Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9717 |
| ensemblid | ENSG00000103184.12 |
| hgncid | 29032 |
| symbol | SEC14L5 |
| name | SEC14 like lipid binding 5 |
| refseq_nuc | NM_014692.2 |
| refseq_prot | NP_055507.1 |
| ensembl_nuc | ENST00000251170.12 |
| ensembl_prot | ENSP00000251170.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 4958330 |
| end | 5019157 |
| strand | + |
| ver | v1.2 |
| region | chr16:4958330-5019157 |
| region5000 | chr16:4953330-5024157 |
| regionname0 | SEC14L5_chr16_4958330_5019157 |
| regionname5000 | SEC14L5_chr16_4953330_5024157 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 696 | 365 | 92 | 69 | 146 | 18 | 38 | 106 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0002 | 0/0 | 425 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(420): Show |
chr16 | 4953330 | 5024157 |
| a0003 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0004 | 0/0 | 696 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0005 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0006 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0007 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0008 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0009 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0010 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0011 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| a0012 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | MVQRY others(691): Show |
chr16 | 4953330 | 5024157 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2088 | 143 | 23 | 12 | 83 | 5 | 19 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0002 | 0/1 | 2088 | 129 | 41 | 29 | 39 | 8 | 11 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0003 | 0/0 | 2088 | 36 | 4 | 17 | 8 | 3 | 4 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0004 | 0/0 | 2088 | 14 | 13 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0005 | 0/0 | 2088 | 12 | 0 | 0 | 12 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0006 | 0/0 | 2088 | 8 | 0 | 8 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0007 | 0/0 | 2088 | 4 | 1 | 0 | 0 | 0 | 3 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0008 | 0/0 | 2088 | 4 | 4 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0009 | 0/0 | 2088 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0010 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0011 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0012 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0015 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0016 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0018 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0020 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0022 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0024 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0026 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0001c0029 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0002c0021 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0003c0030 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0004c0019 | 0/0 | 2088 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0005c0025 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0006c0027 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0007c0028 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0008c0023 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0009c0013 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0010c0031 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0011c0017 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 | ||
| a0012c0014 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | ATGGT others(2083): Show |
chr16 | 4953330 | 5024157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6445 | 74 | 2 | 9 | 42 | 5 | 16 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0002 | 0/0 | 6445 | 11 | 0 | 2 | 9 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0003 | 0/0 | 6445 | 14 | 0 | 0 | 14 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0004 | 0/0 | 6445 | 17 | 0 | 1 | 15 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0006 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0009 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0014 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0016 | 1/0 | 6445 | 3 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0017 | 0/0 | 6455 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6450): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0020 | 0/0 | 6446 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6441): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0021 | 0/0 | 6446 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6441): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0022 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0023 | 0/0 | 6445 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0025 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0031 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0032 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0034 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0038 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0047 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0048 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0051 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0054 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0001t0056 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0001 | 0/0 | 6445 | 10 | 1 | 6 | 1 | 0 | 2 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0002 | 0/0 | 6445 | 54 | 17 | 6 | 26 | 2 | 3 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0003 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0004 | 0/0 | 6445 | 27 | 1 | 13 | 6 | 3 | 4 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0005 | 0/0 | 6445 | 8 | 8 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0006 | 0/0 | 6445 | 5 | 5 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0008 | 0/0 | 6445 | 4 | 0 | 0 | 4 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0009 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0010 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0013 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0014 | 0/0 | 6445 | 2 | 0 | 0 | 0 | 2 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0018 | 0/0 | 6445 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0026 | 0/1 | 6445 | 2 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0030 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0035 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0036 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0040 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0041 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0042 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0045 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0049 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0050 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0002t0055 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0003t0003 | 0/0 | 6445 | 34 | 4 | 16 | 7 | 3 | 4 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0003t0005 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0003t0037 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0004t0007 | 0/0 | 6445 | 6 | 6 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0004t0010 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0004t0012 | 0/0 | 6445 | 3 | 2 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0004t0019 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0004t0033 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0005t0001 | 0/0 | 6445 | 8 | 0 | 0 | 8 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0005t0015 | 0/0 | 6445 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0005t0027 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0006t0003 | 0/0 | 6445 | 8 | 0 | 8 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0007t0001 | 0/0 | 6445 | 2 | 1 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0007t0024 | 0/0 | 6445 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0008t0009 | 0/0 | 6445 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0008t0028 | 0/0 | 6446 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6441): Show |
chr16 | 4953330 | 5024157 |
| a0001c0009t0011 | 0/0 | 6445 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0010t0013 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0010t0046 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0011t0001 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0012t0039 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0015t0025 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0016t0053 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0018t0002 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0020t0052 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0022t0044 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0024t0003 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0026t0043 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0001c0029t0010 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0002c0021t0004 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0003c0030t0003 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0004c0019t0003 | 0/0 | 6445 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0005c0025t0029 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0006c0027t0003 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0007c0028t0001 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0008c0023t0003 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0009c0013t0002 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0010c0031t0003 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0011c0017t0008 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| a0012c0014t0001 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | CTCTC others(6440): Show |
chr16 | 4953330 | 5024157 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0014g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0016g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0016g0348 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0017g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0020g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0021g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0021g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0022g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0023g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0023g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0025g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0031g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0032g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0034g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0038g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0047g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0048g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0051g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0054g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0001t0056g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0009g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0014g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0014g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0018g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0018g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0026g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0026g0358 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0035g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0036g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0040g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0041g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0042g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0045g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0049g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0050g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0002t0055g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0003g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0003t0037g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0012g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0012g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0019g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0019g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0004t0033g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0015g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0015g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0015g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0005t0027g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0006t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0007t0024g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0007t0024g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0008t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0008t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0008t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0008t0028g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0009t0011g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0009t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0009t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0010t0013g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0010t0046g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0011t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0012t0039g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0015t0025g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0016t0053g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0018t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0020t0052g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0022t0044g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0024t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0026t0043g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0001c0029t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0002c0021t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0003c0030t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0004c0019t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0005c0025t0029g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0006c0027t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0007c0028t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0008c0023t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0009c0013t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0010c0031t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0011c0017t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| a0012c0014t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0014 | g0367 | EUR | GBR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0276 | EUR | GBR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0200 | EUR | GBR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | FIN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00323 | hp1 | a0001 | c0002 | t0014 | g0368 | EUR | FIN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00323 | hp2 | a0001 | c0012 | t0039 | g0109 | EUR | FIN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00423 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00423 | hp2 | a0001 | c0003 | t0003 | g0274 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00438 | hp1 | a0002 | c0021 | t0004 | g0136 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00438 | hp2 | a0003 | c0030 | t0003 | g0335 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00544 | hp2 | a0001 | c0009 | t0011 | g0312 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00597 | hp2 | a0001 | c0009 | t0011 | g0221 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0361 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00673 | hp1 | a0001 | c0009 | t0011 | g0305 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0282 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0143 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0287 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0374 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0269 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01074 | hp1 | a0001 | c0006 | t0003 | g0127 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01074 | hp2 | a0001 | c0003 | t0003 | g0149 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0145 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01099 | hp1 | a0001 | c0002 | t0045 | g0352 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01099 | hp2 | a0001 | c0004 | t0012 | g0258 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0343 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0373 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0322 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0329 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0172 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0325 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0328 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01175 | hp1 | a0001 | c0003 | t0037 | g0270 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01175 | hp2 | a0001 | c0006 | t0003 | g0355 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01192 | hp1 | a0001 | c0002 | t0049 | g0364 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01192 | hp2 | a0001 | c0002 | t0040 | g0289 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01243 | hp1 | a0001 | c0016 | t0053 | g0233 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0251 | AMR | PUR | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01255 | hp2 | a0001 | c0002 | t0018 | g0253 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0173 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0318 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01258 | hp1 | a0001 | c0003 | t0003 | g0315 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0357 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01261 | hp1 | a0001 | c0006 | t0003 | g0125 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0350 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01346 | hp1 | a0001 | c0006 | t0003 | g0129 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0123 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0285 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01361 | hp2 | a0001 | c0002 | t0004 | g0248 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0365 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0375 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0144 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01515 | hp2 | a0001 | c0024 | t0003 | g0254 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01516 | hp1 | a0001 | c0002 | t0026 | g0356 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0184 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0185 | EUR | IBS | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01884 | hp1 | a0001 | c0002 | t0013 | g0026 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01884 | hp2 | a0001 | c0022 | t0044 | g0239 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01891 | hp2 | a0001 | c0001 | t0047 | g0231 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01928 | hp1 | a0001 | c0003 | t0003 | g0265 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01952 | hp1 | a0001 | c0006 | t0003 | g0130 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01975 | hp1 | a0001 | c0006 | t0003 | g0131 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01978 | hp1 | a0001 | c0011 | t0001 | g0126 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01978 | hp2 | a0001 | c0003 | t0003 | g0134 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0298 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01981 | hp2 | a0004 | c0019 | t0003 | g0320 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0317 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01993 | hp2 | a0001 | c0002 | t0004 | g0170 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0319 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02015 | hp1 | a0001 | c0003 | t0005 | g0195 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02015 | hp2 | a0001 | c0005 | t0001 | g0223 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02040 | hp1 | a0001 | c0005 | t0027 | g0346 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0075 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0029 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02083 | hp1 | a0001 | c0005 | t0001 | g0028 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02148 | hp1 | a0001 | c0006 | t0003 | g0128 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0199 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0083 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02258 | hp1 | a0001 | c0004 | t0012 | g0113 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02258 | hp2 | a0001 | c0008 | t0009 | g0111 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0153 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02293 | hp2 | a0001 | c0003 | t0003 | g0314 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02300 | hp1 | a0001 | c0006 | t0003 | g0201 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0205 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02451 | hp2 | a0001 | c0002 | t0006 | g0208 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | KHV | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02572 | hp1 | a0001 | c0004 | t0012 | g0114 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0370 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0246 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0263 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0152 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0369 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02622 | hp1 | a0001 | c0008 | t0028 | g0119 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02622 | hp2 | a0005 | c0025 | t0029 | g0121 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0120 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02647 | hp1 | a0001 | c0002 | t0035 | g0038 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02647 | hp2 | a0001 | c0004 | t0007 | g0234 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02683 | hp2 | a0001 | c0002 | t0036 | g0156 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0291 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02698 | hp2 | a0001 | c0001 | t0038 | g0250 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0206 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02717 | hp2 | a0001 | c0004 | t0007 | g0229 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0159 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02723 | hp2 | a0001 | c0001 | t0017 | g0117 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02735 | hp1 | a0001 | c0001 | t0032 | g0044 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02809 | hp1 | a0001 | c0001 | t0051 | g0238 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0098 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02818 | hp2 | a0001 | c0004 | t0033 | g0097 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02886 | hp1 | a0001 | c0008 | t0009 | g0283 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0353 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02895 | hp2 | a0001 | c0010 | t0046 | g0188 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02896 | hp1 | a0001 | c0004 | t0007 | g0241 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0371 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0372 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0096 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02922 | hp2 | a0001 | c0002 | t0018 | g0213 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02965 | hp1 | a0001 | c0001 | t0054 | g0240 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02965 | hp2 | a0001 | c0001 | t0034 | g0214 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02970 | hp1 | a0001 | c0004 | t0019 | g0230 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02970 | hp2 | a0001 | c0002 | t0041 | g0354 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0211 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0085 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0178 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03041 | hp1 | a0001 | c0002 | t0009 | g0362 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0363 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03098 | hp2 | a0001 | c0002 | t0013 | g0025 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03130 | hp1 | a0001 | c0004 | t0019 | g0225 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03139 | hp1 | a0001 | c0008 | t0009 | g0327 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0084 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0212 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03195 | hp2 | a0001 | c0002 | t0042 | g0232 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03209 | hp1 | a0001 | c0001 | t0031 | g0224 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0006 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03225 | hp2 | a0001 | c0004 | t0007 | g0228 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03453 | hp2 | a0001 | c0003 | t0003 | g0139 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0210 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03486 | hp2 | a0001 | c0029 | t0010 | g0237 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03490 | hp1 | a0001 | c0007 | t0024 | g0055 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0313 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0255 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03492 | hp2 | a0001 | c0007 | t0024 | g0056 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0012 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0203 | AFR | ESN | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0347 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03579 | hp2 | a0001 | c0020 | t0052 | g0216 | AFR | MSL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03654 | hp1 | a0001 | c0002 | t0050 | g0168 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0175 | SAS | PJL | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0151 