593G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244870 | ||||||
| chr8:98244949
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0001g0320 | 2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.376+7514G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98244949 | ||||||
| chr8:98245163
|
C | T | 58 | a0001c0001t0002g0037a0001c0001t0002g0139a0001c0001t0002g0160others(55): Show | 59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.376+7300G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245163 | ||||||
| chr8:98245211
|
C | T | 5 | a0001c0001t0003g0118a0001c0001t0003g0290a0001c0002t0005g0114others(2): Show | 5 | HG02486.hp1 HG02965.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+7252G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245211 | ||||||
| chr8:98245224
|
C | A | 4 | a0001c0001t0004g0122a0001c0001t0004g0129a0001c0001t0004g0130others(1): Show | 4 | HG02602.hp2 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+7239G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245224 | ||||||
| chr8:98245232
|
G | A | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376+7231C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245232 | ||||||
| chr8:98245289
|
A | T | 6 | a0001c0001t0008g0291a0001c0001t0008g0292a0001c0001t0008g0307others(3): Show | 6 | HG00733.hp1 HG00738.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+7174T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245289 | ||||||
| chr8:98245680
|
T | C | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+6783A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245680 | ||||||
| chr8:98245808
|
A | G | 1 | a0001c0001t0004g0101 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.376+6655T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245808 | ||||||
| chr8:98245959
|
G | A | 74 | a0001c0001t0002g0037a0001c0001t0002g0110a0001c0001t0002g0139others(71): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.376+6504C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245959 | ||||||
| chr8:98245975
|
TC | T | 5 | a0001c0001t0003g0234a0001c0001t0003g0236a0001c0005t0001g0030others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+6487delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98245975 | ||||||
| chr8:98246006
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376+6457C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246006 | ||||||
| chr8:98246261
|
A | C | 7 | a0001c0001t0002g0085a0001c0001t0003g0024a0001c0001t0003g0025others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+6202T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246261 | ||||||
| chr8:98246388
|
C | T | 5 | a0001c0001t0002g0285a0001c0001t0002g0322a0001c0001t0002g0323others(2): Show | 5 | HG02257.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+6075G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246388 | ||||||
| chr8:98246420
|
A | T | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.376+6043T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246420 | ||||||
| chr8:98246451
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0166a0001c0001t0002g0167 | 3 | NA18944.hp1 NA18957.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.376+6012C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246451 | ||||||
| chr8:98246628
|
G | T | 2 | a0001c0001t0008g0291a0001c0001t0008g0292 | 2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.376+5835C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246628 | ||||||
| chr8:98246785
|
G | C | 1 | a0001c0001t0003g0192 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.376+5678C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246785 | ||||||
| chr8:98246945
|
A | T | 1 | a0002c0004t0001g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.376+5518T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246945 | ||||||
| chr8:98246956
|
C | A | 1 | a0001c0002t0001g0057 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.376+5507G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98246956 | ||||||
| chr8:98247120
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.376+5343G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247120 | ||||||
| chr8:98247346
|
A | C | 1 | a0001c0002t0005g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.376+5117T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247346 | ||||||
| chr8:98247413
|
C | A | 83 | a0001c0001t0002g0033a0001c0001t0002g0036a0001c0001t0002g0045others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.376+5050G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247413 | ||||||
| chr8:98247454
|
T | C | 223 | a0001c0001t0001g0172a0001c0001t0002g0033a0001c0001t0002g0036others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.376+5009A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247454 | ||||||
| chr8:98247564
|
C | T | 12 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0296others(9): Show | 12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+4899G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247564 | ||||||
| chr8:98247723
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+4740C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247723 | ||||||
| chr8:98247736
|
A | C | 2 | a0001c0001t0002g0277a0001c0002t0001g0019 | 2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.376+4727T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98247736 | ||||||
| chr8:98248084
|
A | G | 1 | a0001c0002t0005g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.376+4379T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248084 | ||||||
| chr8:98248088
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+4375G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248088 | ||||||
| chr8:98248137
|
T | C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.376+4326A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248137 | ||||||
| chr8:98248216
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.376+4247G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248216 | ||||||
| chr8:98248976
|
C | A | 7 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.376+3487G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248976 | ||||||
| chr8:98248985
|
T | C | 1 | a0001c0001t0003g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376+3478A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98248985 | ||||||
| chr8:98249097
|
T | A | 3 | a0001c0005t0001g0030a0001c0005t0001g0035a0001c0005t0005g0029 | 3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.376+3366A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249097 | ||||||
| chr8:98249102
|
G | A | 1 | a0001c0002t0027g0321 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.376+3361C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249102 | ||||||
| chr8:98249154
|
T | G | 82 | a0001c0001t0001g0172a0001c0001t0002g0124a0001c0001t0002g0125others(79): Show | 82 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.376+3309A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249154 | ||||||
| chr8:98249220
|
G | C | 1 | a0001c0002t0001g0107 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.376+3243C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249220 | ||||||
| chr8:98249490
|
A | G | 8 | a0001c0001t0002g0036a0001c0001t0004g0048a0001c0001t0004g0239others(5): Show | 9 | HG00280.hp1 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+2973T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249490 | ||||||
| chr8:98249517
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2946C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249517 | ||||||
| chr8:98249598
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2865T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249598 | ||||||
| chr8:98249739
|
C | T | 10 | a0001c0001t0003g0118a0001c0002t0005g0081a0001c0002t0005g0306others(7): Show | 10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+2724G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249739 | ||||||
| chr8:98249802
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2661C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249802 | ||||||
| chr8:98249936
|
A | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2527T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98249936 | ||||||
| chr8:98250003
|
C | T | 5 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+2460G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250003 | ||||||
| chr8:98250217
|
A | G | 132 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(129): Show | 133 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.376+2246T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250217 | ||||||
| chr8:98250289
|
G | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+2174C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250289 | ||||||
| chr8:98250324
|
TAA | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+2137_376+2138d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250324 | ||||||
| chr8:98250336
|
G | A | 31 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0163others(28): Show | 31 | HG00408.hp2 HG00597.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.376+2127C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250336 | ||||||
| chr8:98250411
|
G | T | 2 | a0001c0001t0010g0180a0001c0002t0005g0257 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.376+2052C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250411 | ||||||
| chr8:98250498
|
C | T | 3 | a0001c0001t0003g0235a0001c0001t0004g0169a0001c0002t0001g0186 | 3 | HG00673.hp2 HG02523.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.376+1965G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250498 | ||||||
| chr8:98250510
|
A | G | 5 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+1953T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250510 | ||||||
| chr8:98250659
|
A | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+1804T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250659 | ||||||
| chr8:98250837
|
C | G | 1 | a0001c0002t0005g0079 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.376+1626G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250837 | ||||||
| chr8:98250944
|
C | T | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.376+1519G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98250944 | ||||||
| chr8:98251164
|
A | G | 2 | a0001c0002t0005g0017a0001c0002t0024g0303 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.376+1299T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251164 | ||||||
| chr8:98251190
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+1273G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251190 | ||||||
| chr8:98251191
|
G | A | 1 | a0001c0001t0010g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+1272C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251191 | ||||||
| chr8:98251449
|
T | C | 7 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+1014A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251449 | ||||||
| chr8:98251489
|
G | C | 1 | a0001c0001t0003g0316 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376+974C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251489 | ||||||
| chr8:98251497
|
A | C | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.376+966T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251497 | ||||||
| chr8:98251586
|
A | G | 9 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0040others(6): Show | 9 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+877T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251586 | ||||||
| chr8:98251631
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.376+832T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98251631 | ||||||
| chr8:98252178
|
T | C | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.376+285A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252178 | ||||||
| chr8:98252230
|
C | G | 1 | a0001c0001t0010g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.376+233G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252230 | ||||||
| chr8:98252260
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0276 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.376+203G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252260 | ||||||
| chr8:98252417
|
A | T | 1 | a0001c0001t0004g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+46T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 3/10 | chr8 | 98252417 | ||||||
| chr8:98252733
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.205-99C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98252733 | ||||||
| chr8:98253020
|
T | C | 1 | a0001c0001t0006g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205-386A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253020 | ||||||
| chr8:98253393
|
A | G | 2 | a0001c0001t0004g0178a0001c0001t0004g0276 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.204+626T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253393 | ||||||
| chr8:98253743
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.204+276T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253743 | ||||||
| chr8:98253750
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.204+269G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253750 | ||||||
| chr8:98253876
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+143A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 2/10 | chr8 | 98253876 | ||||||
| chr8:98254511
|
A | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-424T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254511 | ||||||
| chr8:98254559
|
A | G | 12 | a0001c0001t0002g0312a0001c0001t0002g0314a0001c0001t0003g0014others(9): Show | 12 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-472T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254559 | ||||||
| chr8:98254854
|
G | C | 2 | a0001c0001t0003g0025a0001c0002t0005g0114 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.136-767C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254854 | ||||||
