| geneid | 347735 |
|---|---|
| ensemblid | ENSG00000168528.12 |
| hgncid | 23231 |
| symbol | SERINC2 |
| name | serine incorporator 2 |
| refseq_nuc | NM_178865.5 |
| refseq_prot | NP_849196.2 |
| ensembl_nuc | ENST00000373709.8 |
| ensembl_prot | ENSP00000362813.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 31413213 |
| end | 31434678 |
| strand | + |
| ver | v1.2 |
| region | chr1:31413213-31434678 |
| region5000 | chr1:31408213-31439678 |
| regionname0 | SERINC2_chr1_31413213_31434678 |
| regionname5000 | SERINC2_chr1_31408213_31439678 |
| 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 | 0/0 | 456 | 250 | 74 | 42 | 99 | 9 | 26 | 76 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002 | 1/0 | 455 | 102 | 18 | 19 | 47 | 1 | 16 | 32 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0003 | 0/1 | 456 | 11 | 1 | 5 | 0 | 2 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0004 | 0/0 | 456 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0005 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0006 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0007 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0008 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0009 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0010 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0011 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0012 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0013 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1371 | 87 | 55 | 12 | 11 | 5 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0002 | 1/0 | 1368 | 79 | 14 | 13 | 40 | 0 | 11 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0003 | 0/0 | 1371 | 73 | 10 | 15 | 42 | 2 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0004 | 0/0 | 1371 | 63 | 7 | 5 | 37 | 1 | 13 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0005 | 0/0 | 1371 | 19 | 0 | 7 | 9 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0006 | 0/0 | 1368 | 12 | 1 | 3 | 6 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0007 | 0/1 | 1371 | 11 | 1 | 5 | 0 | 2 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0008 | 0/0 | 1368 | 5 | 3 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0009 | 0/0 | 1371 | 4 | 3 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0010 | 0/0 | 1371 | 4 | 0 | 3 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0011 | 0/0 | 1368 | 4 | 0 | 1 | 0 | 1 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0012 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0013 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0014 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0015 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0016 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0017 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0018 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0019 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0020 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0021 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0022 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0023 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0024 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0025 | 0/0 | 1371 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| c0026 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 533 | 100 | 13 | 23 | 47 | 3 | 14 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0002 | 0/1 | 533 | 93 | 8 | 30 | 31 | 10 | 13 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0003 | 0/0 | 533 | 48 | 0 | 3 | 35 | 1 | 9 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0004 | 0/0 | 533 | 45 | 20 | 3 | 21 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0005 | 0/0 | 533 | 18 | 16 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0006 | 1/0 | 533 | 14 | 7 | 2 | 3 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0007 | 0/0 | 533 | 14 | 14 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0008 | 0/0 | 533 | 11 | 0 | 2 | 7 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0009 | 0/0 | 533 | 10 | 8 | 1 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0010 | 0/0 | 533 | 6 | 0 | 2 | 1 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0011 | 0/0 | 533 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0012 | 0/0 | 533 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0013 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0014 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0015 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0016 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0017 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0018 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0019 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0020 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0021 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0022 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0023 | 0/0 | 533 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0024 | 0/0 | 533 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| t0025 | 0/0 | 533 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1371 | 87 | 55 | 12 | 11 | 5 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003 | 0/0 | 1371 | 73 | 10 | 15 | 42 | 2 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004 | 0/0 | 1371 | 63 | 7 | 5 | 37 | 1 | 13 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0005 | 0/0 | 1371 | 19 | 0 | 7 | 9 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0010 | 0/0 | 1371 | 4 | 0 | 3 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0014 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0016 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0023 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0026 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002 | 1/0 | 1368 | 79 | 14 | 13 | 40 | 0 | 11 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0006 | 0/0 | 1368 | 12 | 1 | 3 | 6 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0008 | 0/0 | 1368 | 5 | 3 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0011 | 0/0 | 1368 | 4 | 0 | 1 | 0 | 1 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0017 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0021 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0003c0007 | 0/1 | 1371 | 11 | 1 | 5 | 0 | 2 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0004c0009 | 0/0 | 1371 | 4 | 3 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0005c0012 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0006c0020 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0007c0018 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0008c0024 | 0/0 | 1371 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0009c0019 | 0/0 | 1371 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0010c0022 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0011c0015 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0012c0025 | 0/0 | 1371 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0013c0013 | 0/0 | 1371 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1903 | 16 | 4 | 6 | 4 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0002 | 0/0 | 1903 | 11 | 0 | 1 | 5 | 3 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0004 | 0/0 | 1903 | 19 | 16 | 2 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0005 | 0/0 | 1903 | 15 | 14 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0006 | 0/0 | 1903 | 5 | 0 | 2 | 2 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0007 | 0/0 | 1903 | 13 | 13 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0009 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0011 | 0/0 | 1903 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0018 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0020 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0001t0021 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0001 | 0/0 | 1903 | 6 | 0 | 1 | 5 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0002 | 0/0 | 1903 | 42 | 7 | 14 | 15 | 2 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0004 | 0/0 | 1903 | 21 | 0 | 0 | 21 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0007 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0009 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0019 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0003t0022 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0003 | 0/0 | 1903 | 46 | 0 | 1 | 35 | 1 | 9 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0008 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0009 | 0/0 | 1903 | 6 | 4 | 1 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0010 | 0/0 | 1903 | 6 | 0 | 2 | 1 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0012 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0014 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0015 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0004t0016 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0005t0002 | 0/0 | 1903 | 19 | 0 | 7 | 9 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0010t0002 | 0/0 | 1903 | 4 | 0 | 3 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0014t0009 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0016t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0023t0005 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0001c0026t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0001 | 0/0 | 1900 | 67 | 7 | 13 | 36 | 0 | 11 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0002 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0004 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0006 | 1/0 | 1900 | 7 | 5 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0008 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0023 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0002t0025 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0006t0003 | 0/0 | 1900 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0006t0006 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0006t0008 | 0/0 | 1900 | 9 | 0 | 1 | 6 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0008t0001 | 0/0 | 1900 | 4 | 2 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0008t0017 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0011t0001 | 0/0 | 1900 | 4 | 0 | 1 | 0 | 1 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0017t0001 | 0/0 | 1900 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0002c0021t0001 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0003c0007t0002 | 0/1 | 1903 | 9 | 0 | 4 | 0 | 2 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0003c0007t0004 | 0/0 | 1903 | 2 | 1 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0004c0009t0004 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0004c0009t0005 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0004c0009t0006 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0005c0012t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0006c0020t0002 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0007c0018t0013 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0008c0024t0005 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0009c0019t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0010c0022t0001 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0011c0015t0024 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0012c0025t0002 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| a0013c0013t0002 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | copy fasta | chr1 | 31408213 | 31439678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0018g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0020g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0022g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0008g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0012g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0015g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0014t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0016t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0023t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0026t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0023g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0025g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0011t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0011t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0011t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0017t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0021t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0004c0009t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0004c0009t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0004c0009t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0004c0009t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0005c0012t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0006c0020t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0007c0018t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0008c0024t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0009c0019t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0010c0022t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0011c0015t0024g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0012c0025t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0013c0013t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0019 | t0002 | g0079 | EUR | GBR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00280 | hp2 | a0003 | c0007 | t0002 | g0138 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0106 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00323 | hp2 | a0002 | c0011 | t0001 | g0271 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00408 | hp2 | a0001 | c0003 | t0004 | g0257 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00423 | hp2 | a0006 | c0020 | t0002 | g0089 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00544 | hp1 | a0002 | c0006 | t0008 | g0228 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00544 | hp2 | a0001 | c0004 | t0009 | g0213 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00597 | hp1 | a0001 | c0004 | t0003 | g0173 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00597 | hp2 | a0001 | c0005 | t0002 | g0042 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00609 | hp1 | a0001 | c0003 | t0004 | g0249 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0346 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00621 | hp1 | a0001 | c0004 | t0003 | g0161 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00642 | hp1 | a0002 | c0006 | t0008 | g0208 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00673 | hp1 | a0002 | c0006 | t0008 | g0204 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00673 | hp2 | a0001 | c0004 | t0003 | g0194 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0350 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0084 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0058 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00741 | hp1 | a0001 | c0005 | t0002 | g0060 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00741 | hp2 | a0003 | c0007 | t0002 | g0148 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01069 | hp2 | a0001 | c0004 | t0009 | g0155 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0066 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0050 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01167 | hp1 | a0003 | c0007 | t0002 | g0170 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0365 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01175 | hp1 | a0003 | c0007 | t0002 | g0146 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0072 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0097 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01243 | hp1 | a0002 | c0006 | t0003 | g0207 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01243 | hp2 | a0004 | c0009 | t0005 | g0229 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0077 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01257 | hp1 | a0001 | c0004 | t0008 | g0210 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01261 | hp1 | a0001 | c0010 | t0002 | g0085 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0367 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01346 | hp1 | a0003 | c0007 | t0002 | g0149 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01346 | hp2 | a0002 | c0011 | t0001 | g0270 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01358 | hp1 | a0001 | c0010 | t0002 | g0094 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01358 | hp2 | a0001 | c0005 | t0002 | g0062 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01361 | hp1 | a0002 | c0008 | t0001 | g0051 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0351 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01433 | hp1 | a0001 | c0004 | t0010 | g0223 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0065 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0333 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01517 | hp1 | a0003 | c0007 | t0002 | g0139 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01884 | hp2 | a0002 | c0008 | t0001 | g0125 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01891 | hp2 | a0002 | c0008 | t0001 | g0126 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01928 | hp1 | a0001 | c0005 | t0002 | g0061 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01928 | hp2 | a0002 | c0006 | t0003 | g0209 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01934 | hp1 | a0003 | c0007 | t0004 | g0162 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0358 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0359 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01952 | hp1 | a0001 | c0005 | t0002 | g0059 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01952 | hp2 | a0001 | c0004 | t0010 | g0217 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01981 | hp1 | a0001 | c0010 | t0002 | g0101 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0352 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0364 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02004 | hp2 | a0002 | c0008 | t0001 | g0075 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02015 | hp1 | a0002 | c0006 | t0008 | g0190 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02015 | hp2 | a0001 | c0004 | t0003 | g0186 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02040 | hp1 | a0001 | c0005 | t0002 | g0043 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0151 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02055 | hp2 | a0002 | c0002 | t0006 | g0169 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0166 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02071 | hp1 | a0001 | c0003 | t0004 | g0247 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02071 | hp2 | a0001 | c0004 | t0003 | g0152 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02074 | hp2 | a0001 | c0004 | t0003 | g0188 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02080 | hp1 | a0001 | c0003 | t0004 | g0243 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02080 | hp2 | a0001 | c0004 | t0003 | g0167 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0199 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02129 | hp1 | a0010 | c0022 | t0001 | g0278 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0045 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0258 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02135 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0070 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | CDX | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | CDX | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02257 | hp1 | a0001 | c0004 | t0015 | g0232 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02257 | hp2 | a0002 | c0002 | t0006 | g0212 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0033 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0074 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0096 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0289 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02280 | hp2 | a0003 | c0007 | t0004 | g0163 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02300 | hp1 | a0001 | c0004 | t0003 | g0201 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0339 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0115 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02572 | hp1 | a0001 | c0004 | t0009 | g0160 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0288 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02602 | hp2 | a0002 | c0006 | t0008 | g0225 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0136 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02622 | hp1 | a0002 | c0002 | t0006 | g0240 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0119 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02630 | hp1 | a0002 | c0006 | t0006 | g0128 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0282 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0286 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0198 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0354 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02717 | hp1 | a0004 | c0009 | t0006 | g0206 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02723 | hp1 | a0001 | c0004 | t0016 | g0224 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0028 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02735 | hp1 | a0001 | c0004 | t0003 | g0165 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0080 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0111 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02738 | hp2 | a0001 | c0005 | t0002 | g0114 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0121 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0109 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0145 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02895 | hp2 | a0001 | c0004 | t0009 | g0159 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02896 | hp1 | a0004 | c0009 | t0004 | g0127 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02897 | hp1 | a0004 | c0009 | t0004 | g0129 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0120 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02976 | hp1 | a0008 | c0024 | t0005 | g0020 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03017 | hp2 | a0001 | c0004 | t0003 | g0218 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0048 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0281 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03130 | hp1 | a0001 | c0004 | t0009 | g0144 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03209 | hp1 | a0001 | c0023 | t0005 | g0022 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03225 | hp1 | a0001 | c0014 | t0009 | g0157 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0226 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03239 | hp2 | a0001 | c0016 | t0002 | g0103 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03453 | hp1 | a0007 | c0018 | t0013 | g0153 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03486 | hp1 | a0002 | c0002 | t0006 | g0239 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03486 | hp2 | a0001 | c0004 | t0009 | g0156 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03490 | hp1 | a0003 | c0007 | t0002 | g0003 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03490 | hp2 | a0001 | c0004 | t0010 | g0171 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03491 | hp1 | a0002 | c0011 | t0001 | g0004 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03492 | hp1 | a0002 | c0011 | t0001 | g0004 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03492 | hp2 | a0003 | c0007 | t0002 | g0003 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03540 | hp2 | a0001 | c0004 | t0014 | g0183 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0122 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03654 | hp1 | a0001 | c0004 | t0003 | g0154 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0320 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03669 | hp1 | a0001 | c0004 | t0003 | g0189 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03669 | hp2 | a0001 | c0004 | t0010 | g0231 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03688 | hp1 | a0001 | c0004 | t0010 | g0233 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0292 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03831 | hp1 | a0001 | c0004 | t0003 | g0234 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03831 | hp2 | a0002 | c0006 | t0008 | g0235 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0081 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0272 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04115 | hp1 | a0001 | c0004 | t0012 | g0219 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0368 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0118 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04199 | hp2 | a0001 | c0005 | t0002 | g0063 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04204 | hp1 | a0002 | c0017 | t0001 | g0102 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04204 | hp2 | a0001 | c0005 | t0002 | g0049 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04228 | hp1 | a0001 | c0004 | t0003 | g0220 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18612 | hp1 | a0001 | c0005 | t0002 | g0105 | EAS | CHB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | CHB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18939 | hp2 | a0001 | c0003 | t0004 | g0263 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18940 | hp1 | a0001 | c0004 | t0003 | g0180 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18940 | hp2 | a0013 | c0013 | t0002 | g0093 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0363 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18943 | hp2 | a0001 | c0005 | t0002 | g0055 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0202 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18946 | hp2 | a0001 | c0005 | t0002 | g0073 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18947 | hp1 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18947 | hp2 | a0001 | c0004 | t0003 | g0200 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18952 | hp1 | a0001 | c0003 | t0004 | g0245 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18952 | hp2 | a0002 | c0006 | t0008 | g0221 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18953 | hp1 | a0001 | c0005 | t0002 | g0056 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18959 | hp2 | a0001 | c0004 | t0003 | g0174 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0369 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0349 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18962 | hp1 | a0001 | c0003 | t0004 | g0246 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18962 | hp2 | a0001 | c0004 | t0003 | g0195 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18963 | hp1 | a0002 | c0002 | t0008 | g0158 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0340 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18970 | hp2 | a0001 | c0004 | t0003 | g0191 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18971 | hp1 | a0001 | c0003 | t0004 | g0266 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18971 | hp2 | a0001 | c0003 | t0004 | g0259 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18979 | hp1 | a0002 | c0021 | t0001 | g0041 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18981 | hp1 | a0001 | c0003 | t0004 | g0252 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0360 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0087 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0168 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18986 | hp1 | a0001 | c0003 | t0004 | g0261 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18991 | hp2 | a0001 | c0004 | t0003 | g0196 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0215 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18995 | hp2 | a0001 | c0004 | t0003 | g0175 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18997 | hp1 | a0001 | c0004 | t0003 | g0205 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0361 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0268 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18999 | hp1 | a0001 | c0004 | t0003 | g0164 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19000 | hp1 | a0001 | c0004 | t0003 | g0211 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19003 | hp1 | a0001 | c0003 | t0004 | g0269 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19003 | hp2 | a0001 | c0004 | t0003 | g0181 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19004 | hp2 | a0001 | c0003 | t0004 | g0262 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19005 | hp1 | a0002 | c0002 | t0006 | g0322 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19005 | hp2 | a0002 | c0002 | t0023 | g0353 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0248 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19010 | hp1 | a0001 | c0003 | t0004 | g0265 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19010 | hp2 | a0001 | c0004 | t0003 | g0178 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19012 | hp2 | a0001 | c0004 | t0003 | g0214 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19030 | hp2 | a0001 | c0003 | t0019 | g0086 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0222 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19057 | hp1 | a0001 | c0003 | t0004 | g0264 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19060 | hp1 | a0011 | c0015 | t0024 | g0069 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19060 | hp2 | a0001 | c0004 | t0003 | g0182 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19063 | hp1 | a0002 | c0002 | t0025 | g0311 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19063 | hp2 | a0001 | c0003 | t0002 | g0076 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19064 | hp2 | a0001 | c0004 | t0003 | g0142 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19066 | hp2 | a0002 | c0006 | t0008 | g0227 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19067 | hp2 | a0001 | c0004 | t0003 | g0179 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19068 | hp1 | a0001 | c0004 | t0003 | g0216 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0091 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19070 | hp1 | a0001 | c0003 | t0004 | g0253 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0357 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19074 | hp1 | a0001 | c0004 | t0003 | g0143 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19076 | hp2 | a0001 | c0003 | t0022 | g0260 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19077 | hp1 | a0001 | c0004 | t0003 | g0238 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19081 | hp2 | a0001 | c0005 | t0002 | g0054 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19084 | hp1 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19085 | hp2 | a0002 | c0006 | t0008 | g0176 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19087 | hp1 | a0001 | c0003 | t0004 | g0267 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19089 | hp1 | a0001 | c0005 | t0002 | g0057 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19089 | hp2 | a0001 | c0003 | t0004 | g0255 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19090 | hp1 | a0001 | c0004 | t0010 | g0203 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19091 | hp1 | a0001 | c0005 | t0002 | g0068 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0244 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ASW | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | ASW | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20752 | hp1 | a0005 | c0012 | t0002 | g0117 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20752 | hp2 | a0001 | c0010 | t0002 | g0123 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0172 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0064 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20905 | hp1 | a0001 | c0004 | t0003 | g0197 | SAS | GIH | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20905 | hp2 | a0001 | c0026 | t0002 | g0366 | SAS | GIH | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01123 | hp1 | a0012 | c0025 | t0002 | g0082 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0090 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02109 | hp2 | a0001 | c0003 | t0009 | g0187 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0071 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02559 | hp2 | a0002 | c0008 | t0017 | g0124 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0280 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20300 | hp2 | a0002 | c0002 | t0006 | g0242 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA21309 | hp1 | a0001 | c0003 | t0007 | g0100 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0007 | t0002 | g0150 | REF | REF | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0006 | g0040 | REF | REF | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31423802
|
T | A | 1 | a0005 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.149T>A | p.Val50Glu | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/10 | 202/1900 | 149/1368 | 50/455 | chr1 | 31423802 | ||
| chr1:31424710
|
G | A | 1 | a0013 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.229G>A | p.Gly77Arg | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/10 | 282/1900 | 229/1368 | 77/455 | chr1 | 31424710 | ||
| chr1:31424740
|
G | A | 1 | a0004 | 4 | HG01243.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.259G>A | p.Asp87Asn | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/10 | 312/1900 | 259/1368 | 87/455 | chr1 | 31424740 | ||
| chr1:31424845
|
C | T | 1 | a0012 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.364C>T | p.Arg122Trp | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/10 | 417/1900 | 364/1368 | 122/455 | chr1 | 31424845 | ||
| chr1:31425790
|
G | A | 1 | a0011 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.487G>A | p.Gly163Ser | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/10 | 540/1900 | 487/1368 | 163/455 | chr1 | 31425790 | ||
| chr1:31426674
|
C | T | 1 | a0006 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.631C>T | p.Leu211Phe | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/10 | 684/1900 | 631/1368 | 211/455 | chr1 | 31426674 | ||
| chr1:31429432
|
G | A | 1 | a0003 | 11 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(8): Show |
missense_variant | MODERATE | c.907G>A | p.Gly303Ser | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/10 | 960/1900 | 907/1368 | 303/455 | chr1 | 31429432 | ||
| chr1:31429459
|
G | A | 1 | a0010 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.934G>A | p.Glu312Lys | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/10 | 987/1900 | 934/1368 | 312/455 | chr1 | 31429459 | ||
| chr1:31429510
|
A | G | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.985A>G | p.Ile329Val | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/10 | 1038/1900 | 985/1368 | 329/455 | chr1 | 31429510 | ||
| chr1:31433042
|
A | ACAG | 11 | a0001a0003a0004others(8): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
conservative_inframe_insertion | MODERATE | c.1102_1104dupCAG | p.Gln368dup | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/10 | 1158/1900 | 1105/1368 | 369/455 | INFO_REALIGN_3_PRIME | chr1 | 31433042 | |
| chr1:31434120
|
G | A | 1 | a0008 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1289G>A | p.Cys430Tyr | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 1342/1900 | 1289/1368 | 430/455 | chr1 | 31434120 | ||
| chr1:31434180
|
G | A | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1349G>A | p.Arg450His | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 1402/1900 | 1349/1368 | 450/455 | chr1 | 31434180 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31423761
|
C | T | 1 | a0002c0011 | 4 | HG00323.hp2 HG01346.hp2 HG03491.hp1 others(1): Show |
synonymous_variant | LOW | c.108C>T | p.Thr36Thr | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/10 | 161/1900 | 108/1368 | 36/455 | chr1 | 31423761 | ||
| chr1:31424709
|
C | T | 1 | a0001c0026 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.228C>T | p.Ala76Ala | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/10 | 281/1900 | 228/1368 | 76/455 | chr1 | 31424709 | ||
| chr1:31424796
|
G | A | 3 | a0001c0004a0001c0014a0002c0006 | 76 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(73): Show |
synonymous_variant | LOW | c.315G>A | p.Ala105Ala | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/10 | 368/1900 | 315/1368 | 105/455 | chr1 | 31424796 | ||
| chr1:31425387
|
T | C | 14 | a0001c0003a0001c0005a0001c0010others(11): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
synonymous_variant | LOW | c.450T>C | p.Ile150Ile | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/10 | 503/1900 | 450/1368 | 150/455 | chr1 | 31425387 | ||
| chr1:31425792
|
C | T | 2 | a0001c0010a0012c0025 | 5 | HG01123.hp1 HG01261.hp1 HG01358.hp1 others(2): Show |
synonymous_variant | LOW | c.489C>T | p.Gly163Gly | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/10 | 542/1900 | 489/1368 | 163/455 | chr1 | 31425792 | ||
| chr1:31425840
|
C | T | 3 | a0001c0005a0002c0021a0011c0015 | 21 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
synonymous_variant | LOW | c.537C>T | p.Ile179Ile | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/10 | 590/1900 | 537/1368 | 179/455 | chr1 | 31425840 | ||
| chr1:31429013
|
G | A | 2 | a0001c0016a0002c0017 | 2 | HG03239.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.816G>A | p.Ser272Ser | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 7/10 | 869/1900 | 816/1368 | 272/455 | chr1 | 31429013 | ||
| chr1:31433099
|
C | T | 1 | a0001c0014 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.1146C>T | p.Asp382Asp | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/10 | 1199/1900 | 1146/1368 | 382/455 | chr1 | 31433099 | ||
| chr1:31433168
|
G | A | 1 | a0001c0023 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1215G>A | p.Thr405Thr | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/10 | 1268/1900 | 1215/1368 | 405/455 | chr1 | 31433168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31413231
|
C | G | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 35 | chr1 | 31413231 | |||||
| chr1:31413235
|
C | T | 1 | a0011c0015t0024 | 1 | NA19060.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 31 | chr1 | 31413235 | |||||
| chr1:31413241
|
G | C | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 25 | chr1 | 31413241 | |||||
| chr1:31413243
|
G | C | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 23 | chr1 | 31413243 | |||||
| chr1:31413244
|
C | T | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 22 | chr1 | 31413244 | |||||
| chr1:31413246
|
C | G | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 20 | chr1 | 31413246 | |||||
| chr1:31413248
|
A | G | 1 | a0002c0002t0025 | 1 | NA19063.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 18 | chr1 | 31413248 | |||||
| chr1:31413250
|
