Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 64168 |
|---|---|
| ensemblid | ENSG00000123119.12 |
| hgncid | 20983 |
| symbol | NECAB1 |
| name | N-terminal EF-hand calcium binding protein 1 |
| refseq_nuc | NM_022351.5 |
| refseq_prot | NP_071746.1 |
| ensembl_nuc | ENST00000417640.7 |
| ensembl_prot | ENSP00000387380.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 90791775 |
| end | 90959393 |
| strand | + |
| ver | v1.2 |
| region | chr8:90791775-90959393 |
| region5000 | chr8:90786775-90964393 |
| regionname0 | NECAB1_chr8_90791775_90959393 |
| regionname5000 | NECAB1_chr8_90786775_90964393 |
| 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 | 351 | 247 | 67 | 40 | 108 | 10 | 20 | 84 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0002 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| 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 | 1056 | 247 | 67 | 40 | 108 | 10 | 20 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| c0002 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| 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 | 1/0 | 3994 | 52 | 4 | 11 | 23 | 4 | 9 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0002 | 0/0 | 3992 | 41 | 3 | 7 | 25 | 1 | 5 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0003 | 0/0 | 3999 | 12 | 0 | 1 | 11 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0004 | 0/0 | 4002 | 12 | 10 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0005 | 0/0 | 3999 | 8 | 1 | 0 | 7 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0006 | 0/0 | 4001 | 8 | 2 | 0 | 5 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0007 | 0/0 | 3990 | 8 | 0 | 3 | 3 | 2 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0008 | 0/0 | 3992 | 7 | 0 | 0 | 6 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0009 | 0/0 | 3991 | 6 | 6 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0010 | 0/0 | 3994 | 6 | 0 | 0 | 6 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0011 | 0/0 | 3994 | 6 | 1 | 1 | 4 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0012 | 0/0 | 3993 | 5 | 5 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0013 | 0/0 | 3996 | 5 | 0 | 2 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0014 | 0/0 | 4000 | 5 | 2 | 2 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0015 | 0/0 | 3988 | 5 | 1 | 1 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0016 | 0/0 | 4003 | 4 | 4 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0017 | 0/0 | 3989 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0018 | 0/0 | 3998 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0019 | 0/0 | 3994 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0020 | 0/0 | 3980 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0021 | 0/0 | 3996 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0022 | 0/1 | 3992 | 3 | 0 | 1 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0023 | 0/0 | 4004 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0024 | 0/0 | 3968 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0025 | 0/0 | 3992 | 2 | 1 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0026 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0027 | 0/0 | 3991 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0028 | 0/0 | 4000 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0029 | 0/0 | 4004 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0030 | 0/0 | 3987 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0031 | 0/0 | 3992 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0032 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0033 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0034 | 0/0 | 3999 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0035 | 0/0 | 4002 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0036 | 0/0 | 4004 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0037 | 0/0 | 3990 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0038 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0039 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0040 | 0/0 | 3992 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0041 | 0/0 | 3993 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0042 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0043 | 0/0 | 4002 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0044 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0045 | 0/0 | 3992 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0046 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0047 | 0/0 | 3988 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0048 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0049 | 0/0 | 3993 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0050 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0051 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0052 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0053 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| t0054 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| 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 | 1056 | 247 | 67 | 40 | 108 | 10 | 20 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0002c0002 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5049 | 52 | 4 | 11 | 23 | 4 | 9 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0002 | 0/0 | 5047 | 41 | 3 | 7 | 25 | 1 | 5 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0003 | 0/0 | 5054 | 12 | 0 | 1 | 11 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0004 | 0/0 | 5057 | 12 | 10 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0005 | 0/0 | 5054 | 8 | 1 | 0 | 7 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0006 | 0/0 | 5056 | 8 | 2 | 0 | 5 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0007 | 0/0 | 5045 | 8 | 0 | 3 | 3 | 2 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0008 | 0/0 | 5047 | 7 | 0 | 0 | 6 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0009 | 0/0 | 5046 | 5 | 5 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0010 | 0/0 | 5049 | 6 | 0 | 0 | 6 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0011 | 0/0 | 5049 | 6 | 1 | 1 | 4 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0012 | 0/0 | 5048 | 5 | 5 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0013 | 0/0 | 5051 | 5 | 0 | 2 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0014 | 0/0 | 5055 | 5 | 2 | 2 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0015 | 0/0 | 5043 | 5 | 1 | 1 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0016 | 0/0 | 5058 | 4 | 4 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0017 | 0/0 | 5044 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0018 | 0/0 | 5053 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0019 | 0/0 | 5049 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0020 | 0/0 | 5035 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0021 | 0/0 | 5051 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0022 | 0/1 | 5047 | 3 | 0 | 1 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0023 | 0/0 | 5059 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0024 | 0/0 | 5023 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0025 | 0/0 | 5047 | 2 | 1 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0026 | 0/0 | 5051 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0027 | 0/0 | 5046 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0028 | 0/0 | 5055 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0029 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0030 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0031 | 0/0 | 5047 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0032 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0033 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0034 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0035 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0036 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0037 | 0/0 | 5045 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0038 | 0/0 | 5048 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0039 | 0/0 | 5046 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0040 | 0/0 | 5047 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0041 | 0/0 | 5048 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0042 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0043 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0044 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0045 | 0/0 | 5047 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0046 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0047 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0048 | 0/0 | 5053 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0049 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0050 | 0/0 | 5053 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0051 | 0/0 | 5051 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0052 | 0/0 | 5051 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0053 | 0/0 | 5056 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0001c0001t0054 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| a0002c0002t0009 | 0/0 | 5046 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | copy fasta | chr8 | 90786775 | 90964393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0024g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0024g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0025g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0025g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0026g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0026g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0027g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0027g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0028g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0029g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0030g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0031g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0032g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0033g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0034g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0035g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0036g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0037g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0038g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0039g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0040g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0041g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0042g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0043g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0044g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0045g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0046g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0047g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0048g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0049g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0050g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0051g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0052g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0053g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0054g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0002c0002t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | GBR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00423 | hp1 | a0001 | c0001 | t0034 | g0156 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00621 | hp2 | a0001 | c0001 | t0047 | g0059 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0232 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0160 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00735 | hp1 | a0001 | c0001 | t0021 | g0175 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00741 | hp1 | a0001 | c0001 | t0014 | g0211 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01070 | hp1 | a0001 | c0001 | t0024 | g0220 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01074 | hp2 | a0001 | c0001 | t0024 | g0221 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01099 | hp2 | a0001 | c0001 | t0020 | g0161 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01109 | hp1 | a0001 | c0001 | t0048 | g0129 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0222 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0053 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01256 | hp2 | a0001 | c0001 | t0038 | g0246 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01261 | hp2 | a0001 | c0001 | t0023 | g0169 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01361 | hp2 | a0001 | c0001 | t0041 | g0197 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01515 | hp1 | a0001 | c0001 | t0020 | g0146 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01516 | hp1 | a0001 | c0001 | t0037 | g0225 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0001 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0002 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0100 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0143 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01978 | hp1 | a0001 | c0001 | t0020 | g0162 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02004 | hp1 | a0001 | c0001 | t0014 | g0210 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02056 | hp2 | a0001 | c0001 | t0013 | g0181 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02074 | hp2 | a0001 | c0001 | t0033 | g0013 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02132 | hp1 | a0001 | c0001 | t0010 | g0121 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02145 | hp2 | a0001 | c0001 | t0054 | g0114 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0109 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0138 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02257 | hp2 | a0001 | c0001 | t0019 | g0236 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0133 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02523 | hp1 | a0001 | c0001 | t0027 | g0016 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02615 | hp2 | a0001 | c0001 | t0021 | g0174 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0134 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0127 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0021 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02630 | hp2 | a0001 | c0001 | t0018 | g0141 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0128 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0235 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02738 | hp1 | a0001 | c0001 | t0049 | g0217 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02809 | hp1 | a0001 | c0001 | t0032 | g0136 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02818 | hp1 | a0001 | c0001 | t0035 | g0130 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0173 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0080 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0032 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0240 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0166 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02965 | hp2 | a0001 | c0001 | t0029 | g0131 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0142 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03098 | hp1 | a0001 | c0001 | t0053 | g0010 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03098 | hp2 | a0001 | c0001 | t0021 | g0176 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03130 | hp1 | a0001 | c0001 | t0045 | g0237 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0243 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0126 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0168 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0238 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03239 | hp2 | a0001 | c0001 | t0015 | g0206 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03453 | hp1 | a0002 | c0002 | t0009 | g0124 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03491 | hp1 | a0001 | c0001 | t0013 | g0216 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03540 | hp2 | a0001 | c0001 | t0036 | g0139 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0152 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04228 | hp1 | a0001 | c0001 | t0052 | g0050 | SAS | STU | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0248 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18522 | hp2 | a0001 | c0001 | t0029 | g0132 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0144 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18939 | hp1 | a0001 | c0001 | t0010 | g0122 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18948 | hp2 | a0001 | c0001 | t0039 | g0183 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18964 | hp2 | a0001 | c0001 | t0030 | g0047 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0061 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0113 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0205 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18985 | hp1 | a0001 | c0001 | t0027 | g0108 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18989 | hp2 | a0001 | c0001 | t0026 | g0194 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18991 | hp1 | a0001 | c0001 | t0014 | g0190 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18991 | hp2 | a0001 | c0001 | t0015 | g0019 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18998 | hp2 | a0001 | c0001 | t0040 | g0184 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19007 | hp1 | a0001 | c0001 | t0026 | g0193 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0057 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19030 | hp1 | a0001 | c0001 | t0050 | g0094 | AFR | LWK | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | LWK | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0071 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19075 | hp2 | a0001 | c0001 | t0015 | g0083 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19076 | hp2 | a0001 | c0001 | t0043 | g0150 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19078 | hp1 | a0001 | c0001 | t0010 | g0060 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19079 | hp2 | a0001 | c0001 | t0051 | g0065 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0034 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19084 | hp2 | a0001 | c0001 | t0013 | g0107 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19085 | hp1 | a0001 | c0001 | t0025 | g0009 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19240 | hp2 | a0001 | c0001 | t0042 | g0178 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0110 | EUR | TSI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01123 | hp2 | a0001 | c0001 | t0022 | g0074 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0165 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0179 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0140 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02559 | hp1 | a0001 | c0001 | t0031 | g0242 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02559 | hp2 | a0001 | c0001 | t0044 | g0125 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | USA | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0022 | g0005 | REF | REF | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0208 | REF | REF | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90940849
|
G | A | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.811G>A | p.Ala271Thr | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/13 | 923/5049 | 811/1056 | 271/351 | chr8 | 90940849 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90791841
|
C | T | 1 | a0001c0001t0054 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/13 | 46 | chr8 | 90791841 | |||||
| chr8:90955572
|
G | A | 9 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(6): Show | 30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*60G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 60 | chr8 | 90955572 | |||||
| chr8:90955582
|
A | G | 1 | a0001c0001t0053 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 70 | chr8 | 90955582 | |||||
| chr8:90955787
|
T | C | 1 | a0001c0001t0034 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 275 | chr8 | 90955787 | |||||
| chr8:90955840
|
T | C | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*328T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 328 | chr8 | 90955840 | |||||
| chr8:90956096
|
C | T | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(40): Show | 169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*584C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 584 | chr8 | 90956096 | |||||
| chr8:90956299
|
G | A | 9 | a0001c0001t0005a0001c0001t0006a0001c0001t0016others(6): Show | 28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*787G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 787 | chr8 | 90956299 | |||||
| chr8:90956383
|
A | C | 5 | a0001c0001t0010a0001c0001t0026a0001c0001t0039others(2): Show | 11 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*871A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 871 | chr8 | 90956383 | |||||
| chr8:90956675
|
T | C | 1 | a0001c0001t0044 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1163 | chr8 | 90956675 | |||||
| chr8:90956828
|
T | C | 2 | a0001c0001t0019a0001c0001t0045 | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1316T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1316 | chr8 | 90956828 | |||||
| chr8:90956943
|
C | CGT | 8 | a0001c0001t0005a0001c0001t0013a0001c0001t0026others(5): Show | 20 | HG00423.hp1 HG00558.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1472_*1473dupGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
C | CGTGT | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0029others(3): Show | 25 | HG00673.hp2 HG01167.hp1 HG01243.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1470_*1473dupGTGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
C | CGTGTGT | 3 | a0001c0001t0014a0001c0001t0016a0001c0001t0023 | 12 | HG00741.hp1 HG01261.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1468_*1473dupGTGT others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGT | C | 13 | a0001c0001t0002a0001c0001t0008a0001c0001t0022others(10): Show | 63 | HG00099.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1472_*1473delGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1472 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGT | C | 3 | a0001c0001t0007a0001c0001t0021a0001c0001t0037 | 12 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1470_*1473delGTGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1470 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGT | C | 4 | a0001c0001t0012a0001c0001t0015a0001c0001t0031others(1): Show | 12 | HG00621.hp2 HG01256.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1468_*1473delGTGT others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1468 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGTG others(1): Show |
C | 2 | a0001c0001t0009a0002c0002t0009 | 6 | HG02622.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1466_*1473delGTGT others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1466 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0017 | 3 | HG01891.hp1 HG02965.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1464_*1473delGTGT others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1464 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0030a0001c0001t0046 | 2 | HG02257.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1462_*1473delGTGT others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1462 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0020 | 3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1460_*1473delGTGT others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1460 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90956943
|
CGTGTGTG others(19): Show |
C | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1448_*1473delGTGT others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1448 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | ||||
| chr8:90957104
|
T | C | 1 | a0001c0001t0032 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1592 | chr8 | 90957104 | |||||
| chr8:90957441
|
C | T | 41 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(38): Show | 165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1929 | chr8 | 90957441 | |||||
| chr8:90957729
|
T | TAA | 7 | a0001c0001t0021a0001c0001t0028a0001c0001t0029others(4): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2218_*2219dupAA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2220 | INFO_REALIGN_3_PRIME | chr8 | 90957729 | ||||
| chr8:90958026
|
A | T | 3 | a0001c0001t0008a0001c0001t0047a0001c0001t0052 | 9 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2514A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2514 | chr8 | 90958026 | |||||
| chr8:90958084
|
C | CT | 9 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(6): Show | 30 | HG00621.hp1 HG01361.hp2 HG01891.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2589dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2590 | INFO_REALIGN_3_PRIME | chr8 | 90958084 | ||||
| chr8:90958084
|
CT | C | 10 | a0001c0001t0005a0001c0001t0006a0001c0001t0016others(7): Show | 28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2589delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2589 | INFO_REALIGN_3_PRIME | chr8 | 90958084 | ||||
| chr8:90958441
|
A | G | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(9): Show | 46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2929A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2929 | chr8 | 90958441 | |||||
| chr8:90958635
|
T | A | 1 | a0001c0001t0022 | 3 | HG01123.hp2 NA20805.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3123T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 3123 | chr8 | 90958635 | |||||
| chr8:90958844
|
A | ATTCT | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(25): Show | 85 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*3335_*3338dupCTTT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 3339 | INFO_REALIGN_3_PRIME | chr8 | 90958844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90792243
|
A | C | 1 | a0001c0001t0009g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+258A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792243 | ||||||
| chr8:90792273
|
G | A | 5 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0003others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+288G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792273 | ||||||
| chr8:90792310
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.99+325G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792310 | ||||||
| chr8:90792505
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.99+520T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792505 | ||||||
| chr8:90792555
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.99+570T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792555 | ||||||
| chr8:90792564
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+579C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792564 | ||||||
| chr8:90792577
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(117): Show | 120 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.99+592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792577 | ||||||
| chr8:90792820
|
T | C | 179 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(176): Show | 179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.99+835T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792820 | ||||||
| chr8:90792849
|
C | T | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+864C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792849 | ||||||
| chr8:90792880
|
C | T | 8 | a0001c0001t0001g0120a0001c0001t0002g0118a0001c0001t0002g0119others(5): Show | 8 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+895C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792880 | ||||||
| chr8:90793093
|
A | C | 41 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(38): Show | 41 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.99+1108A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793093 | ||||||
| chr8:90793586
|
A | G | 182 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(179): Show | 182 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+1601A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793586 | ||||||
| chr8:90793597
|
C | A | 1 | a0001c0001t0025g0009 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.99+1612C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793597 | ||||||
| chr8:90793638
|
G | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+1653G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793638 | ||||||
| chr8:90793665
|
G | A | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+1680G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793665 | ||||||
| chr8:90793856
|
G | C | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1871G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793856 | ||||||
| chr8:90793889
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.99+1904G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793889 | ||||||
| chr8:90793989
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+2004C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793989 | ||||||
| chr8:90794004
|
T | C | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99+2019T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794004 | ||||||
| chr8:90794205
|
T | C | 1 | a0001c0001t0013g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+2220T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794205 | ||||||
| chr8:90794569
|
A | T | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+2584A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794569 | ||||||
| chr8:90794603
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+2618T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794603 | ||||||
| chr8:90794720
|
A | C | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+2735A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794720 | ||||||
| chr8:90794828
|
C | T | 40 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(37): Show | 40 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+2843C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794828 | ||||||
| chr8:90795067
|
A | G | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3082A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795067 | ||||||
| chr8:90795220
|
G | A | 120 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(117): Show | 120 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.99+3235G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795220 | ||||||
| chr8:90795286
|
G | A | 5 | a0001c0001t0018g0133a0001c0001t0029g0131a0001c0001t0029g0132others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3301G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795286 | ||||||
| chr8:90795357
|
G | A | 2 | a0001c0001t0039g0183a0001c0001t0040g0184 | 2 | NA18948.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.99+3372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795357 | ||||||
| chr8:90795393
|
A | T | 172 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(169): Show | 172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.99+3408A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795393 | ||||||
| chr8:90795399
|
A | T | 42 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(39): Show | 42 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.99+3414A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795399 | ||||||
| chr8:90795418
|
G | A | 42 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(39): Show | 42 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.99+3433G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795418 | ||||||
| chr8:90795461
|
G | A | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3476G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795461 | ||||||
| chr8:90795484
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+3499C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795484 | ||||||
| chr8:90795539
|
A | T | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+3554A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795539 | ||||||
| chr8:90795669
|
C | CCCCTCTG others(240): Show |
1 | a0001c0001t0010g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+3684_99+3685ins others(247): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795669 | ||||||
| chr8:90795671
|
G | T | 1 | a0001c0001t0010g0185 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+3686G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795671 | ||||||
| chr8:90795701
|
A | ATC | 5 | a0001c0001t0001g0120a0001c0001t0002g0011a0001c0001t0006g0115others(2): Show | 5 | HG00673.hp1 HG01099.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+3723_99+3724dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795701 | |||||
| chr8:90795701
|
A | ATCTC | 102 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0040others(99): Show | 102 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.99+3721_99+3724dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795701 | |||||
| chr8:90795708
|
T | A | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3723T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795708 | ||||||
| chr8:90795708
|
T | TCA | 10 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 10 | HG02615.hp1 HG02738.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+3755_99+3756dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | |||||
| chr8:90795708
|
T | TCACACA | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3751_99+3756dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | |||||
| chr8:90795708
|
T | TCTCTCA | 10 | a0001c0001t0001g0015a0001c0001t0002g0012a0001c0001t0002g0017others(7): Show | 10 | HG01516.hp2 HG01517.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+3724_99+3725ins others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | |||||
| chr8:90795708
|
TCA | T | 14 | a0001c0001t0006g0145a0001c0001t0009g0239a0001c0001t0012g0240others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+3755_99+3756del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | |||||
| chr8:90795708
|
TCACA | T | 37 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(34): Show | 37 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.99+3753_99+3756del others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | |||||
| chr8:90795710
|
A | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0120a0001c0001t0002g0111others(8): Show | 11 | HG01099.hp1 HG01257.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+3725A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795710 | ||||||
| chr8:90795712
|
A | T | 7 | a0001c0001t0002g0111a0001c0001t0006g0115a0001c0001t0006g0145others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+3727A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795712 | ||||||