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03831 | hp2 | a0001 | c0003 | t0003 | g0286 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0366 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0359 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG04184 | hp2 | a0001 | c0018 | t0002 | g0244 | SAS | BEB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG04204 | hp2 | a0001 | c0007 | t0001 | g0057 | SAS | STU | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18522 | hp1 | a0001 | c0001 | t0022 | g0089 | AFR | YRI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0243 | AFR | YRI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | CHB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | CHB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18906 | hp1 | a0001 | c0002 | t0010 | g0091 | AFR | YRI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18906 | hp2 | a0006 | c0027 | t0003 | g0154 | AFR | YRI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18941 | hp2 | a0001 | c0002 | t0008 | g0160 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18945 | hp2 | a0007 | c0028 | t0001 | g0014 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18947 | hp2 | a0008 | c0023 | t0003 | g0337 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18948 | hp1 | a0001 | c0005 | t0001 | g0042 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18948 | hp2 | a0001 | c0002 | t0008 | g0252 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0162 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18957 | hp1 | a0001 | c0002 | t0030 | g0169 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18957 | hp2 | a0001 | c0005 | t0001 | g0013 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18966 | hp2 | a0009 | c0013 | t0002 | g0264 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0148 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18975 | hp2 | a0001 | c0026 | t0043 | g0280 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18980 | hp1 | a0001 | c0005 | t0015 | g0047 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18983 | hp2 | a0010 | c0031 | t0003 | g0267 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18985 | hp1 | a0001 | c0005 | t0001 | g0035 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18988 | hp1 | a0001 | c0002 | t0004 | g0186 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18994 | hp1 | a0011 | c0017 | t0008 | g0142 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18995 | hp1 | a0012 | c0014 | t0001 | g0062 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA18997 | hp2 | a0001 | c0003 | t0003 | g0344 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19009 | hp1 | a0001 | c0002 | t0008 | g0273 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19030 | hp2 | a0001 | c0001 | t0056 | g0236 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19043 | hp1 | a0001 | c0004 | t0007 | g0226 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19043 | hp2 | a0001 | c0001 | t0022 | g0005 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19054 | hp1 | a0001 | c0005 | t0015 | g0048 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19056 | hp1 | a0001 | c0005 | t0001 | g0087 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19056 | hp2 | a0001 | c0001 | t0048 | g0104 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0198 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19065 | hp2 | a0001 | c0005 | t0015 | g0036 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0324 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19077 | hp1 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19078 | hp1 | a0001 | c0002 | t0008 | g0146 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19079 | hp1 | a0001 | c0003 | t0003 | g0304 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19083 | hp1 | a0001 | c0001 | t0023 | g0218 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19083 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19085 | hp1 | a0001 | c0001 | t0023 | g0222 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19087 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20129 | hp1 | a0001 | c0001 | t0025 | g0260 | AFR | ASW | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0116 | AFR | ASW | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0257 | EUR | TSI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0262 | EUR | TSI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0174 | EUR | TSI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20805 | hp2 | a0001 | c0003 | t0003 | g0299 | EUR | TSI | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0360 | SAS | GIH | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | GIH | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0271 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0141 | AMR | CLM | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02109 | hp1 | a0001 | c0004 | t0007 | g0227 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02109 | hp2 | a0001 | c0015 | t0025 | g0095 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0235 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02486 | hp2 | a0001 | c0004 | t0010 | g0202 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0272 | AFR | ACB | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG06807 | hp1 | a0001 | c0002 | t0055 | g0112 | AFR | USA | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | USA | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20300 | hp1 | a0001 | c0007 | t0001 | g0100 | AFR | USA | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | USA | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA21309 | hp1 | a0001 | c0004 | t0010 | g0207 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| NA21309 | hp2 | a0001 | c0010 | t0013 | g0349 | AFR | LWK | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0026 | g0358 | REF | REF | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0016 | g0348 | REF | REF | SEC14L5_chr16_4953330_5024157 | SEC14L5 | chr16 | 4953330 | 5024157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4959385 | C | T | 1 | a0010 | 1 | NA18983.hp2 | missense_variant&splice_region_variant | MODERATE | c.62C>T | p.Ala21Val | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/16 | 229/6445 | 62/2091 | 21/696 | chr16 | 4959385 | |||
| chr16:4988212 | C | T | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.277C>T | p.Leu93Phe | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/16 | 444/6445 | 277/2091 | 93/696 | chr16 | 4988212 | |||
| chr16:4990827 | T | A | 1 | a0009 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.406T>A | p.Ser136Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/16 | 573/6445 | 406/2091 | 136/696 | chr16 | 4990827 | |||
| chr16:4991989 | G | C | 1 | a0012 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.626G>C | p.Arg209Pro | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/16 | 793/6445 | 626/2091 | 209/696 | chr16 | 4991989 | |||
| chr16:4996915 | G | C | 1 | a0011 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.841G>C | p.Ala281Pro | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/16 | 1008/6445 | 841/2091 | 281/696 | chr16 | 4996915 | |||
| chr16:4996918 | C | G | 1 | a0011 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.844C>G | p.Arg282Gly | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/16 | 1011/6445 | 844/2091 | 282/696 | chr16 | 4996918 | |||
| chr16:5000678 | C | T | 1 | a0007 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.994C>T | p.Arg332Cys | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/16 | 1161/6445 | 994/2091 | 332/696 | chr16 | 5000678 | |||
| chr16:5003547 | C | T | 1 | a0002 | 1 | HG00438.hp1 | stop_gained | HIGH | c.1276C>T | p.Arg426* | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/16 | 1443/6445 | 1276/2091 | 426/696 | chr16 | 5003547 | |||
| chr16:5008529 | G | A | 1 | a0008 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.1681G>A | p.Gly561Ser | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/16 | 1848/6445 | 1681/2091 | 561/696 | chr16 | 5008529 | |||
| chr16:5008536 | G | A | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1688G>A | p.Arg563Gln | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/16 | 1855/6445 | 1688/2091 | 563/696 | chr16 | 5008536 | |||
| chr16:5008558 | C | G | 1 | a0006 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1710C>G | p.Ser570Arg | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/16 | 1877/6445 | 1710/2091 | 570/696 | chr16 | 5008558 | |||
| chr16:5011152 | C | A | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1858C>A | p.Pro620Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/16 | 2025/6445 | 1858/2091 | 620/696 | chr16 | 5011152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4987580 | G | A | 1 | a0001c0011 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.87G>A | p.Thr29Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/16 | 254/6445 | 87/2091 | 29/696 | chr16 | 4987580 | |||
| chr16:4987604 | G | A | 2 | a0001c0009 a0001c0012 |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
synonymous_variant | LOW | c.111G>A | p.Leu37Leu | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/16 | 278/6445 | 111/2091 | 37/696 | chr16 | 4987604 | |||
| chr16:4991900 | G | A | 2 | a0001c0009 a0001c0012 |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
synonymous_variant | LOW | c.537G>A | p.Pro179Pro | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/16 | 704/6445 | 537/2091 | 179/696 | chr16 | 4991900 | |||
| chr16:4996397 | G | A | 3 | a0001c0010 a0001c0015 a0001c0016 |
4 | HG01243.hp1 HG02109.hp2 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.717G>A | p.Thr239Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/16 | 884/6445 | 717/2091 | 239/696 | chr16 | 4996397 | |||
| chr16:5000677 | C | T | 2 | a0001c0008 a0001c0029 |
5 | HG02258.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
synonymous_variant | LOW | c.993C>T | p.Leu331Leu | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/16 | 1160/6445 | 993/2091 | 331/696 | chr16 | 5000677 | |||
| chr16:5000719 | G | A | 1 | a0001c0018 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1035G>A | p.Val345Val | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/16 | 1202/6445 | 1035/2091 | 345/696 | chr16 | 5000719 | |||
| chr16:5000719 | G | T | 1 | a0001c0007 | 4 | HG03490.hp1 HG03492.hp2 HG04204.hp2 others(1): Show |
synonymous_variant | LOW | c.1035G>T | p.Val345Val | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/16 | 1202/6445 | 1035/2091 | 345/696 | chr16 | 5000719 | |||
| chr16:5000896 | G | C | 10 | a0001c0002 a0001c0006 a0001c0011 others(7): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
synonymous_variant | LOW | c.1101G>C | p.Gly367Gly | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/16 | 1268/6445 | 1101/2091 | 367/696 | chr16 | 5000896 | |||
| chr16:5005940 | C | T | 1 | a0001c0009 | 3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
synonymous_variant | LOW | c.1329C>T | p.Thr443Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/16 | 1496/6445 | 1329/2091 | 443/696 | chr16 | 5005940 | |||
| chr16:5007420 | G | C | 1 | a0001c0022 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1506G>C | p.Thr502Thr | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/16 | 1673/6445 | 1506/2091 | 502/696 | chr16 | 5007420 | |||
| chr16:5011112 | G | A | 1 | a0001c0024 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1818G>A | p.Arg606Arg | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/16 | 1985/6445 | 1818/2091 | 606/696 | chr16 | 5011112 | |||
| chr16:5011118 | C | T | 1 | a0001c0026 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.1824C>T | p.Pro608Pro | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/16 | 1991/6445 | 1824/2091 | 608/696 | chr16 | 5011118 | |||
| chr16:5011190 | C | T | 2 | a0001c0004 a0001c0029 |
15 | HG01099.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
synonymous_variant | LOW | c.1896C>T | p.Asp632Asp | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/16 | 2063/6445 | 1896/2091 | 632/696 | chr16 | 5011190 | |||
| chr16:5014892 | C | T | 2 | a0001c0005 a0007c0028 |
13 | HG00423.hp1 HG02015.hp2 HG02040.hp1 others(10): Show |
synonymous_variant | LOW | c.2013C>T | p.Ser671Ser | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2180/6445 | 2013/2091 | 671/696 | chr16 | 5014892 | |||
| chr16:5014910 | C | T | 2 | a0001c0016 a0001c0020 |
2 | HG01243.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2031C>T | p.Ser677Ser | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2198/6445 | 2031/2091 | 677/696 | chr16 | 5014910 | |||
| chr16:5014916 | C | T | 7 | a0001c0003 a0001c0006 a0001c0012 others(4): Show |
49 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(46): Show |
synonymous_variant | LOW | c.2037C>T | p.Ala679Ala | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2204/6445 | 2037/2091 | 679/696 | chr16 | 5014916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4958386 | C | G | 1 | a0001c0001t0056 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/16 | 938 | chr16 | 4958386 | ||||||
| chr16:4959303 | C | T | 1 | a0001c0002t0055 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-21C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/16 | 21 | chr16 | 4959303 | ||||||
| chr16:4959305 | T | C | 1 | a0001c0005t0027 | 1 | HG02040.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-19T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/16 | chr16 | 4959305 | |||||||
| chr16:5014982 | G | A | 3 | a0001c0008t0028 a0001c0009t0011 a0005c0025t0029 |
5 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 12 | chr16 | 5014982 | ||||||
| chr16:5015008 | G | GTGTCCAG others(3): Show |
1 | a0001c0001t0017 | 2 | HG02723.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*48_*57dupATGTCCAG others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 58 | INFO_REALIGN_3_PRIME | chr16 | 5015008 | |||||
| chr16:5015178 | C | A | 1 | a0001c0002t0030 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 208 | chr16 | 5015178 | ||||||
| chr16:5015189 | C | T | 1 | a0001c0002t0026 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 219 | chr16 | 5015189 | ||||||
| chr16:5015354 | C | G | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*384C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 384 | chr16 | 5015354 | ||||||
| chr16:5015355 | T | C | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(82): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*385T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 385 | chr16 | 5015355 | ||||||
| chr16:5015422 | T | C | 2 | a0001c0002t0018 a0001c0002t0055 |
3 | HG01255.hp2 HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*452T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 452 | chr16 | 5015422 | ||||||
| chr16:5015429 | G | A | 1 | a0001c0001t0031 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 459 | chr16 | 5015429 | ||||||
| chr16:5015446 | C | T | 1 | a0001c0002t0050 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 476 | chr16 | 5015446 | ||||||
| chr16:5015471 | A | G | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 501 | chr16 | 5015471 | ||||||
| chr16:5015483 | C | T | 1 | a0001c0001t0054 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 513 | chr16 | 5015483 | ||||||
| chr16:5015628 | T | C | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*658T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 658 | chr16 | 5015628 | ||||||
| chr16:5015666 | A | G | 1 | a0001c0002t0049 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 696 | chr16 | 5015666 | ||||||
| chr16:5015724 | C | T | 3 | a0001c0001t0009 a0001c0002t0009 a0001c0008t0009 |
5 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*754C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 754 | chr16 | 5015724 | ||||||
| chr16:5015729 | C | T | 1 | a0001c0001t0048 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 759 | chr16 | 5015729 | ||||||
| chr16:5015831 | T | C | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*861T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 861 | chr16 | 5015831 | ||||||
| chr16:5015990 | A | T | 4 | a0001c0001t0009 a0001c0001t0047 a0001c0002t0009 others(1): Show |
6 | HG01891.hp2 HG02258.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1020A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1020 | chr16 | 5015990 | ||||||
| chr16:5016049 | A | G | 1 | a0001c0010t0046 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1079A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1079 | chr16 | 5016049 | ||||||
| chr16:5016166 | T | C | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(82): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*1196T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1196 | chr16 | 5016166 | ||||||
| chr16:5016302 | C | T | 1 | a0001c0005t0015 | 3 | NA18980.hp1 NA19054.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1332C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1332 | chr16 | 5016302 | ||||||
| chr16:5016312 | G | T | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1342G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1342 | chr16 | 5016312 | ||||||
| chr16:5016350 | G | A | 1 | a0001c0001t0032 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1380 | chr16 | 5016350 | ||||||
| chr16:5016412 | T | C | 3 | a0001c0004t0007 a0001c0004t0019 a0001c0004t0033 |
9 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1442T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1442 | chr16 | 5016412 | ||||||
| chr16:5016529 | C | T | 1 | a0001c0004t0019 | 2 | HG02970.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1559C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1559 | chr16 | 5016529 | ||||||
| chr16:5016534 | A | G | 7 | a0001c0001t0025 a0001c0001t0051 a0001c0001t0054 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1564A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1564 | chr16 | 5016534 | ||||||
| chr16:5016595 | G | C | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0009t0011 |
10 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1625G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1625 | chr16 | 5016595 | ||||||
| chr16:5016690 | A | G | 1 | a0001c0001t0056 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1720A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1720 | chr16 | 5016690 | ||||||
| chr16:5016740 | C | T | 1 | a0001c0007t0024 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 1770 | chr16 | 5016740 | ||||||
| chr16:5017025 | G | A | 7 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0034 others(4): Show |
15 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2055G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2055 | chr16 | 5017025 | ||||||
| chr16:5017050 | A | G | 2 | a0001c0001t0014 a0001c0002t0014 |
3 | HG00099.hp1 HG00323.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2080A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2080 | chr16 | 5017050 | ||||||
| chr16:5017052 | C | G | 1 | a0001c0004t0019 | 2 | HG02970.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2082C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2082 | chr16 | 5017052 | ||||||
| chr16:5017084 | G | A | 1 | a0001c0002t0035 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2114G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2114 | chr16 | 5017084 | ||||||
| chr16:5017184 | G | T | 1 | a0001c0010t0046 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2214G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2214 | chr16 | 5017184 | ||||||
| chr16:5017221 | A | T | 1 | a0001c0010t0046 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2251A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2251 | chr16 | 5017221 | ||||||
| chr16:5017246 | C | A | 2 | a0001c0001t0051 a0001c0001t0056 |
2 | HG02809.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2276 | chr16 | 5017246 | ||||||
| chr16:5017253 | G | T | 1 | a0001c0009t0011 | 3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2283G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2283 | chr16 | 5017253 | ||||||
| chr16:5017254 | T | G | 2 | a0001c0002t0008 a0011c0017t0008 |
5 | NA18941.hp2 NA18948.hp2 NA18994.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2284T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2284 | chr16 | 5017254 | ||||||
| chr16:5017351 | A | C | 3 | a0001c0004t0007 a0001c0004t0019 a0001c0004t0033 |
9 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2381A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2381 | chr16 | 5017351 | ||||||
| chr16:5017471 | C | T | 10 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0051 others(7): Show |
12 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2501C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2501 | chr16 | 5017471 | ||||||
| chr16:5017527 | C | A | 3 | a0001c0004t0007 a0001c0004t0019 a0001c0004t0033 |
9 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2557C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2557 | chr16 | 5017527 | ||||||
| chr16:5017562 | G | T | 4 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0034 others(1): Show |
6 | HG02622.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2592G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2592 | chr16 | 5017562 | ||||||
| chr16:5017586 | C | A | 1 | a0001c0002t0036 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2616C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2616 | chr16 | 5017586 | ||||||
| chr16:5017666 | T | C | 1 | a0001c0003t0037 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2696T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2696 | chr16 | 5017666 | ||||||
| chr16:5017677 | C | T | 3 | a0001c0001t0047 a0001c0002t0013 a0001c0010t0013 |
4 | HG01884.hp1 HG01891.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2707C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 2707 | chr16 | 5017677 | ||||||
| chr16:5018018 | G | T | 1 | a0001c0002t0045 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3048 | chr16 | 5018018 | ||||||
| chr16:5018028 | A | C | 20 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0023 others(17): Show |
68 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3058A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3058 | chr16 | 5018028 | ||||||
| chr16:5018114 | A | G | 1 | a0001c0026t0043 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3144A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3144 | chr16 | 5018114 | ||||||
| chr16:5018151 | C | T | 32 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0014 others(29): Show |
106 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*3181C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3181 | chr16 | 5018151 | ||||||
| chr16:5018247 | C | T | 1 | a0001c0002t0042 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3277C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3277 | chr16 | 5018247 | ||||||
| chr16:5018250 | A | G | 1 | a0005c0025t0029 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3280A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3280 | chr16 | 5018250 | ||||||
| chr16:5018384 | G | A | 6 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0034 others(3): Show |
14 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3414G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3414 | chr16 | 5018384 | ||||||
| chr16:5018387 | C | T | 1 | a0001c0022t0044 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3417C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3417 | chr16 | 5018387 | ||||||
| chr16:5018393 | G | T | 6 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0034 others(3): Show |
14 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3423G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3423 | chr16 | 5018393 | ||||||
| chr16:5018410 | T | C | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0030 others(2): Show |
47 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3440T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3440 | chr16 | 5018410 | ||||||
| chr16:5018446 | C | T | 13 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(10): Show |
66 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3476C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3476 | chr16 | 5018446 | ||||||
| chr16:5018457 | A | G | 6 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0034 others(3): Show |
14 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3487A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3487 | chr16 | 5018457 | ||||||
| chr16:5018476 | G | A | 1 | a0001c0022t0044 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3506G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3506 | chr16 | 5018476 | ||||||
| chr16:5018518 | T | A | 1 | a0001c0002t0026 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3548T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3548 | chr16 | 5018518 | ||||||
| chr16:5018538 | G | C | 1 | a0001c0001t0022 | 2 | NA18522.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3568G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3568 | chr16 | 5018538 | ||||||
| chr16:5018559 | C | T | 1 | a0001c0004t0012 | 3 | HG01099.hp2 HG02258.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3589C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3589 | chr16 | 5018559 | ||||||
| chr16:5018585 | T | C | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(24): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*3615T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3615 | chr16 | 5018585 | ||||||
| chr16:5018614 | C | G | 3 | a0001c0001t0051 a0001c0001t0056 a0001c0016t0053 |
3 | HG01243.hp1 HG02809.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3644C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3644 | chr16 | 5018614 | ||||||
| chr16:5018651 | C | T | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0020t0052 |
8 | HG02451.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3681C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3681 | chr16 | 5018651 | ||||||
| chr16:5018693 | G | T | 1 | a0005c0025t0029 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3723G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3723 | chr16 | 5018693 | ||||||