G | T | 2 | a0002c0002t0023a0002c0002t0025 | 2 | NA19005.hp2 NA19063.hp1 |
5_prime_UTR_variant | MODIFIER | c.-16G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 16 | chr1 | 31413250 | |||||
| chr1:31413254
|
G | C | 15 | a0001c0001t0009a0001c0003t0009a0001c0004t0003others(12): Show | 80 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-12G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/10 | 12 | chr1 | 31413254 | |||||
| chr1:31434255
|
A | G | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(31): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 56 | chr1 | 31434255 | |||||
| chr1:31434266
|
ACCTGCCC others(6): Show |
A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69_*81delCTGCCCCC others(5): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 69 | INFO_REALIGN_3_PRIME | chr1 | 31434266 | ||||
| chr1:31434280
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 81 | chr1 | 31434280 | |||||
| chr1:31434281
|
A | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 82 | chr1 | 31434281 | |||||
| chr1:31434288
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 89 | chr1 | 31434288 | |||||
| chr1:31434289
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 90 | chr1 | 31434289 | |||||
| chr1:31434290
|
A | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 91 | chr1 | 31434290 | |||||
| chr1:31434292
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 93 | chr1 | 31434292 | |||||
| chr1:31434298
|
T | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 99 | chr1 | 31434298 | |||||
| chr1:31434301
|
G | C | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 102 | chr1 | 31434301 | |||||
| chr1:31434308
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 109 | chr1 | 31434308 | |||||
| chr1:31434311
|
C | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 112 | chr1 | 31434311 | |||||
| chr1:31434315
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 116 | chr1 | 31434315 | |||||
| chr1:31434318
|
A | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 119 | chr1 | 31434318 | |||||
| chr1:31434323
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 124 | chr1 | 31434323 | |||||
| chr1:31434340
|
C | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 141 | chr1 | 31434340 | |||||
| chr1:31434345
|
C | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 146 | chr1 | 31434345 | |||||
| chr1:31434348
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 149 | chr1 | 31434348 | |||||
| chr1:31434350
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*151T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 151 | chr1 | 31434350 | |||||
| chr1:31434353
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*154T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 154 | chr1 | 31434353 | |||||
| chr1:31434354
|
C | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 155 | chr1 | 31434354 | |||||
| chr1:31434357
|
A | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*158A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 158 | chr1 | 31434357 | |||||
| chr1:31434359
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 160 | chr1 | 31434359 | |||||
| chr1:31434362
|
C | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 163 | chr1 | 31434362 | |||||
| chr1:31434363
|
T | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 164 | chr1 | 31434363 | |||||
| chr1:31434364
|
T | C | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 165 | chr1 | 31434364 | |||||
| chr1:31434366
|
A | C | 2 | a0001c0001t0011a0001c0004t0016 | 4 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*167A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 167 | chr1 | 31434366 | |||||
| chr1:31434381
|
T | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*182T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 182 | chr1 | 31434381 | |||||
| chr1:31434385
|
G | A | 1 | a0001c0003t0019 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 186 | chr1 | 31434385 | |||||
| chr1:31434393
|
A | C | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 194 | chr1 | 31434393 | |||||
| chr1:31434394
|
G | C | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 195 | chr1 | 31434394 | |||||
| chr1:31434403
|
C | A | 1 | a0001c0004t0012 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 204 | chr1 | 31434403 | |||||
| chr1:31434403
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 204 | chr1 | 31434403 | |||||
| chr1:31434404
|
C | G | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 205 | chr1 | 31434404 | |||||
| chr1:31434406
|
C | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 207 | chr1 | 31434406 | |||||
| chr1:31434408
|
C | A | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 209 | chr1 | 31434408 | |||||
| chr1:31434412
|
A | T | 1 | a0001c0003t0022 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 213 | chr1 | 31434412 | |||||
| chr1:31434423
|
G | A | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 224 | chr1 | 31434423 | |||||
| chr1:31434507
|
C | T | 2 | a0001c0001t0018a0001c0004t0015 | 2 | HG02257.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*308C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 308 | chr1 | 31434507 | |||||
| chr1:31434610
|
A | C | 16 | a0001c0001t0002a0001c0003t0002a0001c0004t0010others(13): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 411 | chr1 | 31434610 | |||||
| chr1:31434610
|
A | G | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(35): Show | 212 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 411 | chr1 | 31434610 | |||||
| chr1:31434663
|
G | A | 9 | a0001c0001t0005a0001c0001t0007a0001c0001t0020others(6): Show | 35 | HG01070.hp1 HG01243.hp2 HG01884.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*464G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 464 | chr1 | 31434663 | |||||
| chr1:31434671
|
G | A | 1 | a0001c0001t0021 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 472 | chr1 | 31434671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:31413316
|
C | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(101): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.39+12C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413316 | ||||||
| chr1:31413533
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+229C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413533 | ||||||
| chr1:31413562
|
G | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+258G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413562 | ||||||
| chr1:31413651
|
A | C | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+347A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413651 | ||||||
| chr1:31413703
|
C | T | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+399C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413703 | ||||||
| chr1:31413717
|
C | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(221): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.39+413C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413717 | ||||||
| chr1:31413767
|
C | G | 1 | a0001c0004t0003g0238 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.39+463C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413767 | ||||||
| chr1:31413903
|
G | GTCCC | 89 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(86): Show | 92 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.39+602_39+605dupCC others(2): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31413903 | |||||
| chr1:31413986
|
T | C | 252 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(249): Show | 257 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.39+682T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31413986 | ||||||
| chr1:31414229
|
A | C | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+925A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414229 | ||||||
| chr1:31414279
|
C | T | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.39+975C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414279 | ||||||
| chr1:31414418
|
G | GTTGTGTG others(7): Show |
1 | a0001c0010t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.39+1114_39+1115ins others(14): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414418 | ||||||
| chr1:31414419
|
G | GTGTGTGT others(6): Show |
1 | a0002c0002t0001g0367 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.39+1115_39+1116ins others(13): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414419 | ||||||
| chr1:31414419
|
G | GTGTGTGT others(8): Show |
2 | a0001c0026t0002g0366a0002c0002t0001g0369 | 2 | NA18961.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.39+1115_39+1116ins others(15): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414419 | ||||||
| chr1:31414419
|
G | GTGTGTGT others(10): Show |
2 | a0002c0002t0001g0283a0002c0002t0001g0368 | 2 | HG04115.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.39+1115_39+1116ins others(17): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414419 | ||||||
| chr1:31414419
|
GGTTGTGT others(2): Show |
G | 3 | a0002c0002t0001g0284a0002c0008t0001g0125a0002c0008t0001g0126 | 3 | HG00423.hp1 HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.39+1118_39+1126del others(9): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414419 | |||||
| chr1:31414420
|
G | T | 3 | a0001c0004t0003g0234a0001c0010t0002g0123a0002c0006t0008g0235 | 3 | HG03831.hp1 HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.39+1116G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414420 | ||||||
| chr1:31414421
|
T | G | 4 | a0001c0004t0003g0234a0001c0010t0002g0123a0002c0006t0008g0235others(1): Show | 4 | HG02559.hp2 HG03831.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1117T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TG | 30 | a0001c0001t0001g0230a0001c0001t0004g0008a0001c0001t0004g0130others(27): Show | 31 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(1): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTG | 4 | a0001c0001t0004g0141a0001c0004t0003g0142a0001c0004t0003g0143others(1): Show | 4 | HG02280.hp1 HG03130.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(3): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTG | 16 | a0001c0001t0004g0147a0001c0004t0003g0151a0001c0004t0003g0152others(13): Show | 16 | HG00741.hp2 HG01069.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(5): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG | 31 | a0001c0001t0005g0236a0001c0001t0009g0184a0001c0001t0009g0185others(28): Show | 31 | HG00597.hp1 HG00621.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(7): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(2): Show |
35 | a0001c0001t0002g0290a0001c0001t0005g0237a0001c0001t0006g0289others(32): Show | 35 | HG00642.hp1 HG00673.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(9): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(4): Show |
22 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0003t0001g0248others(19): Show | 23 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(11): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(6): Show |
29 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(26): Show | 31 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(13): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(8): Show |
30 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(27): Show | 30 | HG00280.hp1 HG00408.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(15): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(10): Show |
32 | a0001c0001t0002g0007a0001c0001t0002g0315a0001c0001t0002g0333others(29): Show | 33 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(17): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(12): Show |
9 | a0001c0001t0001g0356a0001c0003t0004g0261a0001c0003t0022g0260others(6): Show | 9 | HG01433.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(19): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(16): Show |
2 | a0001c0003t0004g0269a0002c0002t0001g0360 | 2 | NA18981.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(23): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(18): Show |
4 | a0002c0002t0001g0282a0002c0002t0001g0361a0002c0002t0001g0362others(1): Show | 4 | HG02004.hp1 HG02630.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1117_39+1118ins others(25): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(20): Show |
1 | a0002c0002t0001g0363 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.39+1117_39+1118ins others(27): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TGTGTGTG others(22): Show |
1 | a0002c0002t0001g0365 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.39+1117_39+1118ins others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414421 | ||||||
| chr1:31414421
|
T | TTGTG | 6 | a0001c0001t0011g0071a0001c0003t0002g0044a0001c0003t0002g0045others(3): Show | 6 | HG00597.hp2 HG02040.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+1148_39+1151dup others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTG | 4 | a0001c0003t0002g0050a0001c0003t0002g0052a0001c0005t0002g0049others(1): Show | 4 | HG01081.hp2 HG01361.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1146_39+1151dup others(6): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(1): Show |
18 | a0001c0001t0001g0110a0001c0003t0002g0064a0001c0003t0002g0065others(15): Show | 18 | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+1144_39+1151dup others(8): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(3): Show |
34 | a0001c0001t0001g0116a0001c0003t0001g0104a0001c0003t0002g0001others(31): Show | 35 | HG00099.hp1 HG00423.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.39+1142_39+1151dup others(10): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(5): Show |
6 | a0001c0001t0001g0108a0001c0001t0007g0002a0001c0003t0002g0106others(3): Show | 7 | HG00323.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+1140_39+1151dup others(12): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0113a0001c0003t0002g0111a0001c0003t0002g0112others(2): Show | 5 | HG01257.hp2 HG02451.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+1138_39+1151dup others(14): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(9): Show |
1 | a0005c0012t0002g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.39+1136_39+1151dup others(16): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(11): Show |
4 | a0001c0003t0002g0118a0001c0003t0002g0119a0001c0003t0002g0120others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1134_39+1151dup others(18): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414421
|
T | TTGTGTGT others(15): Show |
1 | a0001c0003t0002g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.39+1130_39+1151dup others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414421 | |||||
| chr1:31414452
|
T | TGAGAGA | 5 | a0001c0001t0004g0008a0001c0001t0004g0130a0002c0006t0006g0128others(2): Show | 5 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+1149_39+1150ins others(6): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414452 | |||||
| chr1:31414454
|
T | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0130a0001c0003t0001g0250others(15): Show | 18 | HG02071.hp1 HG02080.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.39+1150T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414454 | ||||||
| chr1:31414454
|
T | TGAGA | 21 | a0001c0003t0004g0244a0001c0003t0004g0245a0001c0004t0003g0211others(18): Show | 21 | HG00544.hp1 HG00642.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.39+1168_39+1171dup others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGAGAGA | 44 | a0001c0001t0004g0140a0001c0001t0005g0236a0001c0001t0005g0237others(41): Show | 44 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.39+1166_39+1171dup others(6): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGAGAGAG others(1): Show |
24 | a0001c0001t0004g0147a0001c0003t0009g0187a0001c0004t0003g0151others(21): Show | 25 | HG00673.hp2 HG00741.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.39+1164_39+1171dup others(8): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGAGAGAG others(3): Show |
4 | a0001c0004t0003g0161a0002c0002t0004g0145a0002c0008t0017g0124others(1): Show | 4 | HG00280.hp2 HG00621.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1162_39+1171dup others(10): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGAGAGAG others(5): Show |
9 | a0001c0001t0004g0131a0001c0001t0004g0133a0001c0001t0004g0134others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+1160_39+1171dup others(12): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGAG others(3): Show |
1 | a0001c0004t0003g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(10): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGAG others(15): Show |
1 | a0002c0002t0006g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(5): Show |
1 | a0002c0006t0008g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(12): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0004g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(19): Show |
1 | a0002c0002t0006g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(26): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(3): Show |
1 | a0001c0003t0002g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(10): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(5): Show |
1 | a0001c0003t0002g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(12): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(21): Show |
1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(28): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(17): Show |
1 | a0001c0003t0004g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(24): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(19): Show |
2 | a0001c0001t0001g0230a0001c0004t0010g0231 | 2 | HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.39+1151_39+1152ins others(26): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(21): Show |
1 | a0001c0004t0015g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(28): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414454
|
T | TGTGTGTG others(23): Show |
1 | a0001c0004t0010g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.39+1151_39+1152ins others(30): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31414454 | |||||
| chr1:31414456
|
A | T | 105 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0116others(102): Show | 108 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.39+1152A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414456 | ||||||
| chr1:31414458
|
A | T | 21 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0002g0331others(18): Show | 21 | HG00735.hp1 HG01168.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.39+1154A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414458 | ||||||
| chr1:31414482
|
G | T | 1 | a0002c0002t0001g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.39+1178G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414482 | ||||||
| chr1:31414539
|
G | A | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1235G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414539 | ||||||
| chr1:31414565
|
AAGAGAGC others(6): Show |
A | 1 | a0001c0004t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.39+1262_39+1274del others(13): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414565 | ||||||
| chr1:31414658
|
G | A | 224 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(221): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.39+1354G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414658 | ||||||
| chr1:31414884
|
G | A | 2 | a0001c0003t0004g0243a0001c0003t0004g0246 | 2 | HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.39+1580G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31414884 | ||||||
| chr1:31415469
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+2165C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415469 | ||||||
| chr1:31415501
|
C | G | 1 | a0001c0003t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.39+2197C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415501 | ||||||
| chr1:31415586
|
C | T | 1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.39+2282C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415586 | ||||||
| chr1:31415709
|
G | A | 1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.39+2405G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415709 | ||||||
| chr1:31415731
|
A | G | 1 | a0002c0002t0008g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.39+2427A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415731 | ||||||
| chr1:31415833
|
T | C | 353 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(350): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.39+2529T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415833 | ||||||
| chr1:31415877
|
G | GGAACTGG others(9): Show |
2 | a0002c0008t0001g0125a0002c0008t0001g0126 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.39+2591_39+2606dup others(16): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31415877 | |||||
| chr1:31415878
|
G | C | 1 | a0001c0003t0002g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.39+2574G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415878 | ||||||
| chr1:31415947
|
A | G | 2 | a0001c0004t0003g0186a0001c0004t0003g0194 | 2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.39+2643A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415947 | ||||||
| chr1:31415975
|
G | A | 2 | a0001c0003t0009g0187a0007c0018t0013g0153 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.39+2671G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415975 | ||||||
| chr1:31415989
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(246): Show | 254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.39+2685T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31415989 | ||||||
| chr1:31416076
|
G | C | 1 | a0001c0001t0007g0025 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.39+2772G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416076 | ||||||
| chr1:31416167
|
A | T | 1 | a0001c0001t0005g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+2863A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416167 | ||||||
| chr1:31416333
|
G | A | 1 | a0001c0003t0004g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.39+3029G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416333 | ||||||
| chr1:31416373
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(246): Show | 254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.39+3069T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416373 | ||||||
| chr1:31416507
|
G | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+3203G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416507 | ||||||
| chr1:31416572
|
C | T | 8 | a0001c0001t0004g0131a0001c0001t0004g0133a0001c0001t0004g0134others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+3268C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416572 | ||||||
| chr1:31416641
|
G | A | 8 | a0001c0005t0002g0042a0001c0005t0002g0054a0001c0005t0002g0055others(5): Show | 8 | HG00597.hp2 NA18612.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+3337G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416641 | ||||||
| chr1:31416752
|
GCT | G | 71 | a0001c0004t0003g0142a0001c0004t0003g0143a0001c0004t0003g0151others(68): Show | 71 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.39+3451_39+3452del others(2): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31416752 | |||||
| chr1:31416753
|
C | T | 3 | a0001c0003t0002g0349a0002c0002t0001g0313a0002c0002t0001g0329 | 3 | NA18612.hp2 NA18961.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.39+3449C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416753 | ||||||
| chr1:31416995
|
C | T | 6 | a0001c0003t0002g0109a0001c0003t0002g0115a0001c0003t0002g0119others(3): Show | 6 | HG02451.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+3691C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31416995 | ||||||
| chr1:31417220
|
G | T | 2 | a0002c0008t0001g0125a0002c0008t0001g0126 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.39+3916G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417220 | ||||||
| chr1:31417259
|
A | G | 1 | a0002c0002t0008g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.39+3955A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417259 | ||||||
| chr1:31417309
|
A | G | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+4005A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417309 | ||||||
| chr1:31417481
|
C | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0019others(5): Show | 8 | HG02818.hp2 HG02976.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+4177C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417481 | ||||||
| chr1:31417482
|
G | A | 4 | a0001c0001t0004g0047a0001c0001t0011g0046a0001c0001t0011g0048others(1): Show | 4 | HG02451.hp2 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+4178G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417482 | ||||||
| chr1:31417581
|
T | A | 1 | a0001c0004t0003g0195 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.39+4277T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417581 | ||||||
| chr1:31417723
|
C | T | 2 | a0001c0016t0002g0103a0002c0017t0001g0102 | 2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.39+4419C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31417723 | ||||||
| chr1:31417852
|
C | CT | 76 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(73): Show | 78 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.39+4570dupT | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTT | 30 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(27): Show | 30 | HG00408.hp2 HG00609.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.39+4569_39+4570dup others(2): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTT | 89 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(86): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.39+4568_39+4570dup others(3): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTTT | 46 | a0001c0001t0001g0356a0001c0001t0004g0008a0001c0001t0004g0130others(43): Show | 46 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.39+4567_39+4570dup others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTTTT | 16 | a0001c0001t0004g0137a0001c0001t0004g0147a0001c0001t0005g0237others(13): Show | 16 | HG00741.hp2 HG01346.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.39+4566_39+4570dup others(5): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTTTTT | 17 | a0001c0001t0001g0230a0001c0004t0003g0196a0001c0004t0003g0226others(14): Show | 17 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.39+4565_39+4570dup others(6): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTTTTTT | 43 | a0001c0004t0003g0142a0001c0004t0003g0151a0001c0004t0003g0154others(40): Show | 44 | HG00597.hp1 HG01433.hp1 HG01952.hp2 others(41): Show |
intron_variant | MODIFIER | c.39+4564_39+4570dup others(7): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31417852
|
C | CTTTTTTT others(1): Show |
13 | a0001c0004t0003g0143a0001c0004t0003g0152a0001c0004t0003g0161others(10): Show | 13 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.39+4563_39+4570dup others(8): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31417852 | |||||
| chr1:31418052
|
T | C | 104 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(101): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.39+4748T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418052 | ||||||
| chr1:31418065
|
G | T | 1 | a0001c0003t0004g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.39+4761G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418065 | ||||||
| chr1:31418078
|
C | T | 213 | a0001c0001t0001g0230a0001c0001t0001g0303a0001c0001t0001g0304others(210): Show | 217 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.39+4774C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418078 | ||||||
| chr1:31418249
|
A | G | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+4945A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418249 | ||||||
| chr1:31418403
|
C | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.39+5099C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418403 | ||||||
| chr1:31418405
|
C | T | 8 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0019others(5): Show | 8 | HG02818.hp2 HG02976.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+5101C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418405 | ||||||
| chr1:31418557
|
G | A | 2 | a0001c0004t0003g0214a0001c0004t0003g0215 | 2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.40-5136G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418557 | ||||||
| chr1:31418565
|
G | A | 1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.40-5128G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418565 | ||||||
| chr1:31418666
|
C | T | 1 | a0001c0003t0007g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.40-5027C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418666 | ||||||
| chr1:31418824
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-4869C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418824 | ||||||
| chr1:31418825
|
A | G | 1 | a0001c0003t0009g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.40-4868A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418825 | ||||||
| chr1:31418836
|
C | T | 1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.40-4857C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418836 | ||||||
| chr1:31418866
|
C | T | 1 | a0001c0003t0004g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.40-4827C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418866 | ||||||
| chr1:31418938
|
G | T | 1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-4755G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418938 | ||||||
| chr1:31418966
|
G | T | 1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-4727G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31418966 | ||||||
| chr1:31419092
|
T | C | 1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-4601T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419092 | ||||||
| chr1:31419143
|
G | A | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-4550G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419143 | ||||||
| chr1:31419301
|
T | A | 220 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(217): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.40-4392T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419301 | ||||||
| chr1:31419345
|
C | T | 36 | a0001c0001t0004g0008a0001c0001t0004g0026a0001c0001t0004g0027others(33): Show | 36 | HG00280.hp2 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.40-4348C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419345 | ||||||
| chr1:31419367
|
A | C | 1 | a0001c0005t0002g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.40-4326A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419367 | ||||||
| chr1:31419392
|
T | C | 2 | a0001c0003t0009g0187a0007c0018t0013g0153 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.40-4301T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419392 | ||||||
| chr1:31419509
|
T | C | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-4184T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419509 | ||||||
| chr1:31419653
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.40-4040C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419653 | ||||||
| chr1:31419902
|
C | T | 4 | a0001c0001t0002g0301a0001c0001t0002g0315a0002c0002t0001g0327others(1): Show | 4 | HG02027.hp1 HG02155.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-3791C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419902 | ||||||
| chr1:31420000
|
T | C | 220 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(217): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.40-3693T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420000 | ||||||
| chr1:31420013
|
A | AT | 246 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(243): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.40-3675dupT | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31420013 | |||||
| chr1:31420014
|
T | A | 21 | a0001c0005t0002g0042a0001c0005t0002g0043a0001c0005t0002g0049others(18): Show | 21 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-3679T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420014 | ||||||
| chr1:31420019
|
C | T | 1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-3674C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420019 | ||||||
| chr1:31420054
|
A | G | 1 | a0001c0001t0005g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.40-3639A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420054 | ||||||
| chr1:31420064
|
A | G | 220 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(217): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.40-3629A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420064 | ||||||
| chr1:31420429
|
A | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(2): Show | 6 | HG01255.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-3264A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420429 | ||||||
| chr1:31420523
|
G | A | 37 | a0001c0001t0004g0008a0001c0001t0004g0026a0001c0001t0004g0027others(34): Show | 38 | HG00280.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.40-3170G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420523 | ||||||
| chr1:31420532
|
G | GTTGT | 101 | a0001c0001t0001g0230a0001c0001t0004g0008a0001c0001t0004g0026others(98): Show | 101 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.40-3146_40-3143dup others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31420532 | |||||
| chr1:31420532
|
G | GTTGTTTG others(1): Show |
4 | a0001c0001t0009g0184a0001c0001t0009g0185a0002c0002t0001g0275others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-3150_40-3143dup others(8): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31420532 | |||||
| chr1:31420532
|
GTTGT | G | 12 | a0001c0001t0005g0236a0001c0001t0005g0237a0003c0007t0002g0003others(9): Show | 13 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.40-3146_40-3143del others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31420532 | |||||
| chr1:31420709
|
T | C | 1 | a0002c0002t0001g0276 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.40-2984T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420709 | ||||||
| chr1:31420781
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.40-2912T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420781 | ||||||
| chr1:31420924
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(2): Show | 6 | HG01255.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-2769C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420924 | ||||||
| chr1:31421190
|
G | A | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(4): Show | 8 | HG01255.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-2503G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421190 | ||||||
| chr1:31421293
|
A | T | 1 | a0001c0001t0001g0308 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.40-2400A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421293 | ||||||
| chr1:31421549
|
C | T | 76 | a0001c0001t0001g0230a0001c0004t0003g0142a0001c0004t0003g0143others(73): Show | 76 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.40-2144C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421549 | ||||||
| chr1:31421555
|
G | A | 71 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(68): Show | 72 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.40-2138G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421555 | ||||||
| chr1:31421582
|
G | T | 2 | a0001c0004t0009g0159a0001c0004t0009g0160 | 2 | HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.40-2111G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421582 | ||||||
| chr1:31421747
|
C | T | 178 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(175): Show | 182 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.40-1946C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421747 | ||||||
| chr1:31421808
|
T | C | 2 | a0001c0016t0002g0103a0002c0017t0001g0102 | 2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.40-1885T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421808 | ||||||
| chr1:31421840
|
ACTGT | A | 3 | a0001c0004t0009g0159a0001c0004t0009g0160a0001c0004t0016g0224 | 3 | HG02572.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.40-1849_40-1846del others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31421840 | |||||
| chr1:31421859
|
T | C | 1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.40-1834T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31421859 | ||||||
| chr1:31422037
|
G | A | 28 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.40-1656G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422037 | ||||||
| chr1:31422079
|
G | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(4): Show | 8 | HG01255.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-1614G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422079 | ||||||
| chr1:31422127
|
C | T | 99 | a0001c0001t0001g0230a0001c0003t0001g0248a0001c0003t0001g0250others(96): Show | 99 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.40-1566C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422127 | ||||||
| chr1:31422182
|
C | CAAAGTCT others(9): Show |
1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1511_40-1510ins others(16): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422182 | ||||||
| chr1:31422184
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1509A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422184 | ||||||
| chr1:31422185
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1508G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422185 | ||||||
| chr1:31422187
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1506T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422187 | ||||||
| chr1:31422189
|
C | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1504C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422189 | ||||||
| chr1:31422192
|
A | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1501A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422192 | ||||||
| chr1:31422199
|
T | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1494T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422199 | ||||||
| chr1:31422200
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1493G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422200 | ||||||
| chr1:31422201
|
A | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1492A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422201 | ||||||
| chr1:31422206
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1487G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422206 | ||||||
| chr1:31422209
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1484G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422209 | ||||||
| chr1:31422211
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1482A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422211 | ||||||
| chr1:31422213
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1480G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422213 | ||||||
| chr1:31422214
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1479G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422214 | ||||||