| chr8:90795714
|
A | T | 36 | a0001c0001t0001g0151a0001c0001t0004g0170a0001c0001t0004g0171others(33): Show | 36 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3729A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795714 | ||||||
| chr8:90795716
|
A | T | 2 | a0001c0001t0012g0140a0001c0001t0018g0141 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.99+3731A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795716 | ||||||
| chr8:90796041
|
T | C | 4 | a0001c0001t0014g0235a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4056T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796041 | ||||||
| chr8:90796130
|
C | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0007g0024others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4145C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796130 | ||||||
| chr8:90796303
|
C | T | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+4318C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796303 | ||||||
| chr8:90796308
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+4323C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796308 | ||||||
| chr8:90796554
|
T | G | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+4569T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796554 | ||||||
| chr8:90796619
|
G | T | 3 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0032g0136 | 3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+4634G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796619 | ||||||
| chr8:90796743
|
G | A | 182 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(179): Show | 182 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+4758G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796743 | ||||||
| chr8:90796765
|
G | A | 4 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4780G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796765 | ||||||
| chr8:90796808
|
G | T | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+4823G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796808 | ||||||
| chr8:90796935
|
G | C | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-4756G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796935 | ||||||
| chr8:90797206
|
A | G | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-4485A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797206 | ||||||
| chr8:90797350
|
A | G | 2 | a0001c0001t0029g0131a0001c0001t0029g0132 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.100-4341A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797350 | ||||||
| chr8:90797379
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.100-4312T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797379 | ||||||
| chr8:90797516
|
C | T | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100-4175C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797516 | ||||||
| chr8:90797757
|
G | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.100-3934G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797757 | ||||||
| chr8:90797815
|
A | T | 1 | a0001c0001t0014g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.100-3876A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797815 | ||||||
| chr8:90797963
|
A | G | 1 | a0001c0001t0013g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100-3728A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797963 | ||||||
| chr8:90798206
|
G | C | 2 | a0001c0001t0012g0179a0002c0002t0009g0124 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-3485G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798206 | ||||||
| chr8:90798288
|
C | A | 19 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(16): Show | 19 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-3403C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798288 | ||||||
| chr8:90798346
|
G | A | 2 | a0001c0001t0012g0179a0002c0002t0009g0124 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-3345G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798346 | ||||||
| chr8:90798837
|
A | G | 120 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(117): Show | 120 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.100-2854A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798837 | ||||||
| chr8:90798887
|
T | C | 2 | a0001c0001t0012g0179a0002c0002t0009g0124 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2804T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798887 | ||||||
| chr8:90799074
|
G | A | 2 | a0001c0001t0012g0179a0002c0002t0009g0124 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799074 | ||||||
| chr8:90799157
|
T | G | 1 | a0001c0001t0002g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-2534T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799157 | ||||||
| chr8:90799450
|
C | G | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-2241C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799450 | ||||||
| chr8:90799451
|
G | A | 1 | a0001c0001t0011g0027 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-2240G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799451 | ||||||
| chr8:90799734
|
A | C | 6 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0003g0103others(3): Show | 6 | HG00558.hp1 NA18954.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-1957A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799734 | ||||||
| chr8:90800156
|
A | G | 3 | a0001c0001t0012g0179a0001c0001t0046g0138a0002c0002t0009g0124 | 3 | HG02257.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-1535A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800156 | ||||||
| chr8:90800242
|
G | A | 3 | a0001c0001t0012g0179a0001c0001t0046g0138a0002c0002t0009g0124 | 3 | HG02257.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-1449G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800242 | ||||||
| chr8:90800548
|
T | C | 1 | a0001c0001t0035g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-1143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800548 | ||||||
| chr8:90800554
|
T | G | 8 | a0001c0001t0012g0179a0001c0001t0019g0127a0001c0001t0028g0126others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-1137T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800554 | ||||||
| chr8:90800900
|
A | T | 2 | a0001c0001t0012g0179a0002c0002t0009g0124 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-791A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800900 | ||||||
| chr8:90801004
|
T | C | 2 | a0001c0001t0006g0115a0001c0001t0054g0114 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.100-687T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801004 | ||||||
| chr8:90801037
|
G | A | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-654G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801037 | ||||||
| chr8:90801176
|
T | C | 1 | a0001c0001t0020g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.100-515T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801176 | ||||||
| chr8:90801177
|
A | G | 118 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0028others(115): Show | 118 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.100-514A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801177 | ||||||
| chr8:90801261
|
C | G | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-430C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801261 | ||||||
| chr8:90801442
|
T | C | 5 | a0001c0001t0009g0239a0001c0001t0012g0240a0001c0001t0012g0241others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-249T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801442 | ||||||
| chr8:90801565
|
T | C | 1 | a0001c0001t0002g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-126T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801565 | ||||||
| chr8:90801639
|
T | C | 4 | a0001c0001t0004g0244a0001c0001t0012g0179a0001c0001t0046g0138others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-52T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801639 | ||||||
| chr8:90801668
|
A | T | 1 | a0001c0001t0009g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-23A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801668 | ||||||
| chr8:90802155
|
C | A | 1 | a0001c0001t0012g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+440C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802155 | ||||||
| chr8:90802222
|
C | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+507C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802222 | ||||||
| chr8:90802428
|
C | G | 2 | a0001c0001t0006g0163a0001c0001t0006g0164 | 2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.124+713C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802428 | ||||||
| chr8:90802547
|
G | C | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+832G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802547 | ||||||
| chr8:90802548
|
G | T | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+833G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802548 | ||||||
| chr8:90802655
|
G | A | 25 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0187others(22): Show | 25 | HG01109.hp2 HG01361.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.124+940G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802655 | ||||||
| chr8:90802773
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124+1058C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802773 | ||||||
| chr8:90802864
|
T | C | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.124+1149T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802864 | ||||||
| chr8:90802952
|
A | C | 81 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0078others(78): Show | 81 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.124+1237A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802952 | ||||||
| chr8:90803078
|
G | T | 1 | a0001c0001t0007g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.124+1363G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803078 | ||||||
| chr8:90803169
|
T | G | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1454T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803169 | ||||||
| chr8:90803203
|
A | G | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1488A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803203 | ||||||
| chr8:90803290
|
A | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA19072.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.124+1575A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803290 | ||||||
| chr8:90803576
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1861C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803576 | ||||||
| chr8:90803613
|
G | A | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+1898G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803613 | ||||||
| chr8:90803756
|
C | A | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+2041C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803756 | ||||||
| chr8:90804057
|
C | G | 11 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(8): Show | 11 | HG01884.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+2342C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804057 | ||||||
| chr8:90804146
|
T | C | 3 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0032g0136 | 3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.124+2431T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804146 | ||||||
| chr8:90804181
|
T | C | 1 | a0001c0001t0023g0165 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124+2466T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804181 | ||||||
| chr8:90804360
|
C | T | 3 | a0001c0001t0020g0146a0001c0001t0020g0161a0001c0001t0020g0162 | 3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.124+2645C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804360 | ||||||
| chr8:90804361
|
G | T | 3 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0032g0136 | 3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.124+2646G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804361 | ||||||
| chr8:90804417
|
A | G | 160 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.124+2702A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804417 | ||||||
| chr8:90804484
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.124+2769C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804484 | ||||||
| chr8:90804485
|
A | C | 28 | a0001c0001t0004g0170a0001c0001t0004g0171a0001c0001t0004g0172others(25): Show | 28 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.124+2770A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804485 | ||||||
| chr8:90804700
|
T | A | 1 | a0001c0001t0052g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124+2985T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804700 | ||||||
| chr8:90804761
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.124+3046C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804761 | ||||||
| chr8:90805023
|
T | G | 139 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(136): Show | 139 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+3308T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805023 | ||||||
| chr8:90805169
|
G | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3454G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805169 | ||||||
| chr8:90805365
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0003g0103a0001c0001t0008g0105 | 3 | NA18954.hp2 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.124+3650G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805365 | ||||||
| chr8:90805414
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+3699A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805414 | ||||||
| chr8:90805498
|
A | AT | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3790dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90805498 | |||||
| chr8:90805511
|
G | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+3796G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805511 | ||||||
| chr8:90805531
|
G | A | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+3816G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805531 | ||||||
| chr8:90806052
|
G | T | 1 | a0001c0001t0013g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.124+4337G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806052 | ||||||
| chr8:90806103
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+4388A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806103 | ||||||
| chr8:90806146
|
C | A | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+4431C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806146 | ||||||
| chr8:90806311
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124+4596A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806311 | ||||||
| chr8:90806510
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+4795C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806510 | ||||||
| chr8:90806760
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124+5045C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806760 | ||||||
| chr8:90807123
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+5408G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807123 | ||||||
| chr8:90807241
|
G | A | 12 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+5526G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807241 | ||||||
| chr8:90807461
|
C | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+5746C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807461 | ||||||
| chr8:90807523
|
C | T | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.124+5808C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807523 | ||||||
| chr8:90807596
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+5881A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807596 | ||||||
| chr8:90807632
|
G | C | 1 | a0001c0001t0002g0048 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.124+5917G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807632 | ||||||
| chr8:90807772
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124+6057G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807772 | ||||||
| chr8:90807941
|
C | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+6226C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807941 | ||||||
| chr8:90807960
|
A | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.124+6245A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807960 | ||||||
| chr8:90808018
|
CT | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+6312delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808018 | |||||
| chr8:90808037
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.124+6322A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808037 | ||||||
| chr8:90808204
|
A | G | 105 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(102): Show | 105 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.124+6489A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808204 | ||||||
| chr8:90808348
|
G | A | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+6633G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808348 | ||||||
| chr8:90808437
|
TC | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(122): Show | 125 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.124+6726delC | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808437 | |||||
| chr8:90808560
|
G | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+6845G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808560 | ||||||
| chr8:90808640
|
C | CT | 11 | a0001c0001t0001g0188a0001c0001t0001g0203a0001c0001t0001g0204others(8): Show | 11 | HG01109.hp1 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+6948dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | |||||
| chr8:90808640
|
C | CTT | 34 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0005g0153others(31): Show | 34 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.124+6947_124+6948d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | |||||
| chr8:90808640
|
CT | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(106): Show | 109 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.124+6948delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | |||||
| chr8:90808640
|
CTT | C | 6 | a0001c0001t0001g0015a0001c0001t0002g0052a0001c0001t0002g0106others(3): Show | 6 | HG00558.hp1 HG01256.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+6947_124+6948d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | |||||
| chr8:90808646
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124+6931T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808646 | ||||||
| chr8:90808696
|
A | C | 1 | a0001c0001t0004g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.124+6981A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808696 | ||||||
| chr8:90808895
|
T | A | 1 | a0001c0001t0018g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124+7180T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808895 | ||||||
| chr8:90809183
|
C | A | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+7468C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809183 | ||||||
| chr8:90809225
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124+7510A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809225 | ||||||
| chr8:90809416
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+7701A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809416 | ||||||
| chr8:90809763
|
T | C | 8 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+8048T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809763 | ||||||
| chr8:90809954
|
T | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.124+8239T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809954 | ||||||
| chr8:90810052
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+8337G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810052 | ||||||
| chr8:90810168
|
G | A | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+8453G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810168 | ||||||
| chr8:90810234
|
A | G | 1 | a0001c0001t0014g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.124+8519A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810234 | ||||||
| chr8:90810348
|
T | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+8633T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810348 | ||||||
| chr8:90810860
|
C | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(136): Show | 139 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+9145C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810860 | ||||||
| chr8:90810899
|
G | C | 4 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0008g0152others(1): Show | 4 | HG03710.hp2 NA18989.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+9184G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810899 | ||||||
| chr8:90810951
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124+9236T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810951 | ||||||
| chr8:90810990
|
C | T | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.124+9275C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810990 | ||||||
| chr8:90811171
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.124+9456T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811171 | ||||||
| chr8:90811230
|
C | T | 1 | a0001c0001t0015g0053 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.124+9515C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811230 | ||||||
| chr8:90811237
|
C | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+9522C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811237 | ||||||
| chr8:90811245
|
C | T | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+9530C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811245 | ||||||
| chr8:90811331
|
A | AT | 247 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.124+9619dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90811331 | |||||
| chr8:90811340
|
C | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+9625C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811340 | ||||||
| chr8:90811582
|
T | C | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+9867T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811582 | ||||||
| chr8:90811761
|
T | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.124+10046T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811761 | ||||||
| chr8:90811911
|
T | A | 1 | a0001c0001t0005g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.124+10196T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811911 | ||||||
| chr8:90812178
|
T | A | 7 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0029g0131others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+10463T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812178 | ||||||
| chr8:90812180
|
C | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+10465C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812180 | ||||||
| chr8:90812645
|
T | C | 139 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(136): Show | 139 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.124+10930T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812645 | ||||||
| chr8:90812672
|
T | C | 3 | a0001c0001t0016g0142a0001c0001t0016g0143a0001c0001t0016g0144 | 3 | HG01884.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.124+10957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812672 | ||||||
| chr8:90812789
|
A | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.124+11074A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812789 | ||||||
| chr8:90812890
|
T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+11175T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812890 | ||||||
| chr8:90812937
|
T | TC | 247 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.124+11224dupC | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90812937 | |||||
| chr8:90813174
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.124+11459C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813174 | ||||||
| chr8:90813182
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.124+11467C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813182 | ||||||
| chr8:90813200
|
AAATT | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+11488_124+1149 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813200 | |||||
| chr8:90813203
|
T | C | 105 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(102): Show | 105 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.124+11488T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813203 | ||||||
| chr8:90813227
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11490G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813227 | ||||||
| chr8:90813229
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11488A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813229 | ||||||
| chr8:90813230
|
TATATACA others(3): Show |
T | 2 | a0001c0001t0006g0115a0001c0001t0054g0114 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.125-11485_125-1147 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813230
|
TATATACA others(9): Show |
T | 9 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-11485_125-1147 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813230
|
TATATACA others(11): Show |
T | 4 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813230
|
TATATACA others(13): Show |
T | 14 | a0001c0001t0002g0087a0001c0001t0004g0095a0001c0001t0004g0096others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813230
|
TATATACA others(15): Show |
T | 97 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(94): Show | 97 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813230
|
TATATACA others(17): Show |
T | 5 | a0001c0001t0002g0084a0001c0001t0007g0001a0001c0001t0007g0002others(2): Show | 5 | HG01074.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | |||||
| chr8:90813232
|
T | C | 2 | a0001c0001t0029g0131a0001c0001t0029g0132 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.125-11485T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813232 | ||||||
| chr8:90813232
|
TATACACA others(13): Show |
T | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11483_125-1146 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813232 | |||||
| chr8:90813234
|
T | C | 5 | a0001c0001t0001g0209a0001c0001t0029g0131a0001c0001t0029g0132others(2): Show | 5 | HG00639.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-11483T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813234 | ||||||
| chr8:90813234
|
T | TAC | 6 | a0001c0001t0001g0195a0001c0001t0012g0140a0001c0001t0018g0173others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-11446_125-1144 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
T | TACAC | 4 | a0001c0001t0001g0207a0001c0001t0001g0213a0001c0001t0001g0214others(1): Show | 4 | NA18964.hp1 NA18970.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-11448_125-1144 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
T | TACACAC | 9 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG02155.hp1 HG02723.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-11450_125-1144 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0049a0001c0001t0002g0192a0001c0001t0014g0210others(2): Show | 5 | HG00741.hp1 HG02004.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-11452_125-1144 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
TAC | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0151a0001c0001t0001g0226others(16): Show | 19 | HG00099.hp2 HG01099.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.125-11446_125-1144 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
TACAC | T | 15 | a0001c0001t0001g0231a0001c0001t0005g0147a0001c0001t0005g0153others(12): Show | 15 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-11448_125-1144 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813234
|
TACACAC | T | 4 | a0001c0001t0006g0164a0001c0001t0020g0162a0001c0001t0023g0165others(1): Show | 4 | HG01261.hp2 HG01978.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-11450_125-1144 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | |||||
| chr8:90813236
|
C | T | 2 | a0001c0001t0005g0149a0002c0002t0009g0124 | 2 | HG03453.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.125-11481C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813236 | ||||||
| chr8:90813238
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0008g0152a0001c0001t0043g0150 | 3 | HG03710.hp2 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.125-11479C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813238 | ||||||
| chr8:90813386
|
C | T | 1 | a0001c0001t0008g0113 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.125-11331C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813386 | ||||||
| chr8:90813564
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.125-11153T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813564 | ||||||
| chr8:90813588
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0046g0138 | 2 | HG02165.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.125-11129C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813588 | ||||||
| chr8:90813657
|
G | T | 1 | a0001c0001t0015g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.125-11060G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813657 | ||||||
| chr8:90813658
|
C | G | 1 | a0001c0001t0015g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.125-11059C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813658 | ||||||
| chr8:90813675
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-11042C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813675 | ||||||
| chr8:90813758
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-10959G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813758 | ||||||
| chr8:90814155
|
C | T | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-10562C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814155 | ||||||
| chr8:90814343
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-10374A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814343 | ||||||
| chr8:90814479
|
T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-10238T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814479 | ||||||
| chr8:90814663
|
T | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-10054T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814663 | ||||||
| chr8:90814668
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.125-10049G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814668 | ||||||
| chr8:90814853
|
G | A | 1 | a0001c0001t0029g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125-9864G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814853 | ||||||
| chr8:90815002
|
T | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-9715T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815002 | ||||||
| chr8:90815048
|
C | T | 1 | a0001c0001t0048g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.125-9669C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815048 | ||||||
| chr8:90815144
|
T | C | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-9573T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815144 | ||||||
| chr8:90815241
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125-9476T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815241 | ||||||
| chr8:90815261
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-9456C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815261 | ||||||
| chr8:90815292
|
C | G | 1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125-9425C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815292 | ||||||
| chr8:90815564
|
C | T | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.125-9153C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815564 | ||||||
| chr8:90815596
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA19010.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.125-9121A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815596 | ||||||
| chr8:90815741
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.125-8976A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815741 | ||||||
| chr8:90815790
|
G | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-8927G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815790 | ||||||
| chr8:90815817
|
G | A | 1 | a0001c0001t0050g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-8900G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815817 | ||||||
| chr8:90815823
|
T | C | 1 | a0001c0001t0011g0027 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-8894T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815823 | ||||||
| chr8:90815836
|
T | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-8881T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815836 | ||||||
| chr8:90816431
|
C | A | 5 | a0001c0001t0009g0239a0001c0001t0012g0240a0001c0001t0012g0241others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-8286C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90816431 | ||||||
| chr8:90816966
|
A | G | 5 | a0001c0001t0005g0153a0001c0001t0006g0148a0001c0001t0006g0160others(2): Show | 5 | HG00673.hp2 NA18966.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-7751A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90816966 | ||||||
| chr8:90817252
|
G | T | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-7465G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817252 | ||||||
| chr8:90817261
|
T | G | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125-7456T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817261 | ||||||
| chr8:90817270
|
G | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-7447G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817270 | ||||||
| chr8:90817409
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-7308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817409 | ||||||
| chr8:90817466
|
G | GT | 44 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(41): Show | 44 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-7243dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90817466 | |||||
| chr8:90817466
|
G | GTT | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-7244_125-7243d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90817466 | |||||
| chr8:90817523
|
A | C | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.125-7194A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817523 | ||||||
| chr8:90817855
|
G | A | 1 | a0001c0001t0020g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.125-6862G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817855 | ||||||
| chr8:90817990
|
T | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.125-6727T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817990 | ||||||
| chr8:90818096
|
CT | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-6618delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90818096 | |||||
| chr8:90818229
|
T | C | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-6488T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818229 | ||||||
