Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 456 | 252 | 76 | 42 | 99 | 9 | 26 | 76 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0002 | 1/0 | 455 | 102 | 18 | 19 | 47 | 1 | 16 | 32 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(450): Show |
chr1 | 31408213 | 31439678 |
| a0003 | 0/1 | 456 | 11 | 1 | 5 | 0 | 2 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0004 | 0/0 | 456 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0005 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0006 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0007 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0008 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(450): Show |
chr1 | 31408213 | 31439678 |
| a0009 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0010 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| a0011 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | MGACL others(451): Show |
chr1 | 31408213 | 31439678 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1368 | 87 | 55 | 12 | 11 | 5 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0003 | 0/0 | 1368 | 73 | 10 | 15 | 42 | 2 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0004 | 0/0 | 1368 | 63 | 7 | 5 | 37 | 1 | 13 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0005 | 0/0 | 1368 | 19 | 0 | 7 | 9 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0010 | 0/0 | 1368 | 4 | 0 | 3 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0014 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0016 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0018 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0023 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0024 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0001c0026 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0002 | 1/0 | 1365 | 79 | 14 | 13 | 40 | 0 | 11 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0006 | 0/0 | 1365 | 12 | 1 | 3 | 6 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0008 | 0/0 | 1365 | 5 | 3 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0011 | 0/0 | 1365 | 4 | 0 | 1 | 0 | 1 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0017 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0002c0021 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0003c0007 | 0/1 | 1368 | 11 | 1 | 5 | 0 | 2 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0004c0009 | 0/0 | 1368 | 4 | 3 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0005c0019 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0006c0020 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0007c0025 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0008c0022 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1360): Show |
chr1 | 31408213 | 31439678 | ||
| a0009c0013 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0010c0015 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
chr1 | 31408213 | 31439678 | ||
| a0011c0012 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | ATGGG others(1363): Show |
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 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0002 | 0/0 | 1903 | 11 | 0 | 1 | 5 | 3 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0004 | 0/0 | 1903 | 19 | 16 | 2 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0005 | 0/0 | 1903 | 15 | 14 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0006 | 0/0 | 1903 | 5 | 0 | 2 | 2 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0007 | 0/0 | 1903 | 13 | 13 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0009 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0011 | 0/0 | 1903 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0018 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0019 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0001t0020 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0001 | 0/0 | 1903 | 7 | 1 | 1 | 5 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0002 | 0/0 | 1903 | 42 | 7 | 14 | 15 | 2 | 4 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0004 | 0/0 | 1903 | 21 | 0 | 0 | 21 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0007 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0009 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0003t0021 | 0/0 | 1890 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1885): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0003 | 0/0 | 1903 | 46 | 0 | 1 | 35 | 1 | 9 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0008 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0009 | 0/0 | 1903 | 6 | 4 | 1 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0010 | 0/0 | 1903 | 6 | 0 | 2 | 1 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0012 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0014 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0015 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0004t0016 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0005t0002 | 0/0 | 1903 | 19 | 0 | 7 | 9 | 0 | 3 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0010t0002 | 0/0 | 1903 | 4 | 0 | 3 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0014t0009 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0016t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0018t0013 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0023t0005 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0024t0005 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0001c0026t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0001 | 0/0 | 1900 | 67 | 7 | 13 | 36 | 0 | 11 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0002 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0004 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0006 | 1/0 | 1900 | 7 | 5 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0008 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0022 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0002t0024 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0006t0003 | 0/0 | 1900 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0006t0006 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0006t0008 | 0/0 | 1900 | 9 | 0 | 1 | 6 | 0 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0008t0001 | 0/0 | 1900 | 4 | 2 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0008t0017 | 0/0 | 1900 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0011t0001 | 0/0 | 1900 | 4 | 0 | 1 | 0 | 1 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0017t0001 | 0/0 | 1900 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0002c0021t0001 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0003c0007t0002 | 0/1 | 1903 | 9 | 0 | 4 | 0 | 2 | 2 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0003c0007t0004 | 0/0 | 1903 | 2 | 1 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0004c0009t0004 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0004c0009t0005 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0004c0009t0006 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0005c0019t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0006c0020t0002 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0007c0025t0002 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0008c0022t0001 | 0/0 | 1900 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1895): Show |
chr1 | 31408213 | 31439678 |
| a0009c0013t0002 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0010c0015t0023 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| a0011c0012t0002 | 0/0 | 1903 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | GAGGT others(1898): Show |
chr1 | 31408213 | 31439678 |
| actghapid | grch38/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 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0002g0362 | 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 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0117 | 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 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0138 | 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 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0004g0169 | 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 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0005g0134 | 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 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0019g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0001t0020g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0001g0258 | 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 |
| a0001c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0002g0296 | 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 |
| a0001c0003t0004g0248 | 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 |
| a0001c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0004g0251 | 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 |
| a0001c0003t0004g0254 | 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 |
| a0001c0003t0004g0256 | 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 |
| a0001c0003t0004g0260 | 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 |
| a0001c0003t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0003t0021g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0160 | 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 |
| a0001c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0163 | 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 | 1 | 0 | 0 | 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 |
| a0001c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0176 | 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 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0185 | 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 |
| a0001c0004t0003g0187 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0004t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0204 | 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 |
| a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0003g0230 | 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 |
| a0001c0004t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0004t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0012g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0004t0016g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0005t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0010t0002g0079 | 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 |
| a0001c0014t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0016t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0018t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0023t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0001c0024t0005g0087 | 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 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0278 | 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 |
| a0002c0002t0001g0281 | 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 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0304 | 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 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0345 | 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 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0006g0171 | 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 |
| a0002c0002t0006g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0022g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0002t0024g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0003g0221 | 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 |
| a0002c0006t0008g0157 | 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 |
| a0002c0006t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0006t0008g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0008t0017g0145 | 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 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0011t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0017t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0002c0021t0001g0016 | 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 |
| a0003c0007t0002g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0003c0007t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0003c0007t0004g0148 | 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 |
| a0004c0009t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0004c0009t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0005c0019t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0006c0020t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0007c0025t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0008c0022t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0009c0013t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0010c0015t0023g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| a0011c0012t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | a0005 | c0019 | t0002 | g0037 | EUR | GBR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00280 | hp2 | a0003 | c0007 | t0002 | g0143 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0018 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00323 | hp2 | a0002 | c0011 | t0001 | g0270 | EUR | FIN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00408 | hp2 | a0001 | c0003 | t0004 | g0261 | 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 | g0059 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00544 | hp1 | a0002 | c0006 | t0008 | g0219 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00544 | hp2 | a0001 | c0004 | t0009 | g0175 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00597 | hp1 | a0001 | c0004 | t0003 | g0186 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00597 | hp2 | a0001 | c0005 | t0002 | g0011 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00609 | hp1 | a0001 | c0003 | t0004 | g0260 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00621 | hp1 | a0001 | c0004 | t0003 | g0144 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00642 | hp1 | a0002 | c0006 | t0008 | g0220 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00673 | hp1 | a0002 | c0006 | t0008 | g0202 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00673 | hp2 | a0001 | c0004 | t0003 | g0167 | EAS | CHS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0356 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0121 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0047 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0029 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00741 | hp1 | a0001 | c0005 | t0002 | g0031 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG00741 | hp2 | a0003 | c0007 | t0002 | g0151 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01069 | hp2 | a0001 | c0004 | t0009 | g0223 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0023 | 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 | g0136 | 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 | g0045 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0040 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0046 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01167 | hp1 | a0003 | c0007 | t0002 | g0173 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0007 | 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 | g0007 | 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 | g0149 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0122 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0071 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01243 | hp1 | a0002 | c0006 | t0003 | g0213 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01243 | hp2 | a0004 | c0009 | t0005 | g0211 | AMR | PUR | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0036 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01257 | hp1 | a0001 | c0004 | t0008 | g0222 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0065 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01261 | hp1 | a0001 | c0010 | t0002 | g0050 | 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 | g0153 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01346 | hp2 | a0002 | c0011 | t0001 | g0271 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01358 | hp1 | a0001 | c0010 | t0002 | g0062 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01358 | hp2 | a0001 | c0005 | t0002 | g0033 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01361 | hp1 | a0002 | c0008 | t0001 | g0048 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0358 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01433 | hp1 | a0001 | c0004 | t0010 | g0182 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0307 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0361 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0041 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01517 | hp1 | a0003 | c0007 | t0002 | g0152 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01884 | hp2 | a0002 | c0008 | t0001 | g0124 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01891 | hp2 | a0002 | c0008 | t0001 | g0125 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01928 | hp1 | a0001 | c0005 | t0002 | g0032 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01928 | hp2 | a0002 | c0006 | t0003 | g0221 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01934 | hp1 | a0003 | c0007 | t0004 | g0147 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0308 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0363 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01952 | hp1 | a0001 | c0005 | t0002 | g0030 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01952 | hp2 | a0001 | c0004 | t0010 | g0195 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01981 | hp1 | a0001 | c0010 | t0002 | g0079 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0357 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02004 | hp2 | a0002 | c0008 | t0001 | g0020 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02015 | hp1 | a0002 | c0006 | t0008 | g0157 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02015 | hp2 | a0001 | c0004 | t0003 | g0141 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02040 | hp1 | a0001 | c0005 | t0002 | g0035 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0156 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02055 | hp2 | a0002 | c0002 | t0006 | g0171 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0161 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02071 | hp1 | a0001 | c0003 | t0004 | g0248 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02071 | hp2 | a0001 | c0004 | t0003 | g0165 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02074 | hp2 | a0001 | c0004 | t0003 | g0154 | 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 | g0163 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0185 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02129 | hp1 | a0008 | c0022 | t0001 | g0277 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02135 | hp1 | a0001 | c0003 | t0004 | g0262 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02135 | hp2 | a0001 | c0004 | t0003 | g0191 | EAS | KHV | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0229 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0364 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0078 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | CDX | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0344 | EAS | CDX | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02257 | hp1 | a0001 | c0004 | t0015 | g0234 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02257 | hp2 | a0002 | c0002 | t0006 | g0170 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0106 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0070 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0318 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02280 | hp2 | a0003 | c0007 | t0004 | g0148 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02300 | hp1 | a0001 | c0004 | t0003 | g0196 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0313 | AMR | PEL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0091 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02572 | hp1 | a0001 | c0004 | t0009 | g0132 | 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 | g0215 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0139 | 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 | g0092 | 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 | g0281 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0337 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0297 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0184 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0319 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02717 | hp1 | a0004 | c0009 | t0006 | g0210 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02723 | hp1 | a0001 | c0004 | t0016 | g0212 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02723 | hp2 | a0001 | c0001 | t0019 | g0101 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02735 | hp1 | a0001 | c0004 | t0003 | g0160 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0038 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02738 | hp1 | a0001 | c0003 | t0002 | g0049 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02738 | hp2 | a0001 | c0005 | t0002 | g0076 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0115 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0096 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0095 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0142 | 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 | g0131 | 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 | g0110 | 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 | g0099 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0093 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0111 | 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 | g0102 | 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 | a0001 | c0024 | t0005 | g0087 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0327 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03017 | hp2 | a0001 | c0004 | t0003 | g0197 | 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 | g0104 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0118 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0273 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03130 | hp1 | a0001 | c0004 | t0009 | g0209 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03209 | hp1 | a0001 | c0023 | t0005 | g0089 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03225 | hp1 | a0001 | c0014 | t0009 | g0225 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0216 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03239 | hp2 | a0001 | c0016 | t0002 | g0081 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03453 | hp1 | a0001 | c0018 | t0013 | g0168 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0072 | 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 | g0224 | 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 | g0179 | 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 | g0325 | 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 | g0085 | AFR | ESN | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0088 | 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 | g0214 | AFR | GWD | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0094 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03654 | hp1 | a0001 | c0004 | t0003 | g0194 | 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 | g0155 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03669 | hp2 | a0001 | c0004 | t0010 | g0233 | SAS | PJL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03688 | hp1 | a0001 | c0004 | t0010 | g0235 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0335 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03831 | hp1 | a0001 | c0004 | t0003 | g0230 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03831 | hp2 | a0002 | c0006 | t0008 | g0231 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0042 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0323 | 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 | g0359 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04115 | hp1 | a0001 | c0004 | t0012 | g0200 | 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 | g0080 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0328 | SAS | BEB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04199 | hp2 | a0001 | c0005 | t0002 | g0034 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04204 | hp1 | a0002 | c0017 | t0001 | g0082 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04204 | hp2 | a0001 | c0005 | t0002 | g0028 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04228 | hp1 | a0001 | c0004 | t0003 | g0208 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0331 | SAS | STU | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0276 | 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 | g0010 | EAS | CHB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | CHB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0098 | AFR | YRI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18939 | hp2 | a0001 | c0003 | t0004 | g0256 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18940 | hp1 | a0001 | c0004 | t0003 | g0204 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18940 | hp2 | a0009 | c0013 | t0002 | g0066 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18943 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0198 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18946 | hp2 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18947 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18947 | hp2 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18952 | hp1 | a0001 | c0003 | t0004 | g0255 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18952 | hp2 | a0002 | c0006 | t0008 | g0218 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18953 | hp1 | a0001 | c0005 | t0002 | g0014 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18959 | hp2 | a0001 | c0004 | t0003 | g0188 | 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 | g0296 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18962 | hp1 | a0001 | c0003 | t0004 | g0244 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18962 | hp2 | a0001 | c0004 | t0003 | g0174 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18963 | hp1 | a0002 | c0002 | t0008 | g0227 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18970 | hp2 | a0001 | c0004 | t0003 | g0159 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18971 | hp1 | a0001 | c0003 | t0004 | g0267 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18971 | hp2 | a0001 | c0003 | t0004 | g0265 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18979 | hp1 | a0002 | c0021 | t0001 | g0016 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18981 | hp1 | a0001 | c0003 | t0004 | g0249 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18983 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0164 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18986 | hp1 | a0001 | c0003 | t0004 | g0251 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18991 | hp2 | a0001 | c0004 | t0003 | g0176 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0178 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18995 | hp2 | a0001 | c0004 | t0003 | g0189 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18997 | hp1 | a0001 | c0004 | t0003 | g0203 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0269 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18999 | hp1 | a0001 | c0004 | t0003 | g0158 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19000 | hp1 | a0001 | c0004 | t0003 | g0226 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19000 | hp2 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19003 | hp1 | a0001 | c0003 | t0004 | g0259 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19003 | hp2 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19004 | hp2 | a0001 | c0003 | t0004 | g0263 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19005 | hp1 | a0002 | c0002 | t0006 | g0306 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19005 | hp2 | a0002 | c0002 | t0022 | g0316 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19010 | hp1 | a0001 | c0003 | t0004 | g0266 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19010 | hp2 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19012 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0172 | 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 | g0053 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19060 | hp1 | a0010 | c0015 | t0023 | g0077 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19060 | hp2 | a0001 | c0004 | t0003 | g0207 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19063 | hp1 | a0002 | c0002 | t0024 | g0346 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19063 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19064 | hp2 | a0001 | c0004 | t0003 | g0187 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19066 | hp2 | a0002 | c0006 | t0008 | g0217 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19067 | hp2 | a0001 | c0004 | t0003 | g0199 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19068 | hp1 | a0001 | c0004 | t0003 | g0181 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0063 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19070 | hp1 | a0001 | c0003 | t0004 | g0250 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0360 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19074 | hp1 | a0001 | c0004 | t0003 | g0205 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19076 | hp2 | a0001 | c0003 | t0021 | g0247 | 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 | g0351 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19079 | hp1 | a0001 | c0004 | t0003 | g0162 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19081 | hp2 | a0001 | c0005 | t0002 | g0009 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19084 | hp1 | a0001 | c0004 | t0003 | g0166 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19085 | hp2 | a0002 | c0006 | t0008 | g0190 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19087 | hp1 | a0001 | c0003 | t0004 | g0268 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19089 | hp1 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19089 | hp2 | a0001 | c0003 | t0004 | g0253 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19090 | hp1 | a0001 | c0004 | t0010 | g0201 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19091 | hp1 | a0001 | c0005 | t0002 | g0074 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0254 | EAS | JPT | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0022 | 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 | g0140 | AFR | ASW | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | ASW | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20752 | hp1 | a0011 | c0012 | t0002 | g0044 | 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 | g0183 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0039 | EUR | TSI | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20905 | hp1 | a0001 | c0004 | t0003 | g0180 | 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 | a0007 | c0025 | t0002 | g0043 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0061 | AMR | CLM | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02109 | hp2 | a0001 | c0003 | t0009 | g0146 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG02559 | hp2 | a0002 | c0008 | t0017 | g0145 | AFR | ACB | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | MSL | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | USA | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0282 | 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 | g0075 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| homoSapiens | chm13v2 | a0003 | c0007 | t0002 | g0126 | REF | REF | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0006 | g0113 | REF | REF | SERINC2_chr1_31408213_31439678 | SERINC2 | chr1 | 31408213 | 31439678 |
| view | 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 | a0011 | 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 | a0009 | 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 | a0007 | 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 | a0010 | 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 | 10 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(7): 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 | a0008 | 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 | a0005 | 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 | 9 | a0001 a0003 a0004 others(6): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): 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 | a0001 | 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 | a0001 | 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 |
| view | 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 | a0001c0004 a0001c0014 a0002c0006 |
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 | a0001c0003 a0001c0005 a0001c0010 others(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 | a0001c0010 a0007c0025 |
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 | a0001c0005 a0002c0021 a0010c0015 |
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 | a0001c0016 a0002c0017 |
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 |
| view | 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 | a0002c0002t0024 | 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 | a0010c0015t0023 | 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 | a0002c0002t0024 | 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 | a0002c0002t0024 | 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 | a0002c0002t0024 | 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 | a0002c0002t0024 | 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 | a0002c0002t0024 | 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 | a0002c0002t0022 a0002c0002t0024 |
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 | a0001c0001t0009 a0001c0003t0009 a0001c0004t0003 others(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 | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(30): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0001t0011 a0001c0004t0016 |
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 | a0001c0003t0021 | 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 | a0001c0003t0001 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0003t0021 | 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 | a0001c0001t0019 | 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 | a0001c0001t0018 a0001c0004t0015 |
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 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0010 others(13): Show |
100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): 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 | 37 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(34): 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 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0019 others(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 | a0001c0001t0020 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472G>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 10/10 | 472 | chr1 | 31434671 |
| view | 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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | 223 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(220): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | 251 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(248): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): 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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | a0001c0001t0005g0236 a0001c0001t0005g0237 |
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 | a0001c0026t0002g0366 a0002c0002t0001g0369 |
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 | a0002c0002t0001g0283 a0002c0002t0001g0368 |