| chr16:5018749 | A | G | 24 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0038 others(21): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*3779A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3779 | chr16 | 5018749 | ||||||
| chr16:5018776 | G | A | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0020 others(25): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*3806G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3806 | chr16 | 5018776 | ||||||
| chr16:5018795 | C | CT | 3 | a0001c0001t0020 a0001c0001t0021 a0001c0008t0028 |
5 | HG02622.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3832dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 3833 | INFO_REALIGN_3_PRIME | chr16 | 5018795 | |||||
| chr16:5019013 | C | G | 7 | a0001c0001t0020 a0001c0001t0021 a0001c0002t0041 others(4): Show |
15 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4043C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 4043 | chr16 | 5019013 | ||||||
| chr16:5019021 | C | T | 1 | a0001c0002t0040 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4051C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 4051 | chr16 | 5019021 | ||||||
| chr16:5019057 | T | C | 1 | a0001c0012t0039 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4087T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 16/16 | 4087 | chr16 | 5019057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4958474 | G | GGAGCCC | 254 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-52+30_-52+31insAG others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 4958474 | ||||||
| chr16:4958535 | C | A | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+90C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958535 | |||||||
| chr16:4958755 | C | T | 23 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0249 others(20): Show |
23 | HG00280.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-52+310C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958755 | |||||||
| chr16:4958789 | G | A | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-52+344G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958789 | |||||||
| chr16:4958846 | C | T | 1 | a0001c0002t0042g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-52+401C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958846 | |||||||
| chr16:4958882 | C | T | 254 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-51-391C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958882 | |||||||
| chr16:4958948 | G | A | 2 | a0001c0002t0001g0255 a0001c0002t0001g0256 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-51-325G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4958948 | |||||||
| chr16:4959047 | G | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-51-226G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4959047 | |||||||
| chr16:4959075 | G | A | 1 | a0001c0002t0004g0257 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51-198G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4959075 | |||||||
| chr16:4959231 | C | T | 11 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0249 others(8): Show |
11 | HG00280.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-51-42C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 1/15 | chr16 | 4959231 | |||||||
| chr16:4959432 | G | A | 255 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.63+46G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959432 | |||||||
| chr16:4959461 | C | T | 1 | a0001c0001t0047g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+75C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959461 | |||||||
| chr16:4959475 | C | T | 1 | a0001c0001t0020g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.63+89C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959475 | |||||||
| chr16:4959495 | A | C | 3 | a0001c0002t0002g0242 a0001c0002t0004g0001 a0001c0004t0007g0241 |
3 | HG02896.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+109A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959495 | |||||||
| chr16:4959559 | C | G | 1 | a0001c0001t0054g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+173C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959559 | |||||||
| chr16:4959567 | G | A | 1 | a0001c0005t0001g0002 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.63+181G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959567 | |||||||
| chr16:4959604 | C | G | 43 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.63+218C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959604 | |||||||
| chr16:4959754 | T | C | 1 | a0001c0002t0055g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+368T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959754 | |||||||
| chr16:4959798 | G | A | 1 | a0001c0002t0002g0259 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.63+412G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959798 | |||||||
| chr16:4959857 | T | A | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+471T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959857 | |||||||
| chr16:4959878 | C | T | 3 | a0001c0001t0001g0376 a0001c0003t0003g0374 a0001c0003t0003g0375 |
3 | HG00642.hp2 HG01070.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.63+492C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959878 | |||||||
| chr16:4959905 | C | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(211): Show |
214 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.63+519C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4959905 | |||||||
| chr16:4960119 | T | G | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+733T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960119 | |||||||
| chr16:4960146 | G | A | 3 | a0001c0001t0004g0261 a0001c0003t0003g0262 a0001c0003t0003g0263 |
3 | HG02602.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.63+760G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960146 | |||||||
| chr16:4960172 | G | C | 255 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.63+786G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960172 | |||||||
| chr16:4960188 | G | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+802G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960188 | |||||||
| chr16:4960423 | C | G | 3 | a0001c0002t0002g0242 a0001c0002t0004g0001 a0001c0004t0007g0241 |
3 | HG02896.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+1037C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960423 | |||||||
| chr16:4960512 | T | C | 1 | a0001c0002t0002g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+1126T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960512 | |||||||
| chr16:4960605 | G | T | 1 | a0001c0001t0048g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+1219G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960605 | |||||||
| chr16:4960734 | G | C | 1 | a0001c0004t0012g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.63+1348G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960734 | |||||||
| chr16:4960758 | G | A | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+1372G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960758 | |||||||
| chr16:4960783 | C | T | 1 | a0001c0003t0003g0373 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.63+1397C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960783 | |||||||
| chr16:4960797 | A | G | 2 | a0001c0001t0054g0240 a0001c0022t0044g0239 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.63+1411A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960797 | |||||||
| chr16:4960827 | C | T | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+1441C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960827 | |||||||
| chr16:4960833 | T | C | 255 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.63+1447T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960833 | |||||||
| chr16:4960850 | G | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.63+1464G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960850 | |||||||
| chr16:4960912 | C | T | 255 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.63+1526C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960912 | |||||||
| chr16:4960943 | G | T | 1 | a0001c0002t0002g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+1557G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4960943 | |||||||
| chr16:4961113 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(151): Show |
154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.63+1727T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961113 | |||||||
| chr16:4961118 | G | A | 349 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(346): Show |
349 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.63+1732G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961118 | |||||||
| chr16:4961130 | G | A | 2 | a0001c0002t0018g0253 a0001c0024t0003g0254 |
2 | HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.63+1744G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961130 | |||||||
| chr16:4961286 | G | GCAACAAC others(5): Show |
1 | a0001c0020t0052g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+1907_63+1918dup others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4961286 | ||||||
| chr16:4961302 | C | CA | 99 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(96): Show |
99 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.63+1919dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4961302 | ||||||
| chr16:4961485 | T | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.63+2099T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961485 | |||||||
| chr16:4961532 | T | C | 1 | a0001c0008t0009g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+2146T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961532 | |||||||
| chr16:4961754 | G | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(152): Show |
155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.63+2368G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961754 | |||||||
| chr16:4961989 | A | C | 98 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(95): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.63+2603A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4961989 | |||||||
| chr16:4962141 | GGGCAACA others(18): Show |
G | 1 | a0001c0001t0001g0004 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.63+2756_63+2780del others(25): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962141 | |||||||
| chr16:4962165 | C | CA | 90 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0106 others(87): Show |
90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.63+2796dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962165 | ||||||
| chr16:4962251 | C | T | 1 | a0001c0002t0002g0215 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.63+2865C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962251 | |||||||
| chr16:4962269 | T | C | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+2883T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962269 | |||||||
| chr16:4962331 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.63+2945C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962331 | |||||||
| chr16:4962425 | T | C | 5 | a0001c0001t0009g0115 a0001c0001t0017g0116 a0001c0001t0017g0117 others(2): Show |
5 | HG01099.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+3039T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962425 | |||||||
| chr16:4962482 | G | C | 1 | a0001c0001t0022g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+3096G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962482 | |||||||
| chr16:4962491 | G | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+3105G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962491 | |||||||
| chr16:4962517 | G | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+3131G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962517 | |||||||
| chr16:4962568 | A | T | 1 | a0001c0007t0001g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+3182A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962568 | |||||||
| chr16:4962595 | G | A | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+3209G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962595 | |||||||
| chr16:4962628 | C | T | 1 | a0001c0005t0027g0346 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+3242C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962628 | |||||||
| chr16:4962686 | C | CA | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0220 others(25): Show |
28 | HG00597.hp2 HG01243.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.63+3322dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962686 | ||||||
| chr16:4962686 | C | CAA | 86 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.63+3321_63+3322dup others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962686 | ||||||
| chr16:4962686 | C | CAAA | 19 | a0001c0001t0001g0245 a0001c0001t0021g0120 a0001c0002t0001g0105 others(16): Show |
19 | HG01074.hp1 HG01255.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+3320_63+3322dup others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962686 | ||||||
| chr16:4962686 | CA | C | 18 | a0001c0001t0001g0088 a0001c0001t0002g0345 a0001c0001t0006g0092 others(15): Show |
18 | HG01975.hp2 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+3322delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962686 | ||||||
| chr16:4962686 | CAAAAA | C | 14 | a0001c0001t0016g0206 a0001c0001t0034g0214 a0001c0002t0002g0203 others(11): Show |
14 | HG02145.hp2 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+3318_63+3322del others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4962686 | ||||||
| chr16:4962698 | A | AC | 3 | a0001c0001t0020g0243 a0001c0001t0051g0238 a0001c0029t0010g0237 |
3 | HG02809.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3312_63+3313ins others(1): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962698 | |||||||
| chr16:4962698 | A | C | 1 | a0001c0001t0004g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.63+3312A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962698 | |||||||
| chr16:4962728 | G | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+3342G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962728 | |||||||
| chr16:4962796 | C | T | 1 | a0001c0016t0053g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+3410C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962796 | |||||||
| chr16:4962887 | C | T | 20 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(17): Show |
20 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+3501C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962887 | |||||||
| chr16:4962963 | G | T | 256 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.63+3577G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4962963 | |||||||
| chr16:4963302 | T | C | 2 | a0001c0003t0003g0266 a0010c0031t0003g0267 |
2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.63+3916T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963302 | |||||||
| chr16:4963376 | C | T | 4 | a0001c0002t0002g0370 a0001c0002t0002g0371 a0001c0002t0002g0372 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3990C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963376 | |||||||
| chr16:4963384 | C | T | 1 | a0001c0029t0010g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+3998C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963384 | |||||||
| chr16:4963576 | C | T | 14 | a0001c0001t0006g0086 a0001c0001t0006g0092 a0001c0001t0020g0096 others(11): Show |
14 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+4190C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963576 | |||||||
| chr16:4963591 | C | A | 3 | a0001c0001t0004g0261 a0001c0003t0003g0262 a0001c0003t0003g0263 |
3 | HG02602.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.63+4205C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963591 | |||||||
| chr16:4963611 | G | T | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.63+4225G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963611 | |||||||
| chr16:4963636 | G | T | 19 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+4250G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963636 | |||||||
| chr16:4963655 | CT | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
82 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.63+4275delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4963655 | ||||||
| chr16:4963685 | G | A | 7 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0003g0219 others(4): Show |
7 | HG00597.hp2 HG02015.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+4299G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963685 | |||||||
| chr16:4963752 | C | CAAGCCAT others(11): Show |
3 | a0001c0005t0001g0013 a0001c0005t0001g0015 a0007c0028t0001g0014 |
3 | NA18945.hp2 NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.63+4368_63+4385dup others(18): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4963752 | ||||||
| chr16:4963819 | A | C | 1 | a0001c0001t0001g0004 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.63+4433A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963819 | |||||||
| chr16:4963819 | A | G | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.63+4433A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963819 | |||||||
| chr16:4963857 | T | C | 9 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+4471T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963857 | |||||||
| chr16:4963859 | A | G | 1 | a0001c0020t0052g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+4473A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4963859 | |||||||
| chr16:4964018 | T | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
119 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.63+4632T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964018 | |||||||
| chr16:4964048 | T | C | 2 | a0001c0002t0004g0135 a0002c0021t0004g0136 |
2 | HG00438.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.63+4662T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964048 | |||||||
| chr16:4964068 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0078 a0001c0001t0001g0079 others(11): Show |
14 | HG00621.hp1 HG02004.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+4682A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964068 | |||||||
| chr16:4964214 | C | T | 6 | a0001c0001t0020g0243 a0001c0001t0051g0238 a0001c0002t0002g0242 others(3): Show |
6 | HG02809.hp1 HG02896.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+4828C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964214 | |||||||
| chr16:4964258 | C | T | 5 | a0001c0001t0009g0115 a0001c0001t0017g0116 a0001c0001t0017g0117 others(2): Show |
5 | HG01099.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+4872C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964258 | |||||||
| chr16:4964310 | C | G | 105 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(102): Show |
105 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.63+4924C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964310 | |||||||
| chr16:4964322 | C | T | 25 | a0001c0001t0001g0351 a0001c0002t0001g0361 a0001c0002t0002g0259 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+4936C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964322 | |||||||
| chr16:4964404 | T | G | 257 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(254): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.63+5018T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964404 | |||||||
| chr16:4964461 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(254): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.63+5075T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964461 | |||||||
| chr16:4964463 | G | C | 1 | a0001c0003t0003g0269 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.63+5077G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964463 | |||||||
| chr16:4964508 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63+5122C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964508 | |||||||
| chr16:4964539 | G | A | 1 | a0001c0001t0022g0089 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+5153G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964539 | |||||||
| chr16:4964569 | G | A | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+5183G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964569 | |||||||
| chr16:4964664 | G | A | 2 | a0001c0002t0002g0090 a0001c0002t0010g0091 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+5278G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964664 | |||||||
| chr16:4964678 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(254): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.63+5292T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964678 | |||||||
| chr16:4964766 | T | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00280.hp2 HG02145.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+5380T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964766 | |||||||
| chr16:4964790 | G | A | 108 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(105): Show |
108 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.63+5404G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964790 | |||||||
| chr16:4964849 | C | G | 258 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(255): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.63+5463C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964849 | |||||||
| chr16:4964952 | A | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(117): Show |
120 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+5566A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964952 | |||||||
| chr16:4964980 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(259): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.63+5594T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4964980 | |||||||
| chr16:4965086 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0002g0138 |
2 | NA18941.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.63+5700G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965086 | |||||||
| chr16:4965102 | G | A | 1 | a0001c0001t0054g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5716G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965102 | |||||||
| chr16:4965137 | A | G | 2 | a0001c0001t0001g0196 a0001c0003t0005g0195 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.63+5751A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965137 | |||||||
| chr16:4965174 | T | G | 3 | a0001c0001t0047g0231 a0001c0002t0002g0118 a0001c0008t0028g0119 |
3 | HG01891.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.63+5788T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965174 | |||||||
| chr16:4965193 | C | T | 11 | a0001c0001t0003g0333 a0001c0001t0003g0334 a0001c0001t0003g0336 others(8): Show |
11 | HG00438.hp2 HG02027.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+5807C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965193 | |||||||
| chr16:4965229 | A | G | 3 | a0001c0002t0002g0366 a0001c0002t0014g0367 a0001c0002t0014g0368 |
3 | HG00099.hp1 HG00323.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.63+5843A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965229 | |||||||
| chr16:4965315 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+5929T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965315 | |||||||
| chr16:4965391 | G | A | 2 | a0001c0002t0013g0025 a0001c0002t0013g0026 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.63+6005G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965391 | |||||||
| chr16:4965400 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+6014G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965400 | |||||||
| chr16:4965457 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.63+6071C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965457 | |||||||
| chr16:4965462 | C | G | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(4): Show |
7 | HG02004.hp2 HG02129.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6076C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965462 | |||||||
| chr16:4965523 | T | C | 1 | a0001c0001t0004g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.63+6137T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965523 | |||||||
| chr16:4965529 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.63+6143C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965529 | |||||||
| chr16:4965531 | G | A | 1 | a0001c0001t0054g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+6145G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965531 | |||||||
| chr16:4965546 | A | G | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+6160A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965546 | |||||||
| chr16:4965615 | A | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0061 others(14): Show |
17 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+6229A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965615 | |||||||
| chr16:4965616 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0061 others(13): Show |
16 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+6230G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965616 | |||||||
| chr16:4965658 | C | G | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | NA18981.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.63+6272C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965658 | |||||||
| chr16:4965660 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0024 others(33): Show |
36 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.63+6303dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4965660 | ||||||
| chr16:4965660 | CA | C | 85 | a0001c0001t0001g0106 a0001c0001t0001g0137 a0001c0001t0001g0245 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.63+6303delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4965660 | ||||||
| chr16:4965660 | CAA | C | 155 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0110 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.63+6302_63+6303del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4965660 | ||||||
| chr16:4965660 | CAAA | C | 11 | a0001c0001t0001g0330 a0001c0001t0054g0240 a0001c0001t0056g0236 others(8): Show |
11 | HG02622.hp1 HG02735.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+6301_63+6303del others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4965660 | ||||||
| chr16:4965760 | G | A | 24 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+6374G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965760 | |||||||