| chr8:90818379
|
A | G | 2 | a0001c0001t0009g0137a0002c0002t0009g0124 | 2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.125-6338A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818379 | ||||||
| chr8:90818392
|
T | A | 177 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(174): Show | 177 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.125-6325T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818392 | ||||||
| chr8:90818638
|
T | C | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.125-6079T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818638 | ||||||
| chr8:90818707
|
A | C | 15 | a0001c0001t0005g0177a0001c0001t0009g0137a0001c0001t0012g0140others(12): Show | 15 | HG00735.hp1 HG01261.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.125-6010A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818707 | ||||||
| chr8:90818804
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-5913C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818804 | ||||||
| chr8:90818917
|
T | G | 8 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-5800T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818917 | ||||||
| chr8:90819100
|
G | A | 1 | a0001c0001t0018g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-5617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819100 | ||||||
| chr8:90819153
|
TTC | T | 2 | a0001c0001t0035g0130a0001c0001t0036g0139 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.125-5560_125-5559d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90819153 | |||||
| chr8:90819218
|
T | A | 39 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.125-5499T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819218 | ||||||
| chr8:90819328
|
T | G | 8 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-5389T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819328 | ||||||
| chr8:90819486
|
G | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-5231G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819486 | ||||||
| chr8:90819988
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-4729A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819988 | ||||||
| chr8:90820074
|
C | T | 8 | a0001c0001t0009g0137a0001c0001t0012g0140a0001c0001t0017g0166others(5): Show | 8 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-4643C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820074 | ||||||
| chr8:90820158
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0048a0001c0001t0003g0042others(3): Show | 6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-4559C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820158 | ||||||
| chr8:90820211
|
A | G | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.125-4506A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820211 | ||||||
| chr8:90820214
|
G | A | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-4503G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820214 | ||||||
| chr8:90820269
|
A | AATG | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.125-4446_125-4444d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820269 | |||||
| chr8:90820438
|
C | T | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125-4279C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820438 | ||||||
| chr8:90820679
|
CT | C | 10 | a0001c0001t0004g0244a0001c0001t0006g0115a0001c0001t0018g0133others(7): Show | 10 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-4023delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | |||||
| chr8:90820679
|
CTT | C | 41 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(38): Show | 41 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.125-4024_125-4023d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | |||||
| chr8:90820679
|
CTTT | C | 125 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(122): Show | 125 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.125-4025_125-4023d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | |||||
| chr8:90820795
|
T | A | 1 | a0001c0001t0015g0053 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.125-3922T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820795 | ||||||
| chr8:90820868
|
T | G | 2 | a0001c0001t0014g0210a0001c0001t0014g0211 | 2 | HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.125-3849T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820868 | ||||||
| chr8:90821123
|
C | A | 1 | a0001c0001t0002g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.125-3594C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821123 | ||||||
| chr8:90821203
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0002g0025a0001c0001t0002g0026 | 3 | HG01167.hp2 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.125-3514C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821203 | ||||||
| chr8:90821206
|
A | G | 5 | a0001c0001t0004g0244a0001c0001t0029g0131a0001c0001t0029g0132others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-3511A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821206 | ||||||
| chr8:90821704
|
G | A | 1 | a0001c0001t0052g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125-3013G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821704 | ||||||
| chr8:90822192
|
G | A | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.125-2525G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822192 | ||||||
| chr8:90822464
|
A | G | 1 | a0001c0001t0007g0024 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.125-2253A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822464 | ||||||
| chr8:90822534
|
TAAG | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-2181_125-2179d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822534 | |||||
| chr8:90822541
|
A | G | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-2176A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822541 | ||||||
| chr8:90822593
|
T | A | 2 | a0001c0001t0006g0115a0001c0001t0054g0114 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.125-2124T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822593 | ||||||
| chr8:90822675
|
G | A | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-2042G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822675 | ||||||
| chr8:90822802
|
C | G | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-1915C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822802 | ||||||
| chr8:90822829
|
A | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-1888A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822829 | ||||||
| chr8:90822866
|
AT | A | 9 | a0001c0001t0004g0244a0001c0001t0006g0115a0001c0001t0018g0133others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-1840delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822866 | |||||
| chr8:90822866
|
ATT | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-1841_125-1840d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822866 | |||||
| chr8:90822908
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.125-1809G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822908 | ||||||
| chr8:90822993
|
T | C | 3 | a0001c0001t0010g0121a0001c0001t0010g0122a0001c0001t0010g0123 | 3 | HG02132.hp1 NA18939.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.125-1724T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822993 | ||||||
| chr8:90823200
|
G | A | 38 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-1517G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823200 | ||||||
| chr8:90823262
|
C | G | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125-1455C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823262 | ||||||
| chr8:90823265
|
G | T | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.125-1452G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823265 | ||||||
| chr8:90823326
|
A | C | 1 | a0001c0001t0020g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.125-1391A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823326 | ||||||
| chr8:90823382
|
A | T | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1335A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823382 | ||||||
| chr8:90823385
|
A | G | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-1332A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823385 | ||||||
| chr8:90823388
|
A | AT | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1323dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90823388 | |||||
| chr8:90823505
|
A | G | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1212A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823505 | ||||||
| chr8:90823799
|
T | C | 5 | a0001c0001t0004g0244a0001c0001t0029g0131a0001c0001t0029g0132others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-918T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823799 | ||||||
| chr8:90823836
|
T | C | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-881T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823836 | ||||||
| chr8:90823875
|
A | G | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-842A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823875 | ||||||
| chr8:90824046
|
CA | C | 247 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.125-667delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90824046 | |||||
| chr8:90824094
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.125-623G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90824094 | ||||||
| chr8:90824280
|
T | G | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-437T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90824280 | ||||||
| chr8:90824835
|
T | A | 1 | a0001c0001t0003g0042 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.233+10T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90824835 | ||||||
| chr8:90825524
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.233+699A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825524 | ||||||
| chr8:90825558
|
C | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0013g0216 | 3 | HG01515.hp2 HG01517.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.233+733C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825558 | ||||||
| chr8:90825677
|
C | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+852C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825677 | ||||||
| chr8:90825736
|
T | A | 47 | a0001c0001t0001g0151a0001c0001t0004g0244a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.233+911T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825736 | ||||||
| chr8:90825762
|
T | G | 1 | a0001c0001t0009g0239 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+937T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825762 | ||||||
| chr8:90825782
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01261.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.233+957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825782 | ||||||
| chr8:90825899
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+1074G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825899 | ||||||
| chr8:90826133
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.233+1308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826133 | ||||||
| chr8:90826424
|
C | T | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1599C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826424 | ||||||
| chr8:90826491
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.233+1666G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826491 | ||||||
| chr8:90826567
|
C | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+1742C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826567 | ||||||
| chr8:90826864
|
T | G | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2039T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826864 | ||||||
| chr8:90826953
|
A | G | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2128A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826953 | ||||||
| chr8:90827165
|
C | T | 13 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.233+2340C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827165 | ||||||
| chr8:90827348
|
G | A | 173 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(170): Show | 173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.233+2523G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827348 | ||||||
| chr8:90827351
|
G | A | 1 | a0001c0001t0015g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.233+2526G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827351 | ||||||
| chr8:90827394
|
C | A | 7 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+2569C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827394 | ||||||
| chr8:90827451
|
G | A | 3 | a0001c0001t0002g0104a0001c0001t0003g0103a0001c0001t0008g0105 | 3 | NA18954.hp2 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.233+2626G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827451 | ||||||
| chr8:90827706
|
C | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0086 | 2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.233+2881C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827706 | ||||||
| chr8:90828131
|
G | GT | 167 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(164): Show | 167 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.233+3319dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90828131 | |||||
| chr8:90828236
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+3411T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828236 | ||||||
| chr8:90828254
|
A | G | 2 | a0001c0001t0006g0115a0001c0001t0054g0114 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.233+3429A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828254 | ||||||
| chr8:90828364
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0008g0113a0001c0001t0011g0057 | 3 | NA18966.hp1 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.233+3539G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828364 | ||||||
| chr8:90828443
|
T | G | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.233+3618T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828443 | ||||||
| chr8:90828524
|
T | G | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+3699T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828524 | ||||||
| chr8:90828972
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233+4147T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828972 | ||||||
| chr8:90829481
|
T | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.233+4656T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829481 | ||||||
| chr8:90829521
|
C | T | 1 | a0001c0001t0016g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233+4696C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829521 | ||||||
| chr8:90829799
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.233+4974C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829799 | ||||||
| chr8:90829875
|
T | A | 10 | a0001c0001t0002g0058a0001c0001t0003g0033a0001c0001t0008g0044others(7): Show | 10 | HG00621.hp1 HG00621.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+5050T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829875 | ||||||
| chr8:90829878
|
T | C | 1 | a0001c0001t0041g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.233+5053T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829878 | ||||||
| chr8:90830109
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+5284C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830109 | ||||||
| chr8:90830124
|
A | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.233+5299A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830124 | ||||||
| chr8:90830495
|
G | A | 4 | a0001c0001t0014g0235a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+5670G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830495 | ||||||
| chr8:90830996
|
A | T | 172 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(169): Show | 172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.233+6171A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830996 | ||||||
| chr8:90831238
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.233+6413T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831238 | ||||||
| chr8:90831276
|
C | A | 39 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+6451C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831276 | ||||||
| chr8:90831316
|
C | T | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.233+6491C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831316 | ||||||
| chr8:90831752
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0014g0080 | 3 | HG02717.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.233+6927C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831752 | ||||||
| chr8:90832073
|
C | T | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.233+7248C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832073 | ||||||
| chr8:90832224
|
G | T | 39 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(36): Show | 39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+7399G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832224 | ||||||
| chr8:90832310
|
G | A | 1 | a0001c0001t0009g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+7485G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832310 | ||||||
| chr8:90832935
|
G | A | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0006g0154 | 3 | HG02165.hp1 NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.233+8110G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832935 | ||||||
| chr8:90833299
|
G | A | 6 | a0001c0001t0001g0120a0001c0001t0007g0001a0001c0001t0007g0002others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+8474G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833299 | ||||||
| chr8:90833363
|
A | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.233+8538A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833363 | ||||||
| chr8:90833390
|
C | CA | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.233+8573dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90833390 | |||||
| chr8:90833556
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0008g0152 | 2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.233+8731C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833556 | ||||||
| chr8:90833757
|
G | A | 40 | a0001c0001t0001g0151a0001c0001t0001g0204a0001c0001t0005g0147others(37): Show | 40 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.233+8932G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833757 | ||||||
| chr8:90833833
|
A | G | 172 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(169): Show | 172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.233+9008A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833833 | ||||||
| chr8:90833931
|
G | A | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233+9106G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833931 | ||||||
| chr8:90833960
|
C | T | 3 | a0001c0001t0010g0185a0001c0001t0039g0183a0001c0001t0040g0184 | 3 | NA18948.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.233+9135C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833960 | ||||||
| chr8:90833979
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.233+9154A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833979 | ||||||
| chr8:90834031
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.233+9206C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834031 | ||||||
| chr8:90834088
|
A | G | 133 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.233+9263A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834088 | ||||||
| chr8:90834160
|
G | C | 7 | a0001c0001t0002g0058a0001c0001t0008g0051a0001c0001t0008g0054others(4): Show | 7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9335G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834160 | ||||||
| chr8:90834162
|
CT | C | 7 | a0001c0001t0002g0058a0001c0001t0008g0051a0001c0001t0008g0054others(4): Show | 7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9338delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834162 | ||||||
| chr8:90834164
|
C | A | 7 | a0001c0001t0002g0058a0001c0001t0008g0051a0001c0001t0008g0054others(4): Show | 7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9339C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834164 | ||||||
| chr8:90834164
|
C | CA | 91 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(88): Show | 91 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.233+9363dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | |||||
| chr8:90834164
|
C | CAA | 7 | a0001c0001t0002g0063a0001c0001t0002g0088a0001c0001t0004g0244others(4): Show | 7 | HG02486.hp1 HG02615.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9362_233+9363d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | |||||
| chr8:90834164
|
CA | C | 58 | a0001c0001t0001g0092a0001c0001t0001g0151a0001c0001t0001g0200others(55): Show | 58 | HG00558.hp2 HG00673.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.233+9363delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | |||||
| chr8:90834245
|
A | T | 2 | a0001c0001t0002g0088a0001c0001t0051g0065 | 2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.233+9420A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834245 | ||||||
| chr8:90834686
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 9 | HG00423.hp2 HG00642.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+9861C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834686 | ||||||
| chr8:90834926
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+10101T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834926 | ||||||
| chr8:90835000
|
T | A | 4 | a0001c0001t0001g0040a0001c0001t0002g0198a0001c0001t0013g0107others(1): Show | 4 | HG02148.hp1 HG03491.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+10175T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835000 | ||||||
| chr8:90835000
|
TA | T | 110 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(107): Show | 110 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.233+10181delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90835000 | |||||
| chr8:90835000
|
TAA | T | 14 | a0001c0001t0002g0066a0001c0001t0002g0081a0001c0001t0002g0106others(11): Show | 14 | HG00558.hp1 HG01070.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.233+10180_233+1018 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90835000 | |||||
| chr8:90835001
|
A | T | 42 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0005g0153others(39): Show | 42 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.233+10176A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835001 | ||||||
| chr8:90835002
|
A | T | 102 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(99): Show | 102 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.233+10177A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835002 | ||||||
| chr8:90835012
|
C | T | 6 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(3): Show | 6 | HG00423.hp1 HG00558.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+10187C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835012 | ||||||
| chr8:90835392
|
C | G | 114 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(111): Show | 114 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.233+10567C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835392 | ||||||
| chr8:90835528
|
T | A | 1 | a0001c0001t0027g0108 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.233+10703T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835528 | ||||||
| chr8:90835558
|
A | T | 1 | a0001c0001t0013g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233+10733A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835558 | ||||||
| chr8:90835862
|
C | T | 1 | a0001c0001t0005g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.233+11037C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835862 | ||||||
| chr8:90836225
|
A | G | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+11400A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836225 | ||||||
| chr8:90836236
|
C | T | 1 | a0001c0001t0009g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+11411C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836236 | ||||||
| chr8:90836529
|
C | G | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+11704C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836529 | ||||||
| chr8:90836789
|
G | A | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+11964G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836789 | ||||||
| chr8:90836896
|
A | T | 1 | a0001c0001t0022g0005 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.233+12071A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836896 | ||||||
| chr8:90836944
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.233+12119T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836944 | ||||||
| chr8:90837083
|
C | T | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+12258C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837083 | ||||||
| chr8:90837123
|
G | T | 7 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+12298G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837123 | ||||||
| chr8:90837227
|
G | A | 1 | a0001c0001t0011g0034 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.233+12402G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837227 | ||||||
| chr8:90837251
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+12426T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837251 | ||||||
| chr8:90837329
|
T | C | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+12504T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837329 | ||||||
| chr8:90837380
|
G | T | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+12555G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837380 | ||||||
| chr8:90837661
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+12836A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837661 | ||||||
| chr8:90837833
|
A | G | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+13008A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837833 | ||||||
| chr8:90838098
|
T | A | 2 | a0001c0001t0001g0120a0001c0001t0046g0138 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.233+13273T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838098 | ||||||
| chr8:90838462
|
C | T | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+13637C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838462 | ||||||
| chr8:90838513
|
T | G | 1 | a0001c0001t0045g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.233+13688T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838513 | ||||||
| chr8:90838619
|
G | A | 1 | a0001c0001t0048g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.233+13794G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838619 | ||||||
| chr8:90838664
|
C | T | 3 | a0001c0001t0008g0051a0001c0001t0008g0062a0001c0001t0011g0061 | 3 | NA18968.hp1 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.233+13839C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838664 | ||||||
| chr8:90839281
|
C | G | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+14456C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839281 | ||||||
| chr8:90839348
|
A | G | 1 | a0001c0001t0018g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.233+14523A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839348 | ||||||
| chr8:90839435
|
A | G | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+14610A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839435 | ||||||
| chr8:90839714
|
G | A | 1 | a0001c0001t0004g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.233+14889G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839714 | ||||||
| chr8:90839773
|
G | T | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+14948G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839773 | ||||||
| chr8:90840358
|
T | A | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+15533T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840358 | ||||||
| chr8:90840599
|
T | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+15774T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840599 | ||||||
| chr8:90840713
|
G | A | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+15888G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840713 | ||||||
| chr8:90840871
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233+16046G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840871 | ||||||
| chr8:90840950
|
C | CA | 77 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0040others(74): Show | 77 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.233+16142dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90840950 | |||||
| chr8:90840950
|
C | CAA | 47 | a0001c0001t0001g0151a0001c0001t0001g0207a0001c0001t0005g0147others(44): Show | 47 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.233+16141_233+1614 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90840950 | |||||
| chr8:90840980
|
G | A | 1 | a0001c0001t0008g0113 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.233+16155G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840980 | ||||||
| chr8:90841100
|
C | CA | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+16285dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90841100 | |||||
| chr8:90841215
|
G | A | 1 | a0001c0001t0023g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.233+16390G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841215 | ||||||
| chr8:90841235
|
A | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+16410A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841235 | ||||||
| chr8:90841268
|
T | A | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+16443T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841268 | ||||||
| chr8:90841268
|
TA | T | 164 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(161): Show | 164 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.233+16455delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90841268 | |||||
| chr8:90841269
|
A | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+16444A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841269 | ||||||
| chr8:90841453
|
T | G | 6 | a0001c0001t0001g0120a0001c0001t0007g0001a0001c0001t0007g0002others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+16628T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841453 | ||||||
| chr8:90841507
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0086 | 2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.233+16682A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841507 | ||||||
| chr8:90841617
|
C | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+16792C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841617 | ||||||
| chr8:90841747
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.233+16922C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841747 | ||||||
| chr8:90841787
|
C | G | 1 | a0001c0001t0013g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.233+16962C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841787 | ||||||
| chr8:90842627
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233+17802T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842627 | ||||||
| chr8:90842661
|
C | T | 114 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(111): Show | 114 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.233+17836C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842661 | ||||||
| chr8:90842801
|
G | T | 1 | a0001c0001t0005g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.233+17976G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842801 | ||||||
| chr8:90843042
|
C | T | 1 | a0001c0001t0020g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.233+18217C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843042 | ||||||
| chr8:90843153
|
G | T | 1 | a0001c0001t0012g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233+18328G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843153 | ||||||
| chr8:90843199
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0015g0083 | 2 | NA19075.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.233+18374C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843199 | ||||||
| chr8:90843223
|
A | C | 96 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(93): Show | 96 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.233+18398A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843223 | ||||||
| chr8:90843280
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0043g0150 | 3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.233+18455G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843280 | ||||||
| chr8:90843325
|
G | A | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+18500G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843325 | ||||||
| chr8:90843580
|
C | T | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+18755C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843580 | ||||||
| chr8:90843588
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+18763C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843588 | ||||||
| chr8:90843675
|
G | T | 1 | a0001c0001t0015g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.233+18850G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843675 | ||||||
| chr8:90843705
|
A | G | 1 | a0001c0001t0044g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+18880A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843705 | ||||||
| chr8:90843926
|
G | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+19101G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843926 | ||||||
| chr8:90843947
|
T | C | 163 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+19122T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843947 | ||||||
| chr8:90844353
|
G | A | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+19528G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844353 | ||||||
| chr8:90844471
|
A | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+19646A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844471 | ||||||
| chr8:90844557
|
T | A | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+19732T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844557 | ||||||
| chr8:90844787
|
GTTC | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+19967_233+1996 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90844787 | |||||
| chr8:90845020
|
C | T | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+20195C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845020 | ||||||
| chr8:90845112
|
A | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+20287A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845112 | ||||||
| chr8:90845183
|
A | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+20358A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845183 | ||||||
| chr8:90845222
|
A | T | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.233+20397A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845222 | ||||||
| chr8:90845353