| chr8:98254854
|
G | T | 3 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0028 | 3 | HG01109.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-767C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98254854 | ||||||
| chr8:98255045
|
ATGCTTCT others(15): Show |
A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-980_136-959del others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255045 | ||||||
| chr8:98255417
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-1330G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255417 | ||||||
| chr8:98255520
|
T | C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-1433A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255520 | ||||||
| chr8:98255913
|
G | T | 1 | a0001c0002t0001g0078 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.136-1826C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255913 | ||||||
| chr8:98255968
|
G | A | 1 | a0001c0001t0004g0001 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.136-1881C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98255968 | ||||||
| chr8:98256213
|
G | A | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-2126C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256213 | ||||||
| chr8:98256221
|
G | A | 128 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(125): Show | 129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.136-2134C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256221 | ||||||
| chr8:98256469
|
T | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2382A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256469 | ||||||
| chr8:98256472
|
T | C | 9 | a0001c0001t0003g0192a0001c0001t0004g0126a0001c0001t0006g0191others(6): Show | 9 | HG00558.hp1 HG02056.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-2385A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256472 | ||||||
| chr8:98256621
|
T | C | 1 | a0001c0005t0005g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136-2534A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256621 | ||||||
| chr8:98256631
|
T | TA | 204 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.136-2545dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256631 | ||||||
| chr8:98256706
|
G | A | 3 | a0001c0001t0003g0175a0001c0001t0004g0041a0001c0002t0001g0176 | 3 | HG00735.hp1 HG01433.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.136-2619C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98256706 | ||||||
| chr8:98257056
|
G | T | 1 | a0001c0002t0007g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-2969C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257056 | ||||||
| chr8:98257328
|
T | C | 4 | a0001c0002t0001g0044a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01109.hp2 HG01192.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3241A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257328 | ||||||
| chr8:98257336
|
T | A | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-3249A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257336 | ||||||
| chr8:98257349
|
TTTTTTTT others(24): Show |
T | 204 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.136-3293_136-3263d others(33): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257349 | ||||||
| chr8:98257724
|
T | C | 2 | a0001c0002t0005g0294a0001c0002t0005g0295 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-3637A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257724 | ||||||
| chr8:98257728
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-3641G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257728 | ||||||
| chr8:98257866
|
C | T | 7 | a0001c0001t0002g0283a0001c0001t0003g0024a0001c0001t0003g0025others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-3779G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257866 | ||||||
| chr8:98257899
|
GA | G | 11 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0131others(8): Show | 11 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-3813delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98257899 | ||||||
| chr8:98258399
|
T | C | 5 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4312A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258399 | ||||||
| chr8:98258477
|
A | C | 249 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.136-4390T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258477 | ||||||
| chr8:98258539
|
C | T | 2 | a0001c0002t0001g0194a0001c0002t0001g0240 | 2 | HG00597.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.136-4452G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258539 | ||||||
| chr8:98258612
|
G | A | 1 | a0001c0002t0005g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-4525C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258612 | ||||||
| chr8:98258630
|
A | G | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-4543T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258630 | ||||||
| chr8:98258650
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-4563T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258650 | ||||||
| chr8:98258748
|
A | G | 2 | a0001c0002t0005g0306a0002c0004t0001g0217 | 2 | HG00609.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.136-4661T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258748 | ||||||
| chr8:98258779
|
CT | C | 293 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.136-4693delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258779 | ||||||
| chr8:98258851
|
T | A | 1 | a0001c0001t0004g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.136-4764A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258851 | ||||||
| chr8:98258862
|
C | T | 1 | a0001c0001t0010g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-4775G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258862 | ||||||
| chr8:98258942
|
T | C | 5 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4855A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258942 | ||||||
| chr8:98258951
|
A | T | 5 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-4864T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98258951 | ||||||
| chr8:98259019
|
T | C | 2 | a0001c0002t0001g0308a0001c0002t0020g0309 | 2 | HG00738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.136-4932A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259019 | ||||||
| chr8:98259069
|
C | CTTT | 4 | a0001c0001t0002g0091a0001c0001t0004g0239a0001c0001t0011g0135others(1): Show | 4 | HG01069.hp2 HG01070.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTT | 55 | a0001c0001t0002g0036a0001c0001t0002g0046a0001c0001t0002g0047others(52): Show | 56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTT | 13 | a0001c0001t0002g0045a0001c0001t0002g0052a0001c0001t0002g0100others(10): Show | 13 | HG01346.hp2 HG02080.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-4983_136-4982i others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0005g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(5): Show |
2 | a0001c0002t0005g0114a0001c0002t0005g0304 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-4983_136-4982i others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0322a0001c0001t0002g0324 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(17): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(10): Show |
2 | a0001c0002t0005g0084a0001c0002t0005g0325 | 2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(19): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(12): Show |
3 | a0001c0002t0005g0082a0001c0002t0005g0083a0001c0002t0021g0086 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4983_136-4982i others(21): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0002g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-4983_136-4982i others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0005g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-4983_136-4982i others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCT | C | 4 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0002t0005g0294others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4984_136-4983d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTT | C | 12 | a0001c0001t0002g0258a0001c0001t0003g0147a0001c0001t0003g0192others(9): Show | 12 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-4985_136-4983d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTTT | C | 116 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(113): Show | 117 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.136-4986_136-4983d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTTTT | C | 9 | a0001c0001t0003g0141a0001c0002t0001g0197a0001c0005t0001g0027others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-4987_136-4983d others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTTTTT | C | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4988_136-4983d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTTTTTT others(1): Show |
C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-4990_136-4983d others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259069
|
CCTTTTTT others(3): Show |
C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-4992_136-4983d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259069 | ||||||
| chr8:98259070
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0010g0012a0001c0002t0005g0011 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.136-4993_136-4984d others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | ||||||
| chr8:98259070
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0002g0314a0001c0001t0003g0014a0001c0001t0010g0013others(1): Show | 4 | HG01884.hp1 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-4994_136-4984d others(13): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | ||||||
| chr8:98259070
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0312a0001c0001t0003g0016 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136-4995_136-4984d others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | ||||||
| chr8:98259070
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0005g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-4996_136-4984d others(15): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | ||||||
| chr8:98259070
|
C | T | 88 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(85): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.136-4983G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259070 | ||||||
| chr8:98259107
|
C | T | 75 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(72): Show | 76 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.136-5020G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259107 | ||||||
| chr8:98259108
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-5021C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259108 | ||||||
| chr8:98259138
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-5051C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259138 | ||||||
| chr8:98259163
|
G | A | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-5076C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259163 | ||||||
| chr8:98259222
|
G | A | 10 | a0001c0001t0003g0118a0001c0002t0005g0081a0001c0002t0005g0306others(7): Show | 10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-5135C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259222 | ||||||
| chr8:98259223
|
C | T | 1 | a0001c0001t0003g0038 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136-5136G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259223 | ||||||
| chr8:98259326
|
C | T | 13 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081others(10): Show | 13 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.136-5239G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259326 | ||||||
| chr8:98259355
|
G | A | 74 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.136-5268C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259355 | ||||||
| chr8:98259436
|
T | C | 3 | a0001c0002t0001g0127a0001c0002t0001g0128a0001c0002t0001g0264 | 3 | HG01099.hp1 HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.136-5349A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259436 | ||||||
| chr8:98259523
|
T | A | 2 | a0001c0001t0004g0129a0001c0002t0001g0260 | 2 | HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.136-5436A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259523 | ||||||
| chr8:98259545
|
G | A | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-5458C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259545 | ||||||
| chr8:98259552
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.136-5465A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259552 | ||||||
| chr8:98259567
|
G | T | 4 | a0001c0002t0001g0044a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01109.hp2 HG01192.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-5480C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259567 | ||||||
| chr8:98259575
|
A | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-5488T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259575 | ||||||
| chr8:98259633
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-5546C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259633 | ||||||
| chr8:98259810
|
G | A | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.136-5723C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259810 | ||||||
| chr8:98259923
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0146 | 2 | NA18970.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.136-5836G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98259923 | ||||||
| chr8:98260045
|
G | A | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-5958C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260045 | ||||||
| chr8:98260090
|
A | T | 5 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-6003T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260090 | ||||||
| chr8:98260157
|
A | T | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-6070T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260157 | ||||||