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 | a0002c0002t0001g0284 a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0001c0004t0003g0230 a0001c0010t0002g0123 a0002c0006t0008g0231 |
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 | a0001c0004t0003g0230 a0001c0010t0002g0123 a0002c0006t0008g0231 others(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 | a0001c0001t0001g0232 a0001c0001t0004g0008 a0001c0001t0004g0130 others(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 | a0001c0001t0004g0137 a0001c0004t0003g0187 a0001c0004t0003g0205 others(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 | 15 | a0001c0001t0004g0150 a0001c0004t0003g0156 a0001c0004t0003g0165 others(12): Show |
15 | HG00741.hp2 HG01069.hp2 HG01175.hp1 others(12): 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 | a0001c0001t0005g0236 a0001c0001t0009g0228 a0001c0001t0009g0229 others(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 | a0001c0001t0002g0326 a0001c0001t0005g0237 a0001c0001t0006g0318 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0003t0001g0257 others(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 | a0001c0001t0001g0290 a0001c0001t0001g0310 a0001c0001t0001g0311 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0287 a0001c0001t0002g0294 others(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 | a0001c0001t0001g0342 a0001c0003t0004g0251 a0001c0003t0021g0247 others(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 | a0001c0003t0004g0259 a0002c0002t0001g0300 |
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 | a0002c0002t0001g0281 a0002c0002t0001g0341 a0002c0002t0001g0352 others(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 | a0002c0002t0001g0353 | 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 | a0001c0001t0011g0116 a0001c0003t0002g0053 a0001c0003t0002g0058 others(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 | a0001c0003t0002g0040 a0001c0003t0002g0067 a0001c0005t0002g0028 others(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 | a0001c0001t0001g0119 a0001c0003t0002g0039 a0001c0003t0002g0041 others(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 | a0001c0001t0001g0120 a0001c0003t0001g0051 a0001c0003t0001g0114 others(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 | a0001c0001t0001g0073 a0001c0001t0007g0002 a0001c0003t0002g0018 others(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 | a0001c0001t0001g0072 a0001c0003t0002g0049 a0001c0003t0002g0065 others(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 | a0011c0012t0002g0044 | 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 | a0001c0003t0002g0080 a0001c0003t0002g0092 a0001c0003t0002g0093 others(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 | a0001c0003t0002g0094 | 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 | a0001c0001t0004g0008 a0001c0001t0004g0130 a0002c0006t0006g0128 others(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 | a0001c0001t0004g0008 a0001c0001t0004g0130 a0001c0003t0001g0245 others(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 | a0001c0003t0004g0254 a0001c0003t0004g0255 a0001c0004t0003g0216 others(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 | a0001c0001t0004g0169 a0001c0001t0005g0236 a0001c0001t0005g0237 others(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 |
23 | a0001c0001t0004g0150 a0001c0003t0009g0146 a0001c0004t0003g0154 others(20): Show |
24 | HG00673.hp2 HG00741.hp2 HG01175.hp1 others(21): 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 | a0001c0004t0003g0144 a0002c0002t0004g0142 a0002c0008t0017g0145 others(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 | a0001c0001t0004g0133 a0001c0001t0004g0135 a0001c0001t0004g0136 others(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 | a0001c0004t0003g0230 | 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 | a0002c0006t0008g0231 | 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 | a0001c0003t0002g0121 | 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 | a0001c0003t0002g0122 | 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 | a0001c0003t0004g0269 | 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 | a0001c0001t0001g0232 a0001c0004t0010g0233 |
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 | a0001c0004t0015g0234 | 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 | a0001c0004t0010g0235 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0362 others(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 | a0002c0002t0001g0281 | 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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | a0001c0004t0003g0208 | 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 | 223 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(220): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0003t0004g0243 a0001c0003t0004g0244 |
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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0114 | 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 | a0001c0004t0009g0209 | 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 | a0002c0002t0008g0227 | 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 | 352 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(349): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): 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 | a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0001c0003t0002g0121 | 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 | a0001c0004t0003g0141 a0001c0004t0003g0167 |
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 | a0001c0003t0009g0146 a0001c0018t0013g0168 |
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 | 248 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(245): Show |
253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): 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 | a0001c0001t0007g0098 | 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 | a0001c0001t0005g0097 | 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 | 248 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(245): Show |
253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0004g0133 a0001c0001t0004g0135 a0001c0001t0004g0136 others(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 | a0001c0005t0002g0009 a0001c0005t0002g0010 a0001c0005t0002g0011 others(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 | a0001c0004t0003g0141 a0001c0004t0003g0144 a0001c0004t0003g0154 others(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 | a0001c0003t0002g0296 a0002c0002t0001g0298 a0002c0002t0001g0303 |
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 | a0001c0003t0002g0091 a0001c0003t0002g0092 a0001c0003t0002g0093 others(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 | a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0002c0002t0008g0227 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0086 others(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 | a0001c0001t0004g0117 a0001c0001t0011g0115 a0001c0001t0011g0116 others(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 | a0001c0004t0003g0174 | 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 | a0001c0016t0002g0081 a0002c0017t0001g0082 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0342 a0001c0001t0004g0008 a0001c0001t0004g0130 others(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 | 15 | a0001c0001t0004g0140 a0001c0001t0004g0150 a0001c0001t0005g0237 others(12): Show |
15 | HG00741.hp2 HG01346.hp1 HG01517.hp1 others(12): 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 | a0001c0001t0001g0232 a0001c0004t0003g0176 a0001c0004t0003g0216 others(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 | a0001c0004t0003g0141 a0001c0004t0003g0154 a0001c0004t0003g0155 others(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 | a0001c0004t0003g0144 a0001c0004t0003g0165 a0001c0004t0003g0166 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0003t0004g0265 | 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 | 212 | a0001c0001t0001g0232 a0001c0001t0001g0310 a0001c0001t0001g0311 others(209): Show |
216 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(213): 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0005g0083 a0001c0001t0005g0084 a0001c0001t0005g0086 others(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 | a0001c0004t0003g0177 a0001c0004t0003g0178 |
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 | a0001c0004t0009g0209 | 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 | a0001c0003t0007g0075 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0009g0146 | 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 | a0001c0004t0009g0209 | 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 | a0002c0002t0001g0351 | 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 | a0002c0002t0001g0351 | 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 | a0002c0002t0001g0351 | 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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | 219 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(216): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.40-4392T>A | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31419301 | |||||||
| chr1:31419345 | C | T | 35 | a0001c0001t0004g0008 a0001c0001t0004g0099 a0001c0001t0004g0100 others(32): Show |
35 | HG00280.hp2 HG00741.hp2 HG01069.hp1 others(32): 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 | a0001c0005t0002g0074 | 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 | a0001c0003t0009g0146 a0001c0018t0013g0168 |
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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0002c0002t0001g0349 others(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 | 219 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(216): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.40-3693T>C | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 1/9 | chr1 | 31420000 | |||||||
| chr1:31420013 | A | AT | 245 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(242): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): 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 | a0001c0005t0002g0009 a0001c0005t0002g0010 a0001c0005t0002g0011 others(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 | a0002c0002t0001g0351 | 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 | a0001c0001t0005g0027 | 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 | 219 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(216): Show |
224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | 36 | a0001c0001t0004g0008 a0001c0001t0004g0099 a0001c0001t0004g0100 others(33): Show |
37 | HG00280.hp2 HG00741.hp2 HG01069.hp1 others(34): 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 | a0001c0001t0001g0232 a0001c0001t0004g0008 a0001c0001t0004g0099 others(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 | a0001c0001t0009g0228 a0001c0001t0009g0229 a0002c0002t0001g0280 others(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 | 11 | a0001c0001t0005g0236 a0001c0001t0005g0237 a0003c0007t0002g0003 others(8): Show |
12 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(9): 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 | a0002c0002t0001g0274 | 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 | a0001c0001t0002g0295 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0338 | 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 | a0001c0001t0001g0232 a0001c0004t0003g0141 a0001c0004t0003g0144 others(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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0001c0004t0009g0131 a0001c0004t0009g0132 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0001c0016t0002g0081 a0002c0017t0001g0082 |
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 | a0001c0004t0009g0131 a0001c0004t0009g0132 a0001c0004t0016g0212 |
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 | a0002c0002t0001g0297 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0232 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | 284 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): 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 | a0001c0003t0002g0060 a0002c0002t0001g0322 a0002c0002t0001g0341 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0006g0320 a0001c0003t0002g0055 a0001c0003t0002g0056 |
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 | a0001c0003t0002g0055 a0001c0003t0002g0056 |
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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0298 | 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 | a0002c0002t0001g0337 | 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 | a0001c0003t0002g0092 a0001c0003t0002g0093 a0001c0003t0002g0094 others(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 | 245 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(242): Show |
250 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(247): 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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0005c0019t0002g0037 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0001g0232 a0001c0004t0003g0141 a0001c0004t0003g0144 others(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 | 246 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(243): Show |
251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0004t0010g0235 | 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 | a0001c0004t0003g0198 a0001c0004t0003g0199 a0001c0004t0003g0207 |
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 | a0001c0001t0005g0236 a0001c0001t0005g0237 a0001c0001t0018g0172 others(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 | a0001c0004t0003g0197 | 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 | a0001c0004t0003g0196 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0004t0009g0209 | 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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | 333 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(330): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.202-37A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 2/9 | chr1 | 31424646 | |||||||
| chr1:31424926 | C | T | 7 | a0003c0007t0002g0003 a0003c0007t0002g0143 a0003c0007t0002g0149 others(4): Show |
8 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(5): 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0001g0245 others(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 | a0001c0003t0009g0146 a0001c0018t0013g0168 |
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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0001c0003t0004g0269 | 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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0001c0001t0018g0172 | 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 | 83 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(80): Show |
84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): 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 | a0002c0002t0001g0336 | 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 | a0001c0003t0002g0071 | 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 | a0001c0001t0002g0294 | 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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0001c0003t0002g0092 a0001c0003t0002g0093 a0001c0003t0002g0094 others(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 | a0001c0001t0005g0021 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0001t0004g0133 a0001c0001t0004g0135 a0001c0001t0004g0136 others(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 | a0001c0004t0016g0212 | 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 | a0001c0003t0002g0019 a0001c0003t0002g0068 a0001c0003t0002g0069 others(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 | 334 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(331): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): 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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0001c0004t0003g0141 | 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 | a0001c0001t0019g0101 | 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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0001c0003t0001g0245 a0001c0003t0001g0246 a0001c0003t0001g0252 others(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 | a0002c0002t0001g0299 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0002c0002t0001g0347 a0002c0002t0001g0348 |
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 | a0002c0002t0001g0297 | 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 | a0001c0001t0004g0279 a0002c0002t0001g0278 a0002c0002t0001g0283 |
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 | a0001c0001t0001g0289 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | 266 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0290 others(263): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0004g0241 a0001c0001t0004g0279 a0001c0001t0005g0236 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0002c0002t0001g0300 | 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 | 334 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(331): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): 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 | a0001c0004t0003g0154 | 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 | a0001c0004t0003g0141 a0001c0004t0003g0144 a0001c0004t0003g0154 others(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 | a0001c0003t0002g0067 | 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 | a0001c0023t0005g0089 | 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 | a0001c0003t0009g0146 a0001c0018t0013g0168 |
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 | a0002c0002t0001g0288 a0002c0002t0001g0335 |
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 | a0001c0005t0002g0009 a0001c0005t0002g0010 a0001c0005t0002g0011 others(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 | 80 | a0001c0001t0001g0232 a0001c0001t0005g0236 a0001c0004t0003g0141 others(77): Show |