| chr16:4965789 | C | T | 104 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(101): Show |
104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.63+6403C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965789 | |||||||
| chr16:4965794 | C | A | 1 | a0001c0005t0027g0346 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+6408C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965794 | |||||||
| chr16:4965820 | C | T | 145 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.63+6434C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965820 | |||||||
| chr16:4965855 | A | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+6469A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965855 | |||||||
| chr16:4965926 | C | A | 1 | a0001c0002t0055g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+6540C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965926 | |||||||
| chr16:4965935 | G | A | 115 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0275 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.63+6549G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4965935 | |||||||
| chr16:4966002 | A | T | 145 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.63+6616A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966002 | |||||||
| chr16:4966098 | C | T | 145 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.63+6712C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966098 | |||||||
| chr16:4966123 | G | A | 130 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.63+6737G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966123 | |||||||
| chr16:4966208 | C | T | 3 | a0001c0002t0002g0242 a0001c0002t0004g0001 a0001c0004t0007g0241 |
3 | HG02896.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+6822C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966208 | |||||||
| chr16:4966250 | C | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0039 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.63+6864C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966250 | |||||||
| chr16:4966267 | C | CT | 47 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0037 others(44): Show |
47 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+6905dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4966267 | ||||||
| chr16:4966267 | CT | C | 78 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0040 others(75): Show |
78 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.63+6905delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4966267 | ||||||
| chr16:4966361 | C | T | 1 | a0001c0002t0002g0033 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.63+6975C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966361 | |||||||
| chr16:4966494 | G | T | 128 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.63+7108G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966494 | |||||||
| chr16:4966563 | C | T | 1 | a0001c0003t0003g0265 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.63+7177C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966563 | |||||||
| chr16:4966617 | C | T | 6 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0023g0218 others(3): Show |
6 | HG00597.hp2 HG02015.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+7231C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966617 | |||||||
| chr16:4966793 | G | A | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.63+7407G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966793 | |||||||
| chr16:4966875 | C | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0064 others(2): Show |
5 | NA18949.hp2 NA18951.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7489C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966875 | |||||||
| chr16:4966875 | C | T | 4 | a0001c0007t0001g0057 a0001c0007t0001g0100 a0001c0007t0024g0055 others(1): Show |
4 | HG03490.hp1 HG03492.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+7489C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966875 | |||||||
| chr16:4966876 | G | A | 111 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(108): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.63+7490G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966876 | |||||||
| chr16:4966959 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+7573C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4966959 | |||||||
| chr16:4967242 | C | T | 1 | a0006c0027t0003g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+7856C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967242 | |||||||
| chr16:4967386 | G | A | 83 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(80): Show |
83 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.63+8000G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967386 | |||||||
| chr16:4967404 | A | G | 1 | a0001c0002t0004g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.63+8018A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967404 | |||||||
| chr16:4967525 | G | T | 4 | a0001c0002t0002g0133 a0001c0002t0002g0181 a0001c0002t0002g0182 others(1): Show |
4 | HG00408.hp2 NA18969.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+8139G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967525 | |||||||
| chr16:4967561 | CGTTTT | C | 7 | a0001c0002t0002g0124 a0001c0002t0002g0179 a0001c0002t0008g0146 others(4): Show |
7 | HG01928.hp1 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+8176_63+8180del others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967561 | |||||||
| chr16:4967561 | CGTTTTT | C | 89 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.63+8176_63+8181del others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967561 | |||||||
| chr16:4967561 | CGTTTTTT | C | 4 | a0001c0002t0002g0140 a0001c0002t0002g0189 a0001c0002t0004g0198 others(1): Show |
4 | HG01074.hp1 NA19057.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8176_63+8182del others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967561 | |||||||
| chr16:4967562 | G | GT | 8 | a0001c0001t0001g0281 a0001c0001t0001g0293 a0001c0002t0001g0105 others(5): Show |
8 | HG01123.hp1 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+8206dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967562 | ||||||
| chr16:4967562 | GT | G | 105 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0034 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.63+8206delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967562 | ||||||
| chr16:4967562 | GTT | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.63+8205_63+8206del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967562 | ||||||
| chr16:4967562 | GTTTTT | G | 7 | a0001c0001t0056g0236 a0001c0002t0002g0118 a0001c0002t0002g0203 others(4): Show |
7 | HG02622.hp1 HG03098.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+8202_63+8206del others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967562 | ||||||
| chr16:4967562 | GTTTTTT | G | 13 | a0001c0001t0006g0092 a0001c0001t0020g0243 a0001c0001t0025g0260 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+8201_63+8206del others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967562 | ||||||
| chr16:4967567 | T | A | 7 | a0001c0002t0002g0124 a0001c0002t0002g0179 a0001c0002t0008g0146 others(4): Show |
7 | HG01928.hp1 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+8181T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967567 | |||||||
| chr16:4967568 | T | A | 89 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(86): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.63+8182T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967568 | |||||||
| chr16:4967569 | T | A | 4 | a0001c0002t0002g0140 a0001c0002t0002g0189 a0001c0002t0004g0198 others(1): Show |
4 | HG01074.hp1 NA19057.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8183T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967569 | |||||||
| chr16:4967593 | G | A | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63+8207G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967593 | |||||||
| chr16:4967853 | T | A | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+8467T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967853 | |||||||
| chr16:4967855 | C | T | 113 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(110): Show |
113 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.63+8469C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967855 | |||||||
| chr16:4967875 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+8489G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967875 | |||||||
| chr16:4967884 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.63+8498G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967884 | |||||||
| chr16:4967948 | T | TC | 42 | a0001c0001t0001g0024 a0001c0001t0001g0150 a0001c0001t0001g0157 others(39): Show |
42 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+8569dupC | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4967948 | ||||||
| chr16:4967960 | C | G | 1 | a0001c0001t0004g0319 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.63+8574C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967960 | |||||||
| chr16:4967964 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63+8578C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967964 | |||||||
| chr16:4967965 | C | T | 2 | a0001c0002t0004g0141 a0001c0002t0004g0343 |
2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.63+8579C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967965 | |||||||
| chr16:4967977 | C | T | 4 | a0001c0001t0020g0243 a0001c0001t0051g0238 a0001c0010t0046g0188 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8591C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4967977 | |||||||
| chr16:4968177 | G | T | 1 | a0001c0020t0052g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63+8791G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968177 | |||||||
| chr16:4968240 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.63+8854C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968240 | |||||||
| chr16:4968241 | G | A | 1 | a0001c0005t0001g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+8855G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968241 | |||||||
| chr16:4968244 | A | G | 3 | a0001c0002t0002g0187 a0001c0002t0002g0329 a0001c0002t0004g0328 |
3 | HG01167.hp1 HG01168.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.63+8858A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968244 | |||||||
| chr16:4968267 | C | G | 3 | a0001c0001t0054g0240 a0001c0016t0053g0233 a0001c0022t0044g0239 |
3 | HG01243.hp1 HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.63+8881C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968267 | |||||||
| chr16:4968323 | G | A | 23 | a0001c0001t0001g0351 a0001c0002t0001g0361 a0001c0002t0002g0350 others(20): Show |
23 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+8937G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968323 | |||||||
| chr16:4968337 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.63+8951G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968337 | |||||||
| chr16:4968350 | T | C | 1 | a0001c0001t0002g0016 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.63+8964T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968350 | |||||||
| chr16:4968368 | G | A | 97 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.63+8982G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968368 | |||||||
| chr16:4968545 | C | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+9159C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968545 | |||||||
| chr16:4968707 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.63+9321C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968707 | |||||||
| chr16:4968834 | C | T | 2 | a0001c0001t0001g0321 a0001c0003t0003g0291 |
2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.63+9448C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968834 | |||||||
| chr16:4968835 | G | C | 97 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.63+9449G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968835 | |||||||
| chr16:4968915 | A | AATTTAGC others(4): Show |
1 | a0001c0001t0001g0027 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.63+9530_63+9540dup others(11): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4968915 | ||||||
| chr16:4968986 | T | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+9600T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4968986 | |||||||
| chr16:4969007 | C | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+9621C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969007 | |||||||
| chr16:4969008 | G | A | 7 | a0001c0001t0031g0224 a0001c0004t0007g0226 a0001c0004t0007g0227 others(4): Show |
7 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9622G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969008 | |||||||
| chr16:4969180 | T | C | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+9794T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969180 | |||||||
| chr16:4969616 | TC | T | 11 | a0001c0001t0006g0092 a0001c0001t0020g0243 a0001c0001t0051g0238 others(8): Show |
11 | HG02486.hp1 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+10231delC | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969616 | |||||||
| chr16:4969783 | A | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+10397A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969783 | |||||||
| chr16:4969815 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.63+10429C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969815 | |||||||
| chr16:4969816 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.63+10430T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969816 | |||||||
| chr16:4969818 | TCC | T | 3 | a0001c0002t0002g0371 a0001c0002t0002g0372 a0001c0003t0003g0313 |
3 | HG02896.hp2 HG02897.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.63+10433_63+10434d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969818 | |||||||
| chr16:4969819 | C | T | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.63+10433C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969819 | |||||||
| chr16:4969820 | CT | C | 121 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0049 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+10450delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4969820 | ||||||
| chr16:4969822 | T | C | 3 | a0001c0002t0002g0371 a0001c0002t0002g0372 a0001c0003t0003g0313 |
3 | HG02896.hp2 HG02897.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.63+10436T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969822 | |||||||
| chr16:4969885 | A | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0003g0054 others(1): Show |
4 | NA18939.hp2 NA18987.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+10499A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969885 | |||||||
| chr16:4969974 | T | C | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+10588T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969974 | |||||||
| chr16:4969977 | T | C | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+10591T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969977 | |||||||
| chr16:4969989 | T | C | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+10603T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4969989 | |||||||
| chr16:4970001 | A | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+10615A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970001 | |||||||
| chr16:4970089 | G | A | 2 | a0001c0004t0007g0226 a0001c0004t0007g0227 |
2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.63+10703G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970089 | |||||||
| chr16:4970131 | G | A | 1 | a0001c0003t0003g0274 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.63+10745G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970131 | |||||||
| chr16:4970147 | G | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0275 a0001c0001t0001g0288 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10761G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970147 | |||||||
| chr16:4970169 | G | C | 5 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0008t0009g0111 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+10783G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970169 | |||||||
| chr16:4970173 | A | AG | 6 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0066 others(3): Show |
6 | HG00621.hp2 HG01978.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10792dupG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4970173 | ||||||
| chr16:4970219 | A | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.63+10833A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970219 | |||||||
| chr16:4970301 | G | C | 7 | a0001c0001t0006g0092 a0001c0002t0002g0235 a0001c0002t0002g0242 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+10915G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970301 | |||||||
| chr16:4970403 | T | G | 5 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0008t0009g0111 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+11017T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970403 | |||||||
| chr16:4970513 | T | C | 119 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.63+11127T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970513 | |||||||
| chr16:4970519 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.63+11133C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970519 | |||||||
| chr16:4970538 | A | G | 122 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11152A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970538 | |||||||
| chr16:4970694 | C | T | 1 | a0001c0007t0001g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63+11308C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970694 | |||||||
| chr16:4970696 | C | T | 6 | a0001c0001t0009g0115 a0001c0001t0017g0116 a0001c0001t0017g0117 others(3): Show |
6 | HG01099.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+11310C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970696 | |||||||
| chr16:4970705 | G | A | 1 | a0008c0023t0003g0337 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.63+11319G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970705 | |||||||
| chr16:4970782 | A | G | 122 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11396A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970782 | |||||||
| chr16:4970804 | T | C | 122 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11418T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970804 | |||||||
| chr16:4970811 | C | G | 1 | a0001c0003t0003g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.63+11425C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970811 | |||||||
| chr16:4970842 | G | C | 11 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0004g0287 others(8): Show |
11 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+11456G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970842 | |||||||
| chr16:4970936 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+11550C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970936 | |||||||
| chr16:4970953 | C | A | 119 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.63+11567C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4970953 | |||||||
| chr16:4971004 | G | A | 237 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.63+11618G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971004 | |||||||
| chr16:4971069 | C | T | 1 | a0001c0001t0004g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.63+11683C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971069 | |||||||
| chr16:4971091 | C | CA | 27 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0275 others(24): Show |
27 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.63+11723dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4971091 | ||||||
| chr16:4971126 | G | C | 7 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0002t0002g0118 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+11740G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971126 | |||||||
| chr16:4971145 | T | A | 122 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11759T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971145 | |||||||
| chr16:4971179 | A | G | 121 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+11793A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971179 | |||||||
| chr16:4971276 | C | T | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+11890C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971276 | |||||||
| chr16:4971348 | A | G | 1 | a0001c0004t0007g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+11962A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971348 | |||||||
| chr16:4971376 | T | C | 3 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0008t0009g0111 |
3 | HG02258.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.63+11990T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971376 | |||||||
| chr16:4971381 | G | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+11995G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971381 | |||||||
| chr16:4971384 | A | C | 116 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.63+11998A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971384 | |||||||
| chr16:4971407 | C | T | 1 | a0001c0007t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.63+12021C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971407 | |||||||
| chr16:4971450 | C | T | 1 | a0001c0009t0011g0312 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.63+12064C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971450 | |||||||
| chr16:4971486 | C | G | 1 | a0001c0003t0003g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.63+12100C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971486 | |||||||
| chr16:4971598 | A | T | 3 | a0001c0002t0002g0366 a0001c0002t0014g0367 a0001c0002t0014g0368 |
3 | HG00099.hp1 HG00323.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.63+12212A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971598 | |||||||
| chr16:4971658 | G | A | 110 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(107): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.63+12272G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971658 | |||||||
| chr16:4971660 | G | A | 2 | a0001c0002t0002g0118 a0001c0020t0052g0216 |
2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+12274G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971660 | |||||||
| chr16:4971674 | C | G | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.63+12288C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971674 | |||||||
| chr16:4971732 | G | A | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0025g0260 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12346G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971732 | |||||||
| chr16:4971754 | T | A | 5 | a0001c0002t0002g0235 a0001c0002t0002g0242 a0001c0002t0018g0213 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+12368T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971754 | |||||||
| chr16:4971823 | T | A | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.63+12437T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971823 | |||||||
| chr16:4971982 | A | C | 231 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.63+12596A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4971982 | |||||||
| chr16:4972049 | G | A | 227 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.63+12663G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972049 | |||||||
| chr16:4972152 | C | A | 10 | a0001c0002t0004g0200 a0001c0002t0004g0246 a0001c0003t0003g0134 others(7): Show |
10 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+12766C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972152 | |||||||
| chr16:4972164 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.63+12778G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972164 | |||||||
| chr16:4972313 | G | T | 230 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.63+12927G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972313 | |||||||
| chr16:4972405 | T | A | 1 | a0001c0002t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.63+13019T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972405 | |||||||
| chr16:4972476 | C | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+13090C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972476 | |||||||
| chr16:4972571 | A | G | 371 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.63+13185A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972571 | |||||||
| chr16:4972611 | T | A | 7 | a0001c0001t0031g0224 a0001c0004t0007g0226 a0001c0004t0007g0227 others(4): Show |
7 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+13225T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972611 | |||||||
| chr16:4972748 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.63+13362G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972748 | |||||||
| chr16:4972755 | T | G | 371 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.63+13369T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972755 | |||||||
| chr16:4972827 | C | G | 1 | a0001c0002t0006g0208 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63+13441C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972827 | |||||||
| chr16:4972863 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.63+13477C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4972863 | |||||||
| chr16:4973060 | T | G | 115 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.63+13674T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973060 | |||||||
| chr16:4973225 | G | T | 227 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.63+13839G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973225 | |||||||
| chr16:4973269 | C | T | 121 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+13883C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973269 | |||||||
| chr16:4973287 | T | A | 100 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(97): Show |
100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.63+13901T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973287 | |||||||
| chr16:4973402 | GCTTCCGG others(30): Show |