| chr8:98260286
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6199G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260286 | ||||||
| chr8:98260303
|
G | A | 1 | a0001c0001t0002g0243 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.136-6216C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260303 | ||||||
| chr8:98260326
|
G | T | 4 | a0001c0001t0004g0247a0002c0004t0001g0217a0002c0004t0001g0220others(1): Show | 4 | HG00438.hp1 HG00609.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-6239C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260326 | ||||||
| chr8:98260419
|
G | A | 3 | a0001c0001t0004g0247a0002c0004t0001g0217a0002c0004t0001g0220 | 3 | HG00438.hp1 HG00609.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.136-6332C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260419 | ||||||
| chr8:98260436
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6349G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260436 | ||||||
| chr8:98260534
|
T | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6447A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260534 | ||||||
| chr8:98260550
|
C | T | 1 | a0002c0003t0003g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136-6463G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260550 | ||||||
| chr8:98260594
|
G | A | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-6507C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260594 | ||||||
| chr8:98260639
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.136-6552C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260639 | ||||||
| chr8:98260644
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-6557C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260644 | ||||||
| chr8:98260650
|
T | C | 1 | a0001c0001t0004g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136-6563A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260650 | ||||||
| chr8:98260679
|
C | G | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-6592G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260679 | ||||||
| chr8:98260766
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0003g0311 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.136-6679G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260766 | ||||||
| chr8:98260782
|
A | T | 7 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-6695T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260782 | ||||||
| chr8:98260800
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.136-6713G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260800 | ||||||
| chr8:98260817
|
C | A | 130 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.136-6730G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260817 | ||||||
| chr8:98260850
|
C | G | 1 | a0001c0002t0001g0184 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.136-6763G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98260850 | ||||||
| chr8:98261154
|
T | G | 1 | a0001c0001t0004g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-7067A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261154 | ||||||
| chr8:98261336
|
C | T | 3 | a0001c0001t0003g0147a0001c0001t0003g0232a0003c0007t0002g0231 | 3 | HG00099.hp1 HG00280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.136-7249G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261336 | ||||||
| chr8:98261454
|
A | C | 2 | a0001c0001t0004g0275a0001c0002t0001g0194 | 2 | NA18973.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.136-7367T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261454 | ||||||
| chr8:98261462
|
C | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-7375G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261462 | ||||||
| chr8:98261619
|
G | A | 25 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0272others(22): Show | 27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.136-7532C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261619 | ||||||
| chr8:98261666
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-7579T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261666 | ||||||
| chr8:98261732
|
A | G | 1 | a0001c0002t0001g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.136-7645T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261732 | ||||||
| chr8:98261734
|
C | T | 1 | a0001c0002t0001g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.136-7647G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261734 | ||||||
| chr8:98261744
|
C | A | 2 | a0001c0002t0001g0318a0001c0002t0001g0320 | 2 | HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.136-7657G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261744 | ||||||
| chr8:98261816
|
A | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-7729T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261816 | ||||||
| chr8:98261886
|
G | A | 57 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-7799C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261886 | ||||||
| chr8:98261954
|
G | A | 327 | a0001c0001t0001g0172a0001c0001t0002g0010a0001c0001t0002g0021others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.136-7867C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261954 | ||||||
| chr8:98261959
|
G | C | 11 | a0001c0001t0002g0065a0001c0001t0004g0050a0001c0001t0004g0053others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-7872C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98261959 | ||||||
| chr8:98262041
|
G | A | 1 | a0001c0001t0015g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.136-7954C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262041 | ||||||
| chr8:98262047
|
G | T | 1 | a0001c0001t0003g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136-7960C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262047 | ||||||
| chr8:98262101
|
C | A | 1 | a0001c0006t0002g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.136-8014G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262101 | ||||||
| chr8:98262272
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8185T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262272 | ||||||
| chr8:98262374
|
C | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8287G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262374 | ||||||
| chr8:98262391
|
G | A | 2 | a0001c0001t0004g0129a0001c0002t0001g0260 | 2 | HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.136-8304C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262391 | ||||||
| chr8:98262551
|
A | C | 2 | a0001c0002t0005g0294a0001c0002t0005g0295 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8464T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262551 | ||||||
| chr8:98262553
|
G | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-8466C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262553 | ||||||
| chr8:98262677
|
A | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-8590T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262677 | ||||||
| chr8:98262729
|
A | C | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-8642T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262729 | ||||||
| chr8:98262761
|
C | T | 1 | a0001c0002t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.136-8674G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262761 | ||||||
| chr8:98262840
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.136-8753C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262840 | ||||||
| chr8:98262871
|
C | T | 5 | a0001c0001t0002g0161a0001c0001t0002g0233a0001c0001t0002g0301others(2): Show | 5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-8784G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262871 | ||||||
| chr8:98262897
|
A | C | 2 | a0001c0002t0005g0294a0001c0002t0005g0295 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-8810T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262897 | ||||||
| chr8:98262934
|
G | C | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-8847C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262934 | ||||||
| chr8:98262985
|
C | T | 70 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.136-8898G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262985 | ||||||
| chr8:98262986
|
G | A | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-8899C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98262986 | ||||||
| chr8:98263041
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-8954G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263041 | ||||||
| chr8:98263259
|
G | C | 2 | a0001c0001t0004g0130a0001c0001t0004g0296 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.136-9172C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263259 | ||||||
| chr8:98263376
|
C | T | 2 | a0001c0001t0003g0016a0002c0004t0001g0248 | 2 | HG02451.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.136-9289G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263376 | ||||||
| chr8:98263536
|
T | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9449A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263536 | ||||||
| chr8:98263549
|
G | A | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136-9462C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263549 | ||||||
| chr8:98263574
|
A | C | 1 | a0001c0002t0024g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-9487T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263574 | ||||||
| chr8:98263601
|
G | C | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-9514C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263601 | ||||||
| chr8:98263615
|
T | G | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-9528A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263615 | ||||||
| chr8:98263635
|
C | T | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-9548G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263635 | ||||||
| chr8:98263641
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-9554A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263641 | ||||||
| chr8:98263650
|
C | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-9563G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263650 | ||||||
| chr8:98263727
|
T | C | 1 | a0001c0001t0015g0182 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.136-9640A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263727 | ||||||
| chr8:98263794
|
T | A | 1 | a0001c0002t0005g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-9707A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263794 | ||||||
| chr8:98263823
|
CA | C | 327 | a0001c0001t0001g0172a0001c0001t0002g0010a0001c0001t0002g0021others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.136-9737delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263823 | ||||||
| chr8:98263862
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.136-9775T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263862 | ||||||
| chr8:98263979
|
C | T | 8 | a0001c0001t0002g0143a0001c0001t0003g0148a0001c0001t0003g0151others(5): Show | 8 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-9892G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98263979 | ||||||
| chr8:98264128
|
G | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0023 | 2 | HG01069.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.136-10041C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264128 | ||||||
| chr8:98264158
|
C | A | 1 | a0001c0002t0005g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-10071G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264158 | ||||||
| chr8:98264169
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0023 | 2 | HG01069.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.136-10082A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264169 | ||||||
| chr8:98264277
|
C | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-10190G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264277 | ||||||
| chr8:98264304
|
A | C | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-10217T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264304 | ||||||
| chr8:98264355
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.136-10268G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264355 | ||||||
| chr8:98264384
|
T | A | 1 | a0001c0001t0003g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.136-10297A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264384 | ||||||
| chr8:98264483
|
G | A | 1 | a0003c0007t0002g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.136-10396C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264483 | ||||||
| chr8:98264487
|
T | C | 1 | a0003c0007t0002g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.136-10400A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264487 | ||||||
| chr8:98264518
|
C | T | 57 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.136-10431G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264518 | ||||||
| chr8:98264548
|
A | C | 3 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0254 | 3 | HG02258.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-10461T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264548 | ||||||
| chr8:98264667
|
G | A | 11 | a0001c0001t0002g0143a0001c0001t0003g0098a0001c0001t0003g0141others(8): Show | 11 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-10580C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98264667 | ||||||
| chr8:98265144
|
A | C | 6 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(3): Show | 6 | HG01243.hp2 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-11057T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265144 | ||||||
| chr8:98265154
|
G | C | 1 | a0001c0002t0007g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11067C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265154 | ||||||
| chr8:98265156
|
T | C | 1 | a0001c0002t0007g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11069A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265156 | ||||||
| chr8:98265158