81 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(78): 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 | a0001c0001t0004g0272 a0002c0002t0001g0274 a0002c0002t0001g0337 others(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 | a0001c0001t0007g0102 | 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 | a0001c0003t0001g0252 a0001c0003t0001g0257 a0001c0003t0001g0258 others(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 | 150 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(147): Show |
156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): 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 | a0001c0003t0001g0051 a0001c0003t0001g0114 a0001c0003t0002g0001 others(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 | a0002c0002t0001g0354 | 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 | 148 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(145): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0001t0005g0026 a0001c0004t0015g0234 |
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 | a0001c0004t0003g0141 a0001c0004t0003g0144 a0001c0004t0003g0154 others(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 | a0002c0002t0001g0334 | 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 | 150 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(147): Show |
156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): 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 | a0002c0002t0001g0301 | 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 | a0002c0002t0001g0302 | 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 | a0002c0002t0001g0303 | 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 | a0001c0001t0001g0338 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | a0002c0002t0001g0275 | 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 | a0001c0001t0001g0338 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | a0002c0002t0001g0339 | 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 | a0002c0002t0001g0297 | 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 | a0002c0021t0001g0016 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0009c0013t0002g0066 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | a0001c0001t0019g0101 | 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 | a0001c0001t0002g0332 a0001c0001t0002g0333 |
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 | 155 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(152): Show |
157 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(154): 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 | a0002c0008t0017g0145 | 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 | 23 | a0001c0001t0001g0232 a0001c0001t0004g0008 a0001c0001t0004g0099 others(20): Show |
24 | HG00280.hp2 HG00741.hp2 HG01167.hp1 others(21): 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 | a0001c0001t0007g0103 | 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 | a0001c0004t0003g0141 a0001c0004t0003g0144 a0001c0004t0003g0154 others(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 | a0001c0003t0002g0065 | 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 | 209 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): 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 | a0001c0001t0001g0120 a0001c0001t0004g0138 a0001c0003t0002g0063 others(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 | a0001c0005t0002g0074 | 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 | a0009c0013t0002g0066 | 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 | a0001c0016t0002g0081 a0002c0017t0001g0082 |
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 | a0001c0001t0001g0338 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | a0001c0001t0001g0338 a0001c0003t0001g0245 a0001c0003t0001g0246 others(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 | a0001c0001t0004g0241 a0002c0002t0006g0239 a0002c0002t0006g0240 others(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 | a0001c0004t0014g0214 | 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 | 257 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): 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 | a0002c0002t0001g0282 | 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 | a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0002c0002t0001g0276 | 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 | a0001c0003t0002g0061 a0001c0004t0016g0212 a0002c0008t0001g0124 others(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 | a0001c0001t0019g0101 | 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 | a0001c0003t0002g0061 | 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 | a0001c0003t0002g0296 | 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 | a0001c0001t0004g0022 a0001c0001t0019g0101 a0001c0004t0016g0212 others(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 | a0001c0001t0004g0169 | 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 | a0003c0007t0002g0151 | 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 | a0001c0004t0010g0179 | 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 | a0001c0001t0009g0228 | 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 | a0001c0003t0004g0253 | 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 | a0001c0004t0010g0182 | 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 | a0001c0001t0001g0338 a0001c0003t0021g0247 |
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 | a0001c0003t0004g0244 | 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 | a0002c0006t0008g0231 | 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 | a0001c0004t0003g0167 | 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 | a0001c0003t0004g0256 | 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 | a0001c0004t0003g0163 | 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 | a0001c0003t0004g0249 | 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 | a0001c0003t0004g0251 | 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 | a0001c0003t0004g0269 | 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 | a0001c0003t0001g0246 | 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 | a0001c0003t0004g0266 | 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 | a0001c0003t0004g0260 | 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 | a0001c0003t0004g0265 | 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 | a0001c0003t0004g0262 | 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 | a0001c0004t0003g0185 | 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 | a0001c0004t0003g0186 | 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 | a0001c0004t0003g0204 | 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 | a0001c0004t0003g0205 | 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 | a0002c0006t0003g0221 | 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 | a0001c0004t0003g0197 | 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 | a0001c0003t0002g0122 | 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 | a0001c0001t0004g0117 | 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 | a0008c0022t0001g0277 | 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 | a0002c0011t0001g0271 | 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 | a0002c0002t0001g0319 a0002c0002t0001g0322 |
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 | a0001c0010t0002g0062 | 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 | a0001c0003t0002g0038 | 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 | a0002c0008t0001g0048 | 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 | a0002c0002t0001g0358 | 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 | a0001c0003t0002g0093 | 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 | a0001c0003t0002g0045 | 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 | a0001c0003t0002g0121 | 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 | a0002c0002t0001g0359 | 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 | a0009c0013t0002g0066 | 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 | a0001c0003t0002g0096 | 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 | a0001c0003t0001g0051 | 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 | a0001c0003t0009g0146 | 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 | a0001c0001t0006g0308 | 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 | a0002c0002t0001g0297 | 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 | a0001c0003t0002g0056 | 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 | a0001c0005t0002g0010 | 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 | a0002c0021t0001g0016 | 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 | a0001c0004t0010g0195 | 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 | a0001c0005t0002g0030 | 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 | a0001c0005t0002g0011 | 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 | a0001c0005t0002g0074 | 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 | a0001c0003t0002g0063 | 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 | a0001c0003t0002g0019 | 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 | a0001c0003t0002g0068 | 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 | a0001c0003t0002g0069 | 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 | a0001c0003t0002g0064 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0311 | 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 | a0002c0002t0001g0340 | 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 | a0001c0005t0002g0034 | 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 | a0002c0002t0001g0314 | 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 | a0002c0002t0001g0335 | 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 | a0001c0001t0006g0315 | 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 | a0001c0001t0001g0293 | 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 | a0002c0002t0001g0352 | 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 | a0002c0002t0001g0299 | 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 | a0002c0002t0001g0353 | 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 | a0002c0002t0001g0344 | 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 | a0002c0002t0001g0351 | 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 | a0001c0001t0002g0325 | 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 | a0002c0002t0001g0324 a0002c0002t0001g0334 |
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 | a0002c0002t0001g0323 | 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 | a0002c0002t0001g0331 | 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 | a0002c0002t0008g0227 | 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 | a0002c0002t0001g0327 | 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 | a0002c0002t0001g0328 | 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 | a0002c0002t0001g0302 | 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 | a0002c0002t0024g0346 | 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 | a0002c0002t0001g0339 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0003c0007t0002g0143 | 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 | a0001c0001t0001g0232 | 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 | a0002c0002t0006g0171 | 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 | a0001c0004t0003g0216 | 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 | a0001c0003t0001g0245 | 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 | a0001c0003t0004g0263 | 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 | a0001c0004t0003g0206 | 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 | a0001c0004t0003g0191 | 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 | a0001c0004t0003g0193 | 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 | a0001c0003t0007g0075 | 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 | a0001c0004t0003g0141 | 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 | a0001c0004t0009g0131 | 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 | a0001c0003t0002g0091 | 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 | a0001c0003t0001g0114 | 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 | a0001c0016t0002g0081 | 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 | a0002c0002t0001g0307 | 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 | a0001c0004t0009g0209 | 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 | a0001c0004t0003g0194 | 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 | a0001c0003t0002g0053 | 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 | a0001c0005t0002g0029 | 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 | a0001c0005t0002g0078 | 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 | a0001c0005t0002g0076 | 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 | a0001c0003t0002g0067 | 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 | a0001c0003t0002g0058 | 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 | a0002c0002t0001g0343 | 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 | a0002c0002t0001g0345 | 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 | a0001c0001t0002g0362 | 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 | a0001c0001t0002g0006 | 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 | a0002c0002t0001g0007 | 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 | a0002c0002t0002g0273 | 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 | a0001c0005t0002g0035 | 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 | a0002c0002t0001g0275 a0002c0008t0001g0124 a0002c0008t0001g0125 |
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 | a0001c0001t0004g0022 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0002c0002t0001g0304 | 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 | a0001c0001t0005g0083 | 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 | a0003c0007t0004g0147 | 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 | a0004c0009t0004g0127 a0004c0009t0004g0129 |
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 | a0001c0003t0002g0061 | 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 | a0002c0008t0017g0145 | 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 | a0001c0001t0004g0140 | 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 | a0001c0004t0003g0181 | 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 | a0002c0006t0008g0217 | 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 | a0002c0006t0008g0218 | 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 | a0001c0003t0001g0257 | 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 | a0001c0003t0001g0258 | 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 | a0002c0006t0008g0190 | 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 | a0001c0004t0003g0226 | 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 | a0002c0002t0004g0142 | 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 | a0002c0002t0001g0303 | 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 | a0002c0011t0001g0270 | 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 | a0001c0003t0002g0041 | 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 | a0001c0003t0002g0040 | 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 | a0001c0003t0002g0092 | 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 | a0001c0003t0002g0094 | 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 | a0007c0025t0002g0043 | 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 | a0001c0003t0002g0018 | 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 | a0005c0019t0002g0037 | 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 | a0001c0004t0009g0224 | 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 | a0001c0001t0002g0332 | 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 | a0001c0003t0002g0052 | 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 | a0001c0005t0002g0009 | 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 | a0010c0015t0023g0077 | 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 | a0001c0005t0002g0031 | 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 | a0002c0008t0001g0020 | 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 | a0001c0003t0002g0055 | 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 | a0001c0003t0002g0057 | 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 | a0001c0001t0001g0342 | 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 | a0002c0002t0001g0349 | 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 | a0002c0002t0001g0301 | 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 | a0001c0003t0002g0070 | 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 | a0002c0002t0001g0329 | 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 | a0002c0002t0001g0330 | 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 | a0002c0002t0001g0280 | 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 | a0001c0005t0002g0015 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0002c0002t0006g0306 | 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 | a0003c0007t0002g0152 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0342 a0001c0001t0004g0022 a0001c0001t0004g0279 others(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 | a0001c0003t0002g0055 a0001c0003t0002g0070 a0001c0003t0002g0092 others(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 | a0002c0002t0001g0357 | 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 | a0004c0009t0006g0210 | 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 | a0001c0001t0004g0099 | 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 | a0001c0001t0004g0100 | 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(1109): Show |