G | 118 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.63+14022_63+14058d others(39): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4973402 | ||||||
| chr16:4973492 | T | C | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0025g0260 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-14065T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973492 | |||||||
| chr16:4973520 | C | T | 97 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.64-14037C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973520 | |||||||
| chr16:4973678 | C | T | 93 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(90): Show |
93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.64-13879C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4973678 | |||||||
| chr16:4973680 | C | CT | 16 | a0001c0001t0001g0031 a0001c0001t0001g0059 a0001c0001t0016g0199 others(13): Show |
16 | HG00408.hp1 HG01517.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-13857dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4973680 | ||||||
| chr16:4973680 | CT | C | 49 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0110 others(46): Show |
49 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.64-13857delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4973680 | ||||||
| chr16:4973680 | CTT | C | 85 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(82): Show |
85 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-13858_64-13857d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4973680 | ||||||
| chr16:4974040 | G | A | 117 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.64-13517G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974040 | |||||||
| chr16:4974103 | T | G | 371 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.64-13454T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974103 | |||||||
| chr16:4974141 | T | C | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-13416T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974141 | |||||||
| chr16:4974212 | T | G | 7 | a0001c0001t0056g0236 a0001c0002t0002g0093 a0001c0002t0002g0094 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-13345T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974212 | |||||||
| chr16:4974215 | A | G | 1 | a0008c0023t0003g0337 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-13342A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974215 | |||||||
| chr16:4974269 | G | A | 1 | a0001c0016t0053g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-13288G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974269 | |||||||
| chr16:4974438 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64-13119A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974438 | |||||||
| chr16:4974493 | G | A | 102 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(99): Show |
102 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.64-13064G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974493 | |||||||
| chr16:4974529 | C | T | 120 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-13028C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974529 | |||||||
| chr16:4974549 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-13008A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974549 | |||||||
| chr16:4974561 | T | A | 2 | a0001c0001t0006g0092 a0001c0010t0013g0349 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-12996T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974561 | |||||||
| chr16:4974562 | A | T | 93 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(90): Show |
93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.64-12995A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974562 | |||||||
| chr16:4974585 | A | G | 1 | a0001c0002t0004g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64-12972A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974585 | |||||||
| chr16:4974591 | T | G | 2 | a0001c0001t0006g0092 a0001c0010t0013g0349 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-12966T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974591 | |||||||
| chr16:4974598 | G | A | 1 | a0001c0003t0003g0304 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.64-12959G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974598 | |||||||
| chr16:4974604 | C | CT | 21 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-12943dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4974604 | ||||||
| chr16:4974604 | CT | C | 112 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.64-12943delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4974604 | ||||||
| chr16:4974610 | T | C | 95 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(92): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-12947T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974610 | |||||||
| chr16:4974662 | T | C | 2 | a0001c0002t0002g0161 a0001c0002t0002g0189 |
2 | NA18980.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.64-12895T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974662 | |||||||
| chr16:4974847 | G | A | 3 | a0001c0003t0003g0276 a0001c0003t0003g0286 a0001c0003t0003g0298 |
3 | HG00099.hp2 HG01981.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.64-12710G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974847 | |||||||
| chr16:4974872 | T | A | 2 | a0001c0001t0006g0092 a0001c0010t0013g0349 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-12685T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4974872 | |||||||
| chr16:4975026 | C | A | 2 | a0001c0001t0006g0092 a0001c0010t0013g0349 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-12531C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975026 | |||||||
| chr16:4975341 | T | C | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-12216T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975341 | |||||||
| chr16:4975345 | C | T | 1 | a0001c0002t0055g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-12212C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975345 | |||||||
| chr16:4975362 | A | G | 1 | a0001c0002t0005g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-12195A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975362 | |||||||
| chr16:4975397 | C | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-12160C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975397 | |||||||
| chr16:4975404 | C | A | 2 | a0001c0001t0006g0092 a0001c0010t0013g0349 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-12153C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975404 | |||||||
| chr16:4975405 | A | G | 25 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0001g0351 others(22): Show |
25 | HG00597.hp2 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.64-12152A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975405 | |||||||
| chr16:4975422 | G | A | 1 | a0001c0005t0001g0035 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.64-12135G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975422 | |||||||
| chr16:4975472 | C | CA | 115 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(112): Show |
115 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.64-12065dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4975472 | ||||||
| chr16:4975472 | C | CAA | 116 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.64-12066_64-12065d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4975472 | ||||||
| chr16:4975472 | C | CAAA | 7 | a0001c0002t0002g0215 a0001c0002t0002g0350 a0001c0002t0002g0357 others(4): Show |
7 | HG00741.hp1 HG01258.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-12067_64-12065d others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4975472 | ||||||
| chr16:4975546 | C | A | 217 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(214): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.64-12011C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975546 | |||||||
| chr16:4975566 | T | C | 6 | a0001c0001t0006g0092 a0001c0002t0002g0203 a0001c0002t0002g0204 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-11991T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975566 | |||||||
| chr16:4975689 | T | C | 1 | a0001c0001t0020g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64-11868T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975689 | |||||||
| chr16:4975855 | G | A | 1 | a0001c0002t0004g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.64-11702G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975855 | |||||||
| chr16:4975868 | G | C | 119 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.64-11689G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975868 | |||||||
| chr16:4975899 | T | C | 1 | a0001c0007t0001g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.64-11658T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975899 | |||||||
| chr16:4975953 | C | T | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-11604C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975953 | |||||||
| chr16:4975961 | C | G | 6 | a0001c0001t0006g0092 a0001c0002t0002g0203 a0001c0002t0002g0204 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-11596C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975961 | |||||||
| chr16:4975978 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-11579C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4975978 | |||||||
| chr16:4976006 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.64-11551A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976006 | |||||||
| chr16:4976132 | C | T | 8 | a0001c0001t0001g0351 a0001c0001t0056g0236 a0001c0002t0002g0093 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-11425C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976132 | |||||||
| chr16:4976315 | A | C | 2 | a0001c0002t0002g0242 a0001c0004t0007g0241 |
2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-11242A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976315 | |||||||
| chr16:4976335 | C | T | 1 | a0001c0002t0004g0198 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.64-11222C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976335 | |||||||
| chr16:4976339 | G | T | 2 | a0001c0003t0003g0276 a0001c0003t0003g0298 |
2 | HG00099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.64-11218G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976339 | |||||||
| chr16:4976418 | C | G | 3 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0209 |
3 | HG02145.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.64-11139C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976418 | |||||||
| chr16:4976451 | T | C | 1 | a0011c0017t0008g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-11106T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976451 | |||||||
| chr16:4976483 | T | C | 233 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.64-11074T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976483 | |||||||
| chr16:4976590 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-10967C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976590 | |||||||
| chr16:4976608 | C | T | 2 | a0001c0002t0002g0242 a0001c0004t0007g0241 |
2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-10949C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976608 | |||||||
| chr16:4976910 | G | A | 2 | a0001c0001t0016g0199 a0001c0001t0016g0206 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-10647G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976910 | |||||||
| chr16:4976934 | C | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-10623C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4976934 | |||||||
| chr16:4977075 | T | C | 370 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.64-10482T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977075 | |||||||
| chr16:4977321 | C | G | 22 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(19): Show |
22 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-10236C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977321 | |||||||
| chr16:4977370 | C | T | 8 | a0001c0001t0001g0351 a0001c0001t0056g0236 a0001c0002t0002g0093 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-10187C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977370 | |||||||
| chr16:4977434 | G | A | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-10123G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977434 | |||||||
| chr16:4977442 | G | A | 244 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.64-10115G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977442 | |||||||
| chr16:4977446 | C | CA | 97 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.64-10088dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4977446 | ||||||
| chr16:4977446 | C | CAA | 24 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0001g0275 others(21): Show |
24 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.64-10089_64-10088d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4977446 | ||||||
| chr16:4977463 | A | AAAAAGG | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
111 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-10090_64-10089i others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4977463 | ||||||
| chr16:4977469 | A | G | 120 | a0001c0001t0001g0066 a0001c0001t0001g0106 a0001c0001t0001g0107 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-10088A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977469 | |||||||
| chr16:4977470 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
113 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.64-10087G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977470 | |||||||
| chr16:4977471 | G | A | 233 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.64-10086G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977471 | |||||||
| chr16:4977473 | A | AAAAAAAA others(1): Show |
21 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0006g0092 others(18): Show |
21 | HG00408.hp2 HG00597.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-10079_64-10072d others(10): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4977473 | ||||||
| chr16:4977473 | A | AAAAAAAG | 236 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0066 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.64-10078_64-10077i others(9): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4977473 | ||||||
| chr16:4977473 | A | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
113 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.64-10084A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977473 | |||||||
| chr16:4977511 | T | C | 1 | a0001c0001t0003g0333 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.64-10046T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977511 | |||||||
| chr16:4977538 | C | G | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-10019C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977538 | |||||||
| chr16:4977654 | A | G | 370 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.64-9903A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977654 | |||||||
| chr16:4977661 | G | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-9896G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977661 | |||||||
| chr16:4977666 | G | C | 1 | a0001c0002t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-9891G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977666 | |||||||
| chr16:4977696 | A | C | 8 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0002t0002g0235 others(5): Show |
8 | HG00597.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9861A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977696 | |||||||
| chr16:4977709 | C | A | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-9848C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977709 | |||||||
| chr16:4977714 | C | T | 93 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(90): Show |
93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.64-9843C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977714 | |||||||
| chr16:4977763 | G | A | 4 | a0001c0002t0004g0141 a0001c0002t0004g0248 a0001c0002t0004g0251 others(1): Show |
4 | HG01106.hp2 HG01123.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9794G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977763 | |||||||
| chr16:4977842 | T | C | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.64-9715T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977842 | |||||||
| chr16:4977910 | C | T | 8 | a0001c0001t0001g0351 a0001c0001t0056g0236 a0001c0002t0002g0093 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9647C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977910 | |||||||
| chr16:4977937 | A | G | 3 | a0001c0001t0006g0092 a0001c0003t0003g0153 a0001c0010t0013g0349 |
3 | HG02280.hp2 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-9620A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977937 | |||||||
| chr16:4977947 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-9610C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4977947 | |||||||
| chr16:4978016 | T | C | 1 | a0001c0001t0009g0115 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.64-9541T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978016 | |||||||
| chr16:4978137 | G | A | 1 | a0001c0002t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-9420G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978137 | |||||||
| chr16:4978233 | T | C | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-9324T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978233 | |||||||
| chr16:4978241 | C | T | 1 | a0001c0002t0002g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.64-9316C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978241 | |||||||
| chr16:4978244 | C | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.64-9313C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978244 | |||||||
| chr16:4978269 | T | A | 2 | a0001c0001t0004g0076 a0001c0002t0006g0369 |
2 | HG02132.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.64-9288T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978269 | |||||||
| chr16:4978277 | G | A | 1 | a0009c0013t0002g0264 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64-9280G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978277 | |||||||
| chr16:4978277 | G | T | 1 | a0001c0001t0054g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-9280G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978277 | |||||||
| chr16:4978285 | G | A | 2 | a0001c0001t0001g0294 a0001c0003t0003g0313 |
2 | HG03017.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.64-9272G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978285 | |||||||
| chr16:4978288 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-9269C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978288 | |||||||
| chr16:4978298 | C | T | 2 | a0001c0001t0001g0294 a0001c0003t0003g0313 |
2 | HG03017.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.64-9259C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978298 | |||||||
| chr16:4978300 | C | T | 1 | a0001c0002t0004g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-9257C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978300 | |||||||
| chr16:4978303 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-9254C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978303 | |||||||
| chr16:4978309 | T | C | 2 | a0001c0001t0001g0294 a0001c0003t0003g0313 |
2 | HG03017.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.64-9248T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978309 | |||||||
| chr16:4978338 | A | G | 1 | a0001c0002t0040g0289 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.64-9219A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978338 | |||||||
| chr16:4978341 | C | T | 3 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0047g0231 |
3 | HG01891.hp2 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-9216C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978341 | |||||||
| chr16:4978365 | C | T | 1 | a0001c0004t0007g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-9192C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978365 | |||||||
| chr16:4978403 | T | C | 373 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(370): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.64-9154T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978403 | |||||||
| chr16:4978416 | C | CA | 17 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0001g0351 others(14): Show |
17 | HG00597.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-9131dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4978416 | ||||||
| chr16:4978425 | AAGG | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0137 a0001c0001t0001g0294 others(7): Show |
10 | HG00099.hp2 HG01074.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-9130_64-9128del others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4978425 | ||||||
| chr16:4978426 | AG | A | 4 | a0001c0001t0001g0278 a0001c0002t0002g0205 a0001c0002t0004g0173 others(1): Show |
4 | HG01256.hp1 HG02451.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-9129delG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4978426 | ||||||
| chr16:4978426 | AGG | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
217 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.64-9130_64-9129del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978426 | |||||||
| chr16:4978427 | G | A | 143 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.64-9130G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978427 | |||||||
| chr16:4978428 | G | A | 147 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.64-9129G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978428 | |||||||
| chr16:4978484 | T | C | 1 | a0001c0005t0027g0346 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-9073T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978484 | |||||||
| chr16:4978497 | C | A | 6 | a0001c0001t0001g0351 a0001c0002t0002g0093 a0001c0002t0002g0094 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9060C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978497 | |||||||
| chr16:4978546 | G | A | 8 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0002t0002g0235 others(5): Show |
8 | HG00597.hp2 HG02040.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9011G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978546 | |||||||
| chr16:4978643 | C | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
112 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.64-8914C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978643 | |||||||
| chr16:4978727 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.64-8830C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978727 | |||||||
| chr16:4978741 | T | C | 98 | a0001c0001t0001g0157 a0001c0001t0001g0177 a0001c0001t0001g0196 others(95): Show |
98 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.64-8816T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978741 | |||||||
| chr16:4978760 | G | A | 2 | a0001c0002t0002g0164 a0001c0002t0002g0197 |
2 | HG02071.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.64-8797G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978760 | |||||||
| chr16:4978771 | CTT | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
111 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.64-8783_64-8782del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4978771 | ||||||
| chr16:4978792 | C | T | 1 | a0001c0002t0002g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-8765C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978792 | |||||||
| chr16:4978793 | G | T | 3 | a0001c0005t0001g0013 a0001c0005t0001g0015 a0007c0028t0001g0014 |
3 | NA18945.hp2 NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.64-8764G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978793 | |||||||
| chr16:4978801 | C | T | 1 | a0001c0002t0006g0369 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-8756C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978801 | |||||||
| chr16:4978802 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-8755C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978802 | |||||||
| chr16:4978837 | G | C | 1 | a0001c0003t0003g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-8720G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978837 | |||||||
| chr16:4978959 | G | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(229): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.64-8598G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978959 | |||||||
| chr16:4978989 | A | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.64-8568A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4978989 | |||||||
| chr16:4979242 | G | A | 1 | a0001c0001t0004g0301 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.64-8315G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979242 | |||||||
| chr16:4979250 | C | T | 1 | a0001c0029t0010g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-8307C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979250 | |||||||
| chr16:4979496 | A | G | 130 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.64-8061A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979496 | |||||||
| chr16:4979660 | G | A | 1 | a0001c0003t0003g0324 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-7897G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979660 | |||||||
| chr16:4979727 | C | T | 22 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(19): Show |
22 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-7830C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979727 | |||||||
| chr16:4979731 | T | TGTG | 365 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(362): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.64-7824_64-7823ins others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4979731 | ||||||
| chr16:4979934 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-7623C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979934 | |||||||
| chr16:4979964 | A | C | 1 | a0005c0025t0029g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64-7593A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979964 | |||||||
| chr16:4979978 | C | T | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.64-7579C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4979978 | |||||||