|
G | C | 1 | a0001c0002t0007g0274 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-11071C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265158 | ||||||
| chr8:98265352
|
G | A | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-11265C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265352 | ||||||
| chr8:98265353
|
A | C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-11266T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265353 | ||||||
| chr8:98265405
|
A | C | 1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.136-11318T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265405 | ||||||
| chr8:98265431
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-11344T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265431 | ||||||
| chr8:98265455
|
T | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11368A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265455 | ||||||
| chr8:98265468
|
G | A | 1 | a0001c0002t0024g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-11381C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265468 | ||||||
| chr8:98265504
|
T | A | 2 | a0001c0001t0003g0179a0001c0001t0004g0238 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.136-11417A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265504 | ||||||
| chr8:98265509
|
T | C | 279 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(276): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.136-11422A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265509 | ||||||
| chr8:98265547
|
G | A | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-11460C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265547 | ||||||
| chr8:98265646
|
G | A | 2 | a0001c0002t0005g0294a0001c0002t0005g0295 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-11559C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265646 | ||||||
| chr8:98265747
|
G | A | 4 | a0001c0001t0002g0033a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11660C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265747 | ||||||
| chr8:98265858
|
G | A | 4 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-11771C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265858 | ||||||
| chr8:98265858
|
G | C | 5 | a0001c0001t0003g0120a0001c0001t0004g0115a0001c0001t0004g0116others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-11771C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265858 | ||||||
| chr8:98265864
|
A | G | 3 | a0001c0005t0001g0030a0001c0005t0001g0035a0001c0005t0005g0029 | 3 | HG02145.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.136-11777T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265864 | ||||||
| chr8:98265881
|
C | T | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-11794G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265881 | ||||||
| chr8:98265998
|
T | A | 1 | a0001c0002t0001g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.136-11911A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98265998 | ||||||
| chr8:98266026
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.136-11939C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266026 | ||||||
| chr8:98266048
|
C | T | 4 | a0001c0001t0002g0205a0001c0001t0002g0229a0001c0001t0004g0159others(1): Show | 4 | HG00735.hp2 NA18961.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11961G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266048 | ||||||
| chr8:98266137
|
TG | T | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-12051delC | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266137 | ||||||
| chr8:98266143
|
G | A | 8 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-12056C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266143 | ||||||
| chr8:98266172
|
G | A | 249 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.136-12085C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266172 | ||||||
| chr8:98266202
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12115G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266202 | ||||||
| chr8:98266213
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.136-12126G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266213 | ||||||
| chr8:98266282
|
T | TA | 246 | a0001c0001t0001g0172a0001c0001t0002g0021a0001c0001t0002g0023others(243): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.136-12196dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266282 | ||||||
| chr8:98266282
|
T | TAA | 8 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324others(5): Show | 8 | HG01069.hp2 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-12197_136-1219 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266282 | ||||||
| chr8:98266300
|
GA | G | 16 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-12214delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266300 | ||||||
| chr8:98266327
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12240G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266327 | ||||||
| chr8:98266553
|
C | CA | 29 | a0001c0001t0002g0085a0001c0001t0002g0124a0001c0001t0002g0125others(26): Show | 29 | HG00544.hp1 HG01175.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.136-12467dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266553 | ||||||
| chr8:98266553
|
CA | C | 10 | a0001c0002t0001g0215a0001c0002t0005g0306a0001c0005t0001g0027others(7): Show | 10 | HG02145.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-12467delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266553 | ||||||
| chr8:98266595
|
T | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-12508A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266595 | ||||||
| chr8:98266641
|
G | C | 4 | a0001c0002t0001g0221a0001c0002t0001g0222a0001c0002t0001g0224others(1): Show | 4 | NA18998.hp1 NA19060.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-12554C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266641 | ||||||
| chr8:98266651
|
C | T | 1 | a0002c0003t0002g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.136-12564G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266651 | ||||||
| chr8:98266898
|
C | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-12811G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266898 | ||||||
| chr8:98266973
|
T | A | 4 | a0001c0001t0002g0033a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-12886A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266973 | ||||||
| chr8:98266973
|
TA | T | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(9): Show | 12 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-12887delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98266973 | ||||||
| chr8:98267086
|
T | C | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-12999A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267086 | ||||||
| chr8:98267327
|
CT | C | 6 | a0001c0001t0002g0102a0001c0001t0002g0261a0001c0001t0003g0232others(3): Show | 6 | HG01074.hp1 HG01167.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-13241delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267327 | ||||||
| chr8:98267380
|
G | A | 1 | a0001c0001t0006g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.136-13293C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267380 | ||||||
| chr8:98267415
|
C | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-13328G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267415 | ||||||
| chr8:98267744
|
A | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-13657T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267744 | ||||||
| chr8:98267832
|
T | G | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-13745A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267832 | ||||||
| chr8:98267893
|
T | G | 1 | a0001c0001t0003g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.136-13806A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267893 | ||||||
| chr8:98267901
|
T | C | 1 | a0001c0001t0002g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.136-13814A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98267901 | ||||||
| chr8:98268011
|
T | G | 1 | a0001c0001t0004g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-13924A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268011 | ||||||
| chr8:98268044
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-13957C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268044 | ||||||
| chr8:98268080
|
T | C | 10 | a0001c0001t0002g0091a0001c0001t0002g0094a0001c0001t0002g0095others(7): Show | 10 | HG00408.hp1 NA18747.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-13993A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268080 | ||||||
| chr8:98268296
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136-14209C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268296 | ||||||
| chr8:98268545
|
C | G | 3 | a0001c0001t0004g0001a0001c0001t0004g0281a0001c0001t0004g0282 | 5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-14458G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268545 | ||||||
| chr8:98268549
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.136-14462T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268549 | ||||||
| chr8:98268621
|
AG | A | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-14535delC | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268621 | ||||||
| chr8:98268622
|
GA | G | 135 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0085others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.136-14536delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268622 | ||||||
| chr8:98268637
|
C | G | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-14550G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268637 | ||||||
| chr8:98268647
|
GA | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-14561delT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268647 | ||||||
| chr8:98268666
|
A | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-14579T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268666 | ||||||
| chr8:98268933
|
C | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-14846G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268933 | ||||||
| chr8:98268996
|
C | T | 1 | a0001c0001t0009g0156 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.136-14909G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98268996 | ||||||
| chr8:98269010
|
C | G | 131 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(128): Show | 132 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.136-14923G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269010 | ||||||
| chr8:98269305
|
CTATT | C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136-15222_136-1521 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269305 | ||||||
| chr8:98269435
|
C | T | 1 | a0001c0001t0016g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136-15348G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269435 | ||||||
| chr8:98269615
|
C | G | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-15528G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269615 | ||||||
| chr8:98269697
|
T | C | 205 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.136-15610A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269697 | ||||||
| chr8:98269750
|
C | T | 1 | a0001c0005t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.136-15663G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269750 | ||||||
| chr8:98269809
|
C | A | 1 | a0001c0001t0002g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-15722G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269809 | ||||||
| chr8:98269846
|
C | T | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-15759G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269846 | ||||||
| chr8:98269946
|
C | T | 205 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.136-15859G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269946 | ||||||
| chr8:98269980
|
T | G | 212 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(209): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.136-15893A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98269980 | ||||||
| chr8:98270020
|
TC | T | 4 | a0001c0001t0002g0033a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-15934delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270020 | ||||||
| chr8:98270085
|
T | C | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.136-15998A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270085 | ||||||
| chr8:98270165
|
T | C | 5 | a0001c0001t0002g0161a0001c0001t0002g0233a0001c0001t0002g0301others(2): Show | 5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-16078A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270165 | ||||||
| chr8:98270555
|
C | T | 1 | a0001c0002t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.136-16468G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270555 | ||||||
| chr8:98270743
|
G | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16656C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270743 | ||||||
| chr8:98270766
|
T | TTGC | 6 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-16682_136-1668 others(7): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270766 | ||||||
| chr8:98270769
|
C | T | 12 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0296others(9): Show | 12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-16682G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98270769 | ||||||
| chr8:98271051
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16964G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271051 | ||||||
| chr8:98271449
|
G | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17362C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271449 | ||||||
| chr8:98271522
|
G | A | 4 | a0001c0002t0007g0059a0001c0002t0007g0077a0002c0003t0002g0073others(1): Show | 4 | NA18947.hp2 NA18993.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-17435C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271522 | ||||||