|
G | A | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+20528G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845353 | ||||||
| chr8:90845553
|
G | T | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+20728G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845553 | ||||||
| chr8:90845828
|
G | A | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+21003G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845828 | ||||||
| chr8:90846062
|
C | T | 1 | a0001c0001t0007g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.233+21237C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846062 | ||||||
| chr8:90846179
|
G | A | 109 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(106): Show | 109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+21354G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846179 | ||||||
| chr8:90846461
|
G | C | 46 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(43): Show | 46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+21636G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846461 | ||||||
| chr8:90846500
|
G | A | 109 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(106): Show | 109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+21675G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846500 | ||||||
| chr8:90846601
|
A | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+21776A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846601 | ||||||
| chr8:90846750
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.233+21925C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846750 | ||||||
| chr8:90846842
|
C | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+22017C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846842 | ||||||
| chr8:90846953
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+22128T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846953 | ||||||
| chr8:90847178
|
A | G | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233+22353A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847178 | ||||||
| chr8:90847310
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.233+22485G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847310 | ||||||
| chr8:90847392
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.233+22567C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847392 | ||||||
| chr8:90847417
|
G | A | 96 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(93): Show | 96 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.233+22592G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847417 | ||||||
| chr8:90847443
|
G | A | 2 | a0001c0001t0024g0220a0001c0001t0024g0221 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.233+22618G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847443 | ||||||
| chr8:90847502
|
C | T | 5 | a0001c0001t0019g0127a0001c0001t0028g0126a0001c0001t0028g0128others(2): Show | 5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+22677C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847502 | ||||||
| chr8:90847508
|
G | T | 12 | a0001c0001t0004g0045a0001c0001t0004g0096a0001c0001t0004g0097others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+22683G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847508 | ||||||
| chr8:90847750
|
A | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+22925A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847750 | ||||||
| chr8:90847767
|
C | G | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+22942C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847767 | ||||||
| chr8:90847878
|
T | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(114): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.233+23053T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847878 | ||||||
| chr8:90848126
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.233+23301C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848126 | ||||||
| chr8:90848250
|
A | C | 109 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(106): Show | 109 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+23425A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848250 | ||||||
| chr8:90848442
|
C | T | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+23617C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848442 | ||||||
| chr8:90848469
|
C | T | 30 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.233+23644C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848469 | ||||||
| chr8:90848520
|
AAAG | A | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-23605_234-2360 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90848520 | |||||
| chr8:90848569
|
T | G | 2 | a0001c0001t0001g0218a0001c0001t0025g0009 | 2 | HG04184.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.234-23559T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848569 | ||||||
| chr8:90848574
|
A | C | 14 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-23554A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848574 | ||||||
| chr8:90848638
|
T | A | 13 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(10): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-23490T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848638 | ||||||
| chr8:90848639
|
T | A | 13 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(10): Show | 13 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-23489T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848639 | ||||||
| chr8:90848649
|
T | C | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-23479T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848649 | ||||||
| chr8:90848720
|
C | T | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234-23408C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848720 | ||||||
| chr8:90848986
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.234-23142G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848986 | ||||||
| chr8:90849045
|
C | G | 1 | a0001c0001t0002g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.234-23083C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849045 | ||||||
| chr8:90849047
|
C | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-23081C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849047 | ||||||
| chr8:90849294
|
C | A | 2 | a0001c0001t0002g0088a0001c0001t0051g0065 | 2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.234-22834C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849294 | ||||||
| chr8:90849377
|
G | T | 7 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0207others(4): Show | 7 | NA18954.hp1 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-22751G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849377 | ||||||
| chr8:90849483
|
C | CT | 204 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0038others(201): Show | 204 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.234-22627dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849483 | |||||
| chr8:90849483
|
C | CTT | 36 | a0001c0001t0001g0028a0001c0001t0001g0093a0001c0001t0001g0182others(33): Show | 36 | HG00423.hp1 HG00673.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-22628_234-2262 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849483 | |||||
| chr8:90849534
|
T | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-22594T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849534 | ||||||
| chr8:90849686
|
A | AT | 13 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0234others(10): Show | 13 | HG01074.hp1 HG01256.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.234-22417dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | |||||
| chr8:90849686
|
A | ATT | 92 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(89): Show | 92 | HG00639.hp2 HG00673.hp1 HG01070.hp2 others(89): Show |
intron_variant | MODIFIER | c.234-22418_234-2241 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | |||||
| chr8:90849686
|
A | ATTT | 21 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0076others(18): Show | 21 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.234-22419_234-2241 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | |||||
| chr8:90849686
|
ATTTTTTT others(1): Show |
A | 24 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(21): Show | 24 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.234-22424_234-2241 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | |||||
| chr8:90849686
|
ATTTTTTT others(3): Show |
A | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-22426_234-2241 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | |||||
| chr8:90849870
|
G | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-22258G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849870 | ||||||
| chr8:90850234
|
C | A | 1 | a0001c0001t0013g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.234-21894C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850234 | ||||||
| chr8:90850314
|
G | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-21814G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850314 | ||||||
| chr8:90850344
|
G | T | 14 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-21784G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850344 | ||||||
| chr8:90850579
|
GATACAAG others(3): Show |
G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-21547_234-2153 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90850579 | |||||
| chr8:90850610
|
T | G | 1 | a0001c0001t0050g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234-21518T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850610 | ||||||
| chr8:90850612
|
C | T | 7 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(4): Show | 7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-21516C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850612 | ||||||
| chr8:90850848
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-21280A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850848 | ||||||
| chr8:90850946
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-21182C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850946 | ||||||
| chr8:90851171
|
T | C | 1 | a0001c0001t0004g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.234-20957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851171 | ||||||
| chr8:90851189
|
C | G | 1 | a0001c0001t0044g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-20939C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851189 | ||||||
| chr8:90851421
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-20707C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851421 | ||||||
| chr8:90851435
|
T | C | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-20693T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851435 | ||||||
| chr8:90851912
|
G | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-20216G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851912 | ||||||
| chr8:90852000
|
T | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-20128T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852000 | ||||||
| chr8:90852394
|
T | C | 1 | a0001c0001t0007g0024 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234-19734T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852394 | ||||||
| chr8:90852406
|
AC | A | 147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-19721delC | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852406 | ||||||
| chr8:90852568
|
C | T | 2 | a0001c0001t0010g0185a0001c0001t0027g0108 | 2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.234-19560C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852568 | ||||||
| chr8:90852640
|
G | A | 1 | a0001c0001t0005g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.234-19488G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852640 | ||||||
| chr8:90852825
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234-19303G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852825 | ||||||
| chr8:90853342
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234-18786G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853342 | ||||||
| chr8:90853476
|
G | GA | 88 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(85): Show | 88 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.234-18645dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90853476 | |||||
| chr8:90853530
|
C | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-18598C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853530 | ||||||
| chr8:90853782
|
C | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-18346C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853782 | ||||||
| chr8:90853814
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-18314A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853814 | ||||||
| chr8:90853936
|
A | AG | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-18191dupG | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90853936 | |||||
| chr8:90854034
|
C | A | 1 | a0001c0001t0014g0080 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.234-18094C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854034 | ||||||
| chr8:90854069
|
G | C | 97 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(94): Show | 97 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.234-18059G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854069 | ||||||
| chr8:90854077
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-18051A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854077 | ||||||
| chr8:90854390
|
C | G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-17738C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854390 | ||||||
| chr8:90854502
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-17626A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854502 | ||||||
| chr8:90855322
|
G | T | 6 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(3): Show | 6 | HG00423.hp1 HG00558.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-16806G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855322 | ||||||
| chr8:90855425
|
T | C | 1 | a0001c0001t0006g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.234-16703T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855425 | ||||||
| chr8:90855842
|
T | G | 1 | a0001c0001t0015g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.234-16286T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855842 | ||||||
| chr8:90856052
|
T | C | 1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.234-16076T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856052 | ||||||
| chr8:90856382
|
G | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-15746G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856382 | ||||||
| chr8:90856620
|
A | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-15508A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856620 | ||||||
| chr8:90857188
|
C | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14940C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857188 | ||||||
| chr8:90857605
|
A | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14523A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857605 | ||||||
| chr8:90857683
|
G | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14445G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857683 | ||||||
| chr8:90857684
|
G | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14444G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857684 | ||||||
| chr8:90857728
|
C | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14400C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857728 | ||||||
| chr8:90857776
|
G | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-14352G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857776 | ||||||
| chr8:90857995
|
A | C | 169 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(166): Show | 169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-14133A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857995 | ||||||
| chr8:90858105
|
G | A | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-14023G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858105 | ||||||
| chr8:90858127
|
C | A | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-14001C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858127 | ||||||
| chr8:90858245
|
T | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0082 | 2 | HG01361.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.234-13883T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858245 | ||||||
| chr8:90858624
|
GA | G | 27 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.234-13492delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90858624 | |||||
| chr8:90858664
|
C | G | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-13464C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858664 | ||||||
| chr8:90858962
|
T | C | 25 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(22): Show | 25 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.234-13166T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858962 | ||||||
| chr8:90858980
|
CA | C | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-13141delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90858980 | |||||
| chr8:90859361
|
G | T | 2 | a0001c0001t0023g0165a0001c0001t0023g0169 | 2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-12767G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859361 | ||||||
| chr8:90859451
|
T | C | 29 | a0001c0001t0001g0015a0001c0001t0002g0012a0001c0001t0002g0017others(26): Show | 29 | HG00558.hp1 HG01361.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.234-12677T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859451 | ||||||
| chr8:90859597
|
C | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-12531C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859597 | ||||||
| chr8:90859762
|
C | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-12366C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859762 | ||||||
| chr8:90859820
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0011g0027 | 2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.234-12308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859820 | ||||||
| chr8:90859996
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-12132A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859996 | ||||||
| chr8:90860115
|
T | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-12013T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860115 | ||||||
| chr8:90860238
|
C | CT | 22 | a0001c0001t0002g0087a0001c0001t0004g0095a0001c0001t0004g0172others(19): Show | 22 | HG01070.hp2 HG01167.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-11874dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | |||||
| chr8:90860238
|
C | CTT | 111 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(108): Show | 111 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.234-11875_234-1187 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | |||||
| chr8:90860238
|
CT | C | 29 | a0001c0001t0001g0151a0001c0001t0001g0191a0001c0001t0001g0207others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.234-11874delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | |||||
| chr8:90860243
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-11885T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860243 | ||||||
| chr8:90860586
|
G | A | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-11542G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860586 | ||||||
| chr8:90860661
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.234-11467C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860661 | ||||||
| chr8:90861146
|
C | G | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10982C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861146 | ||||||
| chr8:90861361
|
C | G | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-10767C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861361 | ||||||
| chr8:90861491
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10637C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861491 | ||||||
| chr8:90861515
|
C | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10613C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861515 | ||||||
| chr8:90861533
|
A | G | 1 | a0001c0001t0022g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.234-10595A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861533 | ||||||
| chr8:90861658
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.234-10470T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861658 | ||||||
| chr8:90861817
|
C | G | 7 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(4): Show | 7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-10311C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861817 | ||||||
| chr8:90862235
|
C | T | 1 | a0001c0001t0029g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234-9893C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862235 | ||||||
| chr8:90862409
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.234-9719C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862409 | ||||||
| chr8:90862433
|
C | T | 2 | a0001c0001t0023g0165a0001c0001t0023g0169 | 2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-9695C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862433 | ||||||
| chr8:90862542
|
C | A | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-9586C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862542 | ||||||
| chr8:90862634
|
CTTGT | C | 2 | a0001c0001t0006g0115a0001c0001t0054g0114 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.234-9491_234-9488d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90862634 | |||||
| chr8:90862806
|
T | TTCCCTTA others(19): Show |
147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-9321_234-9296d others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90862806 | |||||
| chr8:90863045
|
C | T | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-9083C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863045 | ||||||
| chr8:90863127
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0051g0065 | 2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.234-9001G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863127 | ||||||
| chr8:90863234
|
C | G | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.234-8894C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863234 | ||||||
| chr8:90863281
|
A | G | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.234-8847A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863281 | ||||||
| chr8:90864051
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0017 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.234-8077G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864051 | ||||||
| chr8:90864088
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.234-8040C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864088 | ||||||
| chr8:90864149
|
G | T | 23 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(20): Show | 23 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.234-7979G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864149 | ||||||
| chr8:90864193
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.234-7935G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864193 | ||||||
| chr8:90864332
|
C | CAAGG | 161 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.234-7792_234-7789d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90864332 | |||||
| chr8:90864500
|
C | T | 1 | a0001c0001t0007g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.234-7628C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864500 | ||||||
| chr8:90864557
|
A | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-7571A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864557 | ||||||
| chr8:90864822
|
T | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0090others(12): Show | 15 | HG02155.hp1 HG04184.hp1 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.234-7306T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864822 | ||||||
| chr8:90865017
|
G | GCCCCACT others(41): Show |
1 | a0001c0001t0001g0187 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.234-7102_234-7101i others(50): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90865017 | |||||
| chr8:90865279
|
A | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.234-6849A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865279 | ||||||
| chr8:90865903
|
T | C | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-6225T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865903 | ||||||
| chr8:90865926
|
A | G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-6202A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865926 | ||||||
| chr8:90866654
|
A | G | 146 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(143): Show | 146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-5474A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866654 | ||||||
| chr8:90866693
|
C | T | 146 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(143): Show | 146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-5435C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866693 | ||||||
| chr8:90866837
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0093 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.234-5291C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866837 | ||||||
| chr8:90867108
|
G | A | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0103others(2): Show | 5 | HG02074.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-5020G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867108 | ||||||
| chr8:90867114
|
C | G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-5014C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867114 | ||||||
| chr8:90867116
|
G | A | 147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-5012G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867116 | ||||||
| chr8:90867126
|
A | T | 1 | a0001c0001t0002g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234-5002A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867126 | ||||||
| chr8:90867305
|
A | T | 11 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(8): Show | 11 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.234-4823A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867305 | ||||||
| chr8:90867533
|
A | G | 147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-4595A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867533 | ||||||
| chr8:90867549
|
TTCTA | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-4572_234-4569d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90867549 | |||||
| chr8:90867639
|
A | T | 147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-4489A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867639 | ||||||
| chr8:90867648
|
A | C | 14 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.234-4480A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867648 | ||||||
| chr8:90867711
|
A | G | 1 | a0001c0001t0032g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.234-4417A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867711 | ||||||
| chr8:90868083
|
CTCTT | C | 98 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(95): Show | 98 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.234-4041_234-4038d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90868083 | |||||
| chr8:90868315
|
A | C | 1 | a0001c0001t0011g0034 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.234-3813A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868315 | ||||||
| chr8:90868355
|
C | T | 2 | a0001c0001t0010g0122a0001c0001t0010g0123 | 2 | NA18939.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.234-3773C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868355 | ||||||
| chr8:90868521
|
A | G | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.234-3607A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868521 | ||||||
| chr8:90868859
|
T | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-3269T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868859 | ||||||
| chr8:90869016
|
T | C | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-3112T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869016 | ||||||
| chr8:90869016
|
T | G | 151 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(148): Show | 151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.234-3112T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869016 | ||||||
| chr8:90869036
|
C | A | 147 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-3092C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869036 | ||||||
| chr8:90869055
|
A | G | 8 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-3073A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869055 | ||||||
| chr8:90869085
|
A | G | 9 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0055others(6): Show | 9 | HG00673.hp1 HG02523.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-3043A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869085 | ||||||
| chr8:90869106
|
T | G | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-3022T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869106 | ||||||
| chr8:90869110
|
A | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.234-3018A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869110 | ||||||
| chr8:90869137
|
T | A | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-2991T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869137 | ||||||
| chr8:90869333
|
G | A | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.234-2795G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869333 | ||||||
| chr8:90869387
|
G | A | 22 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(19): Show | 22 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.234-2741G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869387 | ||||||
| chr8:90869497
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.234-2631G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869497 | ||||||
| chr8:90869920
|
C | T | 2 | a0001c0001t0023g0165a0001c0001t0023g0169 | 2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-2208C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869920 | ||||||
| chr8:90869947
|
G | A | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-2181G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869947 | ||||||
| chr8:90870119
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234-2009C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870119 | ||||||
| chr8:90870136
|
C | T | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-1992C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870136 | ||||||
| chr8:90870505
|
C | T | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-1623C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870505 | ||||||
| chr8:90870539
|
G | A | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-1589G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870539 | ||||||
| chr8:90870805
|
G | A | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.234-1323G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870805 | ||||||
| chr8:90870891
|
A | G | 121 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(118): Show | 121 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.234-1237A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870891 | ||||||
| chr8:90870999
|
T | TTAAAATA others(317): Show |
3 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238 | 3 | HG02257.hp2 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-1116_234-1115i others(326): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90870999 | |||||
| chr8:90871099
|
A | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-1029A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871099 | ||||||
| chr8:90871294
|
T | C | 1 | a0001c0001t0052g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234-834T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871294 | ||||||
| chr8:90871479
|
T | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.234-649T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871479 | ||||||
| chr8:90871756
|
G | A | 1 | a0001c0001t0018g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.234-372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871756 | ||||||
| chr8:90872015
|
A | G | 148 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.234-113A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90872015 | ||||||
| chr8:90872037
|
C | A | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.234-91C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90872037 | ||||||
| chr8:90872159
|
T | A | 1 | a0001c0001t0006g0154 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.259+6T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872159 | ||||||
| chr8:90872181
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0043g0150 | 3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.259+28C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872181 | ||||||
| chr8:90872306
|
G | A | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.259+153G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872306 | ||||||
| chr8:90872412
|
G | C | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+259G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872412 | ||||||
| chr8:90873018
|
T | A | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259+865T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873018 | ||||||
| chr8:90873078
|
C | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+925C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873078 | ||||||
| chr8:90873122
|
A | G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+969A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873122 | ||||||
| chr8:90873224
|
G | A | 11 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0120others(8): Show | 11 | HG00423.hp2 HG00642.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1071G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873224 | ||||||
| chr8:90873257
|
A | G | 1 | a0001c0001t0002g0086 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.259+1104A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873257 | ||||||
| chr8:90873657
|
G | A | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.259+1504G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873657 | ||||||
| chr8:90873891
|
G | GA | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.259+1738_259+1739i others(3): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873891 | ||||||
| chr8:90874020
|
T | C | 1 | a0001c0001t0002g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.259+1867T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874020 | ||||||
| chr8:90874030
|
T | A | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.259+1877T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874030 | ||||||
| chr8:90874285
|
G | A | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.259+2132G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874285 | ||||||