| chr16:4980082 | C | T | 1 | a0001c0004t0019g0230 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64-7475C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980082 | |||||||
| chr16:4980210 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.64-7347G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980210 | |||||||
| chr16:4980265 | G | A | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-7292G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980265 | |||||||
| chr16:4980300 | C | T | 1 | a0009c0013t0002g0264 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64-7257C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980300 | |||||||
| chr16:4980360 | A | T | 8 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0009g0115 others(5): Show |
8 | HG00323.hp2 HG00597.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-7197A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980360 | |||||||
| chr16:4980398 | T | C | 371 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.64-7159T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980398 | |||||||
| chr16:4980521 | C | T | 2 | a0001c0001t0016g0199 a0001c0001t0016g0206 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.64-7036C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980521 | |||||||
| chr16:4980696 | C | T | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-6861C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980696 | |||||||
| chr16:4980769 | GAGGGTGT others(10): Show |
G | 1 | a0009c0013t0002g0264 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64-6784_64-6768del others(17): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4980769 | ||||||
| chr16:4980780 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0032 others(28): Show |
31 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.64-6777G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980780 | |||||||
| chr16:4980793 | A | T | 1 | a0009c0013t0002g0264 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64-6764A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980793 | |||||||
| chr16:4980962 | G | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0009t0011g0221 others(3): Show |
6 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-6595G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4980962 | |||||||
| chr16:4981035 | G | T | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.64-6522G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981035 | |||||||
| chr16:4981036 | T | G | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.64-6521T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981036 | |||||||
| chr16:4981083 | A | AG | 373 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(370): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.64-6472dupG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981083 | ||||||
| chr16:4981123 | A | C | 32 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(29): Show |
32 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.64-6434A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981123 | |||||||
| chr16:4981138 | A | G | 1 | a0001c0016t0053g0233 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64-6419A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981138 | |||||||
| chr16:4981187 | A | G | 264 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.64-6370A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981187 | |||||||
| chr16:4981225 | C | T | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-6332C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981225 | |||||||
| chr16:4981255 | G | GT | 38 | a0001c0001t0016g0199 a0001c0002t0002g0003 a0001c0002t0002g0090 others(35): Show |
38 | HG00438.hp1 HG00741.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.64-6274dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | G | GTT | 8 | a0001c0002t0002g0179 a0001c0002t0002g0184 a0001c0002t0002g0215 others(5): Show |
8 | HG01106.hp2 HG01123.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-6275_64-6274dup others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GT | G | 15 | a0001c0001t0001g0157 a0001c0001t0004g0261 a0001c0002t0001g0122 others(12): Show |
15 | HG00408.hp2 HG00558.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-6274delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTT | G | 26 | a0001c0001t0001g0278 a0001c0001t0001g0294 a0001c0001t0001g0295 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.64-6275_64-6274del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTT | G | 84 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(81): Show |
84 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-6276_64-6274del others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTTT | G | 7 | a0001c0002t0001g0361 a0001c0002t0014g0367 a0001c0002t0045g0352 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6277_64-6274del others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTTTTT | G | 18 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-6279_64-6274del others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTTTTTT | G | 20 | a0001c0001t0001g0217 a0001c0001t0001g0220 a0001c0001t0031g0224 others(17): Show |
20 | HG00323.hp2 HG00544.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-6280_64-6274del others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0001g0058 a0001c0005t0001g0013 |
2 | HG04204.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.64-6287_64-6274del others(14): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981255 | GTTTTTTT others(8): Show |
G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
102 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.64-6288_64-6274del others(15): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4981255 | ||||||
| chr16:4981286 | A | G | 5 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0008t0009g0111 others(2): Show |
5 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6271A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981286 | |||||||
| chr16:4981325 | T | C | 2 | a0001c0002t0002g0205 a0001c0002t0042g0232 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.64-6232T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981325 | |||||||
| chr16:4981417 | A | T | 5 | a0001c0008t0028g0119 a0001c0009t0011g0221 a0001c0009t0011g0305 others(2): Show |
5 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6140A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981417 | |||||||
| chr16:4981447 | A | C | 2 | a0001c0002t0002g0205 a0001c0002t0042g0232 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.64-6110A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981447 | |||||||
| chr16:4981468 | G | A | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-6089G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981468 | |||||||
| chr16:4981485 | T | C | 1 | a0001c0002t0002g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-6072T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981485 | |||||||
| chr16:4981511 | T | C | 16 | a0001c0001t0001g0351 a0001c0001t0025g0260 a0001c0001t0047g0231 others(13): Show |
16 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-6046T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981511 | |||||||
| chr16:4981586 | C | T | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-5971C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981586 | |||||||
| chr16:4981587 | G | C | 1 | a0001c0002t0055g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64-5970G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981587 | |||||||
| chr16:4981623 | A | G | 5 | a0001c0001t0001g0351 a0001c0001t0056g0236 a0001c0002t0002g0118 others(2): Show |
5 | HG01884.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5934A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981623 | |||||||
| chr16:4981668 | G | A | 17 | a0001c0001t0001g0157 a0001c0002t0001g0122 a0001c0002t0001g0132 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-5889G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981668 | |||||||
| chr16:4981682 | A | G | 4 | a0001c0002t0004g0287 a0001c0003t0003g0271 a0001c0003t0003g0322 others(1): Show |
4 | HG00741.hp2 HG01109.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-5875A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981682 | |||||||
| chr16:4981771 | C | T | 1 | a0001c0001t0048g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-5786C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981771 | |||||||
| chr16:4981843 | A | G | 233 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(230): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.64-5714A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981843 | |||||||
| chr16:4981843 | A | T | 1 | a0001c0001t0002g0023 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.64-5714A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981843 | |||||||
| chr16:4981865 | C | T | 1 | a0001c0001t0004g0303 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64-5692C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981865 | |||||||
| chr16:4981914 | G | A | 1 | a0001c0002t0004g0246 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64-5643G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981914 | |||||||
| chr16:4981961 | C | A | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-5596C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981961 | |||||||
| chr16:4981995 | C | T | 2 | a0001c0008t0028g0119 a0005c0025t0029g0121 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.64-5562C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4981995 | |||||||
| chr16:4982135 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0045 others(6): Show |
9 | HG00609.hp1 HG00673.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-5422G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982135 | |||||||
| chr16:4982215 | C | T | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-5342C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982215 | |||||||
| chr16:4982241 | C | A | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-5316C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982241 | |||||||
| chr16:4982258 | G | A | 1 | a0001c0001t0054g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-5299G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982258 | |||||||
| chr16:4982297 | C | A | 76 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(73): Show |
76 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-5260C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982297 | |||||||
| chr16:4982312 | A | G | 1 | a0001c0007t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-5245A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982312 | |||||||
| chr16:4982316 | C | T | 1 | a0001c0001t0048g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-5241C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982316 | |||||||
| chr16:4982362 | A | G | 2 | a0001c0002t0002g0242 a0001c0004t0007g0241 |
2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-5195A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982362 | |||||||
| chr16:4982367 | G | A | 3 | a0001c0002t0002g0118 a0001c0002t0002g0235 a0001c0020t0052g0216 |
3 | HG02486.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.64-5190G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982367 | |||||||
| chr16:4982442 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-5115C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982442 | |||||||
| chr16:4982458 | C | T | 77 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(74): Show |
77 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.64-5099C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982458 | |||||||
| chr16:4982584 | G | C | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-4973G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982584 | |||||||
| chr16:4982630 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.64-4927A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982630 | |||||||
| chr16:4982673 | G | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(117): Show |
120 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-4884G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982673 | |||||||
| chr16:4982774 | G | A | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-4783G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982774 | |||||||
| chr16:4982885 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.64-4672C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982885 | |||||||
| chr16:4982909 | A | G | 229 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(226): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.64-4648A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982909 | |||||||
| chr16:4982929 | T | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
121 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-4628T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982929 | |||||||
| chr16:4982979 | T | C | 12 | a0001c0002t0004g0200 a0001c0002t0004g0246 a0001c0002t0004g0257 others(9): Show |
12 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-4578T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4982979 | |||||||
| chr16:4983065 | C | T | 12 | a0001c0002t0004g0200 a0001c0002t0004g0246 a0001c0002t0004g0257 others(9): Show |
12 | HG00140.hp1 HG01074.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-4492C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983065 | |||||||
| chr16:4983307 | C | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(221): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.64-4250C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983307 | |||||||
| chr16:4983397 | T | C | 5 | a0001c0002t0002g0370 a0001c0002t0002g0371 a0001c0002t0002g0372 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4160T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983397 | |||||||
| chr16:4983440 | TTCTA | T | 28 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(25): Show |
28 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-4111_64-4108del others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983440 | ||||||
| chr16:4983548 | A | T | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.64-4009A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983548 | |||||||
| chr16:4983643 | G | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3914G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983643 | |||||||
| chr16:4983694 | T | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
100 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.64-3863T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983694 | |||||||
| chr16:4983695 | G | T | 1 | a0001c0001t0004g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.64-3862G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983695 | |||||||
| chr16:4983712 | A | G | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-3845A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983712 | |||||||
| chr16:4983748 | G | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-3809G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983748 | |||||||
| chr16:4983761 | C | G | 7 | a0001c0001t0025g0260 a0001c0001t0047g0231 a0001c0001t0056g0236 others(4): Show |
7 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-3796C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983761 | |||||||
| chr16:4983771 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64-3786G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983771 | |||||||
| chr16:4983778 | A | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
109 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.64-3779A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983778 | |||||||
| chr16:4983792 | G | A | 2 | a0001c0002t0002g0090 a0001c0002t0010g0091 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-3765G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983792 | |||||||
| chr16:4983877 | CAAAT | C | 219 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(216): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.64-3642_64-3639del others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983877 | ||||||
| chr16:4983877 | CAAATAAA others(1): Show |
C | 28 | a0001c0001t0001g0351 a0001c0001t0006g0086 a0001c0001t0009g0115 others(25): Show |
28 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.64-3646_64-3639del others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983877 | ||||||
| chr16:4983877 | CAAATAAA others(5): Show |
C | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-3650_64-3639del others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983877 | ||||||
| chr16:4983877 | CAAATAAA others(9): Show |
C | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-3654_64-3639del others(16): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983877 | ||||||
| chr16:4983881 | T | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3676T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983881 | |||||||
| chr16:4983883 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.64-3674A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983883 | |||||||
| chr16:4983902 | AAATAAAT | A | 3 | a0001c0002t0004g0287 a0001c0003t0003g0271 a0001c0003t0037g0270 |
3 | HG00741.hp2 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.64-3652_64-3646del others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983902 | ||||||
| chr16:4983906 | AAAT | A | 73 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(70): Show |
73 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.64-3648_64-3646del others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4983906 | ||||||
| chr16:4983918 | A | AAATT | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-3639_64-3638ins others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983918 | |||||||
| chr16:4983958 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3599C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983958 | |||||||
| chr16:4983981 | A | G | 76 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(73): Show |
76 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-3576A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983981 | |||||||
| chr16:4983992 | C | G | 10 | a0001c0001t0025g0260 a0001c0001t0047g0231 a0001c0001t0056g0236 others(7): Show |
10 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-3565C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4983992 | |||||||
| chr16:4984023 | A | G | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-3534A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984023 | |||||||
| chr16:4984088 | A | G | 228 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(225): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.64-3469A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984088 | |||||||
| chr16:4984198 | A | G | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.64-3359A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984198 | |||||||
| chr16:4984210 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3347C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984210 | |||||||
| chr16:4984278 | A | G | 2 | a0001c0001t0021g0120 a0005c0025t0029g0121 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.64-3279A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984278 | |||||||
| chr16:4984304 | A | C | 1 | a0001c0002t0004g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64-3253A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984304 | |||||||
| chr16:4984329 | A | G | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-3228A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984329 | |||||||
| chr16:4984371 | G | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-3186G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984371 | |||||||
| chr16:4984438 | G | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3119G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984438 | |||||||
| chr16:4984476 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3081C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984476 | |||||||
| chr16:4984483 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
121 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-3074T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984483 | |||||||
| chr16:4984484 | G | A | 1 | a0001c0001t0004g0008 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.64-3073G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984484 | |||||||
| chr16:4984551 | A | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-3006A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984551 | |||||||
| chr16:4984566 | G | A | 9 | a0001c0001t0003g0219 a0001c0001t0003g0333 a0001c0001t0003g0334 others(6): Show |
9 | HG00438.hp2 HG02523.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-2991G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984566 | |||||||
| chr16:4984670 | A | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-2887A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984670 | |||||||
| chr16:4984819 | T | C | 10 | a0001c0001t0025g0260 a0001c0001t0047g0231 a0001c0001t0056g0236 others(7): Show |
10 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2738T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984819 | |||||||
| chr16:4984831 | A | G | 76 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(73): Show |
76 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-2726A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984831 | |||||||
| chr16:4984874 | T | G | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-2683T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984874 | |||||||
| chr16:4984878 | A | G | 26 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.64-2679A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984878 | |||||||
| chr16:4984886 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64-2671A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984886 | |||||||
| chr16:4984895 | T | C | 2 | a0001c0001t0021g0120 a0005c0025t0029g0121 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.64-2662T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984895 | |||||||
| chr16:4984939 | C | G | 1 | a0001c0003t0003g0317 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.64-2618C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4984939 | |||||||
| chr16:4985022 | A | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
109 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.64-2535A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985022 | |||||||
| chr16:4985029 | T | C | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-2528T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985029 | |||||||
| chr16:4985160 | A | G | 2 | a0001c0002t0002g0161 a0001c0002t0002g0189 |
2 | NA18980.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.64-2397A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985160 | |||||||
| chr16:4985249 | G | A | 1 | a0001c0002t0018g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.64-2308G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985249 | |||||||
| chr16:4985392 | A | T | 3 | a0001c0001t0004g0261 a0001c0003t0003g0262 a0001c0003t0003g0263 |
3 | HG02602.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.64-2165A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985392 | |||||||
| chr16:4985400 | C | G | 106 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0106 others(103): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-2157C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985400 | |||||||
| chr16:4985491 | G | T | 1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64-2066G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985491 | |||||||
| chr16:4985546 | A | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-2011A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985546 | |||||||
| chr16:4985559 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0037 |
2 | NA19000.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.64-1998A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985559 | |||||||
| chr16:4985596 | T | C | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1961T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985596 | |||||||
| chr16:4985650 | G | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1907G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985650 | |||||||
| chr16:4985763 | A | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1794A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985763 | |||||||
| chr16:4985799 | AATTAT | A | 4 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0326 others(1): Show |
4 | HG02071.hp2 HG02080.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-1750_64-1746del others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4985799 | ||||||
| chr16:4985967 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(115): Show |
118 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.64-1590A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4985967 | |||||||
| chr16:4986018 | G | C | 1 | a0001c0001t0048g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-1539G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986018 | |||||||
| chr16:4986059 | G | A | 1 | a0001c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64-1498G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986059 | |||||||
| chr16:4986088 | G | T | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.64-1469G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986088 | |||||||
| chr16:4986096 | T | C | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-1461T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986096 | |||||||
| chr16:4986142 | C | CT | 9 | a0001c0001t0021g0120 a0001c0001t0025g0260 a0001c0001t0047g0231 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1401dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4986142 | ||||||
| chr16:4986142 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1415C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986142 | |||||||
| chr16:4986183 | A | G | 7 | a0001c0001t0001g0351 a0001c0001t0054g0240 a0001c0002t0002g0093 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1374A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986183 | |||||||
| chr16:4986228 | T | C | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1329T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986228 | |||||||