| chr8:98271600
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17513A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271600 | ||||||
| chr8:98271660
|
C | T | 5 | a0001c0001t0002g0161a0001c0001t0002g0233a0001c0001t0002g0301others(2): Show | 5 | HG00323.hp2 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-17573G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271660 | ||||||
| chr8:98271711
|
A | C | 7 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-17624T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271711 | ||||||
| chr8:98271866
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.136-17779C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271866 | ||||||
| chr8:98271896
|
T | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-17809A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271896 | ||||||
| chr8:98271938
|
G | A | 1 | a0001c0001t0004g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136-17851C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98271938 | ||||||
| chr8:98272240
|
T | C | 1 | a0001c0002t0005g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136-18153A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272240 | ||||||
| chr8:98272300
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18213C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272300 | ||||||
| chr8:98272346
|
A | G | 2 | a0001c0001t0012g0004a0001c0001t0012g0005 | 2 | NA18942.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.136-18259T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272346 | ||||||
| chr8:98272389
|
G | A | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-18302C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272389 | ||||||
| chr8:98272519
|
A | T | 1 | a0001c0002t0005g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136-18432T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272519 | ||||||
| chr8:98272616
|
CT | C | 7 | a0001c0001t0002g0314a0001c0001t0004g0239a0001c0001t0006g0138others(4): Show | 8 | HG00280.hp1 HG01074.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-18530delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272616 | ||||||
| chr8:98272676
|
A | G | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-18589T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272676 | ||||||
| chr8:98272810
|
A | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18723T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272810 | ||||||
| chr8:98272869
|
C | T | 1 | a0001c0002t0001g0140 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.136-18782G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272869 | ||||||
| chr8:98272909
|
G | A | 7 | a0001c0002t0001g0206a0001c0002t0001g0209a0001c0002t0001g0210others(4): Show | 7 | NA18953.hp2 NA18962.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-18822C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98272909 | ||||||
| chr8:98273017
|
A | T | 2 | a0001c0001t0004g0284a0001c0001t0023g0286 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.136-18930T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273017 | ||||||
| chr8:98273038
|
A | G | 1 | a0001c0001t0006g0002 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.136-18951T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273038 | ||||||
| chr8:98273080
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-18993C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273080 | ||||||
| chr8:98273449
|
T | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19362A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273449 | ||||||
| chr8:98273459
|
T | C | 2 | a0001c0002t0005g0017a0001c0002t0024g0303 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.136-19372A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273459 | ||||||
| chr8:98273646
|
C | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19559G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273646 | ||||||
| chr8:98273659
|
C | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-19572G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273659 | ||||||
| chr8:98273736
|
A | G | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-19649T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273736 | ||||||
| chr8:98273744
|
G | A | 3 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0254 | 3 | HG02258.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-19657C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273744 | ||||||
| chr8:98273830
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-19743A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98273830 | ||||||
| chr8:98274023
|
G | A | 231 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.136-19936C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274023 | ||||||
| chr8:98274250
|
CATCT | C | 3 | a0001c0001t0003g0316a0001c0001t0006g0002a0001c0001t0009g0156 | 4 | HG01256.hp2 HG01258.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+19749_135+1975 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274250 | ||||||
| chr8:98274419
|
C | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19584G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274419 | ||||||
| chr8:98274506
|
A | G | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+19497T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274506 | ||||||
| chr8:98274619
|
G | T | 2 | a0001c0001t0004g0018a0001c0002t0005g0081 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.135+19384C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274619 | ||||||
| chr8:98274742
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19261G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274742 | ||||||
| chr8:98274891
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+19112A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274891 | ||||||
| chr8:98274902
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG01109.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+19101G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98274902 | ||||||
| chr8:98275077
|
A | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18926T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275077 | ||||||
| chr8:98275081
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18922A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275081 | ||||||
| chr8:98275087
|
A | G | 1 | a0001c0002t0005g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.135+18916T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275087 | ||||||
| chr8:98275091
|
C | G | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18912G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275091 | ||||||
| chr8:98275120
|
G | A | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+18883C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275120 | ||||||
| chr8:98275248
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+18755G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275248 | ||||||
| chr8:98275249
|
G | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+18754C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275249 | ||||||
| chr8:98275261
|
T | A | 4 | a0001c0001t0004g0247a0002c0004t0001g0217a0002c0004t0001g0220others(1): Show | 4 | HG00438.hp1 HG00609.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+18742A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275261 | ||||||
| chr8:98275331
|
C | A | 1 | a0001c0001t0003g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.135+18672G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275331 | ||||||
| chr8:98275435
|
A | G | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG00408.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.135+18568T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275435 | ||||||
| chr8:98275547
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.135+18456T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275547 | ||||||
| chr8:98275566
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0010g0012a0001c0001t0010g0013 | 3 | HG02451.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+18437C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275566 | ||||||
| chr8:98275642
|
G | T | 4 | a0001c0005t0001g0027a0001c0005t0001g0030a0001c0005t0001g0035others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+18361C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275642 | ||||||
| chr8:98275647
|
T | C | 1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.135+18356A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275647 | ||||||
| chr8:98275926
|
T | A | 2 | a0001c0001t0003g0188a0001c0001t0010g0180 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18077A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98275926 | ||||||
| chr8:98276268
|
C | G | 1 | a0001c0001t0002g0173 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+17735G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276268 | ||||||
| chr8:98276301
|
A | C | 5 | a0001c0001t0004g0266a0001c0001t0004g0267a0001c0002t0001g0263others(2): Show | 5 | HG00438.hp2 HG02015.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+17702T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276301 | ||||||
| chr8:98276630
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.135+17373C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98276630 | ||||||
| chr8:98277016
|
C | T | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+16987G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277016 | ||||||
| chr8:98277051
|
TGA | T | 70 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.135+16950_135+1695 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277051 | ||||||
| chr8:98277064
|
C | A | 2 | a0001c0001t0003g0141a0001c0001t0003g0142 | 2 | NA18612.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.135+16939G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277064 | ||||||
| chr8:98277115
|
C | T | 1 | a0001c0005t0001g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+16888G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277115 | ||||||
| chr8:98277315
|
G | A | 5 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0010g0012others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+16688C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277315 | ||||||
| chr8:98277427
|
G | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16576C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277427 | ||||||
| chr8:98277451
|
C | A | 57 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+16552G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277451 | ||||||
| chr8:98277478
|
A | T | 1 | a0001c0001t0002g0173 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+16525T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277478 | ||||||
| chr8:98277498
|
T | C | 15 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+16505A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277498 | ||||||
| chr8:98277635
|
G | A | 57 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+16368C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277635 | ||||||
| chr8:98277661
|
G | A | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16342C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277661 | ||||||
| chr8:98277765
|
T | C | 11 | a0001c0001t0003g0192a0001c0001t0004g0126a0001c0001t0006g0191others(8): Show | 11 | HG00558.hp1 HG00597.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+16238A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277765 | ||||||
| chr8:98277841
|
A | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+16162T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277841 | ||||||
| chr8:98277991
|
A | C | 1 | a0001c0002t0001g0278 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+16012T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98277991 | ||||||
| chr8:98278064
|
G | T | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.135+15939C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278064 | ||||||
| chr8:98278224
|
TTTTG | T | 7 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0006g0133others(4): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+15775_135+1577 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278224 | ||||||
| chr8:98278240
|
G | C | 1 | a0001c0001t0004g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.135+15763C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278240 | ||||||
| chr8:98278652
|
G | A | 1 | a0001c0002t0001g0320 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.135+15351C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278652 | ||||||
| chr8:98278653
|
C | T | 130 | a0001c0001t0001g0172a0001c0001t0002g0037a0001c0001t0002g0124others(127): Show | 131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.135+15350G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278653 | ||||||
| chr8:98278837
|
T | G | 1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+15166A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98278837 | ||||||
| chr8:98279222
|
A | G | 12 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0296others(9): Show | 12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+14781T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279222 | ||||||
| chr8:98279361
|
T | C | 3 | a0001c0001t0004g0001a0001c0001t0004g0281a0001c0001t0004g0282 | 5 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+14642A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279361 | ||||||
| chr8:98279578
|
T | C | 3 | a0001c0001t0003g0118a0001c0001t0004g0018a0001c0002t0005g0081 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.135+14425A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279578 | ||||||
| chr8:98279701
|
C | T | 2 | a0002c0004t0001g0076a0002c0004t0001g0297 | 2 | NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.135+14302G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279701 | ||||||
| chr8:98279866
|