| chr1:31422217
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1476T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422217 | ||||||
| chr1:31422218
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1475G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422218 | ||||||
| chr1:31422220
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1473G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422220 | ||||||
| chr1:31422223
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1470C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422223 | ||||||
| chr1:31422224
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1469A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422224 | ||||||
| chr1:31422225
|
G | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1468G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422225 | ||||||
| chr1:31422227
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1466A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422227 | ||||||
| chr1:31422228
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1465G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422228 | ||||||
| chr1:31422229
|
G | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1464G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422229 | ||||||
| chr1:31422231
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1462A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422231 | ||||||
| chr1:31422232
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1461G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422232 | ||||||
| chr1:31422242
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1451T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422242 | ||||||
| chr1:31422243
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1450G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422243 | ||||||
| chr1:31422247
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1446T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422247 | ||||||
| chr1:31422249
|
A | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1444A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422249 | ||||||
| chr1:31422250
|
G | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1443G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422250 | ||||||
| chr1:31422251
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1442A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422251 | ||||||
| chr1:31422253
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1440T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422253 | ||||||
| chr1:31422254
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1439G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422254 | ||||||
| chr1:31422255
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1438C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422255 | ||||||
| chr1:31422259
|
A | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1434A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422259 | ||||||
| chr1:31422261
|
T | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1432T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422261 | ||||||
| chr1:31422272
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1421C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422272 | ||||||
| chr1:31422273
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1420T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422273 | ||||||
| chr1:31422276
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1417G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422276 | ||||||
| chr1:31422278
|
G | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1415G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422278 | ||||||
| chr1:31422287
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1406A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422287 | ||||||
| chr1:31422288
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1405G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422288 | ||||||
| chr1:31422291
|
C | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-1402C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422291 | ||||||
| chr1:31422292
|
C | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1401C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422292 | ||||||
| chr1:31422295
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1398T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422295 | ||||||
| chr1:31422296
|
CTCAAAAA others(25): Show |
C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1396_40-1365del others(32): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422296 | ||||||
| chr1:31422298
|
C | CA | 285 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(282): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.40-1382dupA | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31422298 | |||||
| chr1:31422298
|
C | CAA | 6 | a0001c0003t0002g0078a0002c0002t0001g0334a0002c0002t0001g0361others(3): Show | 6 | HG01517.hp1 HG02559.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-1383_40-1382dup others(2): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31422298 | |||||
| chr1:31422298
|
C | CAAA | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-1384_40-1382dup others(3): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 31422298 | |||||
| chr1:31422312
|
C | A | 3 | a0001c0001t0006g0320a0001c0003t0002g0098a0001c0003t0002g0099 | 3 | HG03654.hp2 NA18970.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.40-1381C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422312 | ||||||
| chr1:31422313
|
A | C | 2 | a0001c0003t0002g0098a0001c0003t0002g0099 | 2 | NA18970.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.40-1380A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422313 | ||||||
| chr1:31422329
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1364A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422329 | ||||||
| chr1:31422332
|
A | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1361A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422332 | ||||||
| chr1:31422333
|
A | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1360A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422333 | ||||||
| chr1:31422336
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1357C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422336 | ||||||
| chr1:31422337
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1356C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422337 | ||||||
| chr1:31422338
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1355C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422338 | ||||||
| chr1:31422341
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1352C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422341 | ||||||
| chr1:31422349
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1344A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422349 | ||||||
| chr1:31422351
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1342G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422351 | ||||||
| chr1:31422354
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1339A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422354 | ||||||
| chr1:31422355
|
C | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1338C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422355 | ||||||
| chr1:31422359
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1334C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422359 | ||||||
| chr1:31422362
|
G | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1331G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422362 | ||||||
| chr1:31422363
|
C | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1330C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422363 | ||||||
| chr1:31422364
|
T | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1329T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422364 | ||||||
| chr1:31422365
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1328A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422365 | ||||||
| chr1:31422368
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1325C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422368 | ||||||
| chr1:31422371
|
C | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1322C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422371 | ||||||
| chr1:31422379
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1314A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422379 | ||||||
| chr1:31422380
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1313T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422380 | ||||||
| chr1:31422385
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1308T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422385 | ||||||
| chr1:31422394
|
T | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1299T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422394 | ||||||
| chr1:31422395
|
G | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1298G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422395 | ||||||
| chr1:31422400
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1293A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422400 | ||||||
| chr1:31422402
|
C | T | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1291C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422402 | ||||||
| chr1:31422408
|
T | A | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1285T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422408 | ||||||
| chr1:31422411
|
T | C | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1282T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422411 | ||||||
| chr1:31422435
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.40-1258T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422435 | ||||||
| chr1:31422452
|
A | G | 1 | a0002c0002t0001g0286 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.40-1241A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422452 | ||||||
| chr1:31422510
|
A | T | 5 | a0001c0003t0002g0109a0001c0003t0002g0119a0001c0003t0002g0120others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.40-1183A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422510 | ||||||
| chr1:31422547
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(243): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.40-1146T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422547 | ||||||
| chr1:31422564
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(175): Show | 182 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.40-1129G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422564 | ||||||
| chr1:31422641
|
G | T | 1 | a0002c0002t0006g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.40-1052G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422641 | ||||||
| chr1:31422738
|
G | A | 1 | a0009c0019t0002g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.40-955G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422738 | ||||||
| chr1:31422809
|
G | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-884G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422809 | ||||||
| chr1:31422869
|
C | G | 77 | a0001c0001t0001g0230a0001c0004t0003g0142a0001c0004t0003g0143others(74): Show | 77 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.40-824C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422869 | ||||||
| chr1:31422878
|
G | A | 1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.40-815G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31422878 | ||||||
| chr1:31423084
|
A | G | 247 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(244): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.40-609A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31423084 | ||||||
| chr1:31423137
|
C | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-556C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31423137 | ||||||
| chr1:31423158
|
G | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-535G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31423158 | ||||||
| chr1:31423237
|
G | T | 1 | a0001c0004t0010g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40-456G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31423237 | ||||||
| chr1:31423687
|
C | T | 3 | a0001c0004t0003g0179a0001c0004t0003g0182a0001c0004t0003g0202 | 3 | NA18945.hp2 NA19060.hp2 NA19067.hp2 |
splice_region_variant&intron_variant | LOW | c.40-6C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31423687 | ||||||
| chr1:31423972
|
C | G | 4 | a0001c0001t0005g0236a0001c0001t0005g0237a0001c0001t0018g0222others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+118C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31423972 | ||||||
| chr1:31424013
|
A | G | 1 | a0001c0004t0003g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.201+159A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424013 | ||||||
| chr1:31424129
|
A | C | 1 | a0001c0004t0003g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.201+275A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424129 | ||||||
| chr1:31424167
|
A | G | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.201+313A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424167 | ||||||
| chr1:31424200
|
C | T | 1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.201+346C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424200 | ||||||
| chr1:31424216
|
G | T | 82 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(79): Show | 83 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.201+362G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424216 | ||||||
| chr1:31424411
|
A | G | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-272A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424411 | ||||||
| chr1:31424446
|
A | G | 88 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(85): Show | 90 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.202-237A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424446 | ||||||
| chr1:31424512
|
CG | C | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.202-169delG | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 31424512 | |||||
| chr1:31424646
|
A | G | 334 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(331): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.202-37A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424646 | ||||||
| chr1:31424926
|
C | T | 8 | a0003c0007t0002g0003a0003c0007t0002g0138a0003c0007t0002g0139others(5): Show | 9 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.392+53C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31424926 | ||||||
| chr1:31425013
|
A | G | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.392+140A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425013 | ||||||
| chr1:31425116
|
C | T | 110 | a0001c0003t0001g0104a0001c0003t0001g0248a0001c0003t0001g0250others(107): Show | 111 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.393-214C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425116 | ||||||
| chr1:31425120
|
C | T | 2 | a0001c0003t0009g0187a0007c0018t0013g0153 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.393-210C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425120 | ||||||
| chr1:31425154
|
G | GT | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-170dupT | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 31425154 | |||||
| chr1:31425285
|
T | C | 83 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.393-45T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425285 | ||||||
| chr1:31425293
|
C | T | 1 | a0001c0003t0004g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.393-37C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425293 | ||||||
| chr1:31425315
|
C | T | 83 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.393-15C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425315 | ||||||
| chr1:31425316
|
G | A | 1 | a0001c0001t0018g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393-14G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 3/9 | chr1 | 31425316 | ||||||
| chr1:31425432
|
A | C | 84 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.472+23A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425432 | ||||||
| chr1:31425515
|
G | A | 1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.472+106G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425515 | ||||||
| chr1:31425556
|
C | T | 1 | a0002c0002t0001g0346 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.472+147C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425556 | ||||||
| chr1:31425594
|
G | T | 1 | a0001c0003t0002g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.473-182G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425594 | ||||||
| chr1:31425615
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.473-161C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425615 | ||||||
| chr1:31425616
|
C | T | 83 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.473-160C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425616 | ||||||
| chr1:31425639
|
C | T | 2 | a0002c0008t0001g0125a0002c0008t0001g0126 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.473-137C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425639 | ||||||
| chr1:31425689
|
C | T | 83 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.473-87C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425689 | ||||||
| chr1:31425700
|
G | A | 5 | a0001c0003t0002g0109a0001c0003t0002g0119a0001c0003t0002g0120others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-76G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 4/9 | chr1 | 31425700 | ||||||
| chr1:31425941
|
G | C | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.610+28G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31425941 | ||||||
| chr1:31426106
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.610+193C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426106 | ||||||
| chr1:31426332
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.611-322C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426332 | ||||||
| chr1:31426389
|
C | A | 9 | a0001c0001t0004g0131a0001c0001t0004g0133a0001c0001t0004g0134others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.611-265C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426389 | ||||||
| chr1:31426400
|
T | G | 1 | a0002c0011t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.611-254T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426400 | ||||||
| chr1:31426445
|
T | C | 1 | a0001c0004t0016g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.611-209T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426445 | ||||||
| chr1:31426475
|
C | T | 5 | a0001c0003t0002g0067a0001c0003t0002g0076a0001c0003t0002g0095others(2): Show | 5 | HG02004.hp2 HG02273.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-179C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 5/9 | chr1 | 31426475 | ||||||
| chr1:31426837
|
A | T | 335 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.780+14A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31426837 | ||||||
| chr1:31426857
|
C | T | 264 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.780+34C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31426857 | ||||||
| chr1:31426990
|
A | G | 1 | a0001c0004t0003g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.780+167A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31426990 | ||||||
| chr1:31427057
|
G | A | 1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.780+234G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427057 | ||||||
| chr1:31427068
|
G | A | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+245G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427068 | ||||||
| chr1:31427211
|
C | T | 27 | a0001c0003t0001g0248a0001c0003t0001g0250a0001c0003t0001g0251others(24): Show | 27 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+388C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427211 | ||||||
| chr1:31427413
|
G | A | 1 | a0002c0002t0001g0335 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.780+590G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427413 | ||||||
| chr1:31427490
|
C | T | 291 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(288): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.780+667C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427490 | ||||||
| chr1:31427596
|
T | A | 104 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(101): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.780+773T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427596 | ||||||
| chr1:31427602
|
G | T | 2 | a0002c0002t0001g0347a0002c0002t0001g0348 | 2 | NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.780+779G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427602 | ||||||
| chr1:31427688
|
T | C | 1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.780+865T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427688 | ||||||
| chr1:31427690
|
C | T | 3 | a0001c0001t0004g0279a0002c0002t0001g0274a0002c0002t0001g0283 | 3 | HG02970.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.780+867C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427690 | ||||||
| chr1:31427824
|
CT | C | 42 | a0001c0001t0001g0294a0001c0003t0001g0248a0001c0003t0001g0250others(39): Show | 42 | HG00408.hp2 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.780+1023delT | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 31427824 | |||||
| chr1:31427824
|
CTT | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0302others(264): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.780+1022_780+1023d others(4): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 31427824 | |||||
| chr1:31427824
|
CTTT | C | 19 | a0001c0001t0004g0241a0001c0001t0004g0279a0001c0001t0005g0236others(16): Show | 19 | HG02004.hp2 HG02486.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.780+1021_780+1023d others(5): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 31427824 | |||||
| chr1:31427824
|
CTTTTT | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(2): Show | 6 | HG01255.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+1019_780+1023d others(7): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 31427824 | |||||
| chr1:31427826
|
T | C | 1 | a0002c0002t0001g0360 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.780+1003T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427826 | ||||||
| chr1:31427922
|
A | G | 335 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(332): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.781-1056A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31427922 | ||||||
| chr1:31428017
|
A | ACACCCAG others(110): Show |
1 | a0001c0004t0003g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.781-948_781-947ins others(117): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 31428017 | |||||
| chr1:31428031
|
A | G | 69 | a0001c0004t0003g0142a0001c0004t0003g0143a0001c0004t0003g0151others(66): Show | 69 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.781-947A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428031 | ||||||
| chr1:31428068
|
C | G | 1 | a0001c0003t0002g0052 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.781-910C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428068 | ||||||
| chr1:31428125
|
C | T | 1 | a0001c0023t0005g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.781-853C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428125 | ||||||
| chr1:31428126
|
G | A | 2 | a0001c0003t0009g0187a0007c0018t0013g0153 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.781-852G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428126 | ||||||
| chr1:31428142
|
C | G | 2 | a0002c0002t0001g0288a0002c0002t0001g0292 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.781-836C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428142 | ||||||
| chr1:31428188
|
C | T | 19 | a0001c0005t0002g0042a0001c0005t0002g0043a0001c0005t0002g0054others(16): Show | 19 | HG00597.hp2 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-790C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428188 | ||||||
| chr1:31428286
|
C | T | 81 | a0001c0001t0001g0230a0001c0001t0005g0236a0001c0004t0003g0142others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.781-692C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428286 | ||||||
| chr1:31428478
|
G | T | 7 | a0001c0001t0004g0272a0002c0002t0001g0276a0002c0002t0001g0286others(4): Show | 8 | HG00323.hp2 HG01346.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-500G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428478 | ||||||
| chr1:31428520
|
G | A | 1 | a0001c0001t0007g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.781-458G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428520 | ||||||
| chr1:31428534
|
C | T | 25 | a0001c0003t0001g0248a0001c0003t0001g0254a0001c0003t0001g0256others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.781-444C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428534 | ||||||
| chr1:31428603
|
T | C | 151 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(148): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.781-375T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428603 | ||||||
| chr1:31428612
|
G | C | 81 | a0001c0003t0001g0104a0001c0003t0002g0001a0001c0003t0002g0044others(78): Show | 82 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.781-366G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428612 | ||||||
| chr1:31428626
|
C | A | 1 | a0002c0002t0001g0352 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.781-352C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428626 | ||||||
| chr1:31428805
|
T | G | 149 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(146): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.781-173T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 6/9 | chr1 | 31428805 | ||||||
| chr1:31429217
|
C | T | 2 | a0001c0001t0005g0014a0001c0004t0015g0232 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.871+149C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 7/9 | chr1 | 31429217 | ||||||
| chr1:31429302
|
G | T | 56 | a0001c0004t0003g0142a0001c0004t0003g0143a0001c0004t0003g0151others(53): Show | 56 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.872-95G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 7/9 | chr1 | 31429302 | ||||||
| chr1:31429304
|
C | G | 1 | a0002c0002t0001g0324 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.872-93C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 7/9 | chr1 | 31429304 | ||||||
| chr1:31429571
|
A | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(148): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1013+33A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429571 | ||||||
| chr1:31429577
|
G | GAGGGCCC others(11): Show |
1 | a0002c0002t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1013+40_1013+57dup others(18): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31429577 | |||||
| chr1:31429747
|
G | A | 1 | a0002c0002t0001g0295 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1013+209G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429747 | ||||||
| chr1:31429870
|
G | A | 1 | a0002c0002t0001g0313 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1013+332G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429870 | ||||||
| chr1:31429905
|
C | T | 28 | a0001c0001t0001g0308a0001c0003t0001g0248a0001c0003t0001g0250others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1013+367C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429905 | ||||||
| chr1:31429966
|
C | A | 1 | a0002c0002t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1013+428C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429966 | ||||||
| chr1:31429970
|
C | G | 28 | a0001c0001t0001g0308a0001c0003t0001g0248a0001c0003t0001g0250others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1013+432C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31429970 | ||||||
| chr1:31430184
|
G | C | 1 | a0001c0001t0004g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1013+646G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430184 | ||||||
| chr1:31430212
|
TGTAAAAC others(11): Show |
T | 1 | a0002c0002t0001g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1013+676_1013+693d others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31430212 | |||||
| chr1:31430302
|
C | A | 1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1013+764C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430302 | ||||||
| chr1:31430462
|
A | T | 1 | a0002c0021t0001g0041 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1013+924A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430462 | ||||||
| chr1:31430498
|
T | TA | 9 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(6): Show | 10 | HG01255.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1013+972dupA | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31430498 | |||||
| chr1:31430519
|
A | G | 1 | a0013c0013t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1013+981A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430519 | ||||||
| chr1:31430544
|
C | A | 131 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0001g0302others(128): Show | 135 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1013+1006C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430544 | ||||||
| chr1:31430571
|
C | T | 1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1013+1033C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430571 | ||||||
| chr1:31430572
|
G | A | 1 | a0002c0002t0006g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1013+1034G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430572 | ||||||
| chr1:31430657
|
T | C | 1 | a0002c0002t0006g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1013+1119T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430657 | ||||||
| chr1:31430771
|
C | T | 2 | a0001c0001t0002g0344a0001c0001t0002g0345 | 2 | NA18948.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1013+1233C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430771 | ||||||
| chr1:31430787
|
T | C | 156 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(153): Show | 158 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.1013+1249T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430787 | ||||||
| chr1:31430839
|
C | T | 1 | a0001c0001t0005g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1013+1301C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430839 | ||||||
| chr1:31430926
|
C | A | 1 | a0002c0008t0017g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1013+1388C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31430926 | ||||||
| chr1:31431065
|
A | C | 24 | a0001c0001t0001g0230a0001c0001t0004g0008a0001c0001t0004g0026others(21): Show | 25 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1013+1527A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431065 | ||||||
| chr1:31431122
|
C | A | 1 | a0001c0001t0007g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1013+1584C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431122 | ||||||
| chr1:31431122
|
C | G | 1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1013+1584C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431122 | ||||||
| chr1:31431181
|
A | G | 55 | a0001c0004t0003g0142a0001c0004t0003g0143a0001c0004t0003g0151others(52): Show | 55 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1013+1643A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431181 | ||||||
| chr1:31431206
|
C | T | 1 | a0001c0003t0002g0112 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1013+1668C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431206 | ||||||
| chr1:31431302
|
A | AT | 210 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(207): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1014-1651dupT | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431302 | |||||
| chr1:31431302
|
A | ATT | 18 | a0001c0001t0001g0116a0001c0001t0004g0135a0001c0003t0002g0091others(15): Show | 18 | HG00280.hp2 HG01358.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1014-1652_1014-165 others(6): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431302 | |||||
| chr1:31431317
|
G | T | 1 | a0001c0005t0002g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1014-1650G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431317 | ||||||
| chr1:31431330
|
G | T | 1 | a0013c0013t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1014-1637G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431330 | ||||||
| chr1:31431343
|
G | A | 2 | a0001c0016t0002g0103a0002c0017t0001g0102 | 2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1014-1624G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431343 | ||||||
| chr1:31431490
|
C | T | 28 | a0001c0001t0001g0308a0001c0003t0001g0248a0001c0003t0001g0250others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1014-1477C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431490 | ||||||
| chr1:31431527
|
G | A | 28 | a0001c0001t0001g0308a0001c0003t0001g0248a0001c0003t0001g0250others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1014-1440G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431527 | ||||||
| chr1:31431556
|
G | C | 4 | a0001c0001t0004g0241a0002c0002t0006g0239a0002c0002t0006g0240others(1): Show | 4 | HG02622.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014-1411G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431556 | ||||||
| chr1:31431734
|
A | G | 1 | a0001c0004t0014g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014-1233A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431734 | ||||||
| chr1:31431737
|
T | C | 258 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1014-1230T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431737 | ||||||
| chr1:31431751
|
T | TAGGGTGG others(3224): Show |
1 | a0002c0002t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1014-1199_1014-119 others(3235): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431751 | |||||
| chr1:31431758
|
G | A | 2 | a0002c0008t0001g0125a0002c0008t0001g0126 | 2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1014-1209G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431758 | ||||||
| chr1:31431760
|
G | GAGGGTGG others(686): Show |
1 | a0002c0002t0001g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1014-1199_1014-119 others(697): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431760 | |||||
| chr1:31431760
|
G | T | 4 | a0001c0003t0002g0090a0001c0004t0016g0224a0002c0008t0001g0125others(1): Show | 4 | HG01123.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-1207G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431760 | ||||||
| chr1:31431767
|
G | A | 1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1014-1200G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431767 | ||||||
| chr1:31431769
|
G | C | 1 | a0001c0003t0002g0090 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1014-1198G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431769 | ||||||
| chr1:31431769
|
G | GAGGGTGG others(65): Show |
1 | a0001c0003t0002g0349 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1014-1192_1014-119 others(76): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431769 | |||||
| chr1:31431769
|
G | GAGGGTGG others(92): Show |
1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1014-1192_1014-119 others(103): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431769 | |||||
| chr1:31431769
|
G | GAGGGTGG others(416): Show |
1 | a0002c0002t0006g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1014-1192_1014-119 others(427): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431769 | |||||
| chr1:31431769
|
G | GAGGGTGG others(2405): Show |
1 | a0002c0002t0006g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1014-1192_1014-119 others(2416): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431769 | |||||
| chr1:31431769
|
G | T | 8 | a0001c0001t0004g0010a0001c0001t0020g0028a0001c0004t0016g0224others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-1198G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431769 | ||||||
| chr1:31431776
|
A | AATAGGGT others(272): Show |
1 | a0001c0001t0004g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(283): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1946): Show |
1 | a0001c0001t0004g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(1957): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2936): Show |
1 | a0003c0007t0002g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(2947): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(506): Show |
1 | a0001c0004t0010g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(632): Show |
1 | a0001c0001t0009g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(643): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(3260): Show |
1 | a0001c0003t0004g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3271): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1685): Show |
1 | a0001c0004t0010g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1696): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1712): Show |
2 | a0001c0001t0001g0308a0001c0003t0022g0260 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(1723): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2684): Show |
1 | a0001c0003t0004g0246 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2695): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(326): Show |
1 | a0002c0006t0008g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(337): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(497): Show |
1 | a0001c0004t0003g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(508): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2792): Show |
1 | a0001c0003t0004g0263 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2803): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(5789): Show |
1 | a0001c0004t0003g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(5800): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(227): Show |
1 | a0001c0003t0004g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(785): Show |
1 | a0001c0003t0004g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(796): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1541): Show |
1 | a0001c0003t0004g0261 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1552): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(479): Show |
1 | a0001c0003t0004g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(490): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1640): Show |
1 | a0001c0003t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1651): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1478): Show |
1 | a0001c0003t0004g0265 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1489): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1541): Show |
1 | a0001c0003t0004g0249 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1552): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(740): Show |
1 | a0001c0003t0004g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(751): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(947): Show |