| chr8:90874318
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0043g0150 | 3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.259+2165G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874318 | ||||||
| chr8:90874583
|
G | A | 15 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(12): Show | 15 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2430G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874583 | ||||||
| chr8:90874797
|
C | T | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.259+2644C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874797 | ||||||
| chr8:90874947
|
A | ATT | 7 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(4): Show | 7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2803_259+2804d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | |||||
| chr8:90874947
|
A | ATTT | 130 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(127): Show | 130 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.259+2802_259+2804d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | |||||
| chr8:90874947
|
A | ATTTT | 15 | a0001c0001t0002g0048a0001c0001t0002g0104a0001c0001t0002g0106others(12): Show | 15 | HG00558.hp1 HG00621.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2801_259+2804d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | |||||
| chr8:90875063
|
C | T | 1 | a0001c0001t0004g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259+2910C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875063 | ||||||
| chr8:90875277
|
C | T | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259+3124C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875277 | ||||||
| chr8:90875388
|
GGA | G | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+3238_259+3239d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875388 | |||||
| chr8:90875429
|
C | T | 1 | a0001c0001t0032g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+3276C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875429 | ||||||
| chr8:90875487
|
C | CA | 59 | a0001c0001t0001g0038a0001c0001t0002g0007a0001c0001t0002g0011others(56): Show | 59 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.259+3362dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | |||||
| chr8:90875487
|
C | CAA | 27 | a0001c0001t0001g0093a0001c0001t0002g0056a0001c0001t0002g0084others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.259+3361_259+3362d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | |||||
| chr8:90875487
|
CA | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0028others(70): Show | 73 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.259+3362delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | |||||
| chr8:90875487
|
CAA | C | 7 | a0001c0001t0009g0137a0001c0001t0012g0140a0001c0001t0017g0166others(4): Show | 7 | HG01070.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+3361_259+3362d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | |||||
| chr8:90875545
|
G | T | 1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+3392G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875545 | ||||||
| chr8:90875739
|
G | A | 1 | a0001c0001t0005g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.259+3586G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875739 | ||||||
| chr8:90875757
|
A | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(127): Show | 130 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.259+3604A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875757 | ||||||
| chr8:90875844
|
C | CA | 98 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(95): Show | 98 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.259+3708dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAA | 9 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(6): Show | 9 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+3706_259+3708d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAA | 5 | a0001c0001t0009g0137a0001c0001t0012g0140a0001c0001t0017g0166others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3705_259+3708d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0151a0001c0001t0005g0149a0001c0001t0005g0177others(6): Show | 9 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+3701_259+3708d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(20): Show | 23 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.259+3700_259+3708d others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0006g0145a0001c0001t0006g0148a0001c0001t0021g0176 | 3 | HG02055.hp2 HG03098.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.259+3699_259+3708d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0032g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+3694_259+3708d others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(9): Show |
12 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0037others(9): Show | 12 | HG01978.hp2 HG02015.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+3693_259+3708d others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875844
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0003g0033a0001c0001t0003g0035a0001c0001t0003g0036 | 3 | HG00621.hp1 HG02056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.259+3692_259+3708d others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | |||||
| chr8:90875864
|
A | AG | 247 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0015others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.259+3711_259+3712i others(3): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875864 | ||||||
| chr8:90875925
|
G | A | 13 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+3772G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875925 | ||||||
| chr8:90876174
|
C | A | 1 | a0001c0001t0032g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+4021C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90876174 | ||||||
| chr8:90876634
|
T | C | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-4399T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90876634 | ||||||
| chr8:90877424
|
A | C | 2 | a0001c0001t0002g0056a0001c0001t0002g0084 | 2 | HG00099.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.260-3609A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877424 | ||||||
| chr8:90877654
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.260-3379G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877654 | ||||||
| chr8:90877701
|
G | C | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-3332G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877701 | ||||||
| chr8:90877942
|
G | T | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-3091G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877942 | ||||||
| chr8:90878040
|
C | A | 15 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(12): Show | 15 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-2993C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878040 | ||||||
| chr8:90878103
|
T | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.260-2930T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878103 | ||||||
| chr8:90878339
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.260-2694G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878339 | ||||||
| chr8:90878340
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.260-2693G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878340 | ||||||
| chr8:90878385
|
A | G | 3 | a0001c0001t0008g0051a0001c0001t0008g0062a0001c0001t0011g0061 | 3 | NA18968.hp1 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.260-2648A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878385 | ||||||
| chr8:90878906
|
C | CCT | 8 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0168others(5): Show | 8 | HG02257.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-2116_260-2115d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878906 | |||||
| chr8:90878906
|
C | CCTCT | 5 | a0001c0001t0009g0239a0001c0001t0012g0240a0001c0001t0012g0241others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-2118_260-2115d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878906 | |||||
| chr8:90878917
|
C | A | 48 | a0001c0001t0001g0202a0001c0001t0002g0111a0001c0001t0003g0014others(45): Show | 48 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.260-2116C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878917 | ||||||
| chr8:90878919
|
A | C | 11 | a0001c0001t0001g0212a0001c0001t0002g0088a0001c0001t0007g0024others(8): Show | 11 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-2114A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878919 | ||||||
| chr8:90878945
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.260-2088T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878945 | ||||||
| chr8:90878968
|
GTC | G | 22 | a0001c0001t0006g0145a0001c0001t0009g0134a0001c0001t0009g0135others(19): Show | 22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.260-2051_260-2050d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878968 | |||||
| chr8:90879062
|
T | TTATATAT others(20): Show |
4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1957_260-1931d others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879062 | |||||
| chr8:90879070
|
AATATATA others(2): Show |
A | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-1945_260-1937d others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879070 | |||||
| chr8:90879136
|
T | G | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-1897T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879136 | ||||||
| chr8:90879193
|
C | CT | 15 | a0001c0001t0001g0187a0001c0001t0009g0134a0001c0001t0009g0135others(12): Show | 15 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-1825dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879193 | |||||
| chr8:90879276
|
C | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-1757C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879276 | ||||||
| chr8:90879379
|
G | C | 2 | a0001c0001t0035g0130a0001c0001t0036g0139 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.260-1654G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879379 | ||||||
| chr8:90879724
|
T | C | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-1309T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879724 | ||||||
| chr8:90880110
|
C | T | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.260-923C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90880110 | ||||||
| chr8:90880247
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260-786A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90880247 | ||||||
| chr8:90880532
|
G | GA | 152 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(149): Show | 152 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.260-487dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90880532 | |||||
| chr8:90881178
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.357+48A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881178 | ||||||
| chr8:90881574
|
T | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.357+444T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881574 | ||||||
| chr8:90881580
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+450C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881580 | ||||||
| chr8:90881667
|
T | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.357+537T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881667 | ||||||
| chr8:90881789
|
G | A | 18 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(15): Show | 18 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+659G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881789 | ||||||
| chr8:90882286
|
T | C | 114 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(111): Show | 114 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.357+1156T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882286 | ||||||
| chr8:90882407
|
T | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.357+1277T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882407 | ||||||
| chr8:90882427
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+1297A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882427 | ||||||
| chr8:90882584
|
G | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.357+1454G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882584 | ||||||
| chr8:90882740
|
C | T | 69 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(66): Show | 69 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.357+1610C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882740 | ||||||
| chr8:90882906
|
T | C | 2 | a0001c0001t0009g0134a0001c0001t0009g0135 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.357+1776T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882906 | ||||||
| chr8:90883205
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.357+2075T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883205 | ||||||
| chr8:90883454
|
C | T | 1 | a0001c0001t0032g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.357+2324C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883454 | ||||||
| chr8:90883660
|
A | C | 26 | a0001c0001t0001g0151a0001c0001t0005g0147a0001c0001t0005g0149others(23): Show | 26 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.357+2530A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883660 | ||||||
| chr8:90883723
|
G | GAACAA | 2 | a0001c0001t0022g0074a0001c0001t0022g0110 | 2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.357+2598_357+2602d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90883723 | |||||
| chr8:90883844
|
A | G | 1 | a0001c0001t0035g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.357+2714A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883844 | ||||||
| chr8:90884057
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.357+2927A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884057 | ||||||
| chr8:90884202
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0017 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.357+3072G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884202 | ||||||
| chr8:90884465
|
G | A | 18 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(15): Show | 18 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+3335G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884465 | ||||||
| chr8:90884637
|
C | T | 1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.357+3507C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884637 | ||||||
| chr8:90884860
|
G | A | 16 | a0001c0001t0002g0070a0001c0001t0003g0014a0001c0001t0003g0031others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.357+3730G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884860 | ||||||
| chr8:90884898
|
A | G | 171 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0078others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.357+3768A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884898 | ||||||
| chr8:90884928
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0030a0001c0001t0011g0027 | 3 | HG01891.hp2 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.357+3798C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884928 | ||||||
| chr8:90885022
|
G | A | 1 | a0001c0001t0006g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.357+3892G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885022 | ||||||
| chr8:90885321
|
T | C | 179 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0040others(176): Show | 179 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.357+4191T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885321 | ||||||
| chr8:90885368
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4238T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885368 | ||||||
| chr8:90885477
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+4347A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885477 | ||||||
| chr8:90885483
|
G | C | 27 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.357+4353G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885483 | ||||||
| chr8:90885585
|
T | G | 171 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0078others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.357+4455T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885585 | ||||||
| chr8:90885592
|
G | A | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357+4462G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885592 | ||||||
| chr8:90885663
|
A | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0078others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.357+4533A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885663 | ||||||
| chr8:90885815
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4685C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885815 | ||||||
| chr8:90886203
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+5073C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886203 | ||||||
| chr8:90886315
|
A | G | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+5185A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886315 | ||||||
| chr8:90886347
|
G | A | 1 | a0001c0001t0010g0060 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.357+5217G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886347 | ||||||
| chr8:90886357
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+5227C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886357 | ||||||
| chr8:90886367
|
C | G | 7 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0207others(4): Show | 7 | NA18954.hp1 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+5237C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886367 | ||||||
| chr8:90886453
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+5323G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886453 | ||||||
| chr8:90886546
|
A | ATGTT | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+5422_357+5425d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90886546 | |||||
| chr8:90886682
|
T | C | 1 | a0001c0001t0016g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357+5552T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886682 | ||||||
| chr8:90887093
|
C | T | 1 | a0001c0001t0015g0019 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+5963C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887093 | ||||||
| chr8:90887155
|
A | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+6025A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887155 | ||||||
| chr8:90887211
|
T | C | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.357+6081T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887211 | ||||||
| chr8:90887277
|
G | A | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+6147G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887277 | ||||||
| chr8:90887420
|
C | A | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+6290C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887420 | ||||||
| chr8:90887475
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.357+6345G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887475 | ||||||
| chr8:90888244
|
C | T | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+7114C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888244 | ||||||
| chr8:90888406
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.357+7276C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888406 | ||||||
| chr8:90888581
|
C | G | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.357+7451C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888581 | ||||||
| chr8:90889121
|
C | T | 30 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(27): Show | 30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.357+7991C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889121 | ||||||
| chr8:90889169
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.357+8039C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889169 | ||||||
| chr8:90889237
|
T | C | 82 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.357+8107T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889237 | ||||||
| chr8:90889452
|
T | C | 2 | a0001c0001t0016g0142a0001c0001t0016g0143 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.357+8322T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889452 | ||||||
| chr8:90889768
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.357+8638G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889768 | ||||||
| chr8:90889956
|
T | TTTGA | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+8826_357+8827i others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889956 | ||||||
| chr8:90889960
|
A | AGT | 161 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(158): Show | 161 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.357+8845_357+8846d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90889960 | |||||
| chr8:90889960
|
A | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+8830A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889960 | ||||||
| chr8:90890238
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+9108T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90890238 | ||||||
| chr8:90890929
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.357+9799T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90890929 | ||||||
| chr8:90891037
|
C | T | 1 | a0001c0001t0018g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.357+9907C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891037 | ||||||
| chr8:90891734
|
C | T | 1 | a0001c0001t0049g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+10604C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891734 | ||||||
| chr8:90891817
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.357+10687C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891817 | ||||||
| chr8:90892091
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.357+10961A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90892091 | ||||||
| chr8:90892266
|
G | GT | 59 | a0001c0001t0002g0088a0001c0001t0003g0014a0001c0001t0003g0031others(56): Show | 59 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.357+11142dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90892266 | |||||
| chr8:90892523
|
G | A | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+11393G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90892523 | ||||||
| chr8:90893047
|
G | C | 7 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0099others(4): Show | 7 | HG01167.hp1 HG02818.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+11917G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893047 | ||||||
| chr8:90893479
|
G | A | 173 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(170): Show | 173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.357+12349G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893479 | ||||||
| chr8:90893627
|
G | C | 29 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.357+12497G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893627 | ||||||
| chr8:90893850
|
A | AT | 140 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(137): Show | 140 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.357+12730dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90893850 | |||||
| chr8:90893850
|
A | ATT | 29 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.357+12729_357+1273 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90893850 | |||||
| chr8:90893887
|
A | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+12757A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893887 | ||||||
| chr8:90893891
|
T | A | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+12761T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893891 | ||||||
| chr8:90894965
|
A | C | 84 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(81): Show | 84 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.357+13835A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90894965 | ||||||
| chr8:90895263
|
C | T | 83 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.357+14133C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90895263 | ||||||
| chr8:90896466
|
G | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+15336G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896466 | ||||||
| chr8:90896521
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+15391C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896521 | ||||||
| chr8:90896554
|
G | A | 169 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(166): Show | 169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.357+15424G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896554 | ||||||
| chr8:90896608
|
A | AAAAAAC | 107 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(104): Show | 107 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.357+15502_357+1550 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90896608 | |||||
| chr8:90896650
|
T | A | 1 | a0001c0001t0015g0019 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+15520T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896650 | ||||||
| chr8:90896669
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.357+15539A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896669 | ||||||
| chr8:90896712
|
A | G | 83 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.357+15582A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896712 | ||||||
| chr8:90896729
|
A | G | 1 | a0002c0002t0009g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.357+15599A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896729 | ||||||
| chr8:90896814
|
C | T | 1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357+15684C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896814 | ||||||
| chr8:90896876
|
CA | C | 15 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0195others(12): Show | 15 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+15747delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896876 | ||||||
| chr8:90896878
|
C | T | 15 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0195others(12): Show | 15 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+15748C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896878 | ||||||
| chr8:90896906
|
T | C | 173 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(170): Show | 173 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.357+15776T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896906 | ||||||
| chr8:90896944
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(21): Show | 24 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.357+15814T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896944 | ||||||
| chr8:90897074
|
T | TA | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.357+15952dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90897074 | |||||
| chr8:90897254
|
A | C | 1 | a0001c0001t0002g0077 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.357+16124A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897254 | ||||||
| chr8:90897394
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.357+16264G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897394 | ||||||
| chr8:90897752
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.357+16622C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897752 | ||||||
| chr8:90897853
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.357+16723C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897853 | ||||||
| chr8:90898078
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+16948C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898078 | ||||||
| chr8:90898265
|
A | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17135A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898265 | ||||||
| chr8:90898640
|
A | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.357+17510A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898640 | ||||||
| chr8:90898661
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17531T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898661 | ||||||
| chr8:90898744
|
T | C | 1 | a0001c0001t0028g0128 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.357+17614T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898744 | ||||||
| chr8:90898747
|
G | A | 3 | a0001c0001t0002g0055a0001c0001t0007g0073a0001c0001t0011g0071 | 3 | NA18998.hp1 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.357+17617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898747 | ||||||
| chr8:90898764
|
C | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0117 | 2 | HG02155.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.357+17634C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898764 | ||||||
| chr8:90898814
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357+17684C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898814 | ||||||
| chr8:90898839
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+17709C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898839 | ||||||
| chr8:90899014
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17884C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899014 | ||||||
| chr8:90899107
|
C | T | 16 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.357+17977C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899107 | ||||||
| chr8:90899148
|
C | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+18018C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899148 | ||||||
| chr8:90899349
|
A | T | 1 | a0001c0001t0048g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.358-18143A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899349 | ||||||
| chr8:90899364
|
T | A | 1 | a0001c0001t0005g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-18128T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899364 | ||||||
| chr8:90899479
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0086 | 2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.358-18013A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899479 | ||||||
| chr8:90899817
|
C | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-17675C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899817 | ||||||
| chr8:90899847
|
T | C | 71 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.358-17645T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899847 | ||||||
| chr8:90899991
|
A | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-17501A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899991 | ||||||
| chr8:90900069
|
C | T | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-17423C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900069 | ||||||
| chr8:90900216
|
T | C | 14 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-17276T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900216 | ||||||
| chr8:90900931
|
G | C | 1 | a0001c0001t0003g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-16561G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900931 | ||||||
| chr8:90900984
|
G | C | 1 | a0001c0001t0003g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-16508G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900984 | ||||||
| chr8:90901235
|
T | TA | 113 | a0001c0001t0001g0078a0001c0001t0002g0007a0001c0001t0002g0011others(110): Show | 113 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.358-16241dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901235 | |||||
| chr8:90901235
|
T | TAA | 50 | a0001c0001t0001g0006a0001c0001t0004g0045a0001c0001t0004g0095others(47): Show | 50 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.358-16242_358-1624 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901235 | |||||
| chr8:90901236
|
A | T | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.358-16256A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901236 | ||||||
| chr8:90901340
|
T | C | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.358-16152T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901340 | ||||||
| chr8:90901832
|
G | A | 75 | a0001c0001t0001g0006a0001c0001t0003g0014a0001c0001t0003g0031others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.358-15660G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901832 | ||||||
| chr8:90901899
|
T | TTG | 10 | a0001c0001t0008g0051a0001c0001t0008g0062a0001c0001t0008g0113others(7): Show | 10 | HG00735.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-15571_358-1557 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901899 | |||||
| chr8:90902056
|
A | G | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.358-15436A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902056 | ||||||
| chr8:90902201
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.358-15291C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902201 | ||||||
| chr8:90902334
|
C | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-15158C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902334 | ||||||
| chr8:90902715
|
T | C | 156 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.358-14777T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902715 | ||||||
| chr8:90902757
|
A | G | 1 | a0001c0001t0043g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.358-14735A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902757 | ||||||
| chr8:90902972
|
A | G | 1 | a0001c0001t0022g0110 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.358-14520A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902972 | ||||||
| chr8:90903383
|
G | GA | 11 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-14102dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90903383 | |||||
| chr8:90903795
|
G | A | 1 | a0001c0001t0052g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.358-13697G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903795 | ||||||
| chr8:90903836
|
T | C | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-13656T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903836 | ||||||
| chr8:90903901
|
G | A | 2 | a0001c0001t0014g0080a0001c0001t0014g0235 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358-13591G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903901 | ||||||
| chr8:90903978
|
G | A | 1 | a0001c0001t0015g0053 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.358-13514G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903978 | ||||||
| chr8:90904031
|
G | C | 1 | a0001c0001t0007g0004 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.358-13461G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904031 | ||||||
| chr8:90904101
|
C | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-13391C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904101 | ||||||
| chr8:90904265
|
CA | C | 165 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(162): Show | 165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.358-13216delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90904265 | |||||
| chr8:90904335
|
A | T | 16 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-13157A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904335 | ||||||
| chr8:90904353
|