G | A | 8 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0002g0111others(5): Show | 8 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+14137C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279866 | ||||||
| chr8:98279945
|
T | G | 1 | a0001c0002t0001g0107 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.135+14058A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98279945 | ||||||
| chr8:98280028
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+13975G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280028 | ||||||
| chr8:98280077
|
C | G | 1 | a0001c0002t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.135+13926G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280077 | ||||||
| chr8:98280217
|
G | A | 1 | a0001c0002t0001g0265 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.135+13786C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280217 | ||||||
| chr8:98280331
|
T | G | 204 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.135+13672A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280331 | ||||||
| chr8:98280339
|
C | T | 17 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(14): Show | 17 | HG01109.hp1 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+13664G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280339 | ||||||
| chr8:98280343
|
T | G | 1 | a0001c0001t0004g0050 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135+13660A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280343 | ||||||
| chr8:98280486
|
T | C | 223 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.135+13517A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280486 | ||||||
| chr8:98280699
|
T | G | 215 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.135+13304A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280699 | ||||||
| chr8:98280736
|
C | CTA | 3 | a0001c0001t0002g0279a0001c0002t0001g0206a0001c0002t0001g0278 | 3 | NA18942.hp2 NA18986.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.135+13265_135+1326 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATA | 4 | a0001c0001t0002g0033a0001c0001t0002g0045a0001c0001t0009g0032others(1): Show | 4 | NA18960.hp1 NA19054.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13263_135+1326 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATATAT others(1): Show |
6 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0071others(3): Show | 6 | HG01099.hp1 HG02132.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13259_135+1326 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATATAT others(3): Show |
2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG01070.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.135+13257_135+1326 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0003g0141 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.135+13243_135+1326 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATATAT others(19): Show |
1 | a0001c0001t0003g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.135+13241_135+1326 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
C | CTATATAT others(23): Show |
1 | a0001c0001t0002g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.135+13266_135+1326 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280736
|
CTA | C | 4 | a0001c0001t0003g0016a0001c0001t0010g0013a0001c0002t0005g0015others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13265_135+1326 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280736 | ||||||
| chr8:98280755
|
T | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0177a0002c0004t0001g0248 | 3 | HG01255.hp2 HG02723.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.135+13248A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280755 | ||||||
| chr8:98280757
|
T | G | 13 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0177others(10): Show | 13 | HG00438.hp1 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.135+13246A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280757 | ||||||
| chr8:98280757
|
T | TAGAGAGA others(3): Show |
1 | a0001c0001t0002g0095 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.135+13245_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280757 | ||||||
| chr8:98280759
|
T | G | 26 | a0001c0001t0002g0091a0001c0001t0002g0094a0001c0001t0002g0095others(23): Show | 27 | HG00438.hp1 HG00609.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.135+13244A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | ||||||
| chr8:98280759
|
T | TAG | 5 | a0001c0001t0004g0001a0001c0001t0004g0281a0001c0001t0004g0282others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+13243_135+1324 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | ||||||
| chr8:98280759
|
T | TAGAGAGA others(3): Show |
2 | a0001c0001t0012g0005a0001c0002t0005g0257 | 2 | HG02886.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.135+13243_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | ||||||
| chr8:98280759
|
T | TAGAGAGA others(5): Show |
3 | a0001c0001t0012g0004a0001c0002t0001g0244a0002c0003t0002g0066 | 3 | HG02523.hp1 NA18992.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.135+13243_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280759 | ||||||
| chr8:98280761
|
T | G | 58 | a0001c0001t0002g0010a0001c0001t0002g0021a0001c0001t0002g0091others(55): Show | 61 | HG00438.hp1 HG00609.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.135+13242A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAG | 4 | a0001c0001t0002g0277a0001c0001t0002g0280a0001c0002t0001g0090others(1): Show | 4 | HG00408.hp1 HG00741.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13240_135+1324 others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAGAG | 5 | a0001c0001t0002g0052a0001c0001t0002g0103a0001c0001t0002g0285others(2): Show | 5 | HG01175.hp1 HG02257.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13238_135+1324 others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAGAGAG | 4 | a0001c0001t0002g0023a0001c0002t0001g0270a0001c0002t0007g0274others(1): Show | 4 | HG00438.hp2 HG04204.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13236_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAGAGAGA others(1): Show |
8 | a0001c0001t0002g0036a0001c0001t0002g0065a0001c0001t0002g0272others(5): Show | 8 | HG00280.hp1 HG00544.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+13234_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAGAGAGA others(3): Show |
2 | a0001c0002t0001g0242a0001c0006t0002g0117 | 2 | HG02976.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.135+13232_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TAGAGAGA others(5): Show |
1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+13230_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATAGAG | 3 | a0001c0001t0004g0267a0001c0002t0001g0127a0001c0002t0001g0268 | 3 | HG02015.hp1 HG02683.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATAGAGA others(1): Show |
8 | a0001c0001t0015g0067a0001c0002t0001g0060a0001c0002t0001g0061others(5): Show | 8 | HG00621.hp1 HG01109.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATAGAGA others(3): Show |
4 | a0001c0001t0003g0311a0001c0002t0001g0093a0001c0002t0001g0199others(1): Show | 4 | HG00558.hp1 HG03471.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATAGAGA others(5): Show |
1 | a0001c0001t0006g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATAGAGA others(13): Show |
2 | a0001c0001t0002g0160a0001c0001t0004g0275 | 2 | HG02451.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAG | 4 | a0001c0001t0004g0126a0001c0001t0006g0191a0001c0002t0001g0216others(1): Show | 4 | HG02056.hp1 NA18979.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(10): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(1): Show |
6 | a0001c0001t0004g0053a0001c0002t0001g0054a0001c0002t0001g0057others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(3): Show |
5 | a0001c0001t0004g0129a0001c0001t0011g0132a0001c0002t0001g0194others(2): Show | 5 | HG00642.hp1 HG02602.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(5): Show |
1 | a0001c0002t0001g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(9): Show |
1 | a0001c0002t0001g0249 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(11): Show |
1 | a0001c0001t0003g0236 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(13): Show |
1 | a0001c0001t0002g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATAGA others(19): Show |
2 | a0001c0001t0004g0276a0001c0002t0001g0328 | 2 | HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(1): Show |
3 | a0001c0001t0004g0050a0001c0001t0004g0101a0001c0001t0004g0266 | 3 | HG01256.hp1 HG02004.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(12): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(3): Show |
3 | a0001c0001t0004g0058a0001c0002t0001g0193a0001c0002t0007g0059 | 3 | HG00099.hp2 NA18966.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(5): Show |
1 | a0001c0002t0001g0092 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(7): Show |
2 | a0001c0001t0011g0134a0001c0001t0011g0135 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(9): Show |
1 | a0001c0002t0001g0222 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(11): Show |
1 | a0001c0001t0002g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(13): Show |
1 | a0001c0002t0001g0224 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
1 | a0001c0001t0019g0158 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
1 | a0001c0001t0004g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
1 | a0001c0001t0004g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(3): Show |
2 | a0001c0001t0003g0192a0001c0002t0001g0240 | 2 | HG00597.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(14): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(5): Show |
2 | a0001c0001t0002g0259a0001c0002t0007g0077 | 2 | NA18997.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(7): Show |
3 | a0001c0001t0004g0130a0001c0001t0006g0133a0001c0002t0001g0260 | 3 | HG03239.hp2 HG03710.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(9): Show |
1 | a0001c0002t0001g0221 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(11): Show |
2 | a0001c0001t0003g0181a0002c0004t0001g0201 | 2 | HG01169.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(13): Show |
5 | a0001c0001t0002g0037a0001c0001t0002g0164a0001c0001t0002g0258others(2): Show | 5 | HG00408.hp2 HG02300.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
3 | a0001c0001t0002g0166a0001c0001t0003g0042a0001c0001t0003g0099 | 3 | HG02896.hp2 HG02897.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
1 | a0001c0005t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(5): Show |
2 | a0001c0001t0004g0296a0002c0004t0001g0051 | 2 | HG01975.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(16): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0172 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(11): Show |
8 | a0001c0001t0003g0118a0001c0001t0003g0179a0001c0001t0004g0178others(5): Show | 8 | HG01167.hp1 HG01517.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(13): Show |
4 | a0001c0001t0002g0139a0001c0001t0002g0168a0001c0001t0003g0152others(1): Show | 4 | HG00323.hp1 HG00597.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
3 | a0001c0001t0003g0121a0001c0001t0003g0155a0001c0002t0025g0226 | 3 | HG00323.hp2 HG03017.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
3 | a0001c0001t0004g0122a0001c0002t0001g0140a0001c0002t0001g0186 | 3 | HG01123.hp1 HG02523.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
4 | a0001c0002t0001g0326a0001c0002t0001g0327a0001c0002t0021g0086others(1): Show | 4 | HG01943.hp2 HG01993.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
2 | a0001c0001t0002g0161a0002c0003t0002g0189 | 2 | HG01257.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0002t0005g0305 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(7): Show |
2 | a0001c0001t0002g0102a0001c0001t0006g0138 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(18): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(9): Show |
1 | a0001c0001t0004g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(11): Show |
2 | a0001c0001t0004g0238a0001c0001t0006g0002 | 3 | HG01256.hp2 HG01258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(13): Show |
3 | a0001c0001t0003g0234a0001c0002t0001g0137a0001c0002t0005g0079 | 3 | HG01515.hp1 HG03209.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(24): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
2 | a0001c0001t0002g0163a0001c0001t0004g0202 | 2 | HG00558.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
2 | a0001c0001t0003g0040a0001c0001t0004g0165 | 2 | HG02258.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
3 | a0001c0001t0003g0237a0001c0001t0006g0228a0001c0002t0001g0069 | 3 | HG03669.hp1 HG03942.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
3 | a0001c0001t0004g0159a0001c0002t0001g0310a0001c0002t0005g0087 | 3 | HG00735.hp2 HG02698.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
1 | a0001c0005t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0001t0003g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(9): Show |
1 | a0002c0003t0002g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(20): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(11): Show |
1 | a0001c0001t0004g0225 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(22): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
2 | a0001c0001t0002g0255a0001c0001t0004g0115 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
4 | a0001c0001t0002g0124a0001c0001t0002g0243a0001c0001t0015g0182others(1): Show | 4 | HG01358.hp2 HG03491.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
4 | a0001c0002t0001g0250a0001c0002t0005g0082a0001c0002t0005g0083others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
4 | a0001c0001t0002g0085a0001c0001t0003g0025a0001c0002t0001g0070others(1): Show | 4 | HG02280.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
2 | a0001c0001t0003g0026a0001c0001t0003g0188 | 2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0002t0005g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