1 | a0001c0003t0004g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(958): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(137): Show |
1 | a0001c0004t0003g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(148): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1523): Show |
1 | a0001c0004t0003g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1534): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1073): Show |
1 | a0001c0004t0003g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1084): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(965): Show |
1 | a0001c0004t0003g0143 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(976): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(146): Show |
1 | a0002c0006t0003g0209 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(157): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(668): Show |
1 | a0001c0004t0003g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(679): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(47): Show |
1 | a0001c0003t0002g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(58): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2027): Show |
1 | a0001c0001t0004g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2038): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1757): Show |
1 | a0010c0022t0001g0278 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1768): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(506): Show |
1 | a0002c0011t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1118): Show |
1 | a0002c0011t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1129): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(38): Show |
2 | a0002c0002t0001g0334a0002c0002t0001g0354 | 2 | HG02698.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(101): Show |
1 | a0001c0010t0002g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(112): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1343): Show |
1 | a0001c0003t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1354): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(65): Show |
1 | a0002c0008t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(76): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(290): Show |
1 | a0002c0002t0001g0351 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(301): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1397): Show |
1 | a0001c0003t0002g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1408): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(578): Show |
1 | a0001c0001t0005g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(589): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(875): Show |
1 | a0001c0003t0002g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(886): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(146): Show |
1 | a0001c0003t0002g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(157): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1910): Show |
1 | a0001c0003t0002g0001 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(1921): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1694): Show |
1 | a0002c0002t0001g0293 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1705): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2234): Show |
1 | a0013c0013t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2245): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(668): Show |
1 | a0001c0003t0002g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(679): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1568): Show |
1 | a0001c0003t0019g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1579): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(92): Show |
1 | a0001c0003t0009g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(103): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1037): Show |
1 | a0001c0001t0006g0337 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1048): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(56): Show |
1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(67): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(74): Show |
1 | a0001c0003t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1298): Show |
1 | a0001c0005t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1309): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(218): Show |
1 | a0002c0021t0001g0041 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(229): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1055): Show |
1 | a0001c0004t0010g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1066): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(3818): Show |
1 | a0001c0005t0002g0059 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3829): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2351): Show |
1 | a0001c0005t0002g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2362): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(254): Show |
1 | a0001c0005t0002g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(265): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1856): Show |
1 | a0001c0003t0002g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1867): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(506): Show |
1 | a0001c0003t0002g0076 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1217): Show |
1 | a0001c0003t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1228): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(290): Show |
1 | a0001c0003t0002g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(301): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1199): Show |
1 | a0001c0003t0002g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1210): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(254): Show |
1 | a0001c0001t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(265): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2558): Show |
1 | a0001c0001t0001g0304 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2569): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(443): Show |
1 | a0002c0002t0001g0309 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(454): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(362): Show |
1 | a0001c0005t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(373): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1028): Show |
1 | a0002c0002t0001g0368 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1039): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(560): Show |
1 | a0002c0002t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(571): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(101): Show |
1 | a0002c0002t0001g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(112): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1379): Show |
1 | a0002c0002t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1390): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1001): Show |
1 | a0001c0001t0006g0340 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1012): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(353): Show |
1 | a0001c0001t0001g0318 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(364): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2882): Show |
1 | a0002c0002t0001g0362 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2893): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(173): Show |
1 | a0002c0002t0001g0335 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(184): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(506): Show |
1 | a0002c0002t0001g0363 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1892): Show |
1 | a0002c0002t0001g0326 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1903): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1559): Show |
1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1570): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(119): Show |
1 | a0001c0001t0002g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(130): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(128): Show |
2 | a0002c0002t0001g0307a0002c0002t0001g0324 | 2 | NA18939.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(139): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2666): Show |
1 | a0002c0002t0001g0297 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2677): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(2279): Show |
1 | a0002c0002t0001g0291 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2290): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(299): Show |
1 | a0002c0002t0008g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(310): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(1469): Show |
1 | a0002c0002t0001g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1480): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(4277): Show |
1 | a0002c0002t0001g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(4288): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(83): Show |
1 | a0002c0002t0001g0295 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(218): Show |
1 | a0002c0002t0025g0311 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(229): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | AATAGGGT others(488): Show |
1 | a0002c0002t0001g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(499): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431776 | |||||
| chr1:31431776
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(19): Show | 24 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1014-1191A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431776 | ||||||
| chr1:31431777
|
A | ATAGGGTG others(2135): Show |
1 | a0003c0007t0002g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(2146): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(92): Show |
1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(103): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(758): Show |
1 | a0002c0002t0006g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(769): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1757): Show |
1 | a0001c0004t0003g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1768): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(380): Show |
1 | a0001c0003t0001g0250 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(391): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(722): Show |
1 | a0001c0003t0004g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(733): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(2486): Show |
1 | a0001c0004t0003g0181 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2497): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(245): Show |
1 | a0001c0004t0003g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(256): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(3125): Show |
1 | a0001c0004t0003g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3136): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(740): Show |
1 | a0001c0003t0007g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(751): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(533): Show |
1 | a0001c0004t0003g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(544): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(11): Show |
1 | a0001c0010t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(659): Show |
1 | a0001c0004t0009g0159 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(670): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(2441): Show |
1 | a0001c0003t0002g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2452): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(713): Show |
1 | a0001c0003t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(724): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(236): Show |
1 | a0001c0016t0002g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(247): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(2144): Show |
1 | a0002c0002t0001g0355 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2155): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(4250): Show |
1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(4261): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1883): Show |
1 | a0001c0004t0003g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1894): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(344): Show |
1 | a0001c0003t0002g0044 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(355): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(803): Show |
1 | a0001c0005t0002g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(814): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1181): Show |
1 | a0001c0005t0002g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1192): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(596): Show |
1 | a0001c0005t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(607): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(236): Show |
1 | a0001c0003t0002g0052 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(247): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(389): Show |
1 | a0001c0003t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(400): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(83): Show |
1 | a0001c0026t0002g0366 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(2900): Show |
1 | a0002c0002t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2911): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1118): Show |
1 | a0002c0002t0001g0310 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1129): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(92): Show |
1 | a0001c0001t0002g0331 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(103): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1046): Show |
1 | a0001c0001t0002g0007 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(1057): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(227): Show |
1 | a0002c0002t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1014-1182_1014-118 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(227): Show |
1 | a0002c0002t0002g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | ATAGGGTG others(1172): Show |
1 | a0001c0005t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1183): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431777 | |||||
| chr1:31431777
|
A | T | 3 | a0002c0002t0001g0273a0002c0008t0001g0125a0002c0008t0001g0126 | 3 | HG01884.hp2 HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1014-1190A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431777 | ||||||
| chr1:31431778
|
T | C | 1 | a0001c0001t0004g0010 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1014-1189T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431778 | ||||||
| chr1:31431778
|
T | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(3): Show | 7 | HG01255.hp2 HG01891.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014-1189T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431778 | ||||||
| chr1:31431778
|
T | TAGGGTGG others(3926): Show |
1 | a0002c0002t0001g0321 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(3937): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(245): Show |
1 | a0001c0001t0005g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1014-1164_1014-116 others(256): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(4034): Show |
1 | a0003c0007t0004g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(4045): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(515): Show |
2 | a0004c0009t0004g0127a0004c0009t0004g0129 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1014-1173_1014-117 others(526): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(83): Show |
1 | a0001c0003t0002g0090 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(119): Show |
1 | a0002c0008t0017g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(130): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(101): Show |
1 | a0001c0001t0004g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(112): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(74): Show |
1 | a0001c0004t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(3161): Show |
1 | a0002c0006t0008g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3172): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1172): Show |
1 | a0002c0006t0008g0221 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1183): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(146): Show |
1 | a0001c0003t0001g0248 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(157): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(3719): Show |
1 | a0001c0003t0001g0256 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3730): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(74): Show |
1 | a0002c0006t0008g0176 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1694): Show |
1 | a0001c0004t0003g0211 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1705): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(3627): Show |
1 | a0001c0004t0003g0238 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(3638): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1091): Show |
1 | a0002c0002t0004g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1102): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(524): Show |
1 | a0002c0002t0001g0313 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(535): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1883): Show |
1 | a0002c0011t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1894): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(101): Show |
1 | a0001c0003t0002g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(112): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1235): Show |
1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1246): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(74): Show |
1 | a0001c0003t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(470): Show |
1 | a0001c0003t0002g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(481): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(128): Show |
1 | a0012c0025t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(139): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(992): Show |
1 | a0001c0003t0002g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1003): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(641): Show |
1 | a0009c0019t0002g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(652): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1280): Show |
1 | a0001c0004t0009g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1291): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(2747): Show |
1 | a0001c0001t0002g0344 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2758): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(47): Show |
1 | a0001c0003t0002g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(58): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(137): Show |
1 | a0001c0005t0002g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(148): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1046): Show |
1 | a0011c0015t0024g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1057): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1658): Show |
1 | a0001c0005t0002g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1669): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(92): Show |
1 | a0002c0008t0001g0075 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(103): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(236): Show |
1 | a0001c0003t0002g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(247): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1460): Show |
1 | a0001c0003t0002g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1471): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(245): Show |
1 | a0001c0001t0001g0356 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(256): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(5843): Show |
1 | a0002c0002t0001g0327 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(5854): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(1910): Show |
1 | a0002c0002t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(1921): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(866): Show |
1 | a0001c0003t0002g0096 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(877): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(200): Show |
1 | a0002c0002t0001g0298 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(211): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(4475): Show |
1 | a0002c0002t0001g0343 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(4486): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(47): Show |
1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(58): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(488): Show |
1 | a0001c0001t0004g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(499): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(218): Show |
1 | a0002c0002t0001g0275 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(229): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431778
|
T | TAGGGTGG others(10055): Show |
1 | a0001c0001t0004g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(10066): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431778 | |||||
| chr1:31431782
|
G | GTGGTTAG others(2387): Show |
1 | a0001c0005t0002g0057 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(2398): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431782 | |||||
| chr1:31431785
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(2): Show | 6 | HG01255.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-1182G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431785 | ||||||
| chr1:31431785
|
G | GATAGGGT others(2243): Show |
1 | a0001c0001t0004g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(2254): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431785 | |||||
| chr1:31431785
|
G | GTTAGGGT others(956): Show |
1 | a0002c0002t0006g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1014-1182_1014-118 others(967): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431785 | ||||||
| chr1:31431786
|
A | ATAGGGTG others(1442): Show |
1 | a0002c0002t0001g0365 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(1453): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431786 | |||||
| chr1:31431786
|
A | ATAGGGTG others(2909): Show |
1 | a0003c0007t0002g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(2920): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431786 | |||||
| chr1:31431786
|
A | T | 139 | a0001c0001t0001g0294a0001c0001t0001g0302a0001c0001t0001g0316others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1014-1181A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431786 | ||||||
| chr1:31431787
|
T | C | 20 | a0001c0001t0001g0356a0001c0001t0004g0010a0001c0001t0004g0279others(17): Show | 20 | HG00099.hp1 HG01123.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1014-1180T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431787 | ||||||
| chr1:31431787
|
T | G | 7 | a0001c0003t0002g0096a0001c0003t0002g0098a0001c0003t0002g0119others(4): Show | 7 | HG01346.hp2 HG02273.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014-1180T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431787 | ||||||
| chr1:31431787
|
T | TAGGGTGG others(776): Show |
1 | a0002c0002t0001g0364 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(787): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431787
|
T | TAGGGTGG others(1352): Show |
1 | a0004c0009t0006g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(1363): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431787
|
T | TAGGGTGG others(191): Show |
1 | a0001c0001t0004g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(202): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431787
|
T | TAGGGTGG others(443): Show |
1 | a0001c0001t0004g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(454): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431787
|
T | TAGGGTGG others(3107): Show |
1 | a0003c0007t0002g0150 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(3118): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431787
|
T | TAGGGTGG others(1109): Show |
1 | a0004c0009t0005g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(1120): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431787 | |||||
| chr1:31431790
|
G | GGTGGTTA others(416): Show |
1 | a0001c0005t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1014-1173_1014-117 others(427): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431790 | |||||
| chr1:31431791
|
G | A | 1 | a0001c0010t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1014-1176G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431791 | ||||||
| chr1:31431795
|
A | ATAGGATG others(2): Show |
16 | a0001c0001t0004g0131a0001c0001t0004g0133a0001c0001t0004g0134others(13): Show | 16 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1168_1014-116 others(13): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | ATAGGATG others(2612): Show |
1 | a0001c0003t0004g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(2623): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | ATAGGATG others(731): Show |
1 | a0001c0003t0004g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(742): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | ATAGGGTG others(1253): Show |
1 | a0002c0002t0001g0358 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(1264): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | ATAGGGTG others(173): Show |
1 | a0001c0001t0005g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(184): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | ATAGGGTG others(947): Show |
1 | a0002c0002t0001g0352 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(958): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431795 | |||||
| chr1:31431795
|
A | T | 82 | a0001c0001t0001g0294a0001c0001t0001g0302a0001c0001t0001g0316others(79): Show | 84 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1014-1172A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431795 | ||||||
| chr1:31431796
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0356a0001c0001t0004g0026others(26): Show | 30 | HG00099.hp1 HG00323.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1014-1171T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431796 | ||||||
| chr1:31431796
|
T | G | 5 | a0001c0003t0002g0119a0001c0004t0003g0200a0002c0002t0001g0343others(2): Show | 5 | HG00558.hp2 HG01261.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-1171T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431796 | ||||||
| chr1:31431796
|
T | TAGGATGG others(2900): Show |
1 | a0001c0004t0003g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(2911): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(9728): Show |
1 | a0001c0001t0004g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(9739): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(1676): Show |
1 | a0001c0004t0003g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(1687): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(155): Show |
1 | a0001c0001t0004g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(166): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(380): Show |
1 | a0001c0003t0001g0254 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(391): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(1073): Show |
1 | a0001c0003t0004g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(1084): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(794): Show |
1 | a0001c0004t0003g0215 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(805): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(578): Show |
1 | a0001c0004t0003g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(589): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(821): Show |
1 | a0001c0004t0003g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(832): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431796
|
T | TAGGATGG others(515): Show |
1 | a0001c0004t0003g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1014-1168_1014-116 others(526): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431796 | |||||
| chr1:31431800
|
G | A | 36 | a0001c0003t0004g0243a0001c0003t0004g0244a0001c0003t0004g0245others(33): Show | 36 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1014-1167G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431800 | ||||||
| chr1:31431804
|
A | ATAGGATG others(128): Show |
1 | a0001c0001t0001g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(139): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGATG others(2): Show |
14 | a0001c0001t0002g0290a0001c0001t0002g0315a0001c0001t0004g0147others(11): Show | 15 | HG01167.hp1 HG01175.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014-1163_1014-116 others(13): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGATG others(1469): Show |
1 | a0003c0007t0004g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(1480): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGATG others(128): Show |
1 | a0002c0002t0006g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(139): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGATG others(659): Show |
1 | a0002c0002t0001g0338 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(670): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGATG others(119): Show |
1 | a0001c0001t0002g0333 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(130): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGGTG others(11): Show |
1 | a0002c0002t0001g0367 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGGTG others(110): Show |
1 | a0001c0001t0005g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(121): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | ATAGGGTG others(164): Show |
1 | a0001c0001t0005g0012 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1014-1163_1014-116 others(175): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431804
|
A | T | 55 | a0001c0001t0004g0038a0001c0001t0005g0009a0001c0001t0005g0011others(52): Show | 56 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1014-1163A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431804 | ||||||
| chr1:31431805
|
C | G | 13 | a0001c0001t0009g0184a0001c0003t0002g0072a0001c0003t0002g0098others(10): Show | 13 | HG00558.hp2 HG01175.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014-1162C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431805 | ||||||
| chr1:31431805
|
C | T | 220 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(217): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1014-1162C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431805 | ||||||
| chr1:31431808
|
G | GATGGTTA others(668): Show |
1 | a0001c0005t0002g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1014-1159_1014-115 others(679): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431808 | ||||||
| chr1:31431809
|
G | A | 50 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0116others(47): Show | 51 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1014-1158G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431809 | ||||||
| chr1:31431813
|
A | ATAGGGTG others(1024): Show |
1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1014-1154_1014-115 others(1035): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431813 | ||||||
| chr1:31431813
|
A | T | 56 | a0001c0001t0001g0294a0001c0001t0001g0302a0001c0001t0001g0316others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.1014-1154A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431813 | ||||||
| chr1:31431814
|
C | CAGGGTGG others(1874): Show |
1 | a0001c0001t0004g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1014-1145_1014-114 others(1885): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431814 | |||||
| chr1:31431814
|
C | CAGGGTGG others(3125): Show |
1 | a0001c0001t0004g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1014-1110_1014-110 others(3136): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431814 | |||||
| chr1:31431814
|
C | G | 6 | a0001c0001t0002g0007a0001c0003t0002g0072a0001c0003t0002g0098others(3): Show | 7 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014-1153C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431814 | ||||||
| chr1:31431814
|
C | T | 177 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(174): Show | 181 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1014-1153C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431814 | ||||||
| chr1:31431818
|
G | A | 2 | a0001c0001t0004g0130a0002c0002t0001g0358 | 2 | HG01934.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1014-1149G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431818 | ||||||
| chr1:31431821
|
G | C | 1 | a0010c0022t0001g0278 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1014-1146G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431821 | ||||||
| chr1:31431822
|
A | ATAGGGTG others(227): Show |
1 | a0001c0001t0007g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1014-1136_1014-113 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431822 | |||||
| chr1:31431822
|
A | ATAGGGTG others(524): Show |
1 | a0002c0008t0001g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1014-1136_1014-113 others(535): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431822 | |||||
| chr1:31431822
|
A | ATAGGGTG others(1496): Show |
1 | a0002c0008t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1014-1137_1014-113 others(1507): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431822 | |||||
| chr1:31431822
|
A | T | 21 | a0001c0001t0001g0308a0001c0001t0004g0130a0001c0001t0004g0137others(18): Show | 22 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014-1145A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431822 | ||||||
| chr1:31431823
|
T | C | 34 | a0001c0001t0002g0342a0001c0001t0006g0340a0001c0003t0002g0052others(31): Show | 34 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1014-1144T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431823 | ||||||
| chr1:31431823
|
T | G | 13 | a0001c0001t0002g0007a0001c0001t0002g0345a0001c0001t0009g0184others(10): Show | 14 | HG01516.hp2 HG01517.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014-1144T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431823 | ||||||
| chr1:31431827
|
G | A | 1 | a0002c0002t0001g0338 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1014-1140G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431827 | ||||||
| chr1:31431831
|
A | ATAGGGTG others(29): Show |
1 | a0001c0001t0011g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(40): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431831 | |||||
| chr1:31431831
|
A | T | 18 | a0001c0001t0002g0342a0001c0003t0004g0261a0001c0003t0004g0262others(15): Show | 18 | HG00735.hp1 HG01361.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1014-1136A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431831 | ||||||
| chr1:31431832
|
T | C | 38 | a0001c0001t0001g0308a0001c0001t0004g0010a0001c0001t0004g0026others(35): Show | 38 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1014-1135T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431832 | ||||||
| chr1:31431832
|
T | G | 7 | a0001c0004t0003g0168a0001c0004t0003g0178a0002c0002t0001g0355others(4): Show | 7 | HG01243.hp2 HG01433.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014-1135T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431832 | ||||||
| chr1:31431832
|
T | TAGGGTGG others(371): Show |
1 | a0001c0001t0005g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(382): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431832 | |||||
| chr1:31431832
|
T | TAGGGTGG others(38): Show |
1 | a0001c0003t0004g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431832 | |||||
| chr1:31431839
|
G | C | 1 | a0002c0011t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1014-1128G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431839 | ||||||
| chr1:31431840
|
A | AGAGGGTG others(11): Show |
1 | a0001c0001t0002g0344 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1014-1127_1014-112 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431840 | ||||||
| chr1:31431840
|
A | ATAGGGTG others(137): Show |
1 | a0001c0005t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1014-1118_1014-111 others(148): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431840 | |||||
| chr1:31431840
|
A | ATAGGGTG others(488): Show |
1 | a0001c0003t0004g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(499): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431840 | |||||
| chr1:31431840
|
A | ATAGGGTG others(20): Show |
1 | a0001c0001t0011g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(31): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431840 | |||||
| chr1:31431840
|
A | T | 20 | a0001c0001t0002g0345a0001c0001t0018g0222a0001c0003t0001g0248others(17): Show | 20 | HG00323.hp2 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1014-1127A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431840 | ||||||
| chr1:31431841
|
T | C | 25 | a0001c0001t0001g0113a0001c0001t0004g0010a0001c0001t0005g0016others(22): Show | 25 | HG00738.hp2 HG01074.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1014-1126T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431841 | ||||||
| chr1:31431841
|
T | G | 6 | a0001c0003t0002g0096a0001c0003t0002g0098a0001c0004t0003g0143others(3): Show | 6 | HG01433.hp1 HG02273.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014-1126T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431841 | ||||||
| chr1:31431841
|
T | TAGGATGG others(398): Show |
1 | a0001c0004t0015g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014-1123_1014-112 others(409): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(1199): Show |
1 | a0001c0001t0007g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(1210): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(4970): Show |
1 | a0001c0001t0007g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(4981): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(2666): Show |
1 | a0001c0004t0003g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1014-1101_1014-110 others(2677): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(74): Show |
1 | a0001c0001t0007g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1014-1110_1014-110 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(29): Show |
1 | a0001c0003t0004g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(40): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431841
|
T | TAGGGTGG others(83): Show |
1 | a0001c0003t0004g0244 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431841 | |||||
| chr1:31431844
|
G | GGTGGTTA others(4403): Show |
1 | a0001c0001t0011g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1014-1119_1014-111 others(4414): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431844 | |||||
| chr1:31431845
|
G | A | 7 | a0001c0003t0002g0050a0001c0004t0003g0151a0001c0005t0002g0068others(4): Show | 8 | HG01081.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1014-1122G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431845 | ||||||
| chr1:31431849
|
A | T | 33 | a0001c0001t0001g0318a0001c0001t0002g0331a0001c0001t0004g0137others(30): Show | 34 | HG00280.hp1 HG00408.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1014-1118A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431849 | ||||||