1 | a0004c0009t0005g0211 | 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 | a0001c0005t0002g0033 | 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 | a0001c0001t0004g0133 a0001c0001t0004g0135 a0001c0001t0004g0136 others(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 | a0001c0003t0004g0268 | 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 | a0001c0003t0004g0261 | 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 | a0002c0002t0001g0355 | 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 | a0001c0001t0005g0097 | 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 | a0002c0002t0001g0354 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0342 a0001c0001t0004g0099 others(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 | a0001c0003t0002g0092 a0001c0004t0003g0193 a0002c0002t0001g0330 others(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 | a0001c0004t0003g0230 | 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 | a0001c0001t0004g0138 | 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 | a0001c0004t0003g0196 | 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 | a0001c0003t0001g0252 | 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 | a0001c0003t0004g0267 | 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 | a0001c0004t0003g0178 | 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 | a0001c0004t0003g0187 | 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 | a0001c0004t0003g0188 | 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 | a0001c0004t0003g0189 | 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 | a0001c0003t0004g0243 a0001c0003t0004g0248 a0001c0003t0004g0250 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0002g0287 a0001c0001t0002g0326 a0001c0001t0004g0150 others(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 | a0003c0007t0004g0148 | 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 | a0002c0002t0006g0170 | 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 | a0002c0002t0001g0309 | 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 | a0001c0001t0002g0294 | 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 | a0001c0001t0005g0025 | 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 | a0001c0001t0005g0024 | 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 | a0001c0001t0004g0111 a0001c0001t0005g0021 a0001c0001t0005g0023 others(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 | a0001c0001t0009g0228 a0001c0003t0002g0055 a0001c0003t0002g0122 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0005t0002g0032 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(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 | a0001c0001t0004g0110 | 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 | a0001c0001t0002g0006 a0001c0003t0002g0055 a0001c0003t0002g0122 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0001t0004g0130 a0002c0002t0001g0355 |
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 | a0008c0022t0001g0277 | 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 | a0001c0001t0007g0104 | 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 | a0002c0008t0001g0125 | 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 | a0002c0008t0001g0124 | 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 | a0001c0001t0001g0338 a0001c0001t0004g0130 a0001c0001t0004g0140 others(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 | a0001c0001t0002g0325 a0001c0001t0006g0315 a0001c0003t0001g0051 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0333 a0001c0001t0009g0228 others(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 | a0002c0002t0001g0309 | 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 | a0001c0001t0011g0115 | 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 | a0001c0001t0002g0325 a0001c0003t0004g0251 a0001c0003t0004g0263 others(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 | a0001c0001t0001g0338 a0001c0001t0004g0022 a0001c0001t0004g0099 others(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 | a0001c0004t0003g0164 a0001c0004t0003g0192 a0002c0002t0001g0307 others(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 | a0001c0001t0005g0026 | 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 | a0001c0003t0004g0259 | 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 | a0002c0011t0001g0271 | 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 | a0001c0001t0002g0332 | 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 | a0001c0005t0002g0034 | 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 | a0001c0001t0011g0116 | 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 | a0001c0001t0002g0333 a0001c0001t0018g0172 a0001c0003t0001g0257 others(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 | a0001c0001t0001g0072 a0001c0001t0004g0022 a0001c0001t0005g0083 others(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 | a0001c0003t0002g0055 a0001c0003t0002g0070 a0001c0004t0003g0193 others(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 | a0001c0004t0015g0234 | 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 | a0001c0001t0007g0105 | 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 | a0001c0001t0007g0107 | 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 | a0001c0004t0003g0166 | 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 | a0001c0001t0007g0103 | 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 | a0001c0003t0004g0250 | 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 | a0001c0003t0004g0254 | 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 | a0001c0001t0011g0118 | 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 | a0001c0003t0002g0040 a0001c0004t0003g0156 a0001c0005t0002g0074 others(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 | a0001c0001t0001g0293 a0001c0001t0002g0362 a0001c0001t0004g0140 others(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 | a0001c0001t0005g0083 a0001c0003t0001g0051 a0001c0003t0002g0042 others(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 | a0001c0003t0002g0055 a0001c0004t0003g0206 a0002c0002t0001g0283 others(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 | a0001c0001t0007g0139 | 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 | a0001c0005t0002g0078 | 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 | a0002c0002t0001g0364 | 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 | a0002c0006t0008g0202 | 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 | a0001c0004t0003g0203 | 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 | a0001c0001t0002g0325 a0001c0001t0004g0008 a0001c0001t0005g0023 others(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 | a0001c0001t0002g0287 a0001c0001t0004g0279 a0001c0001t0007g0104 others(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 | a0001c0001t0019g0101 a0001c0003t0002g0121 a0001c0004t0003g0164 others(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 | a0002c0017t0001g0082 | 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 | a0001c0004t0003g0198 | 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 | a0001c0004t0003g0183 | 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 | a0001c0001t0020g0106 | 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 | a0001c0001t0007g0108 | 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 | a0001c0001t0007g0109 | 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 | a0001c0003t0004g0248 a0001c0003t0004g0255 a0001c0003t0004g0261 others(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 | a0001c0004t0010g0233 | 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 | a0002c0006t0008g0215 | 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 | a0001c0004t0010g0235 | 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 | a0001c0001t0001g0338 a0001c0001t0002g0295 a0001c0001t0002g0326 others(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 | a0001c0001t0002g0286 a0001c0001t0005g0021 a0001c0001t0005g0023 others(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 | a0001c0001t0004g0099 a0001c0001t0004g0100 a0001c0001t0004g0241 others(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 | a0001c0003t0002g0054 | 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 | TAGGGTGG others(3026): Show |
1 | a0001c0023t0005g0089 | 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 | a0001c0001t0005g0088 | 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 | a0001c0004t0003g0165 | 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 | a0001c0003t0004g0259 a0001c0003t0004g0265 a0002c0002t0001g0330 |
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 | a0002c0002t0006g0306 | 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 | a0001c0001t0019g0101 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0002g0333 others(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 | a0001c0003t0004g0262 | 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 | a0002c0002t0001g0361 | 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 | a0001c0001t0004g0241 a0001c0001t0005g0023 a0001c0003t0001g0051 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0002c0002t0001g0337 | 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 | a0001c0001t0004g0150 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0004g0022 | 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 | a0001c0001t0004g0117 a0001c0001t0005g0021 a0001c0001t0005g0024 others(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 | a0001c0001t0004g0169 | 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 | a0001c0003t0002g0060 | 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 | a0001c0004t0014g0214 | 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 | a0002c0002t0001g0341 | 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 | a0001c0003t0001g0114 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0292 | 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 | a0001c0003t0001g0246 | 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 | a0001c0001t0005g0084 | 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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0336 | 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 | a0001c0004t0003g0196 | 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 | a0002c0002t0001g0314 | 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 | a0001c0001t0004g0241 a0001c0003t0002g0041 a0001c0003t0002g0070 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0003t0001g0245 | 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 | a0002c0002t0001g0327 | 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 | a0002c0002t0001g0281 | 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 | a0001c0001t0002g0287 a0001c0001t0002g0294 a0001c0003t0001g0245 others(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 | a0001c0001t0001g0290 a0001c0001t0001g0342 a0001c0001t0002g0325 others(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 | a0001c0001t0004g0099 a0001c0001t0004g0100 a0001c0003t0001g0051 others(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 | a0001c0004t0003g0180 | 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 | a0001c0001t0005g0134 | 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 | a0001c0001t0005g0025 | 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 | a0002c0002t0001g0300 | 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 | a0001c0001t0006g0285 a0001c0003t0002g0040 a0001c0010t0002g0079 |
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 | a0001c0001t0004g0133 | 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 | a0001c0004t0010g0201 | 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 | a0001c0003t0004g0267 | 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 | a0001c0004t0003g0186 | 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 | a0001c0004t0003g0199 | 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 | a0001c0001t0001g0293 a0001c0001t0002g0333 a0001c0001t0006g0285 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0290 a0001c0001t0004g0135 others(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 | a0001c0001t0004g0099 a0001c0001t0004g0100 a0001c0001t0004g0169 others(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 | a0001c0001t0004g0140 | 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 | a0001c0001t0002g0362 | 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 | a0001c0003t0002g0068 | 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 | a0001c0003t0002g0296 | 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0004g0110 a0001c0001t0005g0027 a0001c0001t0005g0097 others(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 | a0001c0001t0002g0362 a0001c0001t0004g0138 a0001c0001t0004g0279 others(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 | a0001c0001t0002g0006 a0001c0001t0004g0241 a0001c0003t0007g0075 others(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 | a0001c0004t0003g0162 | 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 | a0001c0003t0002g0091 | 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 | a0001c0001t0001g0073 a0001c0001t0007g0002 a0001c0003t0001g0245 others(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 | 216 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0232 others(213): Show |
220 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(217): 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 | a0001c0004t0016g0212 | 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 | a0001c0005t0002g0012 | 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 | a0002c0002t0001g0302 | 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 | a0002c0002t0001g0299 | 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 | a0001c0004t0003g0155 | 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 | 35 | a0001c0001t0001g0005 a0001c0001t0002g0326 a0001c0001t0004g0022 others(32): Show |
36 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(33): 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 | a0001c0001t0004g0169 a0001c0004t0003g0164 a0001c0004t0003g0192 others(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 | a0002c0002t0001g0274 | 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 | a0001c0001t0005g0086 a0001c0024t0005g0087 |
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 | a0001c0001t0004g0135 a0001c0001t0004g0136 |
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 | a0001c0001t0007g0098 | 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 | a0002c0002t0001g0358 | 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 | a0001c0003t0002g0058 | 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 | a0001c0004t0003g0185 | 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 | a0001c0001t0001g0072 | 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 | a0002c0002t0001g0301 | 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 | a0002c0008t0017g0145 | 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 | a0001c0005t0002g0009 | 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 | a0001c0001t0002g0006 a0001c0001t0004g0022 a0001c0001t0005g0021 others(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 | a0001c0001t0001g0311 a0001c0001t0002g0295 a0001c0001t0005g0027 others(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 | a0001c0001t0004g0150 a0001c0004t0003g0164 a0001c0004t0003g0181 others(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 | a0001c0003t0002g0057 | 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 | a0001c0004t0003g0194 | 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 | a0001c0004t0003g0174 | 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 | a0002c0002t0001g0343 | 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 | a0001c0004t0008g0222 | 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 | a0001c0001t0006g0308 | 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 | a0002c0002t0001g0358 | 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 | a0001c0001t0001g0293 a0001c0001t0005g0236 a0001c0003t0001g0114 others(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 | a0002c0002t0001g0280 | 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 | a0001c0003t0002g0069 | 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 | a0002c0011t0001g0271 | 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 | 230 | a0001c0001t0001g0072 a0001c0001t0001g0232 a0001c0001t0001g0290 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): 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 | a0001c0001t0001g0311 a0001c0001t0002g0295 a0001c0001t0002g0325 others(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 | a0001c0001t0004g0111 a0001c0003t0002g0296 a0001c0004t0003g0180 others(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 | a0001c0005t0002g0033 | 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 | a0001c0001t0005g0084 | 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 | a0001c0001t0007g0085 | 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 | a0002c0006t0003g0213 | 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 | a0001c0003t0009g0146 | 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 | a0001c0001t0004g0138 a0001c0003t0002g0040 a0001c0005t0002g0034 others(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 | a0001c0004t0003g0178 | 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 | 265 | a0001c0001t0001g0073 a0001c0001t0001g0119 a0001c0001t0001g0120 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): 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 | a0001c0004t0009g0223 | 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 | a0001c0001t0007g0112 | 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 | 25 | a0001c0001t0004g0140 a0001c0001t0005g0021 a0001c0001t0005g0027 others(22): Show |