T | C | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-13139T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904353 | ||||||
| chr8:90904439
|
G | T | 1 | a0001c0001t0016g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-13053G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904439 | ||||||
| chr8:90904631
|
G | C | 22 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(19): Show | 22 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.358-12861G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904631 | ||||||
| chr8:90904649
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0007g0024a0001c0001t0015g0023 | 3 | HG01070.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.358-12843C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904649 | ||||||
| chr8:90904747
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.358-12745T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904747 | ||||||
| chr8:90904778
|
C | CA | 3 | a0001c0001t0020g0146a0001c0001t0020g0161a0001c0001t0020g0162 | 3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.358-12709dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90904778 | |||||
| chr8:90904900
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358-12592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904900 | ||||||
| chr8:90904931
|
C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-12561C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904931 | ||||||
| chr8:90905072
|
T | C | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.358-12420T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905072 | ||||||
| chr8:90905089
|
CAA | C | 81 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.358-12400_358-1239 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90905089 | |||||
| chr8:90905240
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358-12252T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905240 | ||||||
| chr8:90905465
|
T | C | 81 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.358-12027T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905465 | ||||||
| chr8:90905738
|
C | T | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.358-11754C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905738 | ||||||
| chr8:90905761
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.358-11731C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905761 | ||||||
| chr8:90905937
|
C | T | 46 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(43): Show | 46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.358-11555C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905937 | ||||||
| chr8:90906289
|
G | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0120others(4): Show | 7 | HG00642.hp2 HG01099.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-11203G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906289 | ||||||
| chr8:90906874
|
C | CATATATA others(7): Show |
2 | a0001c0001t0019g0236a0001c0001t0019g0238 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.358-10617_358-1061 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(9): Show |
1 | a0001c0001t0045g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(11): Show |
1 | a0001c0001t0019g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(41): Show |
1 | a0001c0001t0018g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(52): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(33): Show |
1 | a0001c0001t0018g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(44): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(37): Show |
1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(48): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906874
|
C | CATATATA others(45): Show |
1 | a0001c0001t0005g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(56): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | |||||
| chr8:90906876
|
C | CAT | 22 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0091others(19): Show | 22 | HG00741.hp1 HG01099.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.358-10583_358-1058 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | CATAT | 5 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0215others(2): Show | 5 | HG00642.hp2 HG01261.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-10585_358-1058 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | CATATAT | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0230others(2): Show | 5 | HG00735.hp2 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-10587_358-1058 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | CATATATA others(1): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0224a0001c0001t0014g0080others(2): Show | 5 | HG01346.hp1 HG02004.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10589_358-1058 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | CATATATA others(3): Show |
1 | a0001c0001t0014g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.358-10591_358-1058 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | CATATATA others(7): Show |
2 | a0001c0001t0001g0038a0001c0001t0006g0046 | 2 | HG02015.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.358-10595_358-1058 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | |||||
| chr8:90906876
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.358-10616C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906876 | ||||||
| chr8:90906877
|
A | ATATATAT others(23): Show |
14 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0004g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.358-10606_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(23): Show |
6 | a0001c0001t0021g0175a0001c0001t0021g0176a0001c0001t0028g0126others(3): Show | 6 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0035g0130a0001c0001t0036g0139 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0021g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906877
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0029g0131a0001c0001t0029g0132 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | |||||
| chr8:90906879
|
A | ATATATAT others(25): Show |
2 | a0001c0001t0005g0158a0001c0001t0018g0133 | 2 | HG00558.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-10602_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0012g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(58): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0017g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(62): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(49): Show |
2 | a0001c0001t0017g0166a0001c0001t0017g0168 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.358-10604_358-1060 others(60): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0012g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(23): Show |
5 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(2): Show | 5 | HG02622.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0012g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(62): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0009g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(23): Show |
14 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0035others(11): Show | 14 | HG01978.hp2 HG02015.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0012g0241a0001c0001t0031g0242 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.358-10606_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906879
|
A | ATATATGT others(21): Show |
1 | a0001c0001t0012g0179 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | |||||
| chr8:90906881
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.358-10586_358-1058 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906881 | |||||
| chr8:90906881
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0005g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.358-10602_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906881 | |||||
| chr8:90906883
|
A | ATATATAT others(21): Show |
12 | a0001c0001t0001g0006a0001c0001t0005g0149a0001c0001t0006g0148others(9): Show | 12 | HG00423.hp1 HG00642.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.358-10602_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | |||||
| chr8:90906883
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-10602_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | |||||
| chr8:90906883
|
A | ATATATGT others(19): Show |
4 | a0001c0001t0005g0147a0001c0001t0005g0155a0001c0001t0005g0157others(1): Show | 4 | NA19004.hp1 NA19007.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | |||||
| chr8:90906885
|
A | ATATATGT others(19): Show |
4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10602_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906885 | |||||
| chr8:90906885
|
A | ATATGTAT others(19): Show |
6 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0069others(3): Show | 6 | HG00423.hp2 HG00558.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906885 | |||||
| chr8:90906887
|
A | ATGTATAT others(19): Show |
1 | a0001c0001t0049g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | ATGTATAT others(25): Show |
1 | a0001c0001t0004g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | ATGTATAT others(17): Show |
68 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(65): Show | 68 | HG00099.hp1 HG00621.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | ATGTATAT others(21): Show |
2 | a0001c0001t0002g0029a0001c0001t0007g0039 | 2 | NA18747.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | ATGTATAT others(43): Show |
1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(54): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | ATGTGTAT others(17): Show |
1 | a0001c0001t0002g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | |||||
| chr8:90906887
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0192 | 2 | HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.358-10605A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906887 | ||||||
| chr8:90906889
|
A | G | 33 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0069others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.358-10603A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906889 | ||||||
| chr8:90906891
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0002g0076a0001c0001t0002g0192 | 2 | HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.358-10588_358-1058 others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906891 | |||||
| chr8:90906891
|
A | G | 100 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(97): Show | 100 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.358-10601A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906891 | ||||||
| chr8:90907122
|
T | TTG | 3 | a0001c0001t0001g0203a0001c0001t0006g0046a0001c0001t0040g0184 | 3 | HG01109.hp2 HG02698.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.358-10341_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | |||||
| chr8:90907122
|
TTG | T | 16 | a0001c0001t0001g0186a0001c0001t0002g0022a0001c0001t0002g0030others(13): Show | 16 | HG00621.hp2 HG00639.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-10341_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | |||||
| chr8:90907122
|
TTGTG | T | 4 | a0001c0001t0004g0045a0001c0001t0028g0126a0001c0001t0044g0125others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10343_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | |||||
| chr8:90907122
|
TTGTGTG | T | 13 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.358-10345_358-1034 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | |||||
| chr8:90907122
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0005g0147a0001c0001t0042g0178 | 2 | NA19078.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.358-10349_358-1034 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | |||||
| chr8:90907141
|
TGTGTGTG others(5): Show |
T | 23 | a0001c0001t0001g0006a0001c0001t0005g0149a0001c0001t0005g0153others(20): Show | 23 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.358-10349_358-1033 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907141 | |||||
| chr8:90907141
|
TGTGTGTG others(13): Show |
T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10349_358-1033 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907141 | |||||
| chr8:90907143
|
T | A | 1 | a0001c0001t0007g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.358-10349T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907143 | ||||||
| chr8:90907143
|
T | TGA | 24 | a0001c0001t0002g0025a0001c0001t0002g0029a0001c0001t0002g0048others(21): Show | 24 | HG00423.hp2 HG00558.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGA | 13 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0026others(10): Show | 13 | HG01099.hp2 HG01167.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGAGA | 5 | a0001c0001t0002g0012a0001c0001t0002g0056a0001c0001t0002g0119others(2): Show | 5 | HG00099.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGAGAG others(1): Show |
3 | a0001c0001t0002g0076a0001c0001t0022g0074a0001c0001t0022g0110 | 3 | HG01123.hp2 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.358-10348_358-1034 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGAGAG others(3): Show |
1 | a0001c0001t0002g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGAGAG others(5): Show |
1 | a0001c0001t0002g0082 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907143
|
T | TGAGAGAG others(9): Show |
1 | a0001c0001t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | |||||
| chr8:90907145
|
T | A | 68 | a0001c0001t0001g0079a0001c0001t0002g0007a0001c0001t0002g0011others(65): Show | 68 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.358-10347T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907145 | ||||||
| chr8:90907145
|
T | TGAGAGAG others(1): Show |
3 | a0001c0001t0021g0174a0001c0001t0022g0005a0001c0001t0036g0139 | 3 | HG02615.hp2 HG03540.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.358-10346_358-1034 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907145 | |||||
| chr8:90907145
|
T | TGAGAGAG others(5): Show |
1 | a0001c0001t0035g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358-10346_358-1034 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907145 | |||||
| chr8:90907145
|
T | TGAGAGAG others(11): Show |
1 | a0001c0001t0021g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.358-10346_358-1034 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907145 | |||||
| chr8:90907147
|
T | A | 90 | a0001c0001t0001g0079a0001c0001t0002g0007a0001c0001t0002g0011others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.358-10345T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907147 | ||||||
| chr8:90907147
|
T | TGAGAGAG others(9): Show |
1 | a0001c0001t0021g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-10344_358-1034 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907147 | |||||
| chr8:90907149
|
T | A | 99 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(96): Show | 99 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.358-10343T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907149 | ||||||
| chr8:90907149
|
T | TGAGA | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0120others(3): Show | 6 | HG01099.hp1 HG01346.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-10342_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907149 | |||||
| chr8:90907149
|
T | TGAGAGAG others(11): Show |
1 | a0001c0001t0003g0031 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.358-10342_358-1034 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907149 | |||||
| chr8:90907151
|
T | A | 133 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0078others(130): Show | 133 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.358-10341T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907151 | ||||||
| chr8:90907151
|
T | TGA | 3 | a0001c0001t0001g0207a0001c0001t0001g0226a0001c0001t0013g0181 | 3 | HG01261.hp1 HG02056.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.358-10304_358-1030 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907151 | |||||
| chr8:90907151
|
T | TGAGAGAG others(7): Show |
1 | a0001c0001t0003g0103 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.358-10316_358-1030 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907151 | |||||
| chr8:90907153
|
A | T | 3 | a0001c0001t0001g0203a0001c0001t0010g0123a0001c0001t0025g0009 | 3 | HG01109.hp2 NA18985.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.358-10339A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907153 | ||||||
| chr8:90907170
|
G | C | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.358-10322G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907170 | ||||||
| chr8:90907181
|
AGAGAGAG | A | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10310_358-1030 others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907181 | ||||||
| chr8:90907188
|
G | GAGAGAGA | 4 | a0001c0001t0009g0137a0001c0001t0012g0240a0001c0001t0031g0242others(1): Show | 4 | HG02559.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907188
|
G | GAGAGAGA others(4): Show |
3 | a0001c0001t0009g0134a0001c0001t0009g0239a0001c0001t0009g0248 | 3 | HG02622.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.358-10303_358-1030 others(15): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907188
|
G | GAGAGAGA others(6): Show |
4 | a0001c0001t0003g0033a0001c0001t0003g0067a0001c0001t0012g0179others(1): Show | 4 | HG00621.hp1 HG02486.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907188
|
G | GAGAGAGA others(8): Show |
4 | a0001c0001t0003g0036a0001c0001t0003g0043a0001c0001t0033g0013others(1): Show | 4 | HG02074.hp2 HG03453.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907188
|
G | GAGAGAGA others(12): Show |
3 | a0001c0001t0003g0037a0001c0001t0003g0042a0001c0001t0003g0117 | 3 | HG02155.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.358-10303_358-1030 others(23): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907188
|
G | GAGAGAGA others(14): Show |
1 | a0001c0001t0003g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-10303_358-1030 others(25): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | |||||
| chr8:90907308
|
G | A | 4 | a0001c0001t0029g0131a0001c0001t0029g0132a0001c0001t0035g0130others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10184G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907308 | ||||||
| chr8:90907322
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0180 | 2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.358-10170A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907322 | ||||||
| chr8:90907909
|
T | C | 10 | a0001c0001t0008g0044a0001c0001t0008g0051a0001c0001t0008g0054others(7): Show | 10 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-9583T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907909 | ||||||
| chr8:90908140
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.358-9352A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908140 | ||||||
| chr8:90908238
|
C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-9254C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908238 | ||||||
| chr8:90908385
|
C | T | 81 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.358-9107C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908385 | ||||||
| chr8:90908403
|
G | C | 2 | a0001c0001t0005g0177a0001c0001t0042g0178 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.358-9089G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908403 | ||||||
| chr8:90908956
|
C | T | 1 | a0001c0001t0005g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-8536C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908956 | ||||||
| chr8:90909312
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-8180A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909312 | ||||||
| chr8:90909375
|
G | GA | 82 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.358-8104dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90909375 | |||||
| chr8:90909424
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.358-8068T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909424 | ||||||
| chr8:90909668
|
GATTTT | G | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-7818_358-7814d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90909668 | |||||
| chr8:90909733
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.358-7759A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909733 | ||||||
| chr8:90909762
|
T | C | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.358-7730T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909762 | ||||||
| chr8:90910010
|
G | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-7482G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910010 | ||||||
| chr8:90910221
|
TATC | T | 81 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.358-7270_358-7268d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910221 | ||||||
| chr8:90910458
|
C | T | 14 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-7034C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910458 | ||||||
| chr8:90910653
|
T | C | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-6839T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910653 | ||||||
| chr8:90910713
|
C | T | 1 | a0001c0001t0018g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358-6779C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910713 | ||||||
| chr8:90910829
|
A | G | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-6663A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910829 | ||||||
| chr8:90910865
|
A | ACCCATTG others(323): Show |
1 | a0001c0001t0018g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-6611_358-6610i others(332): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90910865 | |||||
| chr8:90910866
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-6626C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910866 | ||||||
| chr8:90911192
|
C | T | 1 | a0001c0001t0006g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358-6300C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911192 | ||||||
| chr8:90911326
|
T | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-6166T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911326 | ||||||
| chr8:90911973
|
T | G | 83 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.358-5519T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911973 | ||||||
| chr8:90912677
|
T | TTATTTTT others(313): Show |
1 | a0001c0001t0002g0030 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.358-4800_358-4799i others(322): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90912677 | |||||
| chr8:90913168
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.358-4324A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913168 | ||||||
| chr8:90913371
|
T | A | 1 | a0001c0001t0002g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358-4121T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913371 | ||||||
| chr8:90913372
|
C | CA | 172 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(169): Show | 172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.358-4119dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90913372 | |||||
| chr8:90913613
|
A | G | 3 | a0001c0001t0017g0166a0001c0001t0017g0167a0001c0001t0017g0168 | 3 | HG01891.hp1 HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.358-3879A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913613 | ||||||
| chr8:90913859
|
G | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.358-3633G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913859 | ||||||
| chr8:90913864
|
G | A | 1 | a0001c0001t0008g0054 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.358-3628G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913864 | ||||||
| chr8:90913945
|
C | A | 1 | a0001c0001t0003g0036 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.358-3547C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913945 | ||||||
| chr8:90914254
|
T | G | 16 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-3238T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90914254 | ||||||
| chr8:90915195
|
T | C | 157 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(154): Show | 157 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.358-2297T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915195 | ||||||
| chr8:90915227
|
A | T | 83 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.358-2265A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915227 | ||||||
| chr8:90915665
|
C | T | 15 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.358-1827C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915665 | ||||||
| chr8:90916020
|
A | C | 1 | a0001c0001t0042g0178 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-1472A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916020 | ||||||
| chr8:90916238
|
A | G | 1 | a0001c0001t0006g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358-1254A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916238 | ||||||
| chr8:90916264
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358-1228A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916264 | ||||||
| chr8:90916554
|
G | A | 4 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0003others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-938G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916554 | ||||||
| chr8:90916652
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.358-840G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916652 | ||||||
| chr8:90916920
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.358-572T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916920 | ||||||
| chr8:90917172
|
C | T | 1 | a0001c0001t0014g0190 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.358-320C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90917172 | ||||||
| chr8:90917424
|
GA | G | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.358-56delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90917424 | |||||
| chr8:90917840
|
C | CTA | 15 | a0001c0001t0001g0015a0001c0001t0001g0120a0001c0001t0001g0151others(12): Show | 15 | HG00639.hp1 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.494+242_494+243dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | |||||
| chr8:90917840
|
C | CTATA | 10 | a0001c0001t0001g0093a0001c0001t0001g0186a0001c0001t0001g0200others(7): Show | 10 | HG00642.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+240_494+243dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | |||||
| chr8:90917840
|
C | CTATATA | 8 | a0001c0001t0001g0191a0001c0001t0001g0207a0001c0001t0001g0212others(5): Show | 8 | HG01243.hp2 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+238_494+243dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | |||||
| chr8:90917840
|
CTA | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG02155.hp1 NA19060.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+242_494+243del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | |||||
| chr8:90917870
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0007g0039 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(40): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(38): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0002g0075a0001c0001t0011g0057 | 2 | NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0015g0019 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(38): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0006g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(27): Show |
5 | a0001c0001t0002g0012a0001c0001t0002g0056a0001c0001t0002g0084others(2): Show | 5 | HG00099.hp1 HG00423.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0006g0154a0001c0001t0006g0164 | 2 | HG02165.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(25): Show |
3 | a0001c0001t0002g0052a0001c0001t0002g0066a0001c0001t0007g0004 | 3 | HG01074.hp1 NA18948.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0018g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0043g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0005g0149a0001c0001t0006g0163a0001c0001t0023g0169 | 3 | HG01261.hp2 NA18966.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(21): Show |
12 | a0001c0001t0002g0058a0001c0001t0002g0070a0001c0001t0002g0086others(9): Show | 12 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0002g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0016g0143a0001c0001t0016g0144 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0018g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(19): Show |
5 | a0001c0001t0002g0048a0001c0001t0002g0072a0001c0001t0002g0077others(2): Show | 5 | HG01346.hp2 HG02109.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(15): Show |
3 | a0001c0001t0006g0148a0001c0001t0015g0053a0001c0001t0018g0133 | 3 | HG01256.hp1 HG02280.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(17): Show |
7 | a0001c0001t0001g0078a0001c0001t0002g0011a0001c0001t0002g0192others(4): Show | 7 | HG00673.hp1 HG02523.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0051g0065 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(11): Show |
4 | a0001c0001t0001g0006a0001c0001t0006g0145a0001c0001t0046g0138others(1): Show | 4 | HG00642.hp1 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(15): Show |
8 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0085others(5): Show | 8 | HG01361.hp1 HG01891.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0002g0088a0001c0001t0008g0105 | 2 | NA19011.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(13): Show |
7 | a0001c0001t0002g0007a0001c0001t0002g0017a0001c0001t0008g0044others(4): Show | 7 | HG00621.hp2 HG02132.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0006g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0007g0024 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0037 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(7): Show |
4 | a0001c0001t0005g0177a0001c0001t0012g0179a0001c0001t0021g0175others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(9): Show |
7 | a0001c0001t0002g0022a0001c0001t0003g0014a0001c0001t0003g0031others(4): Show | 7 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(5): Show |
5 | a0001c0001t0009g0137a0001c0001t0012g0243a0001c0001t0020g0161others(2): Show | 5 | HG01099.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(7): Show |
8 | a0001c0001t0003g0042a0001c0001t0003g0117a0001c0001t0028g0126others(5): Show | 8 | HG02074.hp2 HG02155.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(3): Show |
9 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0009g0239others(6): Show | 9 | HG01515.hp1 HG01978.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATAT others(5): Show |
5 | a0001c0001t0003g0067a0001c0001t0029g0131a0001c0001t0029g0132others(2): Show | 5 | HG02559.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATGT others(1): Show |
4 | a0001c0001t0004g0097a0001c0001t0004g0101a0001c0001t0004g0171others(1): Show | 4 | HG01167.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0009g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATG | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATGTG | 4 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0170others(1): Show | 4 | HG01243.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | ATATGTGT others(1): Show |
4 | a0001c0001t0002g0029a0001c0001t0002g0069a0001c0001t0004g0096others(1): Show | 4 | HG03139.hp1 NA18747.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | |||||
| chr8:90917870
|
A | G | 4 | a0001c0001t0001g0195a0001c0001t0010g0185a0001c0001t0039g0183others(1): Show | 4 | NA18948.hp2 NA18950.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+242A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917870 | ||||||
| chr8:90917871
|
TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0017g0166a0001c0001t0017g0167 | 2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.494+248_494+259del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917871 | |||||
| chr8:90917872
|
G | A | 33 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+244G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917872 | ||||||
| chr8:90917873
|
TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0012g0140a0001c0001t0030g0047 | 2 | HG02486.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.494+250_494+259del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917873 | |||||
| chr8:90917874
|
G | A | 31 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(28): Show | 31 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.494+246G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917874 | ||||||
| chr8:90917876
|
G | A | 29 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.494+248G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917876 | ||||||
| chr8:90917878
|
G | A | 28 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.494+250G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917878 | ||||||
| chr8:90917880
|
G | A | 27 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.494+252G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917880 | ||||||
| chr8:90917881
|
T | C | 36 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(33): Show | 36 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.494+253T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917881 | ||||||
| chr8:90917881
|
TGC | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0030a0001c0001t0002g0063others(1): Show | 4 | HG01169.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+255_494+256del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917881 | |||||
| chr8:90917882
|
G | A | 22 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0026others(19): Show | 22 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.494+254G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917882 | ||||||
| chr8:90917883
|
C | T | 23 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0026others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.494+255C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917883 | ||||||
| chr8:90917884
|
G | A | 34 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.494+256G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917884 | ||||||
| chr8:90917886
|
G | A | 34 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.494+258G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917886 | ||||||
| chr8:90917888
|
A | G | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+260A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917888 | ||||||
| chr8:90917890
|
A | G | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+262A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917890 | ||||||
| chr8:90917892
|
A | G | 2 | a0001c0001t0005g0158a0001c0001t0017g0168 | 2 | HG00558.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.494+264A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917892 | ||||||
| chr8:90917894
|
A | G | 2 | a0001c0001t0005g0158a0001c0001t0017g0168 | 2 | HG00558.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.494+266A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917894 | ||||||