| chr1:31431850
|
T | C | 29 | a0001c0001t0005g0016a0001c0003t0002g0081a0001c0003t0002g0087others(26): Show | 29 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.1014-1117T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431850 | ||||||
| chr1:31431850
|
T | G | 4 | a0001c0003t0002g0098a0001c0004t0003g0181a0002c0002t0001g0283others(1): Show | 4 | NA18522.hp2 NA18970.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-1117T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431850 | ||||||
| chr1:31431850
|
T | TAGGGTGG others(4241): Show |
1 | a0002c0006t0006g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(4252): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431850 | |||||
| chr1:31431850
|
T | TAGGGTGG others(1433): Show |
1 | a0001c0001t0007g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1014-1110_1014-110 others(1444): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431850 | |||||
| chr1:31431858
|
A | ACAGGGTG others(821): Show |
1 | a0001c0005t0002g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1014-1109_1014-110 others(832): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431858 | ||||||
| chr1:31431858
|
A | ATAGGATG others(1352): Show |
1 | a0002c0002t0001g0332 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1014-1105_1014-110 others(1363): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431858 | |||||
| chr1:31431858
|
A | ATAGGGTG others(191): Show |
1 | a0002c0006t0008g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(202): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431858 | |||||
| chr1:31431858
|
A | ATAGGGTG others(4430): Show |
1 | a0001c0004t0003g0205 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1014-1101_1014-110 others(4441): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431858 | |||||
| chr1:31431858
|
A | T | 35 | a0001c0001t0002g0342a0001c0001t0004g0008a0001c0001t0005g0011others(32): Show | 35 | HG00323.hp2 HG00609.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1014-1109A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431858 | ||||||
| chr1:31431859
|
T | C | 32 | a0001c0001t0002g0315a0001c0001t0004g0279a0001c0001t0007g0031others(29): Show | 32 | HG00280.hp2 HG01074.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1014-1108T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431859 | ||||||
| chr1:31431859
|
T | G | 10 | a0001c0001t0020g0028a0001c0003t0002g0053a0001c0004t0003g0168others(7): Show | 10 | HG00735.hp2 HG01261.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014-1108T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431859 | ||||||
| chr1:31431859
|
T | TAGGGTGG others(506): Show |
1 | a0002c0017t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431859
|
T | TAGGGTGG others(227): Show |
1 | a0001c0004t0003g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431859
|
T | TAGGGTGG others(227): Show |
1 | a0001c0004t0003g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431859
|
T | TAGGGTGG others(1316): Show |
1 | a0001c0001t0021g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(1327): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431859
|
T | TAGGGTGG others(497): Show |
1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1014-1101_1014-110 others(508): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431859
|
T | TAGGGTGG others(362): Show |
1 | a0001c0001t0007g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1014-1101_1014-110 others(373): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431859 | |||||
| chr1:31431863
|
G | A | 6 | a0001c0003t0004g0245a0001c0003t0004g0247a0001c0003t0004g0257others(3): Show | 6 | HG00408.hp2 HG00735.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-1104G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431863 | ||||||
| chr1:31431866
|
G | C | 1 | a0001c0004t0010g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1014-1101G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431866 | ||||||
| chr1:31431867
|
A | ATAGGGTG others(290): Show |
1 | a0002c0006t0008g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(301): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431867 | |||||
| chr1:31431867
|
A | ATAGGGTG others(245): Show |
1 | a0001c0004t0010g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(256): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431867 | |||||
| chr1:31431867
|
A | T | 41 | a0001c0001t0001g0308a0001c0001t0002g0290a0001c0001t0002g0319others(38): Show | 42 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1014-1100A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431867 | ||||||
| chr1:31431868
|
T | C | 62 | a0001c0001t0002g0301a0001c0001t0005g0009a0001c0001t0005g0011others(59): Show | 62 | HG00280.hp2 HG00609.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1014-1099T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431868 | ||||||
| chr1:31431868
|
T | G | 10 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0241others(7): Show | 11 | HG00741.hp2 HG01934.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014-1099T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431868 | ||||||
| chr1:31431868
|
T | TAGGATGG others(20): Show |
1 | a0001c0003t0002g0088 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1014-1096_1014-109 others(31): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431868 | |||||
| chr1:31431868
|
T | TAGGATGG others(470): Show |
1 | a0003c0007t0002g0150 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1014-1096_1014-109 others(481): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431868 | |||||
| chr1:31431868
|
T | TAGGGTGG others(3026): Show |
1 | a0001c0023t0005g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(3037): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431868 | |||||
| chr1:31431868
|
T | TAGGGTGG others(731): Show |
1 | a0001c0001t0005g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(742): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431868 | |||||
| chr1:31431868
|
T | TAGGGTGG others(173): Show |
1 | a0001c0004t0003g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1014-1092_1014-109 others(184): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431868 | |||||
| chr1:31431872
|
G | A | 3 | a0001c0003t0004g0259a0001c0003t0004g0269a0002c0002t0001g0343 | 3 | HG00558.hp2 NA18971.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1014-1095G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431872 | ||||||
| chr1:31431875
|
G | C | 1 | a0002c0002t0006g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1014-1092G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431875 | ||||||
| chr1:31431876
|
A | ATAGGGTG others(245): Show |
1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1014-1091_1014-109 others(256): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431876 | ||||||
| chr1:31431876
|
A | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0002g0345others(28): Show | 32 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1014-1091A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431876 | ||||||
| chr1:31431877
|
C | CAGGGTGG others(137): Show |
1 | a0001c0003t0004g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(148): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431877 | |||||
| chr1:31431877
|
C | CAGGGTGG others(38): Show |
1 | a0002c0002t0001g0330 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431877 | |||||
| chr1:31431877
|
C | G | 15 | a0001c0001t0004g0241a0001c0001t0005g0011a0001c0003t0002g0065others(12): Show | 15 | HG00741.hp2 HG01070.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1014-1090C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431877 | ||||||
| chr1:31431877
|
C | T | 173 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(170): Show | 177 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.1014-1090C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431877 | ||||||
| chr1:31431885
|
A | AGAGGGTG others(434): Show |
1 | a0002c0002t0001g0286 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(445): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431885 | ||||||
| chr1:31431885
|
A | ATAGGATG others(776): Show |
1 | a0001c0001t0004g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(787): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431885 | ||||||
| chr1:31431885
|
A | ATAGGGTG others(155): Show |
1 | a0001c0001t0001g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(166): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431885 | ||||||
| chr1:31431885
|
A | ATAGGGTG others(128): Show |
1 | a0001c0001t0004g0010 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1014-1082_1014-108 others(139): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431885 | ||||||
| chr1:31431885
|
A | T | 18 | a0001c0001t0004g0047a0001c0001t0005g0009a0001c0001t0005g0012others(15): Show | 19 | HG00735.hp1 HG01168.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1014-1082A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431885 | ||||||
| chr1:31431886
|
C | CAGGATGG others(83): Show |
1 | a0001c0001t0004g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1014-1078_1014-107 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(47): Show |
1 | a0001c0003t0002g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(58): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(5123): Show |
1 | a0001c0004t0014g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(5134): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(290): Show |
1 | a0002c0002t0001g0361 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(301): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(470): Show |
1 | a0001c0003t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(481): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(3944): Show |
1 | a0001c0001t0001g0316 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(3955): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(5528): Show |
1 | a0001c0001t0001g0317 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(5539): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(776): Show |
1 | a0001c0003t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1014-1069_1014-106 others(787): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(11): Show |
1 | a0001c0001t0005g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1014-1064_1014-104 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(2639): Show |
1 | a0002c0002t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1014-1055_1014-105 others(2650): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(317): Show |
1 | a0002c0002t0001g0346 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1014-1056_1014-105 others(328): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(704): Show |
1 | a0001c0004t0003g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1014-1074_1014-107 others(715): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | CAGGGTGG others(506): Show |
1 | a0002c0002t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1014-1074_1014-107 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431886 | |||||
| chr1:31431886
|
C | G | 14 | a0001c0001t0004g0241a0001c0003t0002g0065a0001c0003t0002g0096others(11): Show | 14 | HG00323.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1014-1081C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431886 | ||||||
| chr1:31431886
|
C | T | 161 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0116others(158): Show | 166 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1014-1081C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431886 | ||||||
| chr1:31431890
|
G | A | 1 | a0001c0003t0001g0250 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1014-1077G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431890 | ||||||
| chr1:31431893
|
G | GTTAGGGT others(1136): Show |
1 | a0002c0002t0001g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1014-1074_1014-107 others(1147): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431893 | ||||||
| chr1:31431894
|
A | ACAGGGTG others(182): Show |
1 | a0002c0002t0001g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1014-1073_1014-107 others(193): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431894 | ||||||
| chr1:31431894
|
A | T | 25 | a0001c0001t0002g0315a0001c0001t0002g0333a0001c0003t0001g0250others(22): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1014-1073A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431894 | ||||||
| chr1:31431895
|
T | C | 55 | a0001c0001t0001g0302a0001c0001t0001g0356a0001c0001t0002g0342others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1014-1072T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431895 | ||||||
| chr1:31431895
|
T | G | 10 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0003t0002g0091others(7): Show | 10 | HG02922.hp1 HG03139.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014-1072T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431895 | ||||||
| chr1:31431895
|
T | TAGGGTGG others(443): Show |
1 | a0001c0004t0003g0197 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1014-1064_1014-106 others(454): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431895 | |||||
| chr1:31431895
|
T | TAGGGTGG others(1097): Show |
1 | a0001c0001t0005g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014-1064_1014-106 others(1108): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431895 | |||||
| chr1:31431895
|
T | TAGGGTGG others(20): Show |
1 | a0001c0001t0005g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1014-1065_1014-106 others(31): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431895 | |||||
| chr1:31431895
|
T | TAGGTGGA others(3783): Show |
1 | a0002c0002t0001g0360 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1014-1069_1014-106 others(3794): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431895 | |||||
| chr1:31431899
|
G | A | 3 | a0001c0001t0006g0314a0001c0003t0002g0050a0001c0010t0002g0101 | 3 | HG01081.hp2 HG01981.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1014-1068G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431899 | ||||||
| chr1:31431903
|
A | ACAGGGTG others(2859): Show |
1 | a0001c0001t0004g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1014-1064_1014-106 others(2870): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431903 | ||||||
| chr1:31431903
|
A | ATAGGGTG others(497): Show |
1 | a0001c0004t0010g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1014-1055_1014-105 others(508): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431903 | |||||
| chr1:31431903
|
A | ATAGGGTG others(3179): Show |
1 | a0001c0003t0004g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1014-1047_1014-104 others(3190): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431903 | |||||
| chr1:31431903
|
A | ATAGGGTG others(506): Show |
1 | a0001c0004t0003g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1014-1047_1014-104 others(517): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431903 | |||||
| chr1:31431903
|
A | ATAGGGTG others(11): Show |
1 | a0001c0004t0003g0179 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1014-1056_1014-105 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431903 | |||||
| chr1:31431903
|
A | T | 27 | a0001c0001t0001g0318a0001c0001t0002g0345a0001c0001t0006g0314others(24): Show | 28 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1014-1064A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431903 | ||||||
| chr1:31431904
|
T | C | 43 | a0001c0001t0001g0108a0001c0001t0001g0302a0001c0001t0004g0133others(40): Show | 44 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1014-1063T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431904 | ||||||
| chr1:31431904
|
T | G | 13 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0140others(10): Show | 13 | HG00558.hp1 HG01123.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014-1063T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431904 | ||||||
| chr1:31431904
|
T | TAGGGTGG others(199): Show |
1 | a0001c0001t0004g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014-1047_1014-104 others(210): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431904 | |||||
| chr1:31431904
|
T | TAGGGTGG others(38): Show |
1 | a0001c0001t0002g0331 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1014-1056_1014-105 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431904 | |||||
| chr1:31431908
|
G | A | 1 | a0001c0003t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1014-1059G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431908 | ||||||
| chr1:31431912
|
A | ACAGGGTG others(668): Show |
1 | a0001c0003t0002g0349 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1014-1055_1014-105 others(679): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431912 | ||||||
| chr1:31431912
|
A | ACAGGGTG others(2504): Show |
1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1014-1055_1014-105 others(2515): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431912 | ||||||
| chr1:31431912
|
A | ACAGGGTG others(1757): Show |
1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1014-1055_1014-105 others(1768): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431912 | ||||||
| chr1:31431912
|
A | T | 25 | a0001c0001t0004g0037a0001c0001t0005g0015a0001c0001t0005g0024others(22): Show | 27 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1014-1055A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431912 | ||||||
| chr1:31431913
|
T | C | 35 | a0001c0001t0002g0331a0001c0001t0004g0135a0001c0001t0004g0279others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1014-1054T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431913 | ||||||
| chr1:31431913
|
T | G | 12 | a0001c0001t0002g0007a0001c0001t0004g0241a0001c0003t0007g0100others(9): Show | 13 | HG01123.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014-1054T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431913 | ||||||
| chr1:31431913
|
T | TAGGGTGG others(38): Show |
1 | a0001c0004t0003g0192 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1014-1047_1014-104 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431913 | |||||
| chr1:31431916
|
G | A | 1 | a0001c0003t0002g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1014-1051G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431916 | ||||||
| chr1:31431917
|
G | A | 9 | a0001c0001t0001g0108a0001c0001t0007g0002a0001c0003t0001g0250others(6): Show | 10 | HG01934.hp2 HG02148.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014-1050G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431917 | ||||||
| chr1:31431921
|
T | A | 217 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0230others(214): Show | 221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.1014-1046T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431921 | ||||||
| chr1:31431921
|
T | TTAGGGTG others(407): Show |
1 | a0001c0004t0016g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(418): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431921 | |||||
| chr1:31431921
|
T | TTAGGGTG others(83): Show |
1 | a0001c0005t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(94): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431921 | |||||
| chr1:31431921
|
T | TTAGGGTG others(38): Show |
1 | a0002c0002t0001g0295 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431921 | |||||
| chr1:31431921
|
T | TTAGGGTG others(155): Show |
1 | a0002c0002t0001g0335 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(166): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431921 | |||||
| chr1:31431921
|
T | TTAGGGTG others(677): Show |
1 | a0001c0004t0003g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1014-1038_1014-103 others(688): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431921 | |||||
| chr1:31431922
|
T | C | 36 | a0001c0001t0001g0005a0001c0001t0002g0290a0001c0001t0004g0010others(33): Show | 37 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1014-1045T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431922 | ||||||
| chr1:31431922
|
T | G | 4 | a0001c0001t0004g0140a0001c0004t0003g0168a0001c0004t0003g0178others(1): Show | 4 | HG02109.hp1 NA18984.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-1045T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431922 | ||||||
| chr1:31431922
|
T | TAGGGTGG others(1865): Show |
1 | a0001c0001t0005g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(1876): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431922 | |||||
| chr1:31431922
|
T | TAGGGTGG others(4205): Show |
1 | a0002c0002t0001g0276 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(4216): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431922 | |||||
| chr1:31431922
|
T | TAGGGTGG others(74): Show |
2 | a0001c0001t0005g0019a0008c0024t0005g0020 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1014-1029_1014-102 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431922 | |||||
| chr1:31431922
|
T | TAGGGTGG others(406): Show |
2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1014-1029_1014-102 others(417): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431922 | |||||
| chr1:31431922
|
T | TAGTGTGG others(2180): Show |
1 | a0001c0001t0007g0025 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1014-1043_1014-104 others(2191): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431922 | |||||
| chr1:31431925
|
G | A | 1 | a0002c0002t0001g0351 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1014-1042G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431925 | ||||||
| chr1:31431930
|
A | ACAGGGTG others(2477): Show |
1 | a0001c0003t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(2488): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431930 | ||||||
| chr1:31431930
|
A | ACAGGGTG others(65): Show |
1 | a0001c0004t0003g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(76): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431930 | ||||||
| chr1:31431930
|
A | ACAGGGTG others(10694): Show |
1 | a0001c0001t0001g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1014-1037_1014-103 others(10705): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431930 | ||||||
| chr1:31431930
|
A | ATAGGGTG others(1019): Show |
1 | a0002c0002t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(1030): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431930 | |||||
| chr1:31431930
|
A | ATAGGGTG others(1748): Show |
1 | a0002c0008t0017g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(1759): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431930 | |||||
| chr1:31431930
|
A | ATAGGGTG others(695): Show |
1 | a0001c0005t0002g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(706): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431930 | |||||
| chr1:31431930
|
A | T | 14 | a0001c0001t0002g0007a0001c0001t0004g0010a0001c0001t0005g0009others(11): Show | 15 | HG01516.hp2 HG01517.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014-1037A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431930 | ||||||
| chr1:31431931
|
T | C | 34 | a0001c0001t0001g0304a0001c0001t0002g0319a0001c0001t0005g0015others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.1014-1036T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431931 | ||||||
| chr1:31431931
|
T | G | 15 | a0001c0001t0004g0147a0001c0004t0003g0143a0001c0004t0003g0168others(12): Show | 15 | HG01361.hp2 HG02717.hp1 HG03209.hp2 others(12): Show |
intron_variant | MODIFIER | c.1014-1036T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431931 | ||||||
| chr1:31431931
|
T | TAGGGTGG others(524): Show |
1 | a0001c0003t0002g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(535): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431931
|
T | TAGGGTGG others(1073): Show |
1 | a0001c0004t0003g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(1084): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431931
|
T | TAGGGTGG others(2072): Show |
1 | a0001c0004t0003g0195 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(2083): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431931
|
T | TAGGGTGG others(1388): Show |
1 | a0002c0002t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(1399): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431931
|
T | TAGGGTGG others(497): Show |
1 | a0001c0004t0008g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(508): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431931
|
T | TAGGGTGG others(398): Show |
1 | a0001c0001t0006g0337 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(409): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431931 | |||||
| chr1:31431934
|
G | A | 1 | a0002c0002t0001g0351 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1014-1033G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431934 | ||||||
| chr1:31431935
|
G | A | 16 | a0001c0001t0001g0318a0001c0001t0005g0236a0001c0003t0001g0104others(13): Show | 17 | HG00280.hp1 HG01167.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1014-1032G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431935 | ||||||
| chr1:31431935
|
G | GTGGACAG others(3896): Show |
1 | a0002c0002t0001g0275 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(3907): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431935 | |||||
| chr1:31431935
|
G | GTGGATAG others(335): Show |
1 | a0001c0003t0002g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1014-1029_1014-102 others(346): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431935 | |||||
| chr1:31431938
|
G | C | 1 | a0002c0011t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1014-1029G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431938 | ||||||
| chr1:31431939
|
T | A | 231 | a0001c0001t0001g0113a0001c0001t0001g0230a0001c0001t0001g0302others(228): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1014-1028T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431939 | ||||||
| chr1:31431940
|
T | C | 23 | a0001c0001t0001g0304a0001c0001t0002g0319a0001c0001t0002g0342others(20): Show | 23 | HG00621.hp2 HG01070.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1014-1027T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431940 | ||||||
| chr1:31431940
|
T | G | 6 | a0001c0001t0004g0038a0001c0003t0002g0349a0001c0004t0003g0181others(3): Show | 6 | HG02965.hp1 NA18961.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-1027T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431940 | ||||||
| chr1:31431940
|
T | TAGAGTGG others(335): Show |
1 | a0001c0005t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1014-1025_1014-102 others(346): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431940 | |||||
| chr1:31431940
|
T | TAGGGTGG others(2198): Show |
1 | a0001c0001t0005g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1014-1020_1014-101 others(2209): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431940 | |||||
| chr1:31431940
|
T | TAGGGTGG others(488): Show |
1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1014-1020_1014-101 others(499): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431940 | |||||
| chr1:31431940
|
T | TAGGGTGG others(12620): Show |
1 | a0002c0006t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1014-1020_1014-101 others(12631): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431940 | |||||
| chr1:31431943
|
G | A | 1 | a0001c0003t0009g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1014-1024G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431943 | ||||||
| chr1:31431944
|
G | A | 6 | a0001c0001t0004g0135a0001c0003t0002g0050a0001c0005t0002g0063others(3): Show | 6 | HG01081.hp2 HG01346.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-1023G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431944 | ||||||
| chr1:31431947
|
G | C | 1 | a0001c0004t0003g0215 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1014-1020G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431947 | ||||||
| chr1:31431948
|
T | A | 266 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0116others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1014-1019T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431948 | ||||||
| chr1:31431948
|
T | TTAGGGTG others(1155): Show |
1 | a0001c0004t0009g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(1166): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431948 | |||||
| chr1:31431948
|
T | TTAGTGTG others(7616): Show |
1 | a0001c0001t0007g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1014-1016_1014-101 others(7627): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431948 | |||||
| chr1:31431949
|
T | C | 26 | a0001c0001t0004g0137a0001c0001t0005g0009a0001c0001t0005g0015others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1014-1018T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431949 | ||||||
| chr1:31431949
|
T | G | 12 | a0001c0003t0002g0119a0001c0003t0002g0122a0001c0003t0009g0187others(9): Show | 12 | HG01358.hp1 HG01361.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014-1018T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431949 | ||||||
| chr1:31431949
|
T | TAGAGTGG others(722): Show |
1 | a0001c0005t0002g0359 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1014-1016_1014-101 others(733): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431949 | |||||
| chr1:31431949
|
T | TAGGGTGG others(56): Show |
1 | a0001c0005t0002g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(67): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431949 | |||||
| chr1:31431949
|
T | TAGGGTGG others(470): Show |
1 | a0002c0006t0008g0208 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(481): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431949 | |||||
| chr1:31431949
|
T | TAGTGTGG others(1811): Show |
1 | a0001c0001t0007g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1014-1016_1014-101 others(1822): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431949 | |||||
| chr1:31431952
|
G | A | 1 | a0001c0003t0009g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1014-1015G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431952 | ||||||
| chr1:31431952
|
G | GGTGGAGA others(389): Show |
1 | a0001c0004t0010g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(400): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431952 | |||||
| chr1:31431953
|
G | A | 4 | a0001c0003t0002g0044a0001c0003t0002g0099a0001c0003t0004g0262others(1): Show | 4 | HG01243.hp2 NA19004.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-1014G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431953 | ||||||
| chr1:31431953
|
G | GTGGACAG others(1046): Show |
1 | a0001c0001t0006g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(1057): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431953
|
G | GTGGACAG others(461): Show |
1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(472): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431953
|
G | GTGGATAG others(11): Show |
1 | a0001c0004t0003g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(22): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431953
|
G | GTGGATAG others(29): Show |
1 | a0003c0007t0002g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(40): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431953
|
G | GTGGATAG others(875): Show |
1 | a0002c0002t0001g0327 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1014-1011_1014-101 others(886): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431953
|
G | GTGGTTAG others(47): Show |
1 | a0001c0003t0002g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1014-992_1014-991i others(56): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431953 | |||||
| chr1:31431956
|
G | C | 1 | a0001c0004t0003g0205 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1014-1011G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431956 | ||||||
| chr1:31431957
|
T | A | 241 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0294others(238): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1014-1010T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431957 | ||||||
| chr1:31431957
|
T | TTAGAGTG others(38): Show |
1 | a0001c0005t0002g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1014-1007_1014-100 others(49): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431957 | |||||
| chr1:31431957
|
T | TTAGGGTG others(1892): Show |
1 | a0001c0004t0003g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(1903): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431957 | |||||
| chr1:31431958
|
T | C | 24 | a0001c0001t0004g0141a0001c0001t0005g0016a0001c0001t0005g0236others(21): Show | 25 | HG00099.hp1 HG01943.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1014-1009T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431958 | ||||||
| chr1:31431958
|
T | G | 8 | a0001c0001t0002g0345a0001c0001t0004g0131a0001c0003t0002g0349others(5): Show | 8 | HG01361.hp1 HG02300.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1014-1009T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431958 | ||||||
| chr1:31431958
|
T | TAGGGTGC others(2045): Show |
1 | a0001c0001t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1014-1003_1014-100 others(2056): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(47): Show |
1 | a0001c0003t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(58): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(74): Show |
1 | a0001c0010t0002g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(85): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(227): Show |
1 | a0001c0001t0004g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(238): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(3116): Show |
1 | a0001c0003t0002g0044 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(3127): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(2333): Show |
1 | a0001c0005t0002g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(2344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(3557): Show |
1 | a0002c0002t0004g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(3568): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(137): Show |
1 | a0002c0006t0008g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1014-997_1014-996i others(146): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(20): Show |
1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1014-992_1014-991i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(2351): Show |
1 | a0002c0006t0008g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1014-1002_1014-100 others(2362): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(119): Show |
1 | a0002c0002t0001g0291 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1014-1002_1014-100 others(130): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(2621): Show |
1 | a0001c0004t0003g0165 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1014-1002_1014-100 others(2632): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431958
|
T | TAGGGTGG others(272): Show |
1 | a0002c0002t0001g0354 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1014-1002_1014-100 others(283): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431958 | |||||
| chr1:31431959
|
A | G | 1 | a0001c0003t0002g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1014-1008A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431959 | ||||||
| chr1:31431965
|
G | GACAGGGT others(1037): Show |
1 | a0002c0002t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014-1001_1014-100 others(1048): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431965 | |||||
| chr1:31431966
|
A | ATAGGGTG others(227): Show |
1 | a0001c0001t0006g0314 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431966 | |||||
| chr1:31431966
|
A | ATAGGGTG others(641): Show |
1 | a0002c0002t0001g0309 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(650): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431966 | |||||
| chr1:31431966
|
A | ATAGGGTG others(11495): Show |
1 | a0002c0006t0006g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1014-970_1014-969i others(11504): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431966 | |||||
| chr1:31431966
|
A | ATAGGGTG others(857): Show |
1 | a0002c0002t0001g0328 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(866): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431966 | |||||
| chr1:31431966
|
A | ATAGGGTG others(4673): Show |
1 | a0001c0001t0002g0301 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(4682): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431966 | |||||
| chr1:31431966
|
A | T | 23 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0001g0302others(20): Show | 24 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.1014-1001A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431966 | ||||||
| chr1:31431967
|
T | C | 35 | a0001c0001t0001g0304a0001c0001t0004g0026a0001c0001t0005g0016others(32): Show | 35 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1014-1000T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431967 | ||||||
| chr1:31431967
|
T | G | 9 | a0001c0001t0004g0027a0001c0003t0002g0044a0001c0003t0002g0098others(6): Show | 9 | HG00621.hp1 HG01358.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014-1000T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431967 | ||||||
| chr1:31431967
|
T | TAGGATGG others(254): Show |
1 | a0001c0003t0004g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1014-997_1014-996i others(263): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGATGG others(677): Show |
1 | a0002c0002t0001g0350 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1014-997_1014-996i others(686): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGATGG others(2612): Show |
1 | a0001c0001t0002g0007 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1014-997_1014-996i others(2621): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(164): Show |
1 | a0002c0006t0008g0176 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1014-992_1014-991i others(173): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(227): Show |
1 | a0002c0002t0001g0341 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1014-992_1014-991i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(227): Show |
1 | a0001c0003t0002g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1014-992_1014-991i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(677): Show |
1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1014-983_1014-982i others(686): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(605): Show |
1 | a0001c0003t0004g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(614): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(902): Show |
1 | a0001c0003t0004g0265 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1014-993_1014-992i others(911): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431967
|
T | TAGGGTGG others(992): Show |
1 | a0001c0001t0009g0185 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1014-993_1014-992i others(1001): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431967 | |||||
| chr1:31431970
|
G | A | 1 | a0001c0005t0002g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1014-997G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431970 | ||||||
| chr1:31431971
|