25 | HG00558.hp1 HG00597.hp1 HG01261.hp1 others(22): 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 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0003t0009g0146 others(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 | a0001c0005t0002g0363 | 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 | a0001c0005t0002g0011 | 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 | a0002c0006t0008g0220 | 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 | a0001c0001t0007g0103 | 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 | a0001c0003t0009g0146 | 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 | a0001c0004t0010g0195 | 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 | a0001c0003t0002g0053 a0001c0003t0002g0056 a0001c0003t0004g0263 others(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 | a0001c0001t0006g0318 | 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 | a0001c0003t0002g0040 | 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 | a0001c0004t0003g0198 | 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 | a0003c0007t0002g0149 | 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 | a0002c0002t0001g0349 | 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 | a0001c0003t0002g0121 | 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 | a0001c0004t0003g0203 | 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 | 240 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0289 others(237): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): 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 | a0001c0005t0002g0028 | 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 | a0001c0004t0003g0144 | 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 | a0001c0001t0004g0137 a0001c0001t0005g0083 a0001c0001t0005g0236 others(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 | a0001c0001t0002g0333 a0001c0001t0004g0133 a0001c0003t0002g0296 others(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 | a0001c0001t0001g0310 | 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 | a0001c0003t0002g0092 | 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 | a0001c0010t0002g0079 | 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 | a0001c0001t0004g0100 | 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 | a0001c0003t0002g0053 | 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 | a0001c0005t0002g0031 | 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 | a0002c0002t0004g0142 | 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 | a0002c0006t0008g0157 | 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 | a0001c0001t0005g0021 | 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 | a0002c0006t0008g0219 | 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 | a0002c0002t0001g0331 | 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 | a0001c0004t0003g0160 | 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 | a0002c0002t0001g0319 | 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 | a0001c0003t0002g0039 | 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 | a0001c0001t0006g0285 | 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 | a0002c0002t0001g0340 | 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 | a0002c0002t0001g0350 | 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 | a0001c0001t0002g0286 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0311 a0001c0001t0004g0099 a0001c0001t0005g0083 others(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 | a0001c0001t0004g0100 a0001c0003t0002g0053 a0001c0003t0002g0055 others(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 | a0001c0003t0004g0249 | 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 | a0002c0002t0001g0356 | 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 | a0001c0001t0002g0006 | 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 | a0002c0006t0008g0190 | 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 | a0002c0002t0001g0317 | 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 | a0001c0003t0002g0122 | 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 | a0002c0002t0001g0298 | 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 | a0001c0003t0004g0259 | 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 | a0001c0003t0004g0266 | 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 | a0001c0001t0009g0229 | 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 | a0001c0005t0002g0029 | 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 | a0001c0001t0007g0002 a0001c0004t0003g0181 |
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 | a0001c0001t0007g0103 a0002c0002t0001g0288 a0002c0002t0001g0300 |
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 | a0001c0001t0002g0295 | 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 | a0001c0001t0004g0137 | 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 | a0001c0014t0009g0225 | 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 | a0002c0002t0001g0347 | 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 | a0001c0003t0002g0046 | 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 | a0002c0002t0001g0282 | 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 | a0001c0001t0001g0342 | 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 | a0002c0006t0008g0219 | 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 | a0001c0001t0002g0287 a0001c0001t0004g0140 a0001c0001t0004g0241 others(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 | a0001c0001t0004g0099 a0001c0001t0007g0139 a0001c0001t0009g0229 others(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 | a0001c0003t0002g0053 a0001c0004t0003g0186 a0001c0010t0002g0062 others(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 | a0002c0002t0008g0227 | 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 | a0001c0004t0009g0175 | 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 | a0001c0003t0004g0248 | 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 | a0001c0004t0003g0161 | 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 | a0002c0002t0001g0323 a0002c0011t0001g0004 |
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 | a0003c0007t0002g0173 | 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 | a0011c0012t0002g0044 | 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 | a0001c0001t0002g0294 | 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 | a0001c0003t0002g0036 | 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 | a0001c0003t0002g0063 | 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 | a0002c0002t0001g0324 | 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 | a0001c0004t0016g0212 | 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 | a0002c0006t0008g0219 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0311 a0001c0001t0004g0099 a0001c0001t0005g0084 others(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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0006g0318 others(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 | a0001c0003t0002g0094 | 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 | a0001c0004t0003g0156 | 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 | a0001c0003t0002g0039 | 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 | a0002c0002t0024g0346 | 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 | a0001c0004t0003g0141 | 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 | a0002c0002t0001g0281 | 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 | a0002c0002t0022g0316 | 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 | a0002c0006t0008g0215 | 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 | a0001c0004t0003g0176 | 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 | a0001c0001t0009g0228 | 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 | a0001c0001t0011g0115 | 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 | a0001c0001t0011g0116 | 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 | a0001c0005t0002g0032 | 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 | a0004c0009t0006g0210 | 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 | a0001c0004t0009g0132 | 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 | a0001c0004t0003g0164 | 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 | a0002c0002t0001g0348 | 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 | a0001c0003t0004g0254 | 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 | 23 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0002g0333 others(20): Show |
24 | HG00642.hp2 HG01070.hp1 HG01070.hp2 others(21): 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 | a0001c0001t0001g0073 a0001c0001t0001g0311 a0001c0001t0004g0022 others(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 | a0001c0001t0001g0291 a0001c0001t0004g0100 a0001c0001t0004g0130 others(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 | a0001c0003t0002g0019 | 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 | a0001c0003t0002g0041 | 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 | a0001c0004t0003g0184 | 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 | a0001c0003t0007g0075 | 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 | a0001c0001t0005g0097 | 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 | a0001c0001t0001g0232 | 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 | a0002c0017t0001g0082 | 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 | a0002c0002t0001g0334 | 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 | a0001c0001t0005g0023 | 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 | a0002c0002t0001g0361 | 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 | a0001c0003t0002g0055 | 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 | a0001c0004t0003g0192 | 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 | a0003c0007t0002g0153 | 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 | a0001c0001t0002g0286 a0001c0001t0006g0308 a0001c0004t0003g0180 others(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 | a0001c0001t0005g0027 a0001c0001t0005g0084 a0001c0001t0005g0236 others(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 | a0001c0001t0004g0130 a0001c0001t0005g0023 a0001c0003t0002g0017 others(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 | a0009c0013t0002g0066 | 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 | a0001c0001t0004g0150 | 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 | a0001c0004t0010g0233 | 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 | a0001c0001t0004g0135 | 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 | a0001c0001t0004g0136 | 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 | a0006c0020t0002g0059 | 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 | a0001c0001t0004g0138 | 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 | a0001c0004t0003g0165 | 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 | a0001c0004t0003g0191 | 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 | a0001c0003t0004g0268 | 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0002g0287 | 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 | a0002c0006t0008g0218 | 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 | a0001c0001t0002g0325 | 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 | a0001c0001t0007g0139 | 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 | a0001c0001t0006g0318 a0001c0003t0001g0114 a0002c0002t0001g0283 others(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 | a0001c0004t0003g0199 | 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 | a0001c0001t0005g0090 | 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 | a0001c0001t0007g0109 | 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 | a0001c0004t0010g0182 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0290 a0001c0001t0002g0295 others(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 | a0001c0001t0002g0325 a0001c0001t0004g0022 a0001c0001t0005g0023 others(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 | a0001c0001t0004g0099 a0001c0001t0004g0241 a0001c0001t0005g0021 others(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 | a0001c0004t0003g0162 | 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 | a0001c0003t0002g0060 | 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 | a0001c0003t0002g0052 | 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 | a0002c0002t0002g0273 | 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 | a0001c0005t0002g0012 | 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 | a0001c0004t0003g0155 | 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 | a0002c0002t0001g0328 | 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 | a0003c0007t0002g0149 | 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 | a0002c0002t0006g0170 | 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 | a0001c0001t0001g0338 a0001c0003t0021g0247 |
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 | a0001c0005t0002g0076 | 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 | a0002c0002t0001g0275 | 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 | a0001c0003t0004g0262 | 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 | a0001c0004t0010g0179 | 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 | a0001c0004t0003g0187 | 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 | a0001c0004t0003g0207 | 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 | a0001c0003t0004g0255 | 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 | a0001c0004t0003g0204 | 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 | a0002c0006t0008g0202 | 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 | a0001c0003t0002g0070 | 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 | a0001c0001t0007g0108 | 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 | a0002c0002t0001g0364 | 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 | a0002c0002t0001g0323 | 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 | a0001c0001t0001g0290 a0001c0003t0002g0093 a0001c0003t0002g0094 others(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 | a0001c0018t0013g0168 | 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 | a0001c0001t0004g0169 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0004g0099 a0001c0001t0004g0130 a0001c0001t0004g0150 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0002c0002t0001g0355 | 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 | a0001c0004t0003g0163 a0001c0004t0009g0223 |
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 | a0001c0001t0005g0026 a0001c0001t0005g0134 a0001c0001t0007g0104 others(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 | a0001c0004t0003g0198 | 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 | a0001c0003t0002g0042 | 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 | a0001c0003t0002g0039 | 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 | a0001c0003t0002g0067 | 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 | a0002c0002t0001g0336 | 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 | a0002c0006t0008g0231 | 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 | a0001c0001t0002g0362 | 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 | a0001c0001t0004g0169 a0001c0001t0004g0241 a0001c0001t0005g0237 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0289 others(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 | a0001c0004t0003g0154 | 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 | a0001c0003t0002g0055 | 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 | a0001c0001t0007g0104 | 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 | a0001c0003t0002g0038 a0001c0003t0002g0054 |
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 | a0001c0004t0003g0166 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0289 others(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 | a0003c0007t0002g0151 | 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 | a0002c0002t0001g0360 | 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 | a0001c0001t0002g0333 | 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 | a0001c0004t0003g0161 | 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 | a0002c0002t0001g0305 | 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 | a0001c0005t0002g0013 | 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 | a0001c0001t0011g0118 | 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 | a0001c0001t0001g0290 a0001c0001t0002g0362 a0001c0001t0004g0140 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0003t0002g0018 | 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 | a0001c0005t0002g0015 | 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 | a0001c0003t0001g0257 | 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 | a0002c0002t0006g0306 | 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 | a0001c0004t0003g0206 a0001c0004t0010g0235 a0001c0005t0002g0015 others(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 | a0001c0004t0009g0175 | 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 | a0001c0001t0005g0023 | 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 | a0001c0004t0003g0193 | 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 | a0001c0001t0002g0294 | 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 | a0001c0001t0007g0107 a0001c0003t0001g0051 a0001c0003t0002g0041 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0289 others(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 | a0002c0002t0001g0351 | 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 | a0001c0001t0002g0362 a0001c0001t0018g0172 a0001c0003t0001g0246 others(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 | a0001c0001t0004g0099 | 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 | a0001c0003t0002g0049 | 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 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0005g0237 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0002c0002t0001g0300 | 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 | a0002c0002t0001g0345 | 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 | a0001c0001t0004g0140 a0002c0002t0001g0278 |