2 | a0001c0002t0001g0197a0002c0003t0002g0196 | 2 | HG02080.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
4 | a0001c0001t0002g0125a0001c0001t0003g0290a0001c0001t0004g0116others(1): Show | 4 | HG00738.hp1 HG02257.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
5 | a0001c0001t0003g0227a0001c0001t0003g0235a0001c0001t0003g0302others(2): Show | 5 | HG01106.hp1 HG01433.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0001t0002g0233 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(27): Show |
1 | a0001c0001t0003g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(15): Show |
1 | a0001c0001t0003g0171 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(26): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(17): Show |
2 | a0001c0001t0004g0198a0001c0001t0026g0145 | 2 | HG00733.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(28): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
4 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0002t0001g0184others(1): Show | 4 | HG01884.hp2 HG02165.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
1 | a0001c0002t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0002t0005g0294 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(31): Show |
1 | a0001c0005t0005g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
4 | a0001c0001t0002g0173a0001c0001t0002g0322a0001c0001t0003g0174others(1): Show | 4 | HG00735.hp1 NA18906.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
3 | a0001c0001t0003g0068a0001c0001t0003g0232a0003c0007t0002g0231 | 3 | HG00099.hp1 HG02280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
2 | a0001c0001t0002g0301a0001c0001t0003g0123 | 2 | HG00609.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(27): Show |
1 | a0001c0001t0003g0157 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(19): Show |
2 | a0001c0001t0003g0120a0001c0001t0004g0041 | 2 | HG01975.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(30): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
5 | a0001c0001t0002g0323a0001c0001t0003g0146a0001c0001t0006g0006others(2): Show | 5 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
1 | a0001c0002t0005g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0001t0006g0008 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(21): Show |
1 | a0001c0001t0003g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(32): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
2 | a0001c0001t0003g0147a0001c0002t0001g0176 | 2 | HG00280.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
1 | a0001c0001t0008g0291 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(27): Show |
1 | a0001c0001t0002g0324 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(29): Show |
1 | a0001c0001t0009g0156 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.135+13241_135+1324 others(40): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(25): Show |
3 | a0001c0001t0003g0148a0001c0001t0004g0230a0001c0002t0001g0149 | 3 | HG02135.hp1 NA18947.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(36): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(27): Show |
5 | a0001c0001t0002g0283a0001c0001t0003g0151a0001c0001t0008g0292others(2): Show | 5 | HG00544.hp1 HG00738.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(23): Show |
1 | a0001c0001t0004g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(34): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(27): Show |
1 | a0001c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(38): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(29): Show |
1 | a0001c0002t0007g0241 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(40): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(31): Show |
1 | a0001c0002t0001g0223 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(42): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(37): Show |
1 | a0001c0002t0005g0295 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.135+13241_135+1324 others(48): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280761
|
T | TATATATA others(35): Show |
2 | a0001c0001t0003g0154a0001c0002t0001g0153 | 2 | HG02165.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.135+13241_135+1324 others(46): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280761 | ||||||
| chr8:98280763
|
G | T | 11 | a0001c0001t0002g0205a0001c0001t0003g0141a0001c0001t0003g0142others(8): Show | 11 | HG01070.hp1 HG02273.hp1 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+13240C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280763 | ||||||
| chr8:98280765
|
G | T | 5 | a0001c0001t0002g0205a0001c0001t0003g0141a0001c0001t0003g0142others(2): Show | 5 | NA18612.hp2 NA18992.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+13238C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280765 | ||||||
| chr8:98280792
|
A | AG | 9 | a0001c0001t0002g0139a0001c0001t0002g0168a0001c0001t0003g0026others(6): Show | 9 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+13210_135+1321 others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280792 | ||||||
| chr8:98280921
|
T | C | 6 | a0001c0001t0006g0133a0001c0001t0011g0132a0001c0001t0011g0134others(3): Show | 6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+13082A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280921 | ||||||
| chr8:98280930
|
C | T | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13073G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98280930 | ||||||
| chr8:98281269
|
A | G | 1 | a0001c0001t0006g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+12734T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281269 | ||||||
| chr8:98281406
|
G | C | 1 | a0001c0001t0009g0034 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.135+12597C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281406 | ||||||
| chr8:98281903
|
T | G | 1 | a0001c0001t0015g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.135+12100A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98281903 | ||||||
| chr8:98282336
|
G | T | 1 | a0001c0002t0005g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.135+11667C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282336 | ||||||
| chr8:98282382
|
T | A | 6 | a0001c0001t0002g0085a0001c0002t0005g0082a0001c0002t0005g0083others(3): Show | 6 | HG01243.hp2 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+11621A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282382 | ||||||
| chr8:98282723
|
T | G | 1 | a0001c0001t0004g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.135+11280A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98282723 | ||||||
| chr8:98283192
|
T | C | 3 | a0001c0002t0005g0304a0001c0002t0005g0305a0001c0002t0005g0306 | 3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+10811A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98283192 | ||||||
| chr8:98283436
|
C | A | 57 | a0001c0001t0002g0036a0001c0001t0002g0045a0001c0001t0002g0046others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+10567G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98283436 | ||||||
| chr8:98284058
|
T | A | 1 | a0001c0001t0023g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+9945A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284058 | ||||||
| chr8:98284399
|
TTC | T | 26 | a0001c0001t0002g0243a0001c0001t0003g0121a0001c0001t0003g0192others(23): Show | 26 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.135+9602_135+9603d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284399 | ||||||
| chr8:98284418
|
T | A | 1 | a0001c0001t0004g0225 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+9585A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | ||||||
| chr8:98284418
|
T | TCA | 8 | a0001c0001t0002g0021a0001c0001t0002g0108a0001c0001t0002g0110others(5): Show | 8 | HG01069.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+9583_135+9584d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | ||||||
| chr8:98284418
|
TCA | T | 201 | a0001c0001t0001g0172a0001c0001t0002g0036a0001c0001t0002g0037others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.135+9583_135+9584d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | ||||||
| chr8:98284418
|
TCACACA | T | 16 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+9579_135+9584d others(8): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284418 | ||||||
| chr8:98284420
|
A | T | 5 | a0001c0001t0002g0277a0001c0001t0003g0316a0001c0001t0008g0307others(2): Show | 5 | HG00741.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+9583T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284420 | ||||||
| chr8:98284422
|
A | T | 13 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0166others(10): Show | 13 | HG01884.hp2 HG02015.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+9581T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284422 | ||||||
| chr8:98284593
|
T | C | 3 | a0001c0002t0001g0326a0001c0002t0001g0327a0001c0002t0001g0328 | 3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+9410A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284593 | ||||||
| chr8:98284967
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.135+9036C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284967 | ||||||
| chr8:98284992
|
G | A | 22 | a0001c0001t0002g0312a0001c0001t0002g0314a0001c0001t0003g0014others(19): Show | 22 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.135+9011C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98284992 | ||||||
| chr8:98285259
|
G | C | 1 | a0001c0002t0025g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.135+8744C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285259 | ||||||
| chr8:98285396
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+8607C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285396 | ||||||
| chr8:98285434
|
A | G | 35 | a0001c0001t0002g0037a0001c0001t0002g0139a0001c0001t0002g0143others(32): Show | 36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.135+8569T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285434 | ||||||
| chr8:98285474
|
G | A | 1 | a0001c0001t0003g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.135+8529C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285474 | ||||||
| chr8:98285523
|
C | T | 10 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0004g0115others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+8480G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285523 | ||||||
| chr8:98285535
|
G | A | 11 | a0001c0001t0002g0085a0001c0001t0004g0018a0001c0002t0005g0081others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+8468C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285535 | ||||||
| chr8:98285541
|
G | A | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+8462C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285541 | ||||||
| chr8:98285542
|
C | A | 1 | a0001c0002t0005g0325 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135+8461G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285542 | ||||||
| chr8:98285647
|
A | C | 30 | a0001c0001t0002g0085a0001c0001t0002g0322a0001c0001t0002g0323others(27): Show | 30 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.135+8356T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285647 | ||||||
| chr8:98285676
|
T | C | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0006t0002g0117 | 3 | HG02976.hp1 NA19070.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.135+8327A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285676 | ||||||
| chr8:98285715
|
A | C | 1 | a0001c0002t0001g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.135+8288T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285715 | ||||||
| chr8:98285744
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+8259C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285744 | ||||||
| chr8:98285752
|
C | A | 17 | a0001c0001t0002g0085a0001c0001t0002g0255a0001c0001t0004g0018others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+8251G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285752 | ||||||
| chr8:98285756
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.135+8247G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285756 | ||||||
| chr8:98285913
|
G | A | 1 | a0001c0001t0003g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+8090C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98285913 | ||||||
| chr8:98286214
|
C | A | 5 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0003g0290others(2): Show | 5 | HG02055.hp1 HG02818.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+7789G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286214 | ||||||
| chr8:98286325
|
G | A | 23 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(20): Show | 23 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+7678C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286325 | ||||||
| chr8:98286435
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.135+7568C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286435 | ||||||
| chr8:98286478
|
C | G | 50 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(47): Show | 52 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.135+7525G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286478 | ||||||
| chr8:98286611
|
C | T | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+7392G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286611 | ||||||
| chr8:98286722
|
T | A | 9 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0010g0012others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+7281A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286722 | ||||||
| chr8:98286812
|
C | CA | 43 | a0001c0001t0002g0036a0001c0001t0002g0071a0001c0001t0002g0125others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.135+7190dupT | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286812 | ||||||
| chr8:98286823
|
A | C | 5 | a0001c0001t0002g0312a0001c0001t0002g0314a0001c0001t0003g0311others(2): Show | 5 | HG01884.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+7180T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286823 | ||||||