G | A | 2 | a0001c0001t0007g0002a0001c0004t0003g0216 | 3 | HG02895.hp1 HG02897.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1014-996G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431971 | ||||||
| chr1:31431974
|
G | C | 3 | a0001c0001t0007g0030a0002c0002t0001g0288a0002c0002t0001g0360 | 3 | HG02602.hp1 HG02717.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.1014-993G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431974 | ||||||
| chr1:31431975
|
A | AGAGGGTG others(128): Show |
1 | a0001c0001t0002g0319 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1014-992_1014-991i others(137): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431975
|
A | AGAGGGTG others(640): Show |
1 | a0001c0001t0004g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1014-992_1014-991i others(649): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431975
|
A | AGAGGGTG others(3125): Show |
1 | a0001c0014t0009g0157 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1014-992_1014-991i others(3134): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431975
|
A | AGAGGGTG others(146): Show |
1 | a0002c0002t0001g0348 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1014-992_1014-991i others(155): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431975
|
A | ATAGGGTG others(1811): Show |
1 | a0001c0003t0002g0083 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(1820): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431975 | |||||
| chr1:31431975
|
A | ATAGGGTG others(461): Show |
1 | a0002c0002t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431975 | |||||
| chr1:31431975
|
A | ATAGGGTG others(1460): Show |
1 | a0001c0001t0001g0356 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1014-984_1014-983i others(1469): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431975 | |||||
| chr1:31431975
|
A | G | 1 | a0002c0006t0008g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1014-992A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431975
|
A | T | 21 | a0001c0001t0002g0315a0001c0001t0004g0137a0001c0001t0004g0241others(18): Show | 22 | HG01123.hp2 HG01361.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1014-992A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431975 | ||||||
| chr1:31431976
|
T | C | 30 | a0001c0001t0004g0026a0001c0001t0007g0136a0001c0001t0009g0185others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1014-991T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431976 | ||||||
| chr1:31431976
|
T | G | 10 | a0001c0003t0002g0044a0001c0004t0003g0173a0001c0010t0002g0094others(7): Show | 10 | HG00597.hp1 HG01243.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014-991T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431976 | ||||||
| chr1:31431976
|
T | TAGGGTGG others(731): Show |
1 | a0002c0002t0008g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(740): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431976 | |||||
| chr1:31431976
|
T | TAGGGTGG others(1028): Show |
1 | a0001c0004t0009g0213 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1014-983_1014-982i others(1037): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431976 | |||||
| chr1:31431976
|
T | TAGGGTGG others(1316): Show |
1 | a0001c0003t0004g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1014-984_1014-983i others(1325): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431976 | |||||
| chr1:31431976
|
T | TAGGGTGG others(461): Show |
1 | a0001c0004t0003g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1014-984_1014-983i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431976 | |||||
| chr1:31431983
|
G | C | 2 | a0002c0002t0001g0297a0002c0011t0001g0004 | 3 | HG03491.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1014-984G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431983 | ||||||
| chr1:31431983
|
G | GATAGGGT others(1514): Show |
1 | a0003c0007t0002g0170 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1014-970_1014-969i others(1523): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431983 | |||||
| chr1:31431984
|
A | ACAGGGTG others(461): Show |
1 | a0005c0012t0002g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431984 | ||||||
| chr1:31431984
|
A | ACAGGGTG others(515): Show |
1 | a0001c0001t0002g0333 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(524): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431984 | ||||||
| chr1:31431984
|
A | AGAGGGTG others(3179): Show |
1 | a0001c0003t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1014-983_1014-982i others(3188): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431984 | ||||||
| chr1:31431984
|
A | ATAGGGTG others(371): Show |
1 | a0001c0003t0002g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1014-974_1014-973i others(380): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431984 | |||||
| chr1:31431984
|
A | ATAGGGTG others(317): Show |
1 | a0002c0002t0001g0307 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(326): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431984 | |||||
| chr1:31431984
|
A | ATAGGGTG others(11): Show |
1 | a0001c0004t0016g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-966_1014-965i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431984 | |||||
| chr1:31431984
|
A | G | 1 | a0002c0006t0008g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1014-983A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431984 | ||||||
| chr1:31431984
|
A | T | 23 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0116others(20): Show | 23 | HG01243.hp1 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1014-983A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431984 | ||||||
| chr1:31431985
|
T | C | 33 | a0001c0001t0001g0304a0001c0001t0004g0026a0001c0001t0005g0017others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1014-982T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431985 | ||||||
| chr1:31431985
|
T | G | 15 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0006g0289others(12): Show | 15 | HG00558.hp2 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1014-982T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431985 | ||||||
| chr1:31431985
|
T | TAGGATGG others(560): Show |
1 | a0001c0003t0002g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1014-979_1014-978i others(569): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGATGG others(1928): Show |
1 | a0001c0004t0003g0151 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1014-979_1014-978i others(1937): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGATGG others(2846): Show |
1 | a0001c0001t0005g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1014-979_1014-978i others(2855): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(551): Show |
1 | a0001c0003t0002g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1014-974_1014-973i others(560): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(3647): Show |
1 | a0002c0002t0025g0311 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1014-974_1014-973i others(3656): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(668): Show |
1 | a0001c0004t0003g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1014-974_1014-973i others(677): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(1757): Show |
1 | a0002c0002t0001g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1014-974_1014-973i others(1766): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(47): Show |
1 | a0002c0002t0023g0353 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1014-965_1014-964i others(56): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(218): Show |
1 | a0002c0006t0008g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1014-975_1014-974i others(227): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(1307): Show |
1 | a0001c0004t0003g0196 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1014-975_1014-974i others(1316): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(317): Show |
1 | a0001c0001t0009g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(326): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(38): Show |
1 | a0001c0001t0011g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(47): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431985
|
T | TAGGGTGG others(83): Show |
1 | a0001c0001t0011g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1014-975_1014-974i others(92): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431985 | |||||
| chr1:31431988
|
G | A | 1 | a0001c0005t0002g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1014-979G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431988 | ||||||
| chr1:31431989
|
G | A | 1 | a0004c0009t0006g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1014-978G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431989 | ||||||
| chr1:31431993
|
A | ATAGGGTG others(281): Show |
1 | a0001c0004t0009g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(290): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431993 | |||||
| chr1:31431993
|
A | ATAGGGTG others(1325): Show |
1 | a0001c0004t0003g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(1334): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431993 | |||||
| chr1:31431993
|
A | ATAGGGTG others(533): Show |
1 | a0002c0002t0001g0347 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(542): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431993 | |||||
| chr1:31431993
|
A | ATAGGGTG others(848): Show |
1 | a0001c0003t0004g0244 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(857): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431993 | |||||
| chr1:31431993
|
A | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0294a0001c0001t0002g0345others(21): Show | 25 | HG00642.hp2 HG01070.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1014-974A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431993 | ||||||
| chr1:31431994
|
T | C | 39 | a0001c0001t0001g0108a0001c0001t0001g0304a0001c0001t0004g0010others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1014-973T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431994 | ||||||
| chr1:31431994
|
T | G | 13 | a0001c0001t0001g0316a0001c0001t0004g0027a0001c0001t0004g0130others(10): Show | 13 | HG01081.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.1014-973T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431994 | ||||||
| chr1:31431994
|
T | TAGGGTGG others(875): Show |
1 | a0001c0003t0002g0076 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1014-965_1014-964i others(884): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(1406): Show |
1 | a0001c0003t0002g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1014-965_1014-964i others(1415): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(1136): Show |
1 | a0001c0004t0003g0198 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(1145): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(614): Show |
1 | a0001c0003t0007g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(623): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(668): Show |
1 | a0002c0002t0001g0365 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(677): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(506): Show |
1 | a0001c0001t0005g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014-966_1014-965i others(515): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(1235): Show |
1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014-966_1014-965i others(1244): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(803): Show |
1 | a0002c0017t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1014-966_1014-965i others(812): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431994
|
T | TAGGGTGG others(587): Show |
1 | a0002c0002t0001g0324 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1014-966_1014-965i others(596): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31431994 | |||||
| chr1:31431997
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1014-970G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31431997 | ||||||
| chr1:31432002
|
A | ACAGGGTG others(1757): Show |
1 | a0002c0002t0001g0330 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(1766): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432002 | ||||||
| chr1:31432002
|
A | AGAGGGTG others(56): Show |
1 | a0001c0003t0002g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1014-965_1014-964i others(65): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432002 | ||||||
| chr1:31432002
|
A | ATAGGGTG others(1226): Show |
1 | a0001c0004t0003g0178 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(1235): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432002 | |||||
| chr1:31432002
|
A | ATAGGGTG others(3017): Show |
1 | a0003c0007t0002g0149 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1014-952_1014-951i others(3026): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432002 | |||||
| chr1:31432002
|
A | G | 1 | a0001c0001t0004g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014-965A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432002 | ||||||
| chr1:31432002
|
A | T | 19 | a0001c0001t0002g0301a0001c0001t0006g0337a0001c0004t0003g0197others(16): Show | 19 | HG00741.hp2 HG01261.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1014-965A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432002 | ||||||
| chr1:31432003
|
T | C | 36 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0236others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1014-964T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432003 | ||||||
| chr1:31432003
|
T | G | 17 | a0001c0001t0004g0130a0001c0001t0005g0011a0001c0003t0002g0074others(14): Show | 17 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014-964T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432003 | ||||||
| chr1:31432003
|
T | TAGGATGG others(1343): Show |
1 | a0013c0013t0002g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1014-961_1014-960i others(1352): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(173): Show |
1 | a0001c0001t0004g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(2990): Show |
1 | a0001c0004t0010g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(2999): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(11542): Show |
1 | a0001c0001t0004g0133 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1014-956_1014-955i others(11551): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(11503): Show |
1 | a0001c0001t0004g0134 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1014-956_1014-955i others(11512): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(344): Show |
1 | a0006c0020t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(353): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1703): Show |
1 | a0003c0007t0002g0003 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1014-952_1014-951i others(1712): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(2351): Show |
1 | a0001c0001t0004g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014-952_1014-951i others(2360): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1469): Show |
1 | a0001c0004t0003g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1478): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1730): Show |
1 | a0001c0004t0003g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1739): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1649): Show |
1 | a0001c0003t0004g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1658): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1658): Show |
1 | a0001c0001t0004g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(1667): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(4430): Show |
1 | a0001c0001t0002g0315 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(4439): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(2909): Show |
1 | a0002c0002t0001g0369 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1014-957_1014-956i others(2918): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(857): Show |
1 | a0002c0006t0008g0221 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(866): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1217): Show |
1 | a0001c0001t0002g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(1226): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432003
|
T | TAGGGTGG others(1181): Show |
1 | a0001c0001t0007g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(1190): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432003 | |||||
| chr1:31432007
|
G | A | 5 | a0001c0001t0006g0289a0001c0003t0001g0104a0002c0002t0001g0283others(2): Show | 5 | HG01192.hp2 HG02273.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014-960G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432007 | ||||||
| chr1:31432007
|
G | GTGGTTAG others(443): Show |
1 | a0001c0004t0003g0179 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1014-957_1014-956i others(452): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432007 | |||||
| chr1:31432011
|
A | ACAGGGTG others(182): Show |
1 | a0001c0001t0005g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(191): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432011 | ||||||
| chr1:31432011
|
A | ACAGGGTG others(11): Show |
1 | a0001c0001t0007g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1014-956_1014-955i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432011 | ||||||
| chr1:31432011
|
A | AGAGGGTG others(848): Show |
1 | a0001c0004t0003g0238 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1014-956_1014-955i others(857): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432011 | ||||||
| chr1:31432011
|
A | ATAGGGTG others(488): Show |
1 | a0001c0004t0010g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(497): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432011 | |||||
| chr1:31432011
|
A | G | 1 | a0001c0001t0004g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014-956A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432011 | ||||||
| chr1:31432011
|
A | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0302a0001c0001t0002g0290others(28): Show | 33 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1014-956A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432011 | ||||||
| chr1:31432012
|
T | C | 49 | a0001c0001t0002g0342a0001c0001t0004g0010a0001c0001t0005g0011others(46): Show | 49 | HG00323.hp1 HG00408.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1014-955T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432012 | ||||||
| chr1:31432012
|
T | G | 25 | a0001c0001t0004g0026a0001c0001t0004g0241a0001c0001t0005g0009others(22): Show | 25 | HG00099.hp1 HG00621.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1014-955T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432012 | ||||||
| chr1:31432012
|
T | TAGGATGG others(677): Show |
1 | a0001c0004t0003g0192 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1014-952_1014-951i others(686): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGATGG others(5411): Show |
1 | a0001c0003t0002g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1014-952_1014-951i others(5420): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGATGG others(5222): Show |
1 | a0001c0003t0002g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1014-952_1014-951i others(5231): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(2324): Show |
1 | a0002c0002t0002g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(2333): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(335): Show |
1 | a0001c0005t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1014-939_1014-938i others(344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(830): Show |
1 | a0001c0004t0003g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(839): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(875): Show |
1 | a0002c0002t0001g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(884): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(137): Show |
1 | a0003c0007t0002g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(146): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(389): Show |
1 | a0002c0011t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1014-947_1014-946i others(398): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(524): Show |
1 | a0002c0002t0006g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(533): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(983): Show |
2 | a0001c0001t0001g0308a0001c0003t0022g0260 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1014-947_1014-946i others(992): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(1460): Show |
1 | a0001c0005t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1469): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(200): Show |
1 | a0002c0002t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(209): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(1037): Show |
1 | a0001c0003t0004g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1046): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(353): Show |
1 | a0001c0004t0010g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(362): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(497): Show |
1 | a0001c0004t0003g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(506): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(1127): Show |
1 | a0001c0004t0003g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1014-947_1014-946i others(1136): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(4007): Show |
1 | a0001c0003t0004g0245 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(4016): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(2261): Show |
1 | a0001c0004t0003g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(2270): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(641): Show |
1 | a0002c0006t0008g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014-948_1014-947i others(650): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432012
|
T | TAGGGTGG others(2180): Show |
1 | a0001c0026t0002g0366 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1014-948_1014-947i others(2189): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432012 | |||||
| chr1:31432015
|
G | GGTGGAGA others(227): Show |
1 | a0001c0003t0002g0096 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1014-947_1014-946i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432015 | |||||
| chr1:31432015
|
G | T | 1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1014-952G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432015 | ||||||
| chr1:31432016
|
G | A | 1 | a0002c0002t0001g0332 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1014-951G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432016 | ||||||
| chr1:31432019
|
G | C | 1 | a0002c0002t0001g0297 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1014-948G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432019 | ||||||
| chr1:31432020
|
A | G | 1 | a0001c0001t0004g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014-947A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432020 | ||||||
| chr1:31432020
|
A | T | 15 | a0001c0001t0001g0302a0001c0003t0002g0120a0001c0003t0002g0122others(12): Show | 16 | HG00099.hp2 HG00642.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1014-947A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432020 | ||||||
| chr1:31432021
|
C | CAGGGTGG others(650): Show |
1 | a0001c0010t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1014-929_1014-928i others(659): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432021 | |||||
| chr1:31432021
|
C | CAGGGTGG others(1370): Show |
1 | a0007c0018t0013g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1014-938_1014-937i others(1379): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432021 | |||||
| chr1:31432021
|
C | CAGGGTGG others(101): Show |
1 | a0001c0001t0004g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1014-938_1014-937i others(110): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432021 | |||||
| chr1:31432021
|
C | CAGGGTGG others(2405): Show |
1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014-939_1014-938i others(2414): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432021 | |||||
| chr1:31432021
|
C | G | 31 | a0001c0001t0004g0026a0001c0001t0004g0130a0001c0001t0004g0147others(28): Show | 32 | HG00099.hp1 HG00609.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.1014-946C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432021 | ||||||
| chr1:31432021
|
C | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0116others(134): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1014-946C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432021 | ||||||
| chr1:31432024
|
G | GGTGGTTA others(1082): Show |
1 | a0002c0002t0001g0358 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1014-939_1014-938i others(1091): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432024 | |||||
| chr1:31432025
|
G | A | 2 | a0001c0004t0003g0167a0001c0004t0009g0155 | 2 | HG01069.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1014-942G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432025 | ||||||
| chr1:31432029
|
A | T | 8 | a0001c0001t0005g0014a0001c0001t0005g0132a0001c0001t0007g0031others(5): Show | 8 | HG01884.hp1 HG02080.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014-938A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432029 | ||||||
| chr1:31432030
|
C | CAGGGTGG others(74): Show |
1 | a0001c0004t0003g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(83): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(1262): Show |
1 | a0001c0003t0002g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1014-920_1014-919i others(1271): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(272): Show |
1 | a0001c0003t0002g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1014-921_1014-920i others(281): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(3548): Show |
1 | a0001c0003t0002g0052 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1014-929_1014-928i others(3557): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(1262): Show |
1 | a0002c0002t0001g0346 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1014-930_1014-929i others(1271): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(461): Show |
1 | a0002c0006t0008g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1014-930_1014-929i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(245): Show |
1 | a0001c0001t0002g0331 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1014-930_1014-929i others(254): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | CAGGGTGG others(263): Show |
1 | a0002c0002t0006g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1014-930_1014-929i others(272): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432030 | |||||
| chr1:31432030
|
C | G | 28 | a0001c0001t0004g0140a0001c0001t0004g0241a0001c0001t0005g0237others(25): Show | 28 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1014-937C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432030 | ||||||
| chr1:31432030
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0294others(105): Show | 112 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1014-937C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432030 | ||||||
| chr1:31432031
|
A | AGGGTGGA others(529): Show |
1 | a0001c0004t0003g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1014-929_1014-928i others(538): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432031 | |||||
| chr1:31432033
|
G | A | 1 | a0001c0003t0002g0098 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1014-934G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432033 | ||||||
| chr1:31432033
|
G | T | 1 | a0001c0001t0007g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1014-934G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432033 | ||||||
| chr1:31432034
|
G | A | 2 | a0001c0003t0002g0080a0001c0003t0002g0088 | 2 | HG02735.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1014-933G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432034 | ||||||
| chr1:31432038
|
A | ATAGGGTG others(803): Show |
1 | a0001c0004t0003g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1014-929_1014-928i others(812): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432038 | ||||||
| chr1:31432038
|
A | ATAGGGTG others(3494): Show |
1 | a0001c0001t0004g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1014-929_1014-928i others(3503): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432038 | ||||||
| chr1:31432038
|
A | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0001g0294others(9): Show | 12 | HG00323.hp1 HG00642.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014-929A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432038 | ||||||
| chr1:31432039
|
C | CAGGGTGG others(1352): Show |
1 | a0003c0007t0002g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1361): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(1991): Show |
1 | a0002c0002t0001g0357 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(2000): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(236): Show |
1 | a0001c0001t0002g0345 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(245): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(3287): Show |
1 | a0001c0004t0003g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(3296): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(2972): Show |
1 | a0002c0002t0001g0296 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1014-920_1014-919i others(2981): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(2108): Show |
1 | a0001c0005t0002g0055 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(2117): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | CAGGGTGG others(506): Show |
1 | a0001c0001t0011g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1014-921_1014-920i others(515): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432039 | |||||
| chr1:31432039
|
C | G | 25 | a0001c0001t0001g0302a0001c0001t0002g0331a0001c0001t0004g0137others(22): Show | 25 | HG00099.hp2 HG00423.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1014-928C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432039 | ||||||
| chr1:31432039
|
C | T | 113 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(110): Show | 117 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1014-928C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432039 | ||||||
| chr1:31432042
|
G | GGTGGATA others(1082): Show |
1 | a0001c0003t0002g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1014-920_1014-919i others(1091): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432042 | |||||
| chr1:31432043
|
G | A | 1 | a0001c0005t0002g0057 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1014-924G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432043 | ||||||
| chr1:31432047
|
A | ATAGGGTG others(4592): Show |
1 | a0001c0003t0001g0248 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1014-920_1014-919i others(4601): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432047 | ||||||
| chr1:31432047
|
A | ATAGGGTG others(200): Show |
1 | a0002c0002t0006g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1014-920_1014-919i others(209): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432047 | ||||||
| chr1:31432047
|
A | T | 4 | a0001c0004t0003g0181a0001c0004t0010g0233a0001c0005t0002g0057others(1): Show | 4 | HG03688.hp1 HG03688.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-920A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432047 | ||||||
| chr1:31432048
|
C | CAGGGTGG others(1352): Show |
1 | a0001c0004t0009g0213 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1014-902_1014-901i others(1361): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432048 | |||||
| chr1:31432048
|
C | CAGGGTGG others(866): Show |
1 | a0001c0001t0005g0011 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1014-911_1014-910i others(875): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432048 | |||||
| chr1:31432048
|
C | CAGGGTGG others(470): Show |
1 | a0001c0004t0003g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1014-911_1014-910i others(479): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432048 | |||||
| chr1:31432048
|
C | CAGGGTGG others(173): Show |
1 | a0001c0001t0002g0333 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1014-912_1014-911i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432048 | |||||
| chr1:31432048
|
C | G | 17 | a0001c0001t0007g0034a0001c0003t0002g0065a0001c0003t0002g0098others(14): Show | 17 | HG00423.hp1 HG00735.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1014-919C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432048 | ||||||
| chr1:31432048
|
C | T | 109 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0294others(106): Show | 113 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.1014-919C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432048 | ||||||
| chr1:31432051
|
G | GGTGGTTA others(3145): Show |
1 | a0002c0002t0001g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1014-912_1014-911i others(3154): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432051 | |||||
| chr1:31432056
|
A | T | 14 | a0001c0001t0002g0331a0001c0001t0018g0222a0001c0003t0001g0251others(11): Show | 15 | HG01167.hp2 HG01169.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014-911A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432056 | ||||||
| chr1:31432057
|
C | CAGGGTGG others(1271): Show |
1 | a0001c0001t0004g0026 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1014-902_1014-901i others(1280): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432057 | |||||
| chr1:31432057
|
C | CAGGGTGG others(2432): Show |
1 | a0001c0003t0002g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1014-902_1014-901i others(2441): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432057 | |||||
| chr1:31432057
|
C | G | 23 | a0001c0001t0002g0319a0001c0001t0002g0333a0001c0001t0005g0237others(20): Show | 23 | HG00423.hp1 HG00609.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1014-910C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432057 | ||||||
| chr1:31432057
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0116others(105): Show | 111 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1014-910C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432057 | ||||||
| chr1:31432060
|
G | GGTGGTTA others(1667): Show |
1 | a0002c0002t0001g0360 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1014-903_1014-902i others(1676): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432060 | |||||
| chr1:31432060
|
G | GGTGGTTA others(3305): Show |
1 | a0002c0002t0001g0310 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1014-903_1014-902i others(3314): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432060 | |||||
| chr1:31432061
|
G | A | 2 | a0001c0001t0004g0137a0002c0002t0001g0274 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1014-906G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432061 | ||||||
| chr1:31432064
|
G | A | 1 | a0001c0005t0002g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1014-903G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432064 | ||||||
| chr1:31432065
|
A | ATAGGGTG others(2270): Show |
1 | a0001c0004t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1014-902_1014-901i others(2279): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432065 | ||||||
| chr1:31432065
|
A | ATAGGGTG others(479): Show |
1 | a0001c0003t0002g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1014-902_1014-901i others(488): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432065 | ||||||
| chr1:31432065
|
A | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0116others(10): Show | 15 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1014-902A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432065 | ||||||
| chr1:31432066
|
C | CAGGGTGG others(524): Show |
1 | a0001c0010t0002g0085 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1014-893_1014-892i others(533): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432066 | |||||
| chr1:31432066
|
C | CAGGGTGG others(425): Show |
1 | a0001c0010t0002g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1014-893_1014-892i others(434): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432066 | |||||
| chr1:31432066
|
C | CAGGGTGG others(425): Show |
1 | a0002c0006t0003g0209 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1014-894_1014-893i others(434): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432066 | |||||
| chr1:31432066
|
C | CAGGGTGG others(371): Show |
1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1014-894_1014-893i others(380): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432066 | |||||
| chr1:31432066
|
C | G | 18 | a0001c0001t0001g0230a0001c0001t0002g0319a0001c0001t0004g0131others(15): Show | 18 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1014-901C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432066 | ||||||
| chr1:31432066
|
C | T | 124 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0113others(121): Show | 128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1014-901C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432066 | ||||||
| chr1:31432069
|
G | GGTGGACA others(4961): Show |
1 | a0001c0003t0002g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(4970): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432069 | |||||
| chr1:31432070
|
G | A | 1 | a0001c0003t0004g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1014-897G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432070 | ||||||
| chr1:31432074
|
A | ATAGGGTG others(5843): Show |
1 | a0002c0002t0001g0350 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1014-893_1014-892i others(5852): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432074 | ||||||
| chr1:31432074
|
A | T | 14 | a0001c0001t0001g0302a0001c0001t0002g0290a0001c0001t0004g0133others(11): Show | 14 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014-893A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432074 | ||||||
| chr1:31432075
|
C | CAGGGTGG others(884): Show |
1 | a0001c0001t0007g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(893): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(236): Show |
1 | a0001c0003t0004g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(245): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(1568): Show |
1 | a0001c0005t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1577): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(92): Show |
1 | a0002c0002t0001g0328 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(101): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(1685): Show |
1 | a0001c0004t0010g0217 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1694): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(1154): Show |
1 | a0002c0006t0008g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1163): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(1847): Show |
1 | a0001c0003t0002g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1856): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(3242): Show |
1 | a0001c0001t0002g0344 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(3251): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | CAGGGTGG others(4151): Show |