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 | a0001c0005t0002g0032 | 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 | a0001c0004t0003g0208 | 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 | a0001c0003t0002g0017 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0010t0002g0050 | 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 | a0001c0010t0002g0062 | 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 | a0002c0006t0003g0221 | 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 | a0002c0002t0001g0297 | 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 | a0001c0001t0001g0232 a0001c0001t0002g0295 a0001c0001t0004g0133 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0119 others(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 | a0001c0003t0002g0071 | 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 | a0002c0002t0001g0356 | 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 | a0001c0001t0001g0290 a0001c0001t0002g0326 a0001c0001t0004g0135 others(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 | a0001c0001t0007g0102 | 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 | a0001c0003t0004g0261 | 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 | a0001c0005t0002g0035 | 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 | a0002c0002t0001g0350 | 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 | a0001c0004t0010g0195 | 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 | a0002c0006t0008g0217 | 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 | a0001c0003t0002g0095 | 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 | a0001c0001t0002g0332 | 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 | a0002c0002t0006g0171 | 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 | a0001c0001t0001g0232 a0001c0001t0002g0325 a0001c0001t0004g0117 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0119 others(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 | a0001c0001t0002g0333 a0001c0001t0004g0130 a0001c0001t0004g0140 others(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 | a0001c0004t0003g0158 | 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 | a0001c0004t0003g0159 | 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 | a0001c0003t0002g0063 | 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 | a0001c0001t0019g0101 | 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 | a0001c0003t0002g0057 | 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 | a0001c0004t0009g0209 | 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 | a0001c0003t0004g0250 | 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 | a0001c0003t0002g0038 | 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 | 242 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0291 others(239): Show |
247 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(244): 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 | a0001c0001t0005g0134 | 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 | a0002c0002t0001g0337 | 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 | a0001c0001t0006g0308 | 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 | 67 | a0001c0001t0001g0293 a0001c0001t0001g0311 a0001c0001t0001g0338 others(64): Show |
67 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(64): 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 | a0001c0001t0001g0005 a0001c0001t0002g0325 a0001c0001t0004g0272 others(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 | a0001c0001t0004g0110 | 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 | a0001c0004t0009g0224 | 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 | a0001c0001t0011g0116 | 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 | a0003c0007t0002g0149 | 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 | a0001c0005t0002g0033 | 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 | a0003c0007t0002g0152 | 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 | a0002c0006t0008g0215 | 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 | a0004c0009t0006g0210 | 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 | a0001c0001t0001g0232 | 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 | a0002c0002t0001g0339 | 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 | a0001c0003t0004g0255 | 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 | a0001c0001t0002g0326 a0001c0003t0004g0255 a0001c0003t0004g0267 others(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 | a0002c0002t0001g0345 a0002c0002t0001g0351 |
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 | a0001c0003t0001g0114 | 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 | a0002c0002t0001g0324 | 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 | a0001c0001t0005g0086 | 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 | a0001c0001t0002g0332 a0001c0001t0011g0116 a0001c0003t0002g0039 others(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 | 165 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0119 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(166): 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 | a0001c0005t0002g0014 | 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 | a0001c0003t0002g0092 | 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 | a0002c0006t0003g0213 | 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 | a0002c0008t0001g0124 | 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 | a0001c0001t0018g0172 a0001c0004t0003g0164 a0001c0004t0003g0197 others(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 | a0001c0005t0002g0034 | 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 | a0001c0001t0002g0006 | 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 | a0001c0001t0009g0228 | 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 | a0001c0004t0003g0199 | 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 | a0002c0006t0008g0218 | 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 | a0001c0001t0007g0112 | 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 | a0001c0003t0004g0260 | 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 | a0001c0005t0002g0076 | 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 | a0001c0001t0002g0325 | 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 | a0001c0003t0002g0053 | 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 | a0011c0012t0002g0044 | 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 | a0001c0001t0020g0106 | 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 | a0001c0001t0007g0105 | 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 | a0002c0002t0006g0170 | 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 | a0001c0004t0010g0233 | 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 | a0001c0001t0001g0293 | 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 | a0001c0003t0004g0265 | 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 | a0001c0003t0002g0040 | 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 | a0002c0002t0006g0306 | 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 | a0001c0003t0001g0258 a0001c0003t0002g0041 a0001c0003t0002g0070 others(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 | 148 | a0001c0001t0001g0073 a0001c0001t0001g0119 a0001c0001t0001g0120 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): 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 | a0001c0001t0004g0008 a0001c0001t0004g0099 a0002c0002t0001g0327 |
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 | a0001c0001t0004g0100 | 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 | a0003c0007t0004g0148 | 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 | a0001c0004t0014g0214 | 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 | a0002c0002t0001g0331 | 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 | a0001c0003t0004g0265 | 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 | a0001c0004t0009g0132 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0004g0008 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0286 others(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 | a0001c0001t0005g0084 a0001c0001t0006g0318 a0001c0003t0001g0051 others(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 | a0001c0001t0002g0295 | 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 | a0001c0001t0019g0101 | 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 | a0001c0003t0002g0122 | 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 | a0001c0003t0002g0047 | 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 | a0002c0002t0001g0350 | 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 | a0001c0024t0005g0087 | 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 | a0001c0003t0002g0017 | 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 | a0001c0005t0002g0363 | 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 | a0001c0001t0001g0232 a0001c0001t0002g0326 a0001c0003t0001g0245 others(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 | a0004c0009t0006g0210 | 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 | a0002c0002t0022g0316 | 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 | 255 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0289 others(252): Show |
259 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(256): 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0004g0137 | 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 | a0003c0007t0004g0147 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
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 | a0001c0001t0001g0342 a0001c0001t0002g0294 a0001c0001t0002g0333 others(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 | a0001c0001t0001g0289 a0001c0001t0002g0295 a0001c0003t0001g0051 others(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 | a0007c0025t0002g0043 | 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 | a0001c0005t0002g0078 | 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 | a0001c0003t0002g0069 | 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 | a0001c0003t0001g0252 | 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 | a0001c0003t0002g0096 | 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 | a0001c0003t0002g0065 | 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 | a0001c0005t0002g0028 | 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 | a0001c0001t0004g0022 | 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 | a0001c0005t0002g0014 | 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 | a0001c0005t0002g0015 | 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 | a0001c0003t0002g0296 | 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 | a0001c0001t0001g0338 a0001c0003t0021g0247 |
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 | a0001c0005t0002g0009 | 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 | a0001c0004t0008g0222 | 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 | a0001c0001t0001g0232 | 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 | a0002c0008t0001g0048 | 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 | a0001c0005t0002g0013 | 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 | a0001c0003t0004g0263 | 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 | a0002c0002t0001g0307 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0293 | 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 | a0001c0003t0004g0269 | 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 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0002g0362 others(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 | a0001c0001t0001g0311 a0001c0001t0004g0022 a0001c0001t0004g0111 others(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 | a0001c0001t0006g0315 a0001c0003t0002g0039 a0001c0003t0002g0068 others(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 | a0003c0007t0002g0149 | 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 | a0001c0004t0003g0183 | 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 | a0002c0002t0001g0007 | 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 | a0003c0007t0002g0143 | 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 | a0001c0003t0002g0121 | 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 | a0001c0004t0003g0206 | 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 | a0001c0001t0004g0117 | 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 | a0001c0004t0010g0235 | 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 | a0001c0003t0002g0091 | 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 | a0002c0006t0008g0220 | 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 | a0001c0001t0011g0116 a0001c0003t0002g0049 a0002c0002t0001g0327 others(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 | a0002c0002t0001g0309 | 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 | a0001c0004t0003g0174 | 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 | a0002c0002t0001g0322 | 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 | a0001c0001t0005g0097 a0001c0001t0011g0116 a0001c0003t0002g0049 others(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 | a0001c0004t0016g0212 | 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 | a0001c0003t0002g0095 | 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 | a0001c0003t0002g0096 | 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 | a0004c0009t0004g0127 a0004c0009t0004g0129 |
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 | a0003c0007t0002g0173 | 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 | a0001c0003t0002g0046 | 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 | a0001c0003t0002g0045 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0006g0318 a0001c0003t0001g0252 a0001c0003t0002g0039 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0119 a0001c0001t0001g0120 others(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 | a0001c0005t0002g0035 a0002c0002t0001g0301 a0002c0002t0001g0339 others(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 | a0001c0004t0009g0224 a0001c0014t0009g0225 |
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 | a0002c0002t0001g0276 | 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 | a0002c0002t0001g0348 | 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 | a0002c0002t0001g0347 | 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 | a0002c0002t0001g0298 | 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 | a0008c0022t0001g0277 | 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 | a0001c0004t0003g0226 | 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 | a0001c0004t0010g0201 | 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 | a0002c0002t0001g0340 | 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 | a0002c0002t0001g0353 | 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 | a0002c0002t0001g0357 | 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 | a0001c0001t0002g0332 a0001c0001t0002g0333 a0001c0001t0002g0362 others(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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0314 | 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 | a0005c0019t0002g0037 | 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 | a0002c0008t0001g0020 | 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 | a0002c0002t0001g0303 | 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 | a0002c0002t0001g0354 | 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 | a0002c0006t0008g0202 | 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 | a0002c0021t0001g0016 | 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 | a0002c0002t0001g0350 | 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 | a0001c0010t0002g0079 | 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 | a0001c0005t0002g0029 | 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 | a0002c0008t0001g0125 | 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 | a0002c0006t0008g0190 | 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 | a0001c0003t0002g0018 | 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 | a0001c0001t0001g0342 | 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 | a0001c0004t0009g0131 | 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 | a0001c0005t0002g0031 | 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 | a0001c0001t0006g0318 | 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 | a0002c0002t0001g0304 | 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 | a0001c0005t0002g0010 | 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 | a0001c0005t0002g0011 | 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 | a0001c0023t0005g0089 | 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 | a0002c0002t0001g0007 | 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 | a0001c0004t0009g0209 | 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 | a0001c0004t0003g0198 | 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 | a0001c0001t0004g0008 a0001c0001t0004g0099 a0001c0001t0004g0100 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0001c0001t0011g0115 | 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 | a0001c0001t0001g0073 a0001c0001t0011g0118 a0001c0004t0003g0154 others(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 | a0001c0003t0002g0056 | 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(2468): Show |