| chr8:90917896
|
G | A | 2 | a0001c0001t0005g0157a0001c0001t0005g0159 | 2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.494+268G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917896 | ||||||
| chr8:90917898
|
C | A | 1 | a0001c0001t0005g0159 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.494+270C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917898 | ||||||
| chr8:90917898
|
C | G | 34 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.494+270C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917898 | ||||||
| chr8:90917901
|
T | C | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+273T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917901 | ||||||
| chr8:90917903
|
T | C | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+275T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917903 | ||||||
| chr8:90917906
|
A | G | 35 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(32): Show | 35 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.494+278A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917906 | ||||||
| chr8:90917907
|
T | C | 1 | a0001c0001t0005g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.494+279T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917907 | ||||||
| chr8:90917908
|
A | G | 32 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+280A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917908 | ||||||
| chr8:90917909
|
TATATACA others(1): Show |
T | 4 | a0001c0001t0005g0147a0001c0001t0005g0153a0001c0001t0005g0155others(1): Show | 4 | HG00423.hp1 NA19004.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+283_494+290del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917909 | |||||
| chr8:90917909
|
TATATACA others(9): Show |
T | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+287_494+302del others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917909 | |||||
| chr8:90917910
|
A | G | 26 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(23): Show | 26 | HG00558.hp1 HG00558.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.494+282A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917910 | ||||||
| chr8:90917911
|
TATACACA others(1): Show |
T | 14 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0055others(11): Show | 14 | HG01123.hp2 HG01257.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.494+285_494+292del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917911 | |||||
| chr8:90917912
|
A | G | 8 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0030others(5): Show | 8 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+284A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917912 | ||||||
| chr8:90917913
|
TACACAC | T | 5 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0030others(2): Show | 5 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+293_494+298del others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917913 | |||||
| chr8:90917913
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0005g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.494+287_494+298del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917913 | |||||
| chr8:90917915
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+287C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917915 | ||||||
| chr8:90917915
|
CACACACA others(29): Show |
C | 21 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(18): Show | 21 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.494+302_494+337del others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917915 | |||||
| chr8:90917916
|
A | G | 8 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0009g0134others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+288A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917916 | ||||||
| chr8:90917918
|
A | G | 14 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(11): Show | 14 | HG00423.hp1 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.494+290A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917918 | ||||||
| chr8:90917920
|
A | G | 33 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+292A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917920 | ||||||
| chr8:90917921
|
C | T | 25 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(22): Show | 25 | HG00423.hp1 HG00735.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.494+293C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917921 | ||||||
| chr8:90917922
|
A | G | 33 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+294A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917922 | ||||||
| chr8:90917923
|
C | T | 33 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+295C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917923 | ||||||
| chr8:90917924
|
A | G | 19 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(16): Show | 19 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.494+296A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917924 | ||||||
| chr8:90917925
|
C | T | 33 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+297C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917925 | ||||||
| chr8:90917932
|
G | A | 19 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(16): Show | 19 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.494+304G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917932 | ||||||
| chr8:90917934
|
G | C | 16 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+306G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917934 | ||||||
| chr8:90917936
|
A | C | 19 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(16): Show | 19 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.494+308A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917936 | ||||||
| chr8:90917936
|
A | G | 16 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917936 | ||||||
| chr8:90917936
|
ATGTGTGT others(27): Show |
A | 112 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0002g0007others(109): Show | 112 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.494+327_494+360del others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917936 | |||||
| chr8:90917942
|
G | A | 17 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(14): Show | 17 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.494+314G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917942 | ||||||
| chr8:90917951
|
T | C | 16 | a0001c0001t0003g0043a0001c0001t0003g0103a0001c0001t0005g0147others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+323T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917951 | ||||||
| chr8:90917961
|
C | CACAT | 19 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(16): Show | 19 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.494+334_494+335ins others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917961 | |||||
| chr8:90917970
|
G | A | 56 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0025others(53): Show | 56 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.494+342G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917970 | ||||||
| chr8:90918002
|
G | A | 168 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.494+374G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918002 | ||||||
| chr8:90918051
|
C | A | 1 | a0001c0001t0017g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.494+423C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918051 | ||||||
| chr8:90918166
|
C | T | 2 | a0001c0001t0018g0141a0001c0001t0018g0173 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.494+538C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918166 | ||||||
| chr8:90918200
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.494+572C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918200 | ||||||
| chr8:90918255
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.494+627A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918255 | ||||||
| chr8:90918294
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.494+666A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918294 | ||||||
| chr8:90918345
|
T | G | 1 | a0001c0001t0029g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494+717T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918345 | ||||||
| chr8:90918382
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+754T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918382 | ||||||
| chr8:90918623
|
T | G | 1 | a0001c0001t0016g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.494+995T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918623 | ||||||
| chr8:90918664
|
T | C | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+1036T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918664 | ||||||
| chr8:90918700
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.494+1072A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918700 | ||||||
| chr8:90918972
|
C | G | 2 | a0001c0001t0002g0086a0001c0001t0027g0108 | 2 | NA18985.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.494+1344C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918972 | ||||||
| chr8:90919028
|
A | G | 82 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.494+1400A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919028 | ||||||
| chr8:90919167
|
C | T | 11 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.494+1539C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919167 | ||||||
| chr8:90919342
|
T | C | 46 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(43): Show | 46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.494+1714T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919342 | ||||||
| chr8:90919520
|
C | T | 5 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0022g0005others(2): Show | 5 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+1892C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919520 | ||||||
| chr8:90919908
|
C | T | 171 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.494+2280C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919908 | ||||||
| chr8:90920149
|
T | C | 172 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(169): Show | 172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.494+2521T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920149 | ||||||
| chr8:90920199
|
C | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0112 | 2 | HG01346.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.494+2571C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920199 | ||||||
| chr8:90920310
|
C | A | 1 | a0001c0001t0019g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.494+2682C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920310 | ||||||
| chr8:90920430
|
G | A | 14 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.494+2802G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920430 | ||||||
| chr8:90920522
|
A | G | 1 | a0001c0001t0033g0013 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.494+2894A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920522 | ||||||
| chr8:90920541
|
A | G | 1 | a0001c0001t0026g0194 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.494+2913A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920541 | ||||||
| chr8:90920590
|
C | T | 1 | a0001c0001t0051g0065 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.494+2962C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920590 | ||||||
| chr8:90920640
|
G | A | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+3012G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920640 | ||||||
| chr8:90920916
|
G | A | 16 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.494+3288G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920916 | ||||||
| chr8:90920998
|
C | T | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+3370C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920998 | ||||||
| chr8:90921142
|
G | A | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.494+3514G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921142 | ||||||
| chr8:90921152
|
G | T | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494+3524G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921152 | ||||||
| chr8:90921661
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.495-3874C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921661 | ||||||
| chr8:90921674
|
C | CA | 12 | a0001c0001t0001g0182a0001c0001t0021g0174a0001c0001t0021g0175others(9): Show | 12 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.495-3851dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90921674 | |||||
| chr8:90921706
|
C | T | 1 | a0001c0001t0037g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.495-3829C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921706 | ||||||
| chr8:90921835
|
A | T | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.495-3700A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921835 | ||||||
| chr8:90921862
|
G | A | 3 | a0001c0001t0002g0111a0001c0001t0011g0057a0001c0001t0011g0061 | 3 | NA18966.hp1 NA18968.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.495-3673G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921862 | ||||||
| chr8:90922217
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.495-3318T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922217 | ||||||
| chr8:90922290
|
G | A | 8 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0239others(5): Show | 8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495-3245G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922290 | ||||||
| chr8:90922486
|
A | ATTTT | 12 | a0001c0001t0002g0086a0001c0001t0004g0244a0001c0001t0005g0177others(9): Show | 12 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.495-3028_495-3025d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTT | 55 | a0001c0001t0002g0055a0001c0001t0003g0014a0001c0001t0003g0031others(52): Show | 55 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.495-3029_495-3025d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTT | 18 | a0001c0001t0003g0035a0001c0001t0003g0043a0001c0001t0004g0045others(15): Show | 18 | HG00423.hp1 HG01243.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.495-3030_495-3025d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0007g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.495-3035_495-3025d others(13): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0022g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.495-3036_495-3025d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0045g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.495-3039_495-3025d others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0019g0127a0001c0001t0019g0236 | 2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.495-3040_495-3025d others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0019g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495-3044_495-3025d others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.495-3046_495-3025d others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(16): Show |
21 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0026others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.495-3047_495-3025d others(25): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(17): Show |
33 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0022others(30): Show | 33 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.495-3048_495-3025d others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(18): Show |
7 | a0001c0001t0002g0007a0001c0001t0002g0012a0001c0001t0002g0069others(4): Show | 7 | HG01256.hp1 HG02074.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.495-3025_495-3024i others(27): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(19): Show |
2 | a0001c0001t0015g0019a0001c0001t0047g0059 | 2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(20): Show |
3 | a0001c0001t0002g0084a0001c0001t0002g0119a0001c0001t0007g0024 | 3 | HG01070.hp2 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(21): Show |
3 | a0001c0001t0001g0079a0001c0001t0015g0023a0001c0001t0022g0110 | 3 | HG02717.hp1 NA19030.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(22): Show |
2 | a0001c0001t0002g0056a0001c0001t0022g0005 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(31): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0020g0161 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.495-3025_495-3024i others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(24): Show |
1 | a0001c0001t0007g0039 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.495-3025_495-3024i others(33): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
A | ATTTTTTT others(25): Show |
1 | a0001c0001t0002g0081 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-3025_495-3024i others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922486
|
AT | A | 67 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0028others(64): Show | 67 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.495-3025delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | |||||
| chr8:90922537
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0058a0001c0001t0002g0104 | 3 | NA18954.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.495-2998C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922537 | ||||||
| chr8:90922578
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.495-2957C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922578 | ||||||
| chr8:90922579
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(26): Show | 29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.495-2956G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922579 | ||||||
| chr8:90922606
|
C | T | 16 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-2929C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922606 | ||||||
| chr8:90922853
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2682T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922853 | ||||||
| chr8:90922906
|
A | G | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495-2629A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922906 | ||||||
| chr8:90923004
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.495-2531C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923004 | ||||||
| chr8:90923235
|
G | A | 1 | a0001c0001t0007g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.495-2300G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923235 | ||||||
| chr8:90923332
|
T | A | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2203T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923332 | ||||||
| chr8:90923390
|
A | ACC | 168 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0079others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.495-2144_495-2143i others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90923390 | |||||
| chr8:90924144
|
A | G | 1 | a0001c0001t0020g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.495-1391A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924144 | ||||||
| chr8:90924599
|
T | C | 1 | a0001c0001t0048g0129 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.495-936T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924599 | ||||||
| chr8:90924950
|
TAGTATAT others(3): Show |
T | 1 | a0001c0001t0013g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.495-583_495-574del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90924950 | |||||
| chr8:90924962
|
T | A | 1 | a0001c0001t0013g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.495-573T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924962 | ||||||
| chr8:90925092
|
A | G | 82 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.495-443A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925092 | ||||||
| chr8:90925094
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495-441G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925094 | ||||||
| chr8:90925163
|
G | A | 45 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(42): Show | 45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.495-372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925163 | ||||||
| chr8:90925164
|
C | G | 45 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(42): Show | 45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.495-371C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925164 | ||||||
| chr8:90925272
|
AAC | A | 28 | a0001c0001t0001g0006a0001c0001t0005g0147a0001c0001t0005g0149others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.495-261_495-260del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90925272 | |||||
| chr8:90925295
|
A | C | 11 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.495-240A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925295 | ||||||
| chr8:90925381
|
A | G | 16 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-154A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925381 | ||||||
| chr8:90925399
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.495-136T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925399 | ||||||
| chr8:90925865
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.616+209G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90925865 | ||||||
| chr8:90925887
|
T | C | 15 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(12): Show | 15 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.616+231T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90925887 | ||||||
| chr8:90926086
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.616+430A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926086 | ||||||
| chr8:90926195
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.616+539T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926195 | ||||||
| chr8:90926245
|
T | A | 11 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.616+589T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926245 | ||||||
| chr8:90926286
|
G | A | 1 | a0001c0001t0051g0065 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.616+630G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926286 | ||||||
| chr8:90926384
|
C | T | 166 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.616+728C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926384 | ||||||
| chr8:90926689
|
T | G | 166 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.616+1033T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926689 | ||||||
| chr8:90926799
|
T | C | 4 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0003others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+1143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926799 | ||||||
| chr8:90926870
|
T | C | 83 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(80): Show | 83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.616+1214T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926870 | ||||||
| chr8:90927023
|
C | T | 45 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(42): Show | 45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.617-1200C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927023 | ||||||
| chr8:90927204
|
C | CTCTTTT | 31 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(28): Show | 31 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | |||||
| chr8:90927204
|
C | CTCTTTTT | 31 | a0001c0001t0002g0056a0001c0001t0004g0095a0001c0001t0004g0096others(28): Show | 31 | HG00099.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(9): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | |||||
| chr8:90927204
|
C | CTCTTTTT others(1): Show |
85 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0018others(82): Show | 85 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | |||||
| chr8:90927204
|
C | CTCTTTTT others(2): Show |
16 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0012others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | |||||
| chr8:90927204
|
C | CTCTTTTT others(3): Show |
3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.617-1018_617-1017i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | |||||
| chr8:90927534
|
T | C | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617-689T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927534 | ||||||
| chr8:90927548
|
A | G | 1 | a0001c0001t0019g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.617-675A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927548 | ||||||
| chr8:90927591
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.617-632C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927591 | ||||||
| chr8:90927610
|
T | TAC | 81 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.617-582_617-581dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
T | TACAC | 7 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0018g0133others(4): Show | 7 | HG01257.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.617-584_617-581dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
T | TACACAC | 3 | a0001c0001t0002g0072a0001c0001t0002g0112a0001c0001t0053g0010 | 3 | HG01346.hp2 HG02004.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.617-586_617-581dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
T | TACACACA others(1): Show |
14 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0155others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.617-588_617-581dup others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
T | TACACACA others(3): Show |
5 | a0001c0001t0005g0153a0001c0001t0006g0145a0001c0001t0006g0160others(2): Show | 5 | HG00673.hp2 HG02055.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-590_617-581dup others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
T | TACACACA others(7): Show |
1 | a0001c0001t0006g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.617-594_617-581dup others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927610
|
TAC | T | 54 | a0001c0001t0001g0215a0001c0001t0003g0014a0001c0001t0003g0031others(51): Show | 54 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.617-582_617-581del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | |||||
| chr8:90927664
|
G | C | 1 | a0001c0001t0002g0077 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.617-559G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927664 | ||||||
| chr8:90927802
|
A | ATGGTTTT others(313): Show |
1 | a0001c0001t0007g0024 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.617-407_617-406ins others(320): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | |||||
| chr8:90927802
|
A | ATGGTTTT others(314): Show |
6 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0030others(3): Show | 6 | HG01099.hp2 HG01515.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-407_617-406ins others(321): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | |||||
| chr8:90927802
|
A | ATGGTTTT others(315): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0020g0162 | 3 | HG01978.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.617-407_617-406ins others(322): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | |||||
| chr8:90927805
|
G | GT | 28 | a0001c0001t0003g0043a0001c0001t0005g0147a0001c0001t0005g0149others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.617-407dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927805 | |||||
| chr8:90927863
|
A | G | 1 | a0001c0001t0029g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.617-360A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927863 | ||||||
| chr8:90927970
|
A | T | 1 | a0001c0001t0015g0019 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.617-253A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927970 | ||||||
| chr8:90927985
|
A | G | 5 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(2): Show | 5 | HG02257.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-238A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927985 | ||||||
| chr8:90928009
|
AT | A | 166 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.617-212delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90928009 | |||||
| chr8:90928027
|
G | A | 82 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(79): Show | 82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.617-196G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928027 | ||||||
| chr8:90928057
|
T | C | 166 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.617-166T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928057 | ||||||
| chr8:90928083
|
C | T | 24 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(21): Show | 24 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.617-140C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928083 | ||||||
| chr8:90928114
|
G | C | 1 | a0001c0001t0010g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.617-109G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928114 | ||||||
| chr8:90928218
|
C | T | 109 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(106): Show | 109 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
splice_region_variant&intron_variant | LOW | c.617-5C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928218 | ||||||
| chr8:90928503
|
C | T | 1 | a0001c0001t0011g0027 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.693+204C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90928503 | ||||||
| chr8:90928531
|
G | A | 166 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.693+232G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90928531 | ||||||
| chr8:90928943
|
GGA | G | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+649_693+650del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90928943 | |||||
| chr8:90929468
|
A | T | 1 | a0001c0001t0025g0009 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.693+1169A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90929468 | ||||||
| chr8:90929551
|
CCTT | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1255_693+1257d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90929551 | |||||
| chr8:90929796
|
AGAG | A | 16 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(13): Show | 16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+1500_693+1502d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90929796 | |||||
| chr8:90930040
|
A | C | 16 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+1741A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930040 | ||||||
| chr8:90930162
|
A | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.693+1863A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930162 | ||||||
| chr8:90930358
|
G | A | 171 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0007others(168): Show | 171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.693+2059G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930358 | ||||||
| chr8:90930605
|
G | T | 1 | a0001c0001t0011g0027 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.693+2306G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930605 | ||||||
| chr8:90931014
|
T | TATTTC | 164 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(161): Show | 164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.693+2717_693+2718i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931014 | |||||
| chr8:90931384
|
G | A | 1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.694-2920G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931384 | ||||||
| chr8:90931565
|
A | G | 163 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.694-2739A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931565 | ||||||
| chr8:90931654
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.694-2650G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931654 | ||||||
| chr8:90931680
|
G | GATCA | 9 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0055others(6): Show | 9 | HG00673.hp1 HG02523.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-2623_694-2620d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931680 | |||||
| chr8:90931702
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.694-2602G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931702 | ||||||
| chr8:90931759
|
C | A | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-2545C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931759 | ||||||
| chr8:90931906
|
A | AAAAAT | 27 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(24): Show | 27 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.694-2379_694-2375d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931906 | |||||
| chr8:90931943
|
CA | C | 16 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-2352delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931943 | |||||
| chr8:90931952
|
A | C | 162 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(159): Show | 162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.694-2352A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931952 | ||||||
| chr8:90932199
|
C | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.694-2105C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932199 | ||||||
| chr8:90932237
|
G | A | 168 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.694-2067G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932237 | ||||||
| chr8:90932555
|
G | A | 5 | a0001c0001t0009g0239a0001c0001t0012g0240a0001c0001t0012g0241others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1749G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932555 | ||||||
| chr8:90933617
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0093 | 2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.694-687C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933617 | ||||||
| chr8:90933739
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.694-565A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933739 | ||||||
| chr8:90933760
|
G | A | 168 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.694-544G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933760 | ||||||
| chr8:90934218
|
A | G | 1 | a0001c0001t0013g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.694-86A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90934218 | ||||||
| chr8:90934514
|
G | A | 1 | a0001c0001t0023g0165 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.747+157G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90934514 | ||||||
| chr8:90934846
|
T | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0195others(1): Show | 4 | NA18952.hp1 NA19060.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+489T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90934846 | ||||||
| chr8:90935488
|
G | A | 2 | a0001c0001t0005g0177a0001c0001t0042g0178 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.747+1131G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935488 | ||||||
| chr8:90935545
|
C | T | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.747+1188C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935545 | ||||||
| chr8:90935732
|
T | C | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1375T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935732 | ||||||
| chr8:90935928
|
A | G | 165 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.747+1571A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935928 | ||||||