1 | a0002c0002t0006g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(4160): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432075 | |||||
| chr1:31432075
|
C | G | 32 | a0001c0001t0001g0230a0001c0001t0002g0342a0001c0001t0004g0047others(29): Show | 32 | HG00735.hp2 HG01257.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.1014-892C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432075 | ||||||
| chr1:31432075
|
C | T | 142 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0113others(139): Show | 146 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1014-892C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432075 | ||||||
| chr1:31432079
|
G | A | 11 | a0001c0001t0002g0345a0001c0001t0004g0130a0001c0001t0004g0137others(8): Show | 11 | HG00558.hp2 HG02148.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014-888G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432079 | ||||||
| chr1:31432079
|
G | GTGGACAG others(902): Show |
1 | a0001c0004t0003g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(911): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGACAG others(749): Show |
1 | a0001c0004t0003g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(758): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGACAG others(182): Show |
1 | a0001c0003t0002g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(191): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGACAG others(11): Show |
1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGACAG others(119): Show |
1 | a0001c0003t0002g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(128): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGAGAG others(6509): Show |
1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(6518): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGATAG others(470): Show |
1 | a0001c0003t0004g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1014-885_1014-884i others(479): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432079
|
G | GTGGATAG others(1478): Show |
1 | a0001c0003t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1014-885_1014-884i others(1487): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432079 | |||||
| chr1:31432083
|
T | A | 243 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0303others(240): Show | 248 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1014-884T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432083 | ||||||
| chr1:31432083
|
T | TTAGGGTG others(920): Show |
1 | a0001c0001t0005g0132 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(929): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432083 | |||||
| chr1:31432083
|
T | TTAGGGTG others(992): Show |
1 | a0002c0002t0001g0286 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(1001): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432083 | |||||
| chr1:31432083
|
T | TTAGGGTG others(101): Show |
1 | a0001c0001t0006g0337 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(110): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432083 | |||||
| chr1:31432084
|
T | C | 68 | a0001c0001t0001g0304a0001c0001t0001g0308a0001c0001t0001g0318others(65): Show | 68 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1014-883T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432084 | ||||||
| chr1:31432084
|
T | G | 13 | a0001c0001t0001g0005a0001c0001t0002g0342a0001c0001t0004g0272others(10): Show | 14 | HG01070.hp2 HG01071.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1014-883T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432084 | ||||||
| chr1:31432084
|
T | TAGAGTGG others(2483): Show |
1 | a0001c0001t0004g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1014-881_1014-880i others(2492): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(1667): Show |
1 | a0001c0004t0009g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(1676): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(191): Show |
1 | a0001c0001t0011g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(200): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(38): Show |
1 | a0003c0007t0002g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(47): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(5393): Show |
1 | a0001c0005t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(5402): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(362): Show |
1 | a0003c0007t0002g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(371): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(1136): Show |
1 | a0002c0002t0001g0368 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(1145): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(7994): Show |
1 | a0002c0006t0008g0225 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(8003): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(245): Show |
1 | a0004c0009t0006g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(254): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(74): Show |
1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014-875_1014-874i others(83): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432084
|
T | TAGGGTGG others(1505): Show |
1 | a0002c0002t0001g0300 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1014-876_1014-875i others(1514): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432084 | |||||
| chr1:31432088
|
G | A | 1 | a0001c0003t0004g0245 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1014-879G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432088 | ||||||
| chr1:31432092
|
A | ATAGGGTG others(875): Show |
1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(884): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432092 | ||||||
| chr1:31432092
|
A | ATAGGGTG others(1307): Show |
1 | a0001c0001t0004g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1014-875_1014-874i others(1316): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432092 | ||||||
| chr1:31432092
|
A | T | 7 | a0001c0001t0002g0290a0001c0003t0004g0245a0001c0003t0004g0266others(4): Show | 7 | HG02723.hp1 HG02895.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014-875A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432092 | ||||||
| chr1:31432093
|
C | A | 2 | a0002c0002t0001g0310a0002c0002t0001g0312 | 2 | NA19077.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1014-874C>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432093 | ||||||
| chr1:31432093
|
C | CAGGGTGG others(1217): Show |
1 | a0001c0003t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(1226): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432093 | |||||
| chr1:31432093
|
C | CAGGGTGG others(128): Show |
1 | a0002c0002t0001g0307 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1014-866_1014-865i others(137): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432093 | |||||
| chr1:31432093
|
C | CAGGGTGG others(191): Show |
1 | a0001c0001t0005g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1014-867_1014-866i others(200): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432093 | |||||
| chr1:31432093
|
C | G | 24 | a0001c0001t0002g0344a0001c0001t0011g0071a0001c0003t0002g0044others(21): Show | 24 | HG00642.hp1 HG01496.hp2 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.1014-874C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432093 | ||||||
| chr1:31432093
|
C | T | 166 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(163): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1014-874C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432093 | ||||||
| chr1:31432101
|
A | ATAGGGTG others(4637): Show |
1 | a0001c0005t0002g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1014-866_1014-865i others(4646): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432101 | ||||||
| chr1:31432101
|
A | ATAGGGTG others(461): Show |
1 | a0001c0003t0002g0119 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1014-866_1014-865i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432101 | ||||||
| chr1:31432101
|
A | ATAGGGTG others(92): Show |
1 | a0002c0006t0003g0207 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1014-866_1014-865i others(101): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432101 | ||||||
| chr1:31432101
|
A | ATAGGGTG others(794): Show |
1 | a0002c0008t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1014-866_1014-865i others(803): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432101 | ||||||
| chr1:31432101
|
A | T | 9 | a0001c0001t0018g0222a0001c0004t0003g0168a0001c0004t0003g0218others(6): Show | 9 | HG00323.hp2 HG02040.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014-866A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432101 | ||||||
| chr1:31432102
|
C | CAGGGTGG others(515): Show |
1 | a0001c0005t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(524): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(1316): Show |
1 | a0001c0001t0002g0007 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1014-857_1014-856i others(1325): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(4313): Show |
1 | a0001c0001t0009g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014-857_1014-856i others(4322): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(227): Show |
1 | a0001c0004t0003g0179 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(767): Show |
1 | a0002c0006t0008g0221 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(776): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(3035): Show |
1 | a0001c0001t0007g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1014-857_1014-856i others(3044): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(911): Show |
1 | a0001c0003t0004g0249 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1014-857_1014-856i others(920): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(1118): Show |
1 | a0001c0005t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(1127): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(416): Show |
1 | a0001c0001t0002g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(425): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(731): Show |
1 | a0001c0003t0002g0044 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(740): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(5213): Show |
1 | a0005c0012t0002g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(5222): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(1154): Show |
1 | a0001c0001t0021g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(1163): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(74): Show |
1 | a0001c0001t0007g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(83): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(8660): Show |
1 | a0002c0002t0006g0212 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(8669): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(1325): Show |
1 | a0001c0004t0010g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(1334): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(74): Show |
1 | a0001c0001t0001g0318 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(83): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(902): Show |
1 | a0001c0003t0004g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(911): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(1586): Show |
1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1014-858_1014-857i others(1595): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | CAGGGTGG others(6671): Show |
1 | a0002c0002t0006g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1014-858_1014-857i others(6680): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432102 | |||||
| chr1:31432102
|
C | G | 21 | a0001c0003t0001g0256a0001c0003t0002g0065a0001c0003t0002g0096others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.1014-865C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432102 | ||||||
| chr1:31432102
|
C | T | 149 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0116others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1014-865C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432102 | ||||||
| chr1:31432106
|
G | A | 3 | a0001c0001t0004g0008a0001c0001t0004g0026a0002c0002t0001g0299 | 3 | HG02922.hp1 HG03017.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1014-861G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432106 | ||||||
| chr1:31432109
|
G | C | 1 | a0002c0002t0006g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1014-858G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432109 | ||||||
| chr1:31432110
|
A | ACAGGGTG others(929): Show |
1 | a0001c0001t0004g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1014-857_1014-856i others(938): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432110 | ||||||
| chr1:31432110
|
A | ATAGGATG others(749): Show |
1 | a0003c0007t0004g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1014-853_1014-852i others(758): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432110 | |||||
| chr1:31432110
|
A | ATAGGGTG others(11): Show |
1 | a0001c0004t0014g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432110 | |||||
| chr1:31432110
|
A | ATAGGGTG others(1361): Show |
1 | a0002c0002t0001g0291 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(1370): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432110 | |||||
| chr1:31432110
|
A | ATAGGGTG others(5870): Show |
1 | a0001c0003t0004g0259 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(5879): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432110 | |||||
| chr1:31432110
|
A | ATAGGGTG others(110): Show |
1 | a0001c0004t0009g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(119): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432110 | |||||
| chr1:31432110
|
A | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0004g0008others(17): Show | 22 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1014-857A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432110 | ||||||
| chr1:31432111
|
T | C | 65 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0002g0301others(62): Show | 65 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1014-856T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432111 | ||||||
| chr1:31432111
|
T | G | 14 | a0001c0001t0005g0017a0001c0001t0006g0289a0001c0003t0001g0248others(11): Show | 14 | HG00642.hp1 HG01346.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014-856T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432111 | ||||||
| chr1:31432111
|
T | TAGGGTGC others(2648): Show |
1 | a0001c0001t0002g0319 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1014-850_1014-849i others(2657): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(65): Show |
1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(74): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(1775): Show |
1 | a0001c0003t0002g0072 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(1784): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(3386): Show |
1 | a0001c0003t0002g0084 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(3395): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(2441): Show |
1 | a0002c0002t0001g0328 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(2450): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(245): Show |
1 | a0008c0024t0005g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(254): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(6410): Show |
1 | a0001c0003t0002g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(6419): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432111
|
T | TAGGGTGG others(713): Show |
1 | a0001c0005t0002g0359 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(722): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432111 | |||||
| chr1:31432115
|
G | A | 14 | a0001c0001t0001g0230a0001c0001t0002g0290a0001c0003t0001g0250others(11): Show | 14 | HG00408.hp2 HG01106.hp1 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1014-852G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432115 | ||||||
| chr1:31432115
|
G | GTGGATAG others(9992): Show |
1 | a0004c0009t0006g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1014-849_1014-848i others(10001): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432115 | |||||
| chr1:31432115
|
G | GTGGATAG others(974): Show |
1 | a0001c0001t0006g0320 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1014-849_1014-848i others(983): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432115 | |||||
| chr1:31432115
|
G | GTGGTTAG others(11): Show |
1 | a0002c0002t0023g0353 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1014-835_1014-834i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432115 | |||||
| chr1:31432119
|
T | A | 256 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0294others(253): Show | 260 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.1014-848T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432119 | ||||||
| chr1:31432119
|
T | TTAGGGTG others(8379): Show |
1 | a0001c0001t0004g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(8388): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432119 | |||||
| chr1:31432119
|
T | TTAGGGTG others(9020): Show |
1 | a0001c0001t0004g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(9029): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432119 | |||||
| chr1:31432119
|
T | TTAGGGTG others(362): Show |
1 | a0003c0007t0004g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(371): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432119 | |||||
| chr1:31432119
|
T | TTAGGGTG others(1334): Show |
2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1014-840_1014-839i others(1343): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432119 | |||||
| chr1:31432120
|
T | C | 38 | a0001c0001t0001g0356a0001c0001t0002g0331a0001c0001t0002g0333others(35): Show | 38 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1014-847T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432120 | ||||||
| chr1:31432120
|
T | G | 12 | a0001c0001t0001g0294a0001c0001t0002g0319a0001c0003t0001g0248others(9): Show | 12 | HG00642.hp2 HG01074.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014-847T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432120 | ||||||
| chr1:31432120
|
T | TAGGGTGG others(1424): Show |
1 | a0012c0025t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1014-839_1014-838i others(1433): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(8840): Show |
1 | a0003c0007t0002g0003 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1014-835_1014-834i others(8849): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(2738): Show |
1 | a0001c0001t0004g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1014-832_1014-831i others(2747): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(1631): Show |
1 | a0001c0005t0002g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(1640): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(1118): Show |
1 | a0001c0003t0002g0067 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(1127): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(4088): Show |
1 | a0001c0003t0001g0254 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(4097): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(866): Show |
1 | a0001c0003t0002g0001 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(875): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(461): Show |
1 | a0001c0003t0002g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(3575): Show |
1 | a0001c0003t0002g0112 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(3584): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432120
|
T | TAGGGTGG others(3404): Show |
1 | a0001c0005t0002g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1014-840_1014-839i others(3413): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432120 | |||||
| chr1:31432123
|
G | GATGGTTA others(4196): Show |
1 | a0001c0001t0004g0010 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1014-844_1014-843i others(4205): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432123 | ||||||
| chr1:31432124
|
G | A | 1 | a0001c0005t0002g0056 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1014-843G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432124 | ||||||
| chr1:31432124
|
G | GTGGTTAG others(1577): Show |
1 | a0001c0005t0002g0057 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1014-840_1014-839i others(1586): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432124 | |||||
| chr1:31432128
|
A | ATAGGATG others(2108): Show |
1 | a0001c0003t0002g0349 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1014-835_1014-834i others(2117): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(1289): Show |
2 | a0001c0001t0001g0308a0001c0003t0022g0260 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1014-822_1014-821i others(1298): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(65): Show |
1 | a0001c0005t0002g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(74): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(164): Show |
1 | a0001c0004t0008g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(173): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(6347): Show |
1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(6356): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(4286): Show |
1 | a0002c0008t0001g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(4295): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(677): Show |
1 | a0001c0005t0002g0055 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(686): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(3431): Show |
1 | a0001c0003t0004g0262 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(3440): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(4448): Show |
1 | a0002c0002t0001g0355 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1014-831_1014-830i others(4457): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(1325): Show |
1 | a0001c0001t0001g0302 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1014-831_1014-830i others(1334): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(8471): Show |
1 | a0001c0001t0001g0318 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1014-831_1014-830i others(8480): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | ATAGGGTG others(308): Show |
1 | a0001c0003t0004g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1014-831_1014-830i others(317): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432128 | |||||
| chr1:31432128
|
A | T | 26 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0002g0331others(23): Show | 26 | HG01081.hp1 HG01106.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.1014-839A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432128 | ||||||
| chr1:31432129
|
T | C | 54 | a0001c0001t0001g0304a0001c0001t0004g0010a0001c0001t0004g0038others(51): Show | 54 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1014-838T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432129 | ||||||
| chr1:31432129
|
T | G | 12 | a0001c0001t0006g0340a0001c0003t0002g0064a0001c0003t0002g0072others(9): Show | 12 | HG01175.hp2 HG01346.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014-838T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432129 | ||||||
| chr1:31432129
|
T | TAGGATGG others(5987): Show |
1 | a0003c0007t0002g0146 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1014-835_1014-834i others(5996): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGATGG others(497): Show |
1 | a0001c0004t0003g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1014-835_1014-834i others(506): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(533): Show |
1 | a0002c0002t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1014-830_1014-829i others(542): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(101): Show |
1 | a0003c0007t0002g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(110): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(443): Show |
1 | a0001c0003t0002g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(452): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(1127): Show |
1 | a0001c0004t0003g0181 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(1136): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(2702): Show |
1 | a0002c0011t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1014-830_1014-829i others(2711): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(857): Show |
1 | a0001c0003t0002g0001 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(866): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(2999): Show |
1 | a0001c0001t0004g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(3008): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(227): Show |
1 | a0001c0003t0004g0243 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1014-831_1014-830i others(236): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432129
|
T | TAGGGTGG others(8768): Show |
1 | a0001c0004t0010g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1014-831_1014-830i others(8777): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432129 | |||||
| chr1:31432132
|
G | GGTGGACA others(1442): Show |
1 | a0001c0003t0002g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(1451): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432132 | |||||
| chr1:31432132
|
G | GGTGGATA others(1379): Show |
1 | a0002c0006t0008g0208 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(1388): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432132 | |||||
| chr1:31432133
|
G | A | 5 | a0001c0001t0011g0071a0001c0003t0002g0111a0002c0002t0001g0299others(2): Show | 5 | HG00609.hp2 HG00735.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014-834G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432133 | ||||||
| chr1:31432137
|
A | ATAGGATG others(380): Show |
1 | a0002c0002t0001g0338 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(389): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432137
|
A | ATAGGGTG others(65): Show |
1 | a0001c0001t0006g0320 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(74): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432137
|
A | ATAGGGTG others(2882): Show |
1 | a0001c0001t0004g0279 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(2891): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432137
|
A | ATAGGGTG others(551): Show |
1 | a0001c0004t0003g0195 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1014-830_1014-829i others(560): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432137
|
A | ATAGGGTG others(1262): Show |
1 | a0002c0002t0001g0334 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1014-830_1014-829i others(1271): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432137
|
A | T | 12 | a0001c0001t0005g0024a0001c0001t0011g0071a0001c0003t0002g0111others(9): Show | 12 | HG00673.hp2 HG00735.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1014-830A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432137 | ||||||
| chr1:31432138
|
C | CAGGGTGG others(326): Show |
1 | a0001c0004t0016g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(335): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(20): Show |
1 | a0001c0003t0002g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1014-813_1014-812i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(56): Show |
1 | a0001c0003t0002g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1014-813_1014-812i others(65): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(4475): Show |
2 | a0004c0009t0004g0127a0004c0009t0004g0129 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1014-821_1014-820i others(4484): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(200): Show |
1 | a0003c0007t0002g0170 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(209): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(2639): Show |
1 | a0001c0003t0002g0083 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(2648): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(4556): Show |
1 | a0001c0003t0002g0066 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(4565): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(1613): Show |
1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1014-822_1014-821i others(1622): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | CAGGGTGG others(2882): Show |
1 | a0001c0001t0001g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1014-822_1014-821i others(2891): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432138 | |||||
| chr1:31432138
|
C | G | 22 | a0001c0001t0006g0289a0001c0003t0001g0254a0001c0003t0002g0053others(19): Show | 22 | HG00735.hp2 HG01175.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.1014-829C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432138 | ||||||
| chr1:31432138
|
C | T | 160 | a0001c0001t0001g0110a0001c0001t0001g0113a0001c0001t0001g0116others(157): Show | 163 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1014-829C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432138 | ||||||
| chr1:31432142
|
G | A | 5 | a0001c0005t0002g0043a0002c0002t0001g0300a0002c0002t0001g0327others(2): Show | 5 | HG00558.hp1 HG02027.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014-825G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432142 | ||||||
| chr1:31432145
|
G | A | 2 | a0001c0004t0009g0156a0001c0014t0009g0157 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1014-822G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432145 | ||||||
| chr1:31432146
|
A | AGAGGGTG others(4997): Show |
1 | a0002c0002t0001g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(5006): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | AGAGGGTG others(4421): Show |
1 | a0002c0002t0001g0284 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(4430): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | AGAGGGTG others(1424): Show |
1 | a0002c0002t0001g0347 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1014-821_1014-820i others(1433): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | AGAGGGTG others(3755): Show |
1 | a0002c0002t0001g0348 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(3764): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(1982): Show |
1 | a0002c0002t0001g0329 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1014-821_1014-820i others(1991): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(4961): Show |
1 | a0010c0022t0001g0278 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(4970): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(47): Show |
1 | a0001c0004t0003g0211 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(56): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(299): Show |
1 | a0001c0004t0010g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(308): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(4160): Show |
1 | a0002c0002t0001g0367 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1014-821_1014-820i others(4169): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(1676): Show |
1 | a0002c0002t0001g0309 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(1685): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(119): Show |
1 | a0002c0002t0001g0363 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(128): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | ATAGGGTG others(2684): Show |
1 | a0002c0002t0001g0364 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1014-821_1014-820i others(2693): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432146
|
A | T | 18 | a0001c0001t0002g0331a0001c0001t0002g0344a0001c0001t0002g0345others(15): Show | 18 | HG00408.hp2 HG00558.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1014-821A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432146 | ||||||
| chr1:31432147
|
C | CAGGGTGG others(1316): Show |
1 | a0002c0002t0001g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1325): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(1883): Show |
1 | a0002c0002t0001g0306 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1892): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(650): Show |
1 | a0009c0019t0002g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(659): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(2297): Show |
1 | a0002c0008t0001g0075 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2306): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(2801): Show |
1 | a0002c0002t0001g0313 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2810): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(1181): Show |
1 | a0002c0002t0001g0352 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1190): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(65): Show |
1 | a0002c0006t0008g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(74): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3692): Show |
1 | a0002c0021t0001g0041 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3701): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3413): Show |
1 | a0002c0002t0001g0328 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3422): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(938): Show |
1 | a0001c0010t0002g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(947): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3440): Show |
1 | a0001c0005t0002g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3449): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(1460): Show |
1 | a0002c0008t0001g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(1469): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(7418): Show |
1 | a0002c0006t0008g0176 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(7427): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3017): Show |
1 | a0001c0003t0002g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3026): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(1856): Show |
1 | a0001c0001t0001g0356 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(1865): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(2396): Show |
1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1014-812_1014-811i others(2405): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(9449): Show |
1 | a0001c0004t0009g0159 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(9458): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(668): Show |
1 | a0001c0005t0002g0060 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(677): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3521): Show |
1 | a0001c0001t0006g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3530): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(2801): Show |
1 | a0002c0002t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(2810): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(3260): Show |
1 | a0002c0002t0001g0369 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(3269): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(677): Show |
1 | a0002c0002t0001g0321 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(686): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(605): Show |
1 | a0001c0005t0002g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(614): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(353): Show |
1 | a0001c0005t0002g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(362): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(578): Show |
1 | a0001c0023t0005g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(587): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(10001): Show |
1 | a0002c0002t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1014-813_1014-812i others(10010): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(38567): Show |
1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014-813_1014-812i others(38576): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | CAGGGTGG others(200): Show |
1 | a0001c0004t0003g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1014-813_1014-812i others(209): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432147 | |||||
| chr1:31432147
|
C | G | 37 | a0001c0001t0004g0008a0001c0001t0004g0026a0001c0001t0004g0027others(34): Show | 37 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1014-820C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432147 | ||||||
| chr1:31432147
|
C | T | 124 | a0001c0001t0001g0113a0001c0001t0001g0230a0001c0001t0001g0294others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1014-820C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432147 | ||||||
| chr1:31432155
|
A | AGAGGGTG others(29): Show |
1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1014-812_1014-811i others(38): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432155 | ||||||
| chr1:31432155
|
A | ATAGGGTG others(110): Show |
1 | a0001c0001t0011g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014-812_1014-811i others(119): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432155 | ||||||
| chr1:31432155
|
A | T | 5 | a0001c0001t0001g0108a0001c0001t0011g0048a0001c0004t0003g0188others(2): Show | 6 | HG01928.hp2 HG02074.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-812A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432155 | ||||||
| chr1:31432156
|
C | CAGGGTGG others(4592): Show |
1 | a0001c0003t0002g0099 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(4601): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1280): Show |
1 | a0003c0007t0002g0150 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1289): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2468): Show |
1 | a0001c0016t0002g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2477): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2126): Show |
1 | a0001c0003t0004g0265 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2135): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1190): Show |
1 | a0001c0004t0015g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1199): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(6956): Show |
1 | a0001c0004t0009g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(6965): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(335): Show |
1 | a0002c0002t0001g0335 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(137): Show |
1 | a0001c0003t0004g0246 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(146): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2774): Show |
1 | a0001c0001t0005g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2783): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1343): Show |
1 | a0001c0003t0002g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1352): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(335): Show |
1 | a0001c0003t0002g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(946): Show |
1 | a0001c0003t0004g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(955): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(8426): Show |
1 | a0001c0001t0009g0185 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(8435): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(12188): Show |
1 | a0001c0003t0009g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(12197): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1559): Show |
1 | a0001c0003t0002g0090 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1568): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(9578): Show |