| chr16:4986301 | G | A | 1 | a0001c0002t0045g0352 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.64-1256G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986301 | |||||||
| chr16:4986370 | T | C | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1187T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986370 | |||||||
| chr16:4986448 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1109C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986448 | |||||||
| chr16:4986497 | T | G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-1060T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986497 | |||||||
| chr16:4986534 | C | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-1023C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986534 | |||||||
| chr16:4986757 | G | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-800G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986757 | |||||||
| chr16:4986799 | A | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-758A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986799 | |||||||
| chr16:4986800 | G | T | 1 | a0001c0003t0003g0282 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64-757G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986800 | |||||||
| chr16:4986896 | C | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-661C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986896 | |||||||
| chr16:4986928 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-629C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986928 | |||||||
| chr16:4986945 | G | C | 2 | a0001c0002t0002g0329 a0001c0002t0004g0328 |
2 | HG01167.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.64-612G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986945 | |||||||
| chr16:4986961 | T | C | 3 | a0001c0002t0002g0118 a0001c0002t0002g0235 a0001c0020t0052g0216 |
3 | HG02486.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.64-596T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4986961 | |||||||
| chr16:4987080 | A | G | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-477A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987080 | |||||||
| chr16:4987107 | G | T | 1 | a0001c0002t0002g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.64-450G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987107 | |||||||
| chr16:4987201 | C | CT | 245 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(242): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.64-341dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987201 | ||||||
| chr16:4987201 | C | CTT | 25 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(22): Show |
25 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.64-342_64-341dupTT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987201 | ||||||
| chr16:4987201 | C | CTTT | 61 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(58): Show |
61 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.64-343_64-341dupTT others(1): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987201 | ||||||
| chr16:4987201 | C | CTTTT | 17 | a0001c0001t0001g0278 a0001c0001t0001g0284 a0001c0001t0001g0296 others(14): Show |
17 | HG00738.hp1 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-344_64-341dupTT others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987201 | ||||||
| chr16:4987226 | G | T | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.64-331G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987226 | |||||||
| chr16:4987247 | T | G | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-310T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987247 | |||||||
| chr16:4987264 | A | G | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64-293A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987264 | |||||||
| chr16:4987310 | G | C | 1 | a0001c0002t0008g0273 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.64-247G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987310 | |||||||
| chr16:4987374 | G | A | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-183G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987374 | |||||||
| chr16:4987418 | G | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-139G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987418 | |||||||
| chr16:4987497 | T | TG | 108 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0030 others(105): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.64-49dupG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987497 | T | TGG | 95 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0041 others(92): Show |
95 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-50_64-49dupGG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987497 | T | TGGA | 24 | a0001c0001t0001g0150 a0001c0001t0001g0278 a0001c0001t0001g0284 others(21): Show |
24 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-58_64-57insAGG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987497 | T | TGGAG | 40 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0281 others(37): Show |
40 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-58_64-57insAGGG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987497 | T | TGGG | 27 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0021g0120 others(24): Show |
27 | HG00140.hp1 HG00323.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-51_64-49dupGGG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987497 | T | TGGGCGGC others(3): Show |
1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-57_64-56insCGGC others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 4987497 | ||||||
| chr16:4987521 | C | G | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-36C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987521 | |||||||
| chr16:4987522 | C | G | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.64-35C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987522 | |||||||
| chr16:4987525 | A | C | 1 | a0001c0002t0005g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-32A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 2/15 | chr16 | 4987525 | |||||||
| chr16:4987752 | G | C | 7 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+46G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987752 | |||||||
| chr16:4987753 | A | G | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+47A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987753 | |||||||
| chr16:4987771 | C | T | 2 | a0001c0001t0025g0260 a0001c0001t0047g0231 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+65C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987771 | |||||||
| chr16:4987863 | C | CGGGACCC others(7): Show |
1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.213+163_213+164ins others(14): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 4987863 | ||||||
| chr16:4987867 | A | C | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+161A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987867 | |||||||
| chr16:4987955 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.214-194G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987955 | |||||||
| chr16:4987975 | G | C | 1 | a0001c0002t0004g0148 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.214-174G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4987975 | |||||||
| chr16:4988111 | G | A | 1 | a0001c0003t0003g0029 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.214-38G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 3/15 | chr16 | 4988111 | |||||||
| chr16:4988294 | A | G | 18 | a0001c0001t0001g0351 a0001c0001t0006g0092 a0001c0001t0054g0240 others(15): Show |
18 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.345+14A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988294 | |||||||
| chr16:4988409 | A | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.345+129A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988409 | |||||||
| chr16:4988448 | A | G | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.345+168A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988448 | |||||||
| chr16:4988638 | C | T | 1 | a0001c0009t0011g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.345+358C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988638 | |||||||
| chr16:4988782 | C | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+502C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988782 | |||||||
| chr16:4988832 | G | C | 2 | a0001c0004t0012g0114 a0001c0004t0012g0258 |
2 | HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.345+552G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988832 | |||||||
| chr16:4988875 | C | G | 16 | a0001c0001t0001g0351 a0001c0001t0006g0092 a0001c0002t0002g0093 others(13): Show |
16 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.345+595C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988875 | |||||||
| chr16:4988906 | C | T | 17 | a0001c0001t0001g0351 a0001c0001t0054g0240 a0001c0002t0002g0093 others(14): Show |
17 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.345+626C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988906 | |||||||
| chr16:4988940 | G | T | 4 | a0001c0002t0002g0003 a0001c0002t0002g0090 a0001c0002t0002g0103 others(1): Show |
4 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+660G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988940 | |||||||
| chr16:4988967 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.345+687A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988967 | |||||||
| chr16:4988987 | G | T | 2 | a0001c0008t0009g0283 a0001c0008t0009g0327 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.345+707G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4988987 | |||||||
| chr16:4989218 | C | T | 6 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(3): Show |
6 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+938C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989218 | |||||||
| chr16:4989247 | A | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(223): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.345+967A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989247 | |||||||
| chr16:4989298 | G | GT | 13 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(10): Show |
13 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.345+1029dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 4989298 | ||||||
| chr16:4989298 | GT | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.345+1029delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 4989298 | ||||||
| chr16:4989299 | T | G | 17 | a0001c0001t0001g0351 a0001c0001t0006g0092 a0001c0001t0054g0240 others(14): Show |
17 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.345+1019T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989299 | |||||||
| chr16:4989306 | T | G | 5 | a0001c0001t0003g0307 a0001c0001t0031g0224 a0001c0002t0002g0242 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+1026T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989306 | |||||||
| chr16:4989310 | G | T | 3 | a0001c0001t0003g0054 a0001c0003t0003g0373 a0001c0010t0046g0188 |
3 | HG01109.hp1 HG02895.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.345+1030G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989310 | |||||||
| chr16:4989326 | TG | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0017g0116 others(1): Show |
4 | HG02723.hp2 NA18949.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+1047delG | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989326 | |||||||
| chr16:4989327 | GT | G | 327 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(324): Show |
327 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.345+1058delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 4989327 | ||||||
| chr16:4989331 | T | G | 3 | a0001c0001t0031g0224 a0001c0002t0002g0242 a0001c0004t0007g0241 |
3 | HG02896.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.345+1051T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989331 | |||||||
| chr16:4989338 | T | G | 16 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0107 others(13): Show |
16 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.345+1058T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989338 | |||||||
| chr16:4989339 | G | T | 16 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0107 others(13): Show |
16 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.345+1059G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989339 | |||||||
| chr16:4989341 | T | C | 1 | a0001c0002t0002g0235 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.345+1061T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989341 | |||||||
| chr16:4989343 | G | T | 225 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.345+1063G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989343 | |||||||
| chr16:4989394 | A | G | 226 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(223): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.345+1114A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989394 | |||||||
| chr16:4989472 | G | A | 18 | a0001c0001t0001g0351 a0001c0001t0006g0092 a0001c0002t0002g0093 others(15): Show |
18 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.345+1192G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989472 | |||||||
| chr16:4989472 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.345+1192G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989472 | |||||||
| chr16:4989504 | A | G | 77 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(74): Show |
77 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.345+1224A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989504 | |||||||
| chr16:4989606 | C | G | 1 | a0001c0002t0004g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.346-1161C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989606 | |||||||
| chr16:4989616 | G | T | 1 | a0001c0003t0003g0317 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.346-1151G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989616 | |||||||
| chr16:4989637 | G | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.346-1130G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989637 | |||||||
| chr16:4989827 | C | T | 21 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.346-940C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989827 | |||||||
| chr16:4989997 | A | T | 75 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(72): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.346-770A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4989997 | |||||||
| chr16:4990081 | C | A | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.346-686C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990081 | |||||||
| chr16:4990081 | C | T | 107 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.346-686C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990081 | |||||||
| chr16:4990166 | A | G | 1 | a0001c0002t0045g0352 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.346-601A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990166 | |||||||
| chr16:4990169 | AT | A | 75 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(72): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.346-588delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 4990169 | ||||||
| chr16:4990249 | G | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
126 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.346-518G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990249 | |||||||
| chr16:4990265 | C | T | 6 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(3): Show |
6 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-502C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990265 | |||||||
| chr16:4990353 | G | C | 8 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(5): Show |
8 | HG01099.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.346-414G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990353 | |||||||
| chr16:4990377 | C | G | 85 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(82): Show |
85 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.346-390C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990377 | |||||||
| chr16:4990432 | G | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.346-335G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990432 | |||||||
| chr16:4990572 | G | C | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.346-195G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990572 | |||||||
| chr16:4990716 | C | T | 76 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(73): Show |
76 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.346-51C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990716 | |||||||
| chr16:4990720 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.346-47G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 4/15 | chr16 | 4990720 | |||||||
| chr16:4990902 | G | A | 1 | a0001c0005t0001g0087 | 1 | NA19056.hp1 | splice_region_variant&intron_variant | LOW | c.474+7G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4990902 | |||||||
| chr16:4990962 | A | T | 1 | a0001c0001t0022g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474+67A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4990962 | |||||||
| chr16:4990969 | CT | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(110): Show |
113 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.474+75delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4990969 | |||||||
| chr16:4990970 | T | C | 33 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.474+75T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4990970 | |||||||
| chr16:4990997 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.474+102C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4990997 | |||||||
| chr16:4991086 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.474+191C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991086 | |||||||
| chr16:4991162 | C | CT | 28 | a0001c0001t0001g0040 a0001c0001t0001g0295 a0001c0001t0006g0092 others(25): Show |
28 | HG00438.hp1 HG00558.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.474+292dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 4991162 | ||||||
| chr16:4991162 | CT | C | 23 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0032 others(20): Show |
23 | HG01433.hp1 HG02027.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.474+292delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 4991162 | ||||||
| chr16:4991162 | CTT | C | 116 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(113): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.474+291_474+292del others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 4991162 | ||||||
| chr16:4991162 | CTTT | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0064 others(16): Show |
19 | HG00323.hp2 HG01099.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.474+290_474+292del others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 4991162 | ||||||
| chr16:4991249 | C | G | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.474+354C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991249 | |||||||
| chr16:4991285 | A | C | 1 | a0001c0002t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474+390A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991285 | |||||||
| chr16:4991294 | A | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
150 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.474+399A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991294 | |||||||
| chr16:4991327 | G | T | 2 | a0001c0002t0002g0259 a0001c0002t0002g0363 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.474+432G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991327 | |||||||
| chr16:4991376 | C | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.475-462C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991376 | |||||||
| chr16:4991472 | A | G | 2 | a0001c0001t0021g0120 a0005c0025t0029g0121 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.475-366A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991472 | |||||||
| chr16:4991499 | G | C | 1 | a0001c0001t0002g0060 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.475-339G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991499 | |||||||
| chr16:4991633 | C | G | 2 | a0001c0010t0013g0349 a0001c0010t0046g0188 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.475-205C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991633 | |||||||
| chr16:4991774 | T | G | 8 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(5): Show |
8 | HG01099.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.475-64T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991774 | |||||||
| chr16:4991777 | T | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(284): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.475-61T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 5/15 | chr16 | 4991777 | |||||||
| chr16:4992146 | G | A | 1 | a0001c0001t0004g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.667+116G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992146 | |||||||
| chr16:4992167 | C | T | 97 | a0001c0001t0001g0196 a0001c0001t0001g0306 a0001c0001t0004g0261 others(94): Show |
97 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.667+137C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992167 | |||||||
| chr16:4992233 | TTCTTTTC others(5): Show |
T | 8 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(5): Show |
8 | HG01099.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.667+217_667+228del others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4992233 | ||||||
| chr16:4992286 | T | C | 5 | a0001c0001t0025g0260 a0001c0001t0047g0231 a0001c0002t0002g0118 others(2): Show |
5 | HG01891.hp2 HG02486.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+256T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992286 | |||||||
| chr16:4992290 | T | G | 171 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(168): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.667+260T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992290 | |||||||
| chr16:4992303 | C | T | 1 | a0001c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.667+273C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992303 | |||||||
| chr16:4992327 | T | G | 1 | a0001c0001t0004g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.667+297T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992327 | |||||||
| chr16:4992610 | C | T | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+580C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992610 | |||||||
| chr16:4992826 | C | T | 75 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(72): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.667+796C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992826 | |||||||
| chr16:4992840 | A | G | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+810A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992840 | |||||||
| chr16:4992842 | A | G | 255 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.667+812A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992842 | |||||||
| chr16:4992859 | T | C | 25 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(22): Show |
25 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.667+829T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992859 | |||||||
| chr16:4992990 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0296 |
2 | HG00735.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.667+960C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4992990 | |||||||
| chr16:4993025 | TAACTA | T | 10 | a0001c0001t0020g0243 a0001c0002t0006g0208 a0001c0002t0006g0210 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.667+997_667+1001de others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4993025 | ||||||
| chr16:4993049 | ATTAT | A | 14 | a0001c0002t0002g0184 a0001c0002t0002g0185 a0001c0002t0004g0141 others(11): Show |
14 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.667+1027_667+1030d others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4993049 | ||||||
| chr16:4993110 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.667+1080G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993110 | |||||||
| chr16:4993113 | T | C | 36 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(33): Show |
36 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.667+1083T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993113 | |||||||
| chr16:4993265 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.667+1235G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993265 | |||||||
| chr16:4993467 | C | G | 33 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(30): Show |
33 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.667+1437C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993467 | |||||||
| chr16:4993478 | G | A | 1 | a0001c0020t0052g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667+1448G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993478 | |||||||
| chr16:4993495 | G | C | 3 | a0001c0001t0001g0306 a0001c0002t0002g0164 a0001c0002t0002g0187 |
3 | HG02132.hp2 NA18945.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.667+1465G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993495 | |||||||
| chr16:4993542 | G | A | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+1512G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993542 | |||||||
| chr16:4993603 | C | T | 37 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(34): Show |
37 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.667+1573C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993603 | |||||||
| chr16:4993613 | T | C | 1 | a0001c0002t0008g0273 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.667+1583T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993613 | |||||||
| chr16:4993623 | C | A | 1 | a0001c0002t0002g0118 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667+1593C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993623 | |||||||
| chr16:4993623 | C | T | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+1593C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993623 | |||||||
| chr16:4993652 | T | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(294): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.667+1622T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993652 | |||||||