1 | a0001c0016t0002g0081 | 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 | a0001c0003t0004g0266 | 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 | a0001c0004t0015g0234 | 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 | a0001c0004t0009g0132 | 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 | a0002c0002t0001g0299 | 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 | a0001c0003t0004g0244 | 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 | a0001c0003t0002g0064 | 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 | a0001c0003t0002g0068 | 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 | a0001c0003t0004g0267 | 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 | a0001c0001t0009g0229 | 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 | a0001c0003t0009g0146 | 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 | a0001c0003t0002g0061 | 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 | a0002c0006t0008g0157 | 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 | a0002c0002t0001g0344 | 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 | a0002c0002t0001g0313 | 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 | a0001c0003t0001g0051 | 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 | a0001c0001t0004g0138 | 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 | a0001c0003t0002g0080 | 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 | a0001c0001t0005g0027 | 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 | a0001c0001t0002g0286 | 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 | a0001c0001t0002g0287 | 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 | a0002c0002t0001g0343 | 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 | a0002c0002t0001g0335 | 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 | a0002c0002t0001g0359 | 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 | a0001c0001t0019g0101 | 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 | a0002c0017t0001g0082 | 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 | a0001c0003t0001g0246 | 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 | a0001c0003t0002g0042 | 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 | a0001c0005t0002g0035 | 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 | a0001c0001t0005g0025 | 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 | a0001c0004t0008g0222 | 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 | a0001c0001t0002g0362 | 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 | a0010c0015t0023g0077 | 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 | a0002c0002t0001g0324 | 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 | a0002c0002t0001g0334 | 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 | a0002c0002t0001g0330 | 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 | a0001c0001t0004g0169 | 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 | a0002c0002t0001g0305 | 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 | a0002c0002t0001g0319 | 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 | a0001c0001t0002g0325 | 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 | a0001c0003t0004g0259 | 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 | a0001c0003t0001g0258 | 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 | a0001c0001t0004g0133 | 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 | a0001c0003t0004g0262 | 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 | a0001c0001t0001g0310 | 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 | a0002c0002t0001g0297 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0120 | 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 | a0001c0004t0010g0182 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0338 a0001c0001t0002g0006 others(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 | a0001c0001t0005g0237 a0001c0001t0020g0106 a0001c0004t0003g0163 |
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 | a0001c0004t0003g0144 | 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 | a0001c0001t0006g0315 | 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 | a0001c0001t0005g0083 | 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 | a0001c0004t0003g0155 | 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 | a0001c0004t0003g0159 | 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 | a0001c0004t0012g0200 | 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 | a0001c0001t0005g0090 | 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 | a0004c0009t0005g0211 | 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 | a0001c0001t0004g0111 | 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 | a0001c0004t0003g0199 | 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 | a0001c0004t0003g0184 | 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 | a0001c0001t0004g0150 | 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 | a0001c0001t0007g0109 | 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 | a0001c0001t0007g0104 | 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 | a0001c0001t0007g0108 | 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 | a0001c0001t0005g0024 | 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 | a0001c0003t0002g0093 | 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 | a0002c0002t0001g0361 | 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 | a0001c0004t0010g0179 | 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 | a0001c0004t0003g0194 | 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 | a0001c0001t0007g0103 | 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 | a0001c0004t0003g0216 | 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 | a0001c0001t0005g0084 | 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 | a0001c0001t0005g0023 | 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 | a0001c0001t0007g0098 | 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 | a0001c0001t0005g0134 a0001c0001t0007g0102 a0001c0001t0007g0105 |
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 | a0001c0001t0007g0107 | 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 | a0001c0001t0005g0086 | 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 | a0002c0002t0001g0358 | 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 | a0001c0001t0007g0139 | 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 | a0002c0002t0001g0352 | 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 | a0001c0001t0005g0088 | 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 | a0001c0001t0007g0085 | 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 | a0002c0011t0001g0270 | 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 | a0002c0002t0001g0353 | 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 | a0001c0024t0005g0087 | 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 | a0001c0001t0005g0097 | 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 | a0001c0001t0004g0133 a0001c0001t0005g0237 a0001c0001t0006g0285 others(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 | a0001c0001t0002g0332 a0001c0001t0004g0137 a0001c0001t0006g0315 others(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 | a0002c0002t0001g0299 | 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 | a0001c0003t0007g0075 | 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 | a0001c0001t0001g0289 a0001c0001t0001g0310 a0001c0001t0001g0342 others(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 | a0002c0002t0001g0360 | 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 | a0001c0004t0003g0191 | 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 | a0002c0002t0001g0302 | 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 | a0001c0004t0003g0207 | 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 | a0001c0004t0003g0203 | 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 | a0001c0010t0002g0062 | 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 | a0002c0002t0001g0341 | 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 | a0001c0003t0002g0040 | 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 | a0001c0001t0005g0021 | 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 | a0002c0002t0001g0282 | 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 | a0002c0002t0001g0356 | 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 | a0002c0002t0008g0227 | 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 | a0002c0006t0008g0219 | 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 | a0002c0002t0001g0321 | 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 | a0002c0002t0001g0329 | 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 | a0002c0002t0022g0316 | 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 | a0001c0004t0009g0223 | 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 | a0002c0002t0001g0322 | 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 | a0002c0002t0001g0323 | 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 | a0001c0004t0003g0186 | 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 | a0001c0004t0003g0166 | 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 | a0001c0004t0003g0196 | 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 | a0002c0002t0001g0275 | 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 | a0001c0004t0016g0212 | 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 | a0001c0001t0002g0326 | 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 | a0001c0018t0013g0168 | 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 | a0001c0001t0011g0118 a0001c0001t0018g0172 a0002c0002t0001g0278 |
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 | 75 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0006 others(72): Show |
77 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(74): 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 | a0001c0005t0002g0012 | 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 | a0002c0002t0001g0007 | 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 | a0002c0002t0001g0335 | 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 | a0001c0004t0003g0162 | 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 | a0002c0002t0004g0142 | 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 | a0001c0001t0002g0294 | 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 | a0001c0003t0002g0001 a0001c0003t0002g0038 a0001c0003t0002g0039 others(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 | a0002c0002t0001g0328 | 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 | a0001c0004t0003g0167 | 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 | a0001c0005t0002g0074 | 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 | a0001c0003t0002g0036 | 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 | a0001c0004t0003g0161 | 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 | a0001c0001t0001g0311 | 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 | a0001c0004t0003g0160 | 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 | a0001c0004t0003g0197 | 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 | a0001c0004t0003g0178 | 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 | a0001c0003t0004g0250 | 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 | a0001c0004t0003g0176 | 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 | a0002c0006t0008g0202 | 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 | a0001c0004t0003g0174 a0001c0004t0003g0180 |
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 | a0001c0004t0003g0158 | 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 | a0001c0003t0002g0067 | 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 | a0001c0004t0010g0201 | 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 | a0001c0004t0003g0165 | 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 | a0001c0004t0003g0198 | 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 | a0001c0004t0003g0156 | 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 | a0001c0001t0002g0326 | 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 | a0001c0004t0003g0204 | 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 | a0001c0001t0001g0073 | 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 | a0001c0003t0002g0058 | 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 | a0001c0004t0003g0192 | 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 | a0001c0004t0003g0164 | 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 | a0001c0001t0001g0072 | 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 | a0001c0004t0003g0187 | 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 | a0001c0001t0002g0333 | 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 | a0001c0004t0003g0188 | 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 | a0001c0003t0002g0063 | 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 | a0001c0003t0002g0054 | 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 | a0002c0002t0001g0336 | 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 | a0001c0003t0002g0057 | 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 | a0001c0004t0003g0141 | 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 | a0001c0004t0003g0230 | 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 | a0002c0011t0001g0271 | 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 | a0001c0004t0003g0189 | 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 | a0001c0001t0006g0308 | 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 | a0001c0004t0003g0185 | 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 | a0001c0004t0003g0183 | 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 | a0002c0002t0001g0317 | 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 | a0001c0004t0003g0181 | 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 | a0001c0004t0003g0206 | 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 | a0001c0004t0003g0193 | 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 | a0001c0001t0006g0285 | 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 | a0006c0020t0002g0059 | 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 | a0001c0004t0003g0177 | 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 | a0001c0001t0005g0026 | 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 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0004t0003g0206 others(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 | a0001c0005t0002g0074 a0002c0002t0001g0278 |
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 | a0001c0004t0003g0205 | 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 | a0001c0001t0004g0138 | 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 | a0001c0001t0018g0172 | 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 | a0001c0004t0003g0154 | 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 | a0001c0001t0001g0310 a0001c0001t0001g0338 a0001c0001t0001g0342 others(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 | a0001c0003t0004g0268 | 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 | a0001c0003t0004g0253 | 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 | a0001c0003t0004g0256 | 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 | a0001c0003t0004g0249 | 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 | a0001c0003t0004g0251 | 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 | a0001c0003t0004g0248 | 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 | a0001c0003t0004g0261 | 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 | a0001c0003t0004g0269 | 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 | a0001c0003t0001g0245 | 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 | a0001c0001t0011g0116 | 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 | a0001c0003t0004g0254 | 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 | a0001c0001t0011g0115 | 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 | a0001c0001t0007g0002 a0001c0004t0009g0209 a0001c0005t0002g0074 others(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 | a0003c0007t0002g0143 | 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 | a0001c0001t0007g0002 a0002c0002t0001g0278 a0002c0002t0001g0281 |
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 | a0002c0002t0002g0273 | 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 | a0001c0001t0001g0072 a0001c0001t0007g0002 a0001c0003t0002g0092 others(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 | a0001c0004t0003g0144 a0001c0004t0009g0209 a0003c0007t0002g0143 others(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 | a0001c0001t0004g0279 a0001c0004t0003g0144 a0001c0004t0009g0209 others(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 | a0001c0005t0002g0074 a0002c0002t0001g0278 a0002c0002t0001g0281 others(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 | a0001c0003t0002g0067 a0001c0010t0002g0050 a0001c0010t0002g0062 others(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 | a0003c0007t0002g0152 | 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 | a0001c0005t0002g0012 | 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 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0338 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0289 others(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 | a0002c0002t0004g0142 | 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 | a0002c0002t0004g0142 | 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 | a0001c0004t0009g0209 | 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 | a0001c0001t0006g0285 a0001c0001t0006g0308 a0001c0001t0006g0315 others(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 | a0001c0018t0013g0168 | 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 | a0001c0001t0002g0326 | 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 | a0002c0002t0006g0306 | 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 | a0003c0007t0004g0147 a0003c0007t0004g0148 |
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 | a0001c0003t0002g0058 | 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 | 248 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(245): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): 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 | a0001c0001t0004g0022 a0001c0001t0004g0111 |
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 | a0001c0001t0006g0285 a0001c0001t0006g0308 a0001c0001t0006g0315 others(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 | a0002c0002t0001g0301 a0002c0002t0001g0349 a0002c0002t0001g0350 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0342 others(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 | a0002c0008t0017g0145 | 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 | a0001c0003t0002g0038 | 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 | a0001c0001t0011g0115 a0001c0001t0011g0116 a0001c0001t0011g0118 others(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 | a0001c0001t0004g0008 a0001c0001t0004g0099 a0001c0001t0004g0100 others(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 | 307 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(304): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.1233-29A>G | SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 9/9 | chr1 | 31434035 |