1 | a0002c0006t0008g0190 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(9587): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1361): Show |
1 | a0002c0002t0001g0326 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1370): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4421): Show |
1 | a0002c0002t0001g0339 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(4430): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1118): Show |
1 | a0001c0003t0019g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1127): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(272): Show |
1 | a0001c0001t0004g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(281): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(3494): Show |
1 | a0001c0003t0002g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(3503): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2090): Show |
1 | a0001c0001t0005g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2099): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(47): Show |
1 | a0001c0001t0002g0301 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(56): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(119): Show |
1 | a0001c0001t0002g0315 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(128): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(569): Show |
1 | a0002c0002t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(578): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(641): Show |
1 | a0002c0002t0001g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(650): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(758): Show |
1 | a0002c0002t0001g0293 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(767): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(11): Show |
1 | a0001c0001t0020g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1082): Show |
1 | a0001c0010t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(1091): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4160): Show |
1 | a0002c0017t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(4169): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(515): Show |
1 | a0001c0003t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(524): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(3017): Show |
1 | a0001c0003t0002g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(3026): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(11): Show |
1 | a0001c0005t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(11): Show |
1 | a0002c0002t0006g0242 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1014-794_1014-777d others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1667): Show |
1 | a0001c0001t0005g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(1676): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(12499): Show |
1 | a0001c0004t0008g0210 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(12508): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(7652): Show |
1 | a0001c0001t0002g0331 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1014-778_1014-777i others(7661): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4016): Show |
1 | a0011c0015t0024g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4025): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(10073): Show |
1 | a0002c0002t0001g0307 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(10082): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(10991): Show |
1 | a0002c0002t0001g0324 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(11000): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1028): Show |
1 | a0002c0002t0001g0343 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1037): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4196): Show |
1 | a0001c0001t0004g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4205): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2999): Show |
1 | a0002c0002t0001g0296 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(3008): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2387): Show |
1 | a0002c0002t0001g0354 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(2396): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(6338): Show |
1 | a0001c0001t0002g0342 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1014-795_1014-794i others(6347): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(5483): Show |
1 | a0001c0003t0004g0269 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1014-795_1014-794i others(5492): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(173): Show |
1 | a0001c0003t0001g0256 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1014-795_1014-794i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(362): Show |
1 | a0001c0001t0004g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(371): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(2315): Show |
1 | a0001c0003t0004g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(2324): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(785): Show |
1 | a0001c0001t0001g0303 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(794): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(8885): Show |
1 | a0002c0002t0001g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1014-804_1014-803i others(8894): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4178): Show |
1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1014-804_1014-803i others(4187): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(1748): Show |
1 | a0001c0001t0001g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(1757): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(7157): Show |
1 | a0002c0002t0006g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(7166): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | CAGGGTGG others(4133): Show |
1 | a0001c0004t0010g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1014-804_1014-803i others(4142): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432156 | |||||
| chr1:31432156
|
C | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0302others(33): Show | 38 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1014-811C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432156 | ||||||
| chr1:31432156
|
C | T | 118 | a0001c0001t0001g0108a0001c0001t0001g0308a0001c0001t0002g0007others(115): Show | 121 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1014-811C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432156 | ||||||
| chr1:31432160
|
G | A | 3 | a0001c0001t0005g0237a0001c0001t0021g0033a0001c0004t0003g0167 | 3 | HG02080.hp2 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1014-807G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432160 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(1388): Show |
1 | a0001c0004t0003g0161 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1397): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(5105): Show |
1 | a0001c0001t0006g0340 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(5114): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(2666): Show |
1 | a0001c0001t0005g0016 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2675): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(9020): Show |
1 | a0001c0004t0003g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(9029): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(1811): Show |
1 | a0001c0004t0003g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1820): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(2000): Show |
1 | a0001c0004t0012g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2009): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(9425): Show |
1 | a0001c0001t0005g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(9434): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(173): Show |
1 | a0004c0009t0005g0229 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(1226): Show |
1 | a0001c0001t0004g0038 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1235): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(6986): Show |
1 | a0001c0004t0003g0179 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(6995): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(623): Show |
1 | a0001c0004t0003g0198 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(632): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(83): Show |
1 | a0001c0001t0004g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(92): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(3710): Show |
1 | a0001c0001t0007g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(3719): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(2000): Show |
1 | a0001c0001t0007g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2009): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(8894): Show |
1 | a0001c0001t0007g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(8903): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(2432): Show |
1 | a0001c0001t0005g0012 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(2441): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(173): Show |
1 | a0001c0003t0002g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(3809): Show |
1 | a0002c0002t0001g0330 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(3818): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ACAGGGTG others(7589): Show |
1 | a0001c0004t0010g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(7598): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | AGAGGGTG others(1316): Show |
1 | a0001c0004t0003g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1325): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | AGAGGGTG others(1757): Show |
1 | a0001c0001t0007g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1766): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | AGAGGGTG others(92): Show |
1 | a0001c0004t0003g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(101): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | AGAGGGTG others(1604): Show |
1 | a0001c0001t0005g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(1613): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432164
|
A | ATAGGGTG others(11045): Show |
1 | a0001c0001t0005g0011 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(11054): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(2036): Show |
1 | a0001c0001t0007g0025 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(2045): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(11): Show |
3 | a0001c0001t0005g0132a0001c0001t0007g0029a0001c0001t0007g0032 | 3 | HG01884.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1014-790_1014-789i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(353): Show |
1 | a0001c0001t0007g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(362): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(5915): Show |
1 | a0001c0001t0005g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5924): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(1514): Show |
1 | a0002c0002t0001g0351 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1523): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(380): Show |
1 | a0001c0001t0007g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(389): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(767): Show |
1 | a0002c0002t0001g0362 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(776): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(4025): Show |
1 | a0001c0001t0005g0021 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4034): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(4889): Show |
1 | a0001c0001t0007g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4898): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(38): Show |
1 | a0002c0011t0001g0271 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(47): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(5816): Show |
1 | a0002c0002t0001g0363 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1014-773_1014-772i others(5825): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(9524): Show |
1 | a0008c0024t0005g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1014-786_1014-785i others(9533): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | ATAGGGTG others(1685): Show |
1 | a0001c0001t0005g0024 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1014-795_1014-794i others(1694): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432164 | |||||
| chr1:31432164
|
A | T | 10 | a0001c0001t0004g0131a0001c0001t0005g0237a0001c0001t0006g0314others(7): Show | 10 | HG01517.hp1 HG02080.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014-803A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432164 | ||||||
| chr1:31432165
|
T | C | 60 | a0001c0001t0002g0344a0001c0001t0004g0141a0001c0001t0006g0289others(57): Show | 60 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1014-802T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432165 | ||||||
| chr1:31432165
|
T | CAGGGTGG others(9137): Show |
1 | a0002c0002t0001g0335 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1014-803_1014-802i others(9146): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432165 | ||||||
| chr1:31432165
|
T | CAGGGTGG others(11765): Show |
1 | a0001c0003t0007g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1014-803_1014-802i others(11774): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432165 | ||||||
| chr1:31432165
|
T | G | 11 | a0001c0001t0001g0294a0001c0001t0001g0303a0001c0001t0001g0356others(8): Show | 11 | HG00642.hp2 HG01261.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1014-802T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432165 | ||||||
| chr1:31432165
|
T | TAGGATGG others(11): Show |
1 | a0002c0002t0001g0357 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1014-799_1014-798i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(7814): Show |
1 | a0001c0004t0003g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(7823): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(1730): Show |
1 | a0002c0002t0001g0295 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(1739): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(3557): Show |
1 | a0001c0004t0003g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(3566): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(174): Show |
1 | a0001c0004t0003g0205 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(183): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(2333): Show |
1 | a0001c0004t0003g0238 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(2342): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(335): Show |
1 | a0001c0010t0002g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1014-794_1014-793i others(344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(1199): Show |
1 | a0002c0002t0001g0361 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(1208): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(11): Show |
1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(1334): Show |
1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(1343): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(533): Show |
1 | a0002c0002t0001g0280 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(542): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(20): Show |
1 | a0002c0002t0001g0350 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1014-781_1014-780i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(12071): Show |
1 | a0002c0002t0008g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(12080): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(938): Show |
1 | a0002c0006t0008g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(947): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(2207): Show |
1 | a0002c0002t0001g0323 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2216): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(3215): Show |
1 | a0002c0002t0001g0298 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(3224): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(6428): Show |
1 | a0002c0002t0023g0353 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(6437): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(2171): Show |
1 | a0001c0004t0009g0155 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2180): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(13844): Show |
1 | a0002c0002t0001g0334 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1014-773_1014-772i others(13853): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(1955): Show |
1 | a0002c0002t0001g0297 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(1964): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(1739): Show |
1 | a0001c0004t0003g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1014-795_1014-794i others(1748): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(2243): Show |
1 | a0001c0004t0003g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1014-795_1014-794i others(2252): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(506): Show |
1 | a0001c0004t0003g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1014-795_1014-794i others(515): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432165
|
T | TAGGGTGG others(3098): Show |
1 | a0002c0002t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1014-795_1014-794i others(3107): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432165 | |||||
| chr1:31432173
|
A | ATAGGGTG others(5726): Show |
1 | a0001c0004t0016g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(5735): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432173 | |||||
| chr1:31432173
|
A | ATAGGGTG others(812): Show |
1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(821): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432173 | |||||
| chr1:31432173
|
A | ATAGGGTG others(263): Show |
1 | a0007c0018t0013g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(272): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432173 | |||||
| chr1:31432173
|
A | T | 3 | a0001c0001t0011g0048a0001c0001t0018g0222a0002c0002t0001g0274 | 3 | HG03098.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1014-794A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432173 | ||||||
| chr1:31432174
|
T | C | 76 | a0001c0001t0001g0110a0001c0001t0001g0116a0001c0001t0002g0007others(73): Show | 78 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1014-793T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432174 | ||||||
| chr1:31432174
|
T | CAGGGTGG others(5150): Show |
1 | a0001c0005t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(5159): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432174 | ||||||
| chr1:31432174
|
T | G | 1 | a0002c0002t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1014-793T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432174 | ||||||
| chr1:31432174
|
T | GAGGGTGG others(8939): Show |
1 | a0002c0002t0001g0292 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1014-794_1014-793i others(8948): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432174 | ||||||
| chr1:31432174
|
T | TAGAGTGG others(1424): Show |
1 | a0001c0004t0003g0192 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1014-791_1014-790i others(1433): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGATGG others(515): Show |
1 | a0002c0002t0001g0365 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1014-790_1014-789i others(524): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGATGG others(173): Show |
1 | a0002c0002t0004g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014-790_1014-789i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGC others(7436): Show |
1 | a0001c0001t0002g0333 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1014-787_1014-786i others(7445): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2): Show |
14 | a0001c0003t0002g0001a0001c0003t0002g0053a0001c0003t0002g0064others(11): Show | 14 | HG00099.hp1 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014-785_1014-784i others(11): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1379): Show |
1 | a0002c0002t0001g0287 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(1388): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1640): Show |
1 | a0001c0004t0003g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(1649): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(695): Show |
1 | a0001c0005t0002g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(704): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3413): Show |
1 | a0001c0003t0002g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(3422): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2639): Show |
1 | a0001c0004t0003g0166 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(2648): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(740): Show |
1 | a0001c0001t0001g0304 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(749): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(731): Show |
1 | a0001c0004t0003g0165 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(740): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3395): Show |
1 | a0001c0004t0003g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(3404): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1532): Show |
1 | a0001c0004t0003g0215 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(1541): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(920): Show |
1 | a0001c0003t0004g0253 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(929): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(758): Show |
1 | a0001c0004t0003g0196 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1014-785_1014-784i others(767): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(13520): Show |
1 | a0002c0006t0008g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1014-785_1014-784i others(13529): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(20): Show |
2 | a0001c0004t0003g0195a0001c0004t0003g0197 | 2 | NA18962.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1014-781_1014-780i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1559): Show |
1 | a0001c0004t0003g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1014-781_1014-780i others(1568): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3557): Show |
1 | a0001c0003t0002g0052 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1014-781_1014-780i others(3566): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(11): Show |
1 | a0001c0004t0010g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(20): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3800): Show |
1 | a0001c0004t0003g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(3809): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(9065): Show |
1 | a0001c0004t0003g0202 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(9074): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1775): Show |
1 | a0001c0004t0003g0151 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1784): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(18407): Show |
1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(18416): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(461): Show |
1 | a0001c0004t0003g0180 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(470): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1847): Show |
1 | a0001c0001t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1856): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1487): Show |
1 | a0001c0003t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1496): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(5213): Show |
1 | a0001c0004t0003g0178 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5222): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(5924): Show |
1 | a0001c0004t0003g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5933): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2216): Show |
1 | a0001c0001t0001g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2225): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(5663): Show |
1 | a0001c0004t0003g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5672): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(6779): Show |
1 | a0001c0001t0002g0345 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(6788): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1154): Show |
1 | a0001c0004t0003g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1163): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(299): Show |
1 | a0001c0003t0002g0091 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(308): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(20): Show |
1 | a0001c0003t0002g0088 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(335): Show |
1 | a0002c0002t0001g0346 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(344): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2000): Show |
1 | a0001c0003t0002g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2009): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2351): Show |
1 | a0001c0004t0003g0186 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2360): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(164): Show |
1 | a0001c0004t0003g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(173): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3107): Show |
1 | a0002c0011t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(3116): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1046): Show |
1 | a0001c0004t0003g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1055): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(5762): Show |
1 | a0001c0001t0006g0337 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5771): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(5672): Show |
1 | a0001c0004t0003g0199 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(5681): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(6023): Show |
1 | a0001c0004t0003g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1014-773_1014-772i others(6032): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2126): Show |
1 | a0002c0002t0001g0341 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(2135): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(875): Show |
1 | a0001c0004t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1014-786_1014-785i others(884): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(20): Show |
1 | a0001c0004t0003g0181 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1014-786_1014-785i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(1568): Show |
1 | a0001c0004t0003g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1014-786_1014-785i others(1577): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(3458): Show |
1 | a0001c0001t0006g0314 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1014-786_1014-785i others(3467): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(4988): Show |
1 | a0006c0020t0002g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1014-786_1014-785i others(4997): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432174
|
T | TAGGGTGG others(2180): Show |
1 | a0001c0004t0003g0214 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1014-786_1014-785i others(2189): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432174 | |||||
| chr1:31432182
|
A | ATAGGGTG others(4583): Show |
1 | a0001c0001t0005g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4592): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432182 | |||||
| chr1:31432183
|
T | C | 5 | a0001c0003t0002g0119a0001c0003t0002g0122a0001c0004t0003g0181others(2): Show | 5 | HG01346.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-784T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432183 | ||||||
| chr1:31432183
|
T | G | 2 | a0001c0005t0002g0068a0002c0002t0001g0274 | 2 | NA19091.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1014-784T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432183 | ||||||
| chr1:31432183
|
T | TAGGGTGG others(2981): Show |
1 | a0001c0004t0003g0143 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2990): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432183 | |||||
| chr1:31432183
|
T | TAGGGTGG others(173): Show |
1 | a0001c0001t0004g0241 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(182): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432183 | |||||
| chr1:31432183
|
T | TAGGGTGG others(20): Show |
1 | a0001c0001t0004g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014-773_1014-772i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432183 | |||||
| chr1:31432183
|
T | TAGGGTGG others(146): Show |
1 | a0001c0001t0018g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(155): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432183 | |||||
| chr1:31432184
|
A | AGGGTGGA others(4992): Show |
1 | a0001c0004t0003g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(5001): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432184 | |||||
| chr1:31432187
|
G | A | 24 | a0001c0001t0001g0303a0001c0001t0001g0308a0001c0001t0001g0356others(21): Show | 24 | HG00544.hp2 HG00609.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.1014-780G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432187 | ||||||
| chr1:31432187
|
G | GTGGACAG others(1784): Show |
1 | a0001c0003t0004g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1793): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGACAG others(191): Show |
1 | a0001c0003t0004g0255 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(200): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(533): Show |
1 | a0001c0003t0004g0263 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(542): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(929): Show |
1 | a0001c0003t0004g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(938): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(884): Show |
1 | a0001c0003t0004g0261 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(893): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(2385): Show |
1 | a0001c0003t0004g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2394): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(8786): Show |
1 | a0001c0003t0004g0257 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(8795): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(2315): Show |
1 | a0001c0003t0004g0268 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(2324): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(4268): Show |
1 | a0001c0003t0004g0264 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(4277): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(1361): Show |
1 | a0001c0003t0001g0250 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(1370): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(6185): Show |
1 | a0001c0001t0011g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1014-777_1014-776i others(6194): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGATAG others(74): Show |
1 | a0001c0003t0004g0244 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1014-777_1014-776i others(83): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432187
|
G | GTGGTTAG others(6014): Show |
1 | a0001c0001t0011g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1014-773_1014-772i others(6023): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432187 | |||||
| chr1:31432191
|
T | A | 6 | a0001c0001t0007g0002a0001c0004t0009g0144a0001c0005t0002g0068others(3): Show | 7 | HG00280.hp2 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014-776T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432191 | ||||||
| chr1:31432192
|
T | C | 1 | a0003c0007t0002g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1014-775T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432192 | ||||||
| chr1:31432192
|
T | G | 3 | a0001c0001t0007g0002a0002c0002t0001g0274a0002c0002t0001g0282 | 4 | HG02630.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-775T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432192 | ||||||
| chr1:31432192
|
T | TAGGGTGG others(380): Show |
1 | a0002c0002t0002g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(389): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432192 | |||||
| chr1:31432192
|
T | TAGGGTGG others(20): Show |
1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1014-773_1014-772i others(29): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432192 | |||||
| chr1:31432195
|
A | G | 13 | a0001c0001t0001g0113a0001c0001t0007g0002a0001c0003t0002g0119others(10): Show | 14 | HG00280.hp2 HG01517.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014-772A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432195 | ||||||
| chr1:31432200
|
A | T | 1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1014-767A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432200 | ||||||
| chr1:31432201
|
G | C | 4 | a0001c0004t0003g0161a0001c0004t0009g0144a0003c0007t0002g0138others(1): Show | 4 | HG00280.hp2 HG00621.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014-766G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432201 | ||||||
| chr1:31432201
|
G | T | 1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1014-766G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432201 | ||||||
| chr1:31432204
|
A | G | 10 | a0001c0001t0004g0279a0001c0004t0003g0161a0001c0004t0009g0144others(7): Show | 10 | HG00280.hp2 HG00621.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1014-763A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432204 | ||||||
| chr1:31432204
|
A | GGTGGACA others(6950): Show |
1 | a0001c0001t0007g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1014-764_1014-763i others(6959): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432204 | ||||||
| chr1:31432210
|
C | G | 5 | a0001c0005t0002g0068a0002c0002t0001g0274a0002c0002t0001g0282others(2): Show | 5 | HG02630.hp2 HG03098.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-757C>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432210 | ||||||
| chr1:31432219
|
G | C | 5 | a0001c0003t0002g0052a0001c0010t0002g0085a0001c0010t0002g0094others(2): Show | 5 | HG00280.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1014-748G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432219 | ||||||
| chr1:31432219
|
G | GGGTGGAC others(2754): Show |
1 | a0003c0007t0002g0139 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1014-748_1014-747i others(2763): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432219 | ||||||
| chr1:31432254
|
G | T | 1 | a0001c0005t0002g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1014-713G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432254 | ||||||
| chr1:31432300
|
C | CCTT | 33 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0308others(30): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1014-666_1014-664d others(5): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 31432300 | |||||
| chr1:31432326
|
A | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0230a0001c0001t0001g0294others(92): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1014-641A>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432326 | ||||||
| chr1:31432360
|
A | G | 1 | a0002c0002t0004g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014-607A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432360 | ||||||
| chr1:31432361
|
T | G | 1 | a0002c0002t0004g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014-606T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432361 | ||||||
| chr1:31432415
|
A | G | 1 | a0001c0004t0009g0144 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1014-552A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432415 | ||||||
| chr1:31432435
|
A | C | 11 | a0001c0001t0006g0289a0001c0001t0006g0314a0001c0001t0006g0337others(8): Show | 11 | HG01943.hp1 HG02083.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.1014-532A>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432435 | ||||||
| chr1:31432465
|
G | T | 1 | a0007c0018t0013g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1014-502G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432465 | ||||||
| chr1:31432505
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1014-462C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432505 | ||||||
| chr1:31432528
|
T | G | 1 | a0002c0002t0006g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1014-439T>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432528 | ||||||
| chr1:31432817
|
G | A | 2 | a0003c0007t0004g0162a0003c0007t0004g0163 | 2 | HG01934.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1014-150G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432817 | ||||||
| chr1:31432875
|
C | T | 1 | a0001c0003t0002g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1014-92C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432875 | ||||||
| chr1:31432883
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(246): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1014-84T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432883 | ||||||
| chr1:31432905
|
T | C | 2 | a0001c0001t0004g0010a0001c0001t0004g0038 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1014-62T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432905 | ||||||
| chr1:31432920
|
G | C | 55 | a0001c0001t0006g0289a0001c0001t0006g0314a0001c0001t0006g0320others(52): Show | 55 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1014-47G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | chr1 | 31432920 | ||||||
| chr1:31433196
|
G | A | 3 | a0002c0002t0001g0327a0002c0002t0001g0328a0002c0002t0001g0336 | 3 | HG00558.hp1 HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1232+11G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433196 | ||||||
| chr1:31433230
|
G | A | 39 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0113others(36): Show | 40 | HG01070.hp1 HG01243.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.1232+45G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433230 | ||||||
| chr1:31433253
|
G | A | 29 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0356others(26): Show | 29 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1232+68G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433253 | ||||||
| chr1:31433292
|
G | C | 1 | a0002c0008t0017g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1232+107G>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433292 | ||||||
| chr1:31433449
|
C | T | 1 | a0001c0003t0002g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1232+264C>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433449 | ||||||
| chr1:31433745
|
G | A | 4 | a0001c0001t0011g0046a0001c0001t0011g0048a0001c0001t0011g0071others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233-319G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433745 | ||||||
| chr1:31433979
|
G | T | 8 | a0001c0001t0004g0008a0001c0001t0004g0026a0001c0001t0004g0027others(5): Show | 8 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-85G>T | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31433979 | ||||||
| chr1:31434035
|
A | G | 308 | a0001c0001t0001g0005a0001c0001t0001g0108a0001c0001t0001g0110others(305): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1233-29A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31434035 |