| chr8:98286824
|
A | AC | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324 | 3 | HG03098.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+7178_135+7179i others(3): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286824 | ||||||
| chr8:98286824
|
A | C | 10 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0006g0131others(7): Show | 10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+7179T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286824 | ||||||
| chr8:98286828
|
A | C | 1 | a0001c0001t0002g0021 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.135+7175T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286828 | ||||||
| chr8:98286829
|
A | C | 41 | a0001c0001t0002g0023a0001c0001t0002g0033a0001c0001t0002g0272others(38): Show | 43 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.135+7174T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286829 | ||||||
| chr8:98286830
|
A | C | 33 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(30): Show | 33 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.135+7173T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286830 | ||||||
| chr8:98286831
|
AAAAC | A | 9 | a0001c0001t0003g0014a0001c0001t0003g0016a0001c0001t0010g0012others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+7168_135+7171d others(6): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286831 | ||||||
| chr8:98286832
|
AAAC | A | 9 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0028others(6): Show | 9 | HG02280.hp1 HG02486.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+7168_135+7170d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286832 | ||||||
| chr8:98286834
|
AC | A | 41 | a0001c0001t0002g0023a0001c0001t0002g0033a0001c0001t0002g0272others(38): Show | 43 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.135+7168delG | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286834 | ||||||
| chr8:98286835
|
C | A | 37 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(34): Show | 37 | HG01243.hp1 HG01243.hp2 HG02004.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+7168G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98286835 | ||||||
| chr8:98287051
|
G | T | 1 | a0001c0002t0005g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+6952C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287051 | ||||||
| chr8:98287052
|
A | G | 4 | a0001c0001t0003g0120a0001c0001t0003g0290a0001c0002t0005g0294others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+6951T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287052 | ||||||
| chr8:98287434
|
G | A | 17 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+6569C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287434 | ||||||
| chr8:98287507
|
A | C | 1 | a0001c0001t0004g0001 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.135+6496T>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287507 | ||||||
| chr8:98287741
|
T | C | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+6262A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287741 | ||||||
| chr8:98287753
|
C | G | 25 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0272others(22): Show | 27 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.135+6250G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287753 | ||||||
| chr8:98287754
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.135+6249C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287754 | ||||||
| chr8:98287853
|
T | G | 29 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(26): Show | 29 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+6150A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287853 | ||||||
| chr8:98287952
|
T | C | 4 | a0001c0001t0006g0006a0001c0001t0006g0007a0001c0001t0006g0008others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+6051A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98287952 | ||||||
| chr8:98288094
|
G | T | 1 | a0001c0001t0004g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.135+5909C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288094 | ||||||
| chr8:98288146
|
C | T | 17 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+5857G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288146 | ||||||
| chr8:98288147
|
G | A | 1 | a0001c0002t0005g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.135+5856C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288147 | ||||||
| chr8:98288230
|
C | T | 2 | a0001c0001t0004g0115a0001c0001t0004g0116 | 2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.135+5773G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288230 | ||||||
| chr8:98288231
|
T | C | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG00408.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.135+5772A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288231 | ||||||
| chr8:98288309
|
C | T | 3 | a0001c0001t0003g0016a0001c0001t0010g0012a0001c0001t0010g0013 | 3 | HG02451.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+5694G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288309 | ||||||
| chr8:98288330
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.135+5673C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288330 | ||||||
| chr8:98288411
|
A | G | 1 | a0001c0002t0001g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.135+5592T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288411 | ||||||
| chr8:98288502
|
C | T | 1 | a0004c0008t0004g0262 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+5501G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288502 | ||||||
| chr8:98288503
|
G | A | 15 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+5500C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288503 | ||||||
| chr8:98288610
|
C | T | 3 | a0001c0002t0005g0304a0001c0002t0005g0305a0001c0002t0005g0306 | 3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+5393G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288610 | ||||||
| chr8:98288828
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | NA18953.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.135+5175G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288828 | ||||||
| chr8:98288831
|
G | A | 25 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(22): Show | 25 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.135+5172C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288831 | ||||||
| chr8:98288893
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.135+5110T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98288893 | ||||||
| chr8:98289009
|
T | C | 1 | a0001c0002t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.135+4994A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289009 | ||||||
| chr8:98289051
|
A | T | 15 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+4952T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289051 | ||||||
| chr8:98289256
|
T | G | 29 | a0001c0001t0002g0085a0001c0001t0002g0108a0001c0001t0002g0110others(26): Show | 29 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+4747A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289256 | ||||||
| chr8:98289514
|
CT | C | 65 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(62): Show | 67 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.135+4488delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289514 | ||||||
| chr8:98289569
|
T | G | 3 | a0001c0001t0003g0300a0001c0001t0004g0299a0001c0002t0001g0298 | 3 | NA18945.hp2 NA18990.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.135+4434A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289569 | ||||||
| chr8:98289640
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.135+4363G>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98289640 | ||||||
| chr8:98290081
|
G | T | 2 | a0001c0001t0003g0121a0001c0001t0004g0122 | 2 | HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.135+3922C>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290081 | ||||||
| chr8:98290102
|
A | T | 55 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(52): Show | 57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3901T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290102 | ||||||
| chr8:98290103
|
T | A | 10 | a0001c0001t0002g0091a0001c0001t0002g0094a0001c0001t0002g0095others(7): Show | 10 | HG00408.hp1 NA18747.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+3900A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290103 | ||||||
| chr8:98290498
|
G | A | 4 | a0001c0001t0002g0033a0001c0001t0009g0031a0001c0001t0009g0032others(1): Show | 4 | NA18960.hp1 NA19062.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+3505C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290498 | ||||||
| chr8:98290556
|
G | A | 1 | a0001c0002t0001g0096 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+3447C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290556 | ||||||
| chr8:98290557
|
T | G | 55 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(52): Show | 57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3446A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290557 | ||||||
| chr8:98290642
|
G | C | 2 | a0001c0001t0004g0275a0001c0001t0004g0276 | 2 | HG01169.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.135+3361C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290642 | ||||||
| chr8:98290670
|
A | G | 1 | a0001c0001t0008g0307 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.135+3333T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290670 | ||||||
| chr8:98290756
|
G | A | 55 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(52): Show | 57 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3247C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98290756 | ||||||
| chr8:98291071
|
T | A | 1 | a0001c0002t0001g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.135+2932A>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291071 | ||||||
| chr8:98291299
|
C | A | 1 | a0002c0004t0001g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.135+2704G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291299 | ||||||
| chr8:98291442
|
T | C | 2 | a0001c0001t0002g0288a0001c0001t0003g0289 | 2 | NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.135+2561A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291442 | ||||||
| chr8:98291921
|
C | A | 6 | a0001c0001t0003g0120a0001c0001t0003g0290a0001c0001t0008g0291others(3): Show | 6 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+2082G>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98291921 | ||||||
| chr8:98292484
|
A | G | 3 | a0001c0002t0005g0304a0001c0002t0005g0305a0001c0002t0005g0306 | 3 | HG02559.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+1519T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292484 | ||||||
| chr8:98292575
|
A | G | 47 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(44): Show | 47 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.135+1428T>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292575 | ||||||
| chr8:98292726
|
A | AT | 23 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0103others(20): Show | 23 | HG00280.hp1 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+1276dupA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | ||||||
| chr8:98292726
|
A | ATT | 66 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0045others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.135+1275_135+1276d others(4): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | ||||||
| chr8:98292726
|
A | ATTT | 9 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0324others(6): Show | 9 | HG02630.hp2 HG02698.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+1274_135+1276d others(5): Show |
NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | ||||||
| chr8:98292726
|
AT | A | 6 | a0001c0001t0003g0290a0001c0001t0008g0291a0001c0001t0008g0292others(3): Show | 6 | HG00733.hp1 HG00738.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+1276delA | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292726 | ||||||
| chr8:98292768
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.135+1235A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292768 | ||||||
| chr8:98292794
|
T | C | 4 | a0001c0001t0003g0300a0001c0001t0004g0299a0001c0002t0001g0298others(1): Show | 4 | NA18945.hp2 NA18990.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+1209A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98292794 | ||||||
| chr8:98293135
|
G | A | 35 | a0001c0001t0002g0021a0001c0001t0002g0023a0001c0001t0002g0033others(32): Show | 35 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.135+868C>T | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293135 | ||||||
| chr8:98293272
|
T | C | 2 | a0001c0001t0002g0301a0001c0001t0003g0302 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.135+731A>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293272 | ||||||
| chr8:98293311
|
A | T | 49 | a0001c0001t0002g0010a0001c0001t0002g0021a0001c0001t0002g0023others(46): Show | 49 | HG00738.hp1 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.135+692T>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293311 | ||||||
| chr8:98293406
|
T | G | 23 | a0001c0001t0002g0312a0001c0001t0002g0314a0001c0001t0002g0322others(20): Show | 23 | HG00738.hp1 HG01175.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+597A>C | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293406 | ||||||
| chr8:98293667
|
G | C | 3 | a0001c0002t0001g0326a0001c0002t0001g0327a0001c0002t0001g0328 | 3 | HG01943.hp2 HG01993.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.135+336C>G | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293667 | ||||||
| chr8:98293699
|
C | T | 5 | a0001c0001t0002g0010a0001c0001t0006g0006a0001c0001t0006g0007others(2): Show | 5 | HG02698.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+304G>A | NIPAL2 | ENSG00000104361.10 | transcript | ENST00000430223.7 | protein_coding | 1/10 | chr8 | 98293699 |