| chr8:90935948
|
C | T | 4 | a0001c0001t0007g0001a0001c0001t0007g0002a0001c0001t0007g0003others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1591C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935948 | ||||||
| chr8:90936032
|
T | C | 1 | a0001c0001t0045g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.747+1675T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936032 | ||||||
| chr8:90936304
|
A | G | 1 | a0001c0001t0007g0039 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.747+1947A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936304 | ||||||
| chr8:90936340
|
T | C | 1 | a0001c0001t0011g0034 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.747+1983T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936340 | ||||||
| chr8:90936503
|
T | C | 1 | a0001c0001t0005g0149 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.747+2146T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936503 | ||||||
| chr8:90936618
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.747+2261G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936618 | ||||||
| chr8:90936871
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.747+2514C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936871 | ||||||
| chr8:90937376
|
G | T | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.747+3019G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937376 | ||||||
| chr8:90937377
|
C | T | 1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.747+3020C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937377 | ||||||
| chr8:90937473
|
A | T | 11 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176others(8): Show | 11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+3116A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937473 | ||||||
| chr8:90937672
|
G | A | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-3114G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937672 | ||||||
| chr8:90937994
|
G | T | 180 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0078others(177): Show | 180 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.748-2792G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937994 | ||||||
| chr8:90938036
|
C | G | 165 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(162): Show | 165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.748-2750C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938036 | ||||||
| chr8:90938174
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-2612A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938174 | ||||||
| chr8:90938728
|
A | T | 1 | a0001c0001t0043g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.748-2058A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938728 | ||||||
| chr8:90938803
|
G | C | 75 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.748-1983G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938803 | ||||||
| chr8:90938974
|
A | C | 46 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(43): Show | 46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.748-1812A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938974 | ||||||
| chr8:90938987
|
C | A | 79 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.748-1799C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938987 | ||||||
| chr8:90939230
|
T | C | 170 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.748-1556T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939230 | ||||||
| chr8:90939446
|
A | G | 1 | a0001c0001t0053g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.748-1340A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939446 | ||||||
| chr8:90939661
|
T | C | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.748-1125T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939661 | ||||||
| chr8:90940494
|
T | C | 1 | a0001c0001t0016g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.748-292T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90940494 | ||||||
| chr8:90940910
|
G | A | 80 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(77): Show | 80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.860+12G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90940910 | ||||||
| chr8:90941096
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.860+198G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941096 | ||||||
| chr8:90941429
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.860+531G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941429 | ||||||
| chr8:90941896
|
C | T | 1 | a0001c0001t0008g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.860+998C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941896 | ||||||
| chr8:90942226
|
C | A | 75 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(72): Show | 75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.860+1328C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942226 | ||||||
| chr8:90942270
|
C | G | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.860+1372C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942270 | ||||||
| chr8:90942392
|
T | A | 2 | a0001c0001t0002g0063a0001c0001t0002g0064 | 2 | NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.860+1494T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942392 | ||||||
| chr8:90942460
|
T | C | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1562T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942460 | ||||||
| chr8:90942650
|
G | A | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.860+1752G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942650 | ||||||
| chr8:90942659
|
A | G | 170 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.860+1761A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942659 | ||||||
| chr8:90942666
|
G | A | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1768G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942666 | ||||||
| chr8:90942679
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.860+1781C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942679 | ||||||
| chr8:90942710
|
C | T | 4 | a0001c0001t0019g0127a0001c0001t0019g0236a0001c0001t0019g0238others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1812C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942710 | ||||||
| chr8:90942836
|
C | T | 1 | a0001c0001t0005g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.860+1938C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942836 | ||||||
| chr8:90942931
|
G | C | 2 | a0001c0001t0012g0241a0001c0001t0031g0242 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.860+2033G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942931 | ||||||
| chr8:90943044
|
T | TA | 74 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(71): Show | 74 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.860+2152dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90943044 | |||||
| chr8:90943093
|
T | C | 21 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(18): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.860+2195T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943093 | ||||||
| chr8:90943115
|
G | A | 1 | a0001c0001t0008g0054 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.860+2217G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943115 | ||||||
| chr8:90943127
|
C | G | 1 | a0001c0001t0052g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.860+2229C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943127 | ||||||
| chr8:90943411
|
A | G | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.860+2513A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943411 | ||||||
| chr8:90943601
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.860+2703C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943601 | ||||||
| chr8:90943940
|
C | T | 2 | a0001c0001t0005g0177a0001c0001t0042g0178 | 2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.860+3042C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943940 | ||||||
| chr8:90943941
|
G | A | 30 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(27): Show | 30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.860+3043G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943941 | ||||||
| chr8:90944339
|
T | C | 170 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.860+3441T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944339 | ||||||
| chr8:90944357
|
A | G | 80 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(77): Show | 80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.860+3459A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944357 | ||||||
| chr8:90944458
|
T | C | 14 | a0001c0001t0009g0134a0001c0001t0009g0135a0001c0001t0009g0137others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.860+3560T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944458 | ||||||
| chr8:90945418
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.861-4389T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90945418 | ||||||
| chr8:90945669
|
C | T | 1 | a0001c0001t0023g0165 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861-4138C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90945669 | ||||||
| chr8:90946259
|
T | C | 4 | a0001c0001t0012g0140a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-3548T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90946259 | ||||||
| chr8:90947081
|
C | T | 1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.861-2726C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947081 | ||||||
| chr8:90947296
|
C | CAACTA | 52 | a0001c0001t0003g0014a0001c0001t0003g0031a0001c0001t0003g0033others(49): Show | 52 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947296 | |||||
| chr8:90947297
|
A | AACTAAAA others(18): Show |
2 | a0001c0001t0002g0070a0001c0001t0002g0077 | 2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.861-2508_861-2507i others(27): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947297 | |||||
| chr8:90947297
|
A | AACTAAAA others(20): Show |
1 | a0001c0001t0027g0108 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.861-2508_861-2507i others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947297 | |||||
| chr8:90947299
|
C | CT | 4 | a0001c0001t0009g0135a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(3): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947299
|
C | CTAA | 7 | a0001c0001t0002g0085a0001c0001t0009g0137a0001c0001t0012g0140others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947299
|
C | CTAAAA | 86 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(83): Show | 86 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947299
|
CA | C | 13 | a0001c0001t0009g0134a0001c0001t0009g0239a0001c0001t0009g0248others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2507delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947299
|
CACA | C | 3 | a0001c0001t0005g0177a0001c0001t0018g0173a0001c0001t0042g0178 | 3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2507_861-2505d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947299
|
CACATACA others(10): Show |
C | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2507_861-2491d others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | ||||||
| chr8:90947301
|
C | A | 5 | a0001c0001t0002g0085a0001c0001t0009g0135a0001c0001t0017g0166others(2): Show | 5 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-2506C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947301 | ||||||
| chr8:90947301
|
C | T | 13 | a0001c0001t0009g0134a0001c0001t0009g0239a0001c0001t0009g0248others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2506C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947301 | ||||||
| chr8:90947303
|
T | A | 13 | a0001c0001t0009g0134a0001c0001t0009g0239a0001c0001t0009g0248others(10): Show | 13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2504T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947303 | ||||||
| chr8:90947303
|
T | C | 14 | a0001c0001t0002g0070a0001c0001t0002g0077a0001c0001t0002g0085others(11): Show | 14 | HG01891.hp1 HG02486.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.861-2504T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947303 | ||||||
| chr8:90947303
|
T | TAC | 22 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0090others(19): Show | 22 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.861-2456_861-2455d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | |||||
| chr8:90947303
|
T | TACAC | 6 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0120others(3): Show | 6 | HG01099.hp1 HG01261.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.861-2458_861-2455d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | |||||
| chr8:90947303
|
TAC | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0093others(7): Show | 10 | HG00735.hp2 HG00741.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.861-2456_861-2455d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | |||||
| chr8:90947303
|
TACAC | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0187others(4): Show | 7 | HG02717.hp1 HG03453.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.861-2458_861-2455d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | |||||
| chr8:90947305
|
C | A | 3 | a0001c0001t0005g0177a0001c0001t0018g0173a0001c0001t0042g0178 | 3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2502C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947305 | ||||||
| chr8:90947305
|
C | T | 7 | a0001c0001t0002g0085a0001c0001t0009g0137a0001c0001t0012g0140others(4): Show | 7 | HG02486.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-2502C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947305 | ||||||
| chr8:90947307
|
C | T | 4 | a0001c0001t0009g0135a0001c0001t0017g0166a0001c0001t0017g0167others(1): Show | 4 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-2500C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947307 | ||||||
| chr8:90947309
|
C | T | 12 | a0001c0001t0009g0134a0001c0001t0009g0239a0001c0001t0009g0248others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-2498C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947309 | ||||||
| chr8:90947311
|
C | T | 3 | a0001c0001t0005g0177a0001c0001t0018g0173a0001c0001t0042g0178 | 3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2496C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947311 | ||||||
| chr8:90947317
|
C | T | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2490C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947317 | ||||||
| chr8:90947319
|
C | A | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2488C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947319 | ||||||
| chr8:90947325
|
C | T | 1 | a0001c0001t0030g0047 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2482C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947325 | ||||||
| chr8:90947351
|
C | CACACACA others(11): Show |
7 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0082others(4): Show | 7 | HG01891.hp2 HG02132.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACACA others(9): Show |
14 | a0001c0001t0002g0007a0001c0001t0002g0052a0001c0001t0002g0063others(11): Show | 14 | HG00558.hp1 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACACA others(7): Show |
10 | a0001c0001t0002g0011a0001c0001t0002g0018a0001c0001t0002g0056others(7): Show | 10 | HG00099.hp1 HG00673.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACACA others(5): Show |
16 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0029others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACACA others(3): Show |
6 | a0001c0001t0002g0020a0001c0001t0002g0081a0001c0001t0002g0088others(3): Show | 6 | HG03239.hp2 NA19010.hp2 NA19068.hp1 others(3): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACACA others(1): Show |
16 | a0001c0001t0002g0012a0001c0001t0002g0022a0001c0001t0002g0112others(13): Show | 16 | HG00423.hp2 HG01074.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACACAG | 10 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0192others(7): Show | 10 | HG00639.hp2 HG01070.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CACAG | 12 | a0001c0001t0002g0119a0001c0001t0003g0033a0001c0001t0004g0045others(9): Show | 12 | HG00621.hp1 HG00621.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | CAG | 21 | a0001c0001t0003g0031a0001c0001t0003g0035a0001c0001t0003g0036others(18): Show | 21 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | |||||
| chr8:90947351
|
C | G | 53 | a0001c0001t0002g0070a0001c0001t0002g0077a0001c0001t0002g0085others(50): Show | 53 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.861-2456C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947351 | ||||||
| chr8:90947404
|
TTC | T | 21 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(18): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2401_861-2400d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947404 | |||||
| chr8:90947406
|
CT | C | 143 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0012others(140): Show | 143 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.861-2389delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947406 | |||||
| chr8:90947407
|
T | C | 21 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(18): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2400T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947407 | ||||||
| chr8:90947761
|
G | A | 180 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0078others(177): Show | 180 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.861-2046G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947761 | ||||||
| chr8:90947772
|
T | C | 1 | a0001c0001t0046g0138 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.861-2035T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947772 | ||||||
| chr8:90947774
|
G | A | 16 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0096others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.861-2033G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947774 | ||||||
| chr8:90947852
|
T | A | 1 | a0001c0001t0016g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.861-1955T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947852 | ||||||
| chr8:90948470
|
G | C | 4 | a0001c0001t0006g0145a0001c0001t0016g0142a0001c0001t0016g0143others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-1337G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948470 | ||||||
| chr8:90948498
|
A | G | 3 | a0001c0001t0004g0097a0001c0001t0004g0171a0001c0001t0004g0172 | 3 | HG01167.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.861-1309A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948498 | ||||||
| chr8:90948534
|
C | T | 1 | a0001c0001t0054g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861-1273C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948534 | ||||||
| chr8:90948856
|
T | C | 5 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0103others(2): Show | 5 | HG02074.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-951T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948856 | ||||||
| chr8:90949003
|
C | T | 9 | a0001c0001t0008g0044a0001c0001t0008g0051a0001c0001t0008g0054others(6): Show | 9 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.861-804C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949003 | ||||||
| chr8:90949080
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.861-727C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949080 | ||||||
| chr8:90949145
|
TTTGTGTG | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0063others(2): Show | 5 | HG02074.hp1 HG02132.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-660_861-654del others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949145 | |||||
| chr8:90949146
|
T | TG | 4 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0004g0096others(1): Show | 4 | HG02132.hp1 HG03139.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-661_861-660ins others(1): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949146 | ||||||
| chr8:90949146
|
T | TTG | 23 | a0001c0001t0001g0040a0001c0001t0001g0090a0001c0001t0001g0091others(20): Show | 23 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.861-611_861-610dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
T | TTGTG | 6 | a0001c0001t0005g0147a0001c0001t0005g0153a0001c0001t0006g0145others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.861-613_861-610dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTG | T | 38 | a0001c0001t0001g0038a0001c0001t0001g0078a0001c0001t0001g0186others(35): Show | 38 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.861-611_861-610del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTG | T | 22 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0224others(19): Show | 22 | HG00735.hp1 HG01070.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.861-613_861-610del others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTGTG | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0120others(30): Show | 33 | HG00621.hp1 HG00642.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.861-615_861-610del others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTGTGT others(1): Show |
T | 57 | a0001c0001t0001g0226a0001c0001t0002g0011a0001c0001t0002g0018others(54): Show | 57 | HG00099.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.861-617_861-610del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0002g0007a0001c0001t0006g0115a0001c0001t0018g0133 | 3 | HG02055.hp1 HG02280.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.861-619_861-610del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0106a0001c0001t0020g0146a0001c0001t0054g0114 | 3 | HG00558.hp1 HG01515.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.861-621_861-610del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949146
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0011g0232 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.861-623_861-610del others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | |||||
| chr8:90949551
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.861-256T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949551 | ||||||
| chr8:90950085
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.938+201A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950085 | ||||||
| chr8:90950105
|
T | C | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.938+221T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950105 | ||||||
| chr8:90950113
|
T | C | 1 | a0001c0001t0021g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.938+229T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950113 | ||||||
| chr8:90950118
|
AT | A | 3 | a0001c0001t0006g0115a0001c0001t0018g0133a0001c0001t0054g0114 | 3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.938+238delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 90950118 | |||||
| chr8:90950181
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.938+297G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950181 | ||||||
| chr8:90950210
|
G | C | 1 | a0001c0001t0002g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.938+326G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950210 | ||||||
| chr8:90950387
|
TTAAAA | T | 3 | a0001c0001t0008g0051a0001c0001t0008g0062a0001c0001t0008g0113 | 3 | NA18968.hp2 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.938+508_938+512del others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 90950387 | |||||
| chr8:90951238
|
CT | C | 59 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0020others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1030+38delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90951238 | |||||
| chr8:90951244
|
T | G | 59 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0020others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1030+40T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951244 | ||||||
| chr8:90951313
|
T | C | 1 | a0001c0001t0028g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030+109T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951313 | ||||||
| chr8:90951328
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1030+124T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951328 | ||||||
| chr8:90951347
|
T | C | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951347 | ||||||
| chr8:90951435
|
G | A | 2 | a0001c0001t0024g0220a0001c0001t0024g0221 | 2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1030+231G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951435 | ||||||
| chr8:90951765
|
G | GA | 170 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0007others(167): Show | 170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1030+571dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90951765 | |||||
| chr8:90951776
|
C | A | 1 | a0001c0001t0043g0150 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1030+572C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951776 | ||||||
| chr8:90952116
|
G | A | 2 | a0001c0001t0014g0080a0001c0001t0014g0235 | 2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1030+912G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952116 | ||||||
| chr8:90952221
|
G | GA | 6 | a0001c0001t0004g0045a0001c0001t0004g0095a0001c0001t0004g0244others(3): Show | 6 | HG01261.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1030+1030dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952221 | |||||
| chr8:90952330
|
G | A | 16 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(13): Show | 16 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1030+1126G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952330 | ||||||
| chr8:90952498
|
G | T | 1 | a0001c0001t0017g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1030+1294G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952498 | ||||||
| chr8:90952505
|
G | A | 81 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0007others(78): Show | 81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1030+1301G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952505 | ||||||
| chr8:90952509
|
T | A | 1 | a0001c0001t0011g0071 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1030+1305T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952509 | ||||||
| chr8:90952790
|
TAATAAAA others(9): Show |
T | 1 | a0001c0001t0023g0032 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1030+1595_1030+161 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952790 | |||||
| chr8:90952792
|
ATAAAAT | A | 50 | a0001c0001t0002g0082a0001c0001t0002g0111a0001c0001t0003g0014others(47): Show | 50 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1030+1595_1030+160 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952792 | |||||
| chr8:90952798
|
T | TAAAA | 79 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0007others(76): Show | 79 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | ||||||
| chr8:90952798
|
T | TAAAATAA others(2): Show |
21 | a0001c0001t0002g0020a0001c0001t0002g0030a0001c0001t0005g0147others(18): Show | 21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(13): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | ||||||
| chr8:90952798
|
T | TAAAATAA others(7): Show |
10 | a0001c0001t0005g0157a0001c0001t0006g0115a0001c0001t0018g0133others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | ||||||
| chr8:90952798
|
T | TAAAATAA others(12): Show |
3 | a0001c0001t0005g0177a0001c0001t0036g0139a0001c0001t0054g0114 | 3 | HG02145.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(23): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | ||||||
| chr8:90952798
|
T | TAAAATAA others(17): Show |
3 | a0001c0001t0021g0174a0001c0001t0021g0175a0001c0001t0021g0176 | 3 | HG00735.hp1 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | ||||||
| chr8:90953046
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1030+1842C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953046 | ||||||
| chr8:90953098
|
T | G | 1 | a0001c0001t0013g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1030+1894T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953098 | ||||||
| chr8:90953105
|
A | C | 1 | a0001c0001t0007g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1030+1901A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953105 | ||||||
| chr8:90953124
|
G | A | 1 | a0001c0001t0008g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1030+1920G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953124 | ||||||
| chr8:90953245
|
G | A | 4 | a0001c0001t0005g0177a0001c0001t0018g0141a0001c0001t0018g0173others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+2041G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953245 | ||||||
| chr8:90953530
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1031-1957C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953530 | ||||||
| chr8:90954067
|
A | AAAAT | 24 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0078others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1031-1374_1031-137 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | |||||
| chr8:90954067
|
AAAAT | A | 62 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0227others(59): Show | 62 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1031-1374_1031-137 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | |||||
| chr8:90954067
|
AAAATAAA others(1): Show |
A | 4 | a0001c0001t0006g0148a0001c0001t0009g0137a0001c0001t0014g0190others(1): Show | 4 | HG02723.hp2 HG03239.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031-1378_1031-137 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | |||||
| chr8:90954067
|
AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | NA19010.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1031-1382_1031-137 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | |||||
| chr8:90954367
|
A | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0078others(6): Show | 9 | HG00642.hp2 HG01099.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1031-1120A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90954367 | ||||||
| chr8:90954498
|
C | T | 28 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1031-989C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90954498 | ||||||
| chr8:90955004
|
CAT | C | 92 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0007others(89): Show | 92 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1031-480_1031-479d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955004 | |||||
| chr8:90955063
|
A | C | 2 | a0001c0001t0018g0141a0001c0001t0018g0173 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1031-424A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955063 | ||||||
| chr8:90955112
|
T | TTA | 20 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0186others(17): Show | 20 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1031-339_1031-338d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTAATTAT others(3): Show |
1 | a0001c0001t0004g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1031-373_1031-372i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTAATTAT others(5): Show |
6 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0098others(3): Show | 6 | HG01243.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1031-373_1031-372i others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTAATTAT others(7): Show |
4 | a0001c0001t0004g0095a0001c0001t0004g0172a0001c0001t0004g0244others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-373_1031-372i others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTAATTAT others(9): Show |
1 | a0001c0001t0004g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1031-373_1031-372i others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTAATTAT others(11): Show |
1 | a0001c0001t0004g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1031-373_1031-372i others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATA | 18 | a0001c0001t0001g0038a0001c0001t0001g0191a0001c0001t0001g0201others(15): Show | 18 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1031-341_1031-338d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATA | 31 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0001g0214others(28): Show | 31 | HG00558.hp1 HG01256.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1031-343_1031-338d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATAT others(1): Show |
24 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0227others(21): Show | 24 | HG01070.hp2 HG01516.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1031-345_1031-338d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATAT others(3): Show |
26 | a0001c0001t0001g0215a0001c0001t0001g0224a0001c0001t0002g0011others(23): Show | 26 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1031-347_1031-338d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATAT others(5): Show |
14 | a0001c0001t0001g0120a0001c0001t0002g0055a0001c0001t0002g0063others(11): Show | 14 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1031-349_1031-338d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0002g0048a0001c0001t0002g0089a0001c0001t0007g0039others(2): Show | 5 | HG02896.hp1 HG03834.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-351_1031-338d others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0040 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1031-357_1031-338d others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTA | T | 26 | a0001c0001t0001g0151a0001c0001t0001g0180a0001c0001t0001g0182others(23): Show | 26 | HG01123.hp1 HG01361.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1031-339_1031-338d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTATA | T | 3 | a0001c0001t0001g0203a0001c0001t0002g0056a0001c0001t0002g0084 | 3 | HG00099.hp1 HG01109.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1031-341_1031-338d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTATATA | T | 2 | a0001c0001t0009g0134a0001c0001t0009g0135 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1031-343_1031-338d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTATATAT others(1): Show |
T | 10 | a0001c0001t0002g0081a0001c0001t0009g0137a0001c0001t0009g0239others(7): Show | 10 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1031-345_1031-338d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0016g0100 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1031-347_1031-338d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955112
|
TTATATAT others(5): Show |
T | 26 | a0001c0001t0005g0147a0001c0001t0005g0149a0001c0001t0005g0153others(23): Show | 26 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.1031-349_1031-338d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | |||||
| chr8:90955377
|
T | A | 1 | a0001c0001t0015g0019 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1031-110T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955377 | ||||||
| chr8:90955430
|
T | C | 167 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0007others(164): Show | 167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1031-57T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955430 |