| chr16:4993708 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0004g0102 others(1): Show |
4 | NA18952.hp1 NA19010.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+1678T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993708 | |||||||
| chr16:4993834 | C | T | 1 | a0001c0002t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.667+1804C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993834 | |||||||
| chr16:4993852 | G | C | 1 | a0001c0003t0003g0373 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.667+1822G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993852 | |||||||
| chr16:4993959 | T | C | 372 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(369): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.667+1929T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4993959 | |||||||
| chr16:4993966 | C | CT | 219 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0106 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.667+1953dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4993966 | ||||||
| chr16:4993966 | C | CTT | 19 | a0001c0001t0001g0351 a0001c0001t0014g0272 a0001c0001t0017g0116 others(16): Show |
19 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.667+1952_667+1953d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4993966 | ||||||
| chr16:4993966 | CT | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0004g0300 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.667+1953delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4993966 | ||||||
| chr16:4994014 | C | G | 1 | a0001c0003t0003g0299 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.667+1984C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994014 | |||||||
| chr16:4994035 | C | T | 2 | a0001c0002t0002g0259 a0001c0002t0002g0363 |
2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.667+2005C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994035 | |||||||
| chr16:4994045 | G | A | 5 | a0001c0002t0002g0124 a0001c0002t0002g0155 a0001c0002t0002g0165 others(2): Show |
5 | HG00558.hp2 NA18970.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+2015G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994045 | |||||||
| chr16:4994187 | C | G | 1 | a0010c0031t0003g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.667+2157C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994187 | |||||||
| chr16:4994240 | A | G | 2 | a0001c0008t0009g0111 a0001c0008t0028g0119 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.668-2108A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994240 | |||||||
| chr16:4994260 | C | G | 106 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(103): Show |
106 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.668-2088C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994260 | |||||||
| chr16:4994283 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.668-2065C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994283 | |||||||
| chr16:4994412 | C | T | 1 | a0001c0002t0004g0257 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.668-1936C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994412 | |||||||
| chr16:4994489 | G | A | 2 | a0001c0002t0006g0208 a0001c0002t0006g0211 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.668-1859G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994489 | |||||||
| chr16:4994504 | C | T | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.668-1844C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994504 | |||||||
| chr16:4994644 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.668-1704C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994644 | |||||||
| chr16:4994648 | T | G | 75 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0150 others(72): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.668-1700T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994648 | |||||||
| chr16:4994682 | A | AT | 24 | a0001c0001t0001g0351 a0001c0001t0017g0116 a0001c0001t0017g0117 others(21): Show |
24 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.668-1652dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4994682 | ||||||
| chr16:4994682 | A | ATT | 23 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-1653_668-1652d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4994682 | ||||||
| chr16:4994704 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.668-1644C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994704 | |||||||
| chr16:4994715 | G | T | 4 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(1): Show |
4 | HG02486.hp1 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-1633G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994715 | |||||||
| chr16:4994720 | C | G | 1 | a0001c0001t0003g0336 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.668-1628C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994720 | |||||||
| chr16:4994731 | G | A | 12 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(9): Show |
12 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.668-1617G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994731 | |||||||
| chr16:4994866 | C | T | 4 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(1): Show |
4 | HG02486.hp1 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-1482C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994866 | |||||||
| chr16:4994867 | T | A | 16 | a0001c0001t0023g0218 a0001c0001t0023g0222 a0001c0003t0003g0029 others(13): Show |
16 | HG00423.hp1 HG02015.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.668-1481T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994867 | |||||||
| chr16:4994869 | C | T | 1 | a0001c0001t0002g0016 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.668-1479C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994869 | |||||||
| chr16:4994981 | C | T | 4 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(1): Show |
4 | HG02486.hp1 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-1367C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4994981 | |||||||
| chr16:4995018 | A | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
115 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.668-1330A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995018 | |||||||
| chr16:4995030 | G | A | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-1318G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995030 | |||||||
| chr16:4995052 | T | G | 1 | a0001c0002t0008g0146 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.668-1296T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995052 | |||||||
| chr16:4995172 | C | A | 1 | a0001c0002t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.668-1176C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995172 | |||||||
| chr16:4995231 | C | T | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668-1117C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995231 | |||||||
| chr16:4995296 | G | A | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.668-1052G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995296 | |||||||
| chr16:4995360 | C | T | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-988C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995360 | |||||||
| chr16:4995395 | G | A | 18 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0001g0361 others(15): Show |
18 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.668-953G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995395 | |||||||
| chr16:4995447 | C | T | 2 | a0001c0007t0024g0055 a0001c0007t0024g0056 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.668-901C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995447 | |||||||
| chr16:4995475 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.668-873A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995475 | |||||||
| chr16:4995490 | G | A | 12 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(9): Show |
12 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.668-858G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995490 | |||||||
| chr16:4995552 | T | C | 45 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.668-796T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995552 | |||||||
| chr16:4995624 | C | CT | 39 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0107 others(36): Show |
39 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.668-704dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4995624 | ||||||
| chr16:4995624 | CT | C | 29 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0066 others(26): Show |
29 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.668-704delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 4995624 | ||||||
| chr16:4995626 | T | C | 69 | a0001c0001t0001g0040 a0001c0001t0001g0150 a0001c0001t0001g0281 others(66): Show |
69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.668-722T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995626 | |||||||
| chr16:4995627 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0003g0326 a0001c0001t0003g0338 others(2): Show |
5 | HG01070.hp2 HG01168.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.668-721T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995627 | |||||||
| chr16:4995690 | A | C | 5 | a0001c0001t0001g0351 a0001c0009t0011g0221 a0001c0009t0011g0305 others(2): Show |
5 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.668-658A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995690 | |||||||
| chr16:4995783 | C | T | 1 | a0001c0002t0041g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.668-565C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995783 | |||||||
| chr16:4995849 | A | T | 1 | a0001c0002t0002g0187 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.668-499A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995849 | |||||||
| chr16:4995875 | C | T | 17 | a0001c0001t0001g0157 a0001c0002t0001g0122 a0001c0002t0001g0132 others(14): Show |
17 | HG00408.hp2 HG00558.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.668-473C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995875 | |||||||
| chr16:4995991 | G | T | 138 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0001g0306 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.668-357G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4995991 | |||||||
| chr16:4996023 | G | C | 8 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(5): Show |
8 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-325G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996023 | |||||||
| chr16:4996059 | C | T | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.668-289C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996059 | |||||||
| chr16:4996088 | C | T | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.668-260C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996088 | |||||||
| chr16:4996121 | G | A | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-227G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996121 | |||||||
| chr16:4996145 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.668-203C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996145 | |||||||
| chr16:4996201 | T | A | 30 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.668-147T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996201 | |||||||
| chr16:4996207 | C | A | 30 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(27): Show |
30 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.668-141C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996207 | |||||||
| chr16:4996240 | C | T | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-108C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996240 | |||||||
| chr16:4996309 | G | A | 1 | a0001c0002t0018g0253 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.668-39G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996309 | |||||||
| chr16:4996317 | C | G | 20 | a0001c0001t0020g0243 a0001c0002t0002g0003 a0001c0002t0002g0090 others(17): Show |
20 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.668-31C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 6/15 | chr16 | 4996317 | |||||||
| chr16:4996476 | A | G | 1 | a0001c0002t0004g0151 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.780+16A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996476 | |||||||
| chr16:4996498 | G | T | 2 | a0001c0010t0013g0349 a0001c0010t0046g0188 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.780+38G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996498 | |||||||
| chr16:4996520 | C | G | 4 | a0001c0002t0002g0370 a0001c0002t0002g0371 a0001c0002t0002g0372 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+60C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996520 | |||||||
| chr16:4996540 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.780+80C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996540 | |||||||
| chr16:4996541 | G | A | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.780+81G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996541 | |||||||
| chr16:4996566 | TCTTG | T | 3 | a0001c0002t0002g0350 a0001c0002t0002g0357 a0001c0002t0002g0360 |
3 | HG01258.hp2 HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.780+110_780+113del others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 4996566 | ||||||
| chr16:4996647 | C | G | 20 | a0001c0001t0020g0243 a0001c0002t0002g0003 a0001c0002t0002g0090 others(17): Show |
20 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.780+187C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996647 | |||||||
| chr16:4996786 | G | C | 142 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0001g0306 others(139): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.781-69G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996786 | |||||||
| chr16:4996809 | G | C | 2 | a0001c0001t0021g0120 a0005c0025t0029g0121 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.781-46G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996809 | |||||||
| chr16:4996848 | C | T | 1 | a0001c0005t0027g0346 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.781-7C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996848 | |||||||
| chr16:4996850 | C | G | 2 | a0001c0004t0010g0202 a0001c0004t0010g0207 |
2 | HG02486.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.781-5C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 7/15 | chr16 | 4996850 | |||||||
| chr16:4997095 | A | C | 1 | a0001c0015t0025g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.970+51A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997095 | |||||||
| chr16:4997146 | T | G | 4 | a0001c0002t0005g0347 a0001c0002t0005g0353 a0001c0002t0009g0362 others(1): Show |
4 | HG02886.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+102T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997146 | |||||||
| chr16:4997172 | C | G | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.970+128C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997172 | |||||||
| chr16:4997182 | T | C | 1 | a0011c0017t0008g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.970+138T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997182 | |||||||
| chr16:4997375 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.970+331C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997375 | |||||||
| chr16:4997406 | C | T | 1 | a0001c0002t0014g0367 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.970+362C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997406 | |||||||
| chr16:4997442 | A | C | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.970+398A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997442 | |||||||
| chr16:4997466 | C | A | 1 | a0001c0003t0003g0262 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.970+422C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997466 | |||||||
| chr16:4997599 | G | C | 9 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(6): Show |
9 | HG01099.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.970+555G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997599 | |||||||
| chr16:4997620 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.970+576G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997620 | |||||||
| chr16:4997701 | C | G | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+657C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997701 | |||||||
| chr16:4997740 | C | T | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.970+696C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997740 | |||||||
| chr16:4997800 | A | C | 1 | a0011c0017t0008g0142 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.970+756A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997800 | |||||||
| chr16:4997801 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.970+757C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997801 | |||||||
| chr16:4997915 | T | C | 2 | a0001c0002t0008g0273 a0001c0003t0003g0263 |
2 | HG02602.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.970+871T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997915 | |||||||
| chr16:4997929 | C | T | 6 | a0001c0006t0003g0125 a0001c0006t0003g0127 a0001c0006t0003g0128 others(3): Show |
6 | HG01074.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.970+885C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4997929 | |||||||
| chr16:4998002 | T | TC | 204 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0196 others(201): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.970+959dupC | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998002 | ||||||
| chr16:4998003 | C | CCT | 161 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.970+959_970+960ins others(2): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998003 | |||||||
| chr16:4998003 | C | CCTT | 5 | a0001c0001t0004g0065 a0001c0002t0004g0075 a0001c0002t0005g0083 others(2): Show |
5 | HG00597.hp2 HG02074.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+959_970+960ins others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998003 | |||||||
| chr16:4998004 | T | C | 2 | a0001c0002t0004g0198 a0001c0002t0026g0356 |
2 | HG01516.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.970+960T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998004 | |||||||
| chr16:4998006 | T | C | 1 | a0001c0002t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.970+962T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998006 | |||||||
| chr16:4998116 | C | G | 83 | a0001c0001t0001g0150 a0001c0001t0001g0278 a0001c0001t0001g0281 others(80): Show |
83 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.970+1072C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998116 | |||||||
| chr16:4998126 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.970+1082C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998126 | |||||||
| chr16:4998129 | C | T | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+1085C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998129 | |||||||
| chr16:4998165 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.970+1121T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998165 | |||||||
| chr16:4998223 | C | A | 2 | a0001c0004t0012g0114 a0001c0004t0012g0258 |
2 | HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.970+1179C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998223 | |||||||
| chr16:4998229 | A | C | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+1185A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998229 | |||||||
| chr16:4998327 | C | T | 1 | a0006c0027t0003g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.970+1283C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998327 | |||||||
| chr16:4998366 | C | G | 1 | a0001c0002t0041g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.970+1322C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998366 | |||||||
| chr16:4998423 | C | G | 2 | a0001c0002t0014g0367 a0001c0002t0014g0368 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.970+1379C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998423 | |||||||
| chr16:4998463 | G | A | 6 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(3): Show |
6 | HG02109.hp1 HG02717.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.970+1419G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998463 | |||||||
| chr16:4998481 | G | A | 1 | a0001c0003t0003g0313 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.970+1437G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998481 | |||||||
| chr16:4998520 | C | T | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+1476C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998520 | |||||||
| chr16:4998596 | G | A | 4 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0015t0025g0095 others(1): Show |
4 | HG01243.hp1 HG02109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+1552G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998596 | |||||||
| chr16:4998601 | A | G | 1 | a0001c0008t0009g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.970+1557A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998601 | |||||||
| chr16:4998670 | G | A | 13 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(10): Show |
13 | HG01099.hp2 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.970+1626G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998670 | |||||||
| chr16:4998688 | A | C | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.970+1644A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998688 | |||||||
| chr16:4998693 | C | G | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.970+1649C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998693 | |||||||
| chr16:4998694 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.970+1650C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998694 | |||||||
| chr16:4998737 | CA | C | 136 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0024 others(133): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.970+1722delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998737 | ||||||
| chr16:4998737 | CAA | C | 130 | a0001c0001t0001g0321 a0001c0001t0004g0261 a0001c0001t0017g0116 others(127): Show |
130 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.970+1721_970+1722d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998737 | ||||||
| chr16:4998737 | CAAA | C | 8 | a0001c0001t0031g0224 a0001c0002t0004g0145 a0001c0002t0004g0198 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+1720_970+1722d others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998737 | ||||||
| chr16:4998737 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0196 a0001c0003t0005g0195 |
2 | HG02015.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.970+1710_970+1722d others(15): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998737 | ||||||
| chr16:4998737 | CAAAAAAA others(10): Show |
C | 75 | a0001c0001t0001g0150 a0001c0001t0001g0278 a0001c0001t0001g0281 others(72): Show |
75 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.970+1706_970+1722d others(19): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 4998737 | ||||||
| chr16:4998748 | A | T | 2 | a0001c0010t0013g0349 a0001c0010t0046g0188 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.970+1704A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998748 | |||||||
| chr16:4998753 | A | T | 2 | a0001c0010t0013g0349 a0001c0010t0046g0188 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.970+1709A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998753 | |||||||
| chr16:4998754 | A | T | 2 | a0001c0002t0001g0361 a0001c0002t0049g0364 |
2 | HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.970+1710A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998754 | |||||||
| chr16:4998755 | A | T | 7 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.970+1711A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998755 | |||||||
| chr16:4998756 | A | T | 2 | a0001c0004t0012g0114 a0001c0004t0012g0258 |
2 | HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.970+1712A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998756 | |||||||
| chr16:4998757 | A | T | 4 | a0001c0001t0001g0050 a0001c0001t0004g0065 a0001c0001t0004g0300 others(1): Show |
4 | HG03654.hp2 NA18983.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.970+1713A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998757 | |||||||
| chr16:4998762 | A | T | 2 | a0001c0002t0002g0329 a0001c0002t0004g0328 |
2 | HG01167.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.970+1718A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998762 | |||||||
| chr16:4998772 | G | A | 2 | a0001c0007t0024g0055 a0001c0007t0024g0056 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.970+1728G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998772 | |||||||
| chr16:4998936 | T | C | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.971-1719T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4998936 | |||||||
| chr16:4999006 | G | C | 4 | a0001c0001t0025g0260 a0001c0002t0002g0118 a0001c0002t0002g0235 others(1): Show |
4 | HG02486.hp1 HG03098.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-1649G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999006 | |||||||
| chr16:4999063 | C | G | 6 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0047g0231 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.971-1592C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999063 | |||||||
| chr16:4999073 | C | T | 38 | a0001c0002t0001g0122 a0001c0002t0001g0132 a0001c0002t0001g0163 others(35): Show |
38 | HG00408.hp2 HG00558.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.971-1582C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999073 | |||||||
| chr16:4999139 | C | G | 1 | a0001c0001t0020g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.971-1516C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999139 | |||||||
| chr16:4999159 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.971-1496C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999159 | |||||||
| chr16:4999230 | C | G | 2 | a0001c0001t0047g0231 a0001c0022t0044g0239 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.971-1425C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999230 | |||||||
| chr16:4999247 | C | T | 11 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(8): Show |
11 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.971-1408C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999247 | |||||||
| chr16:4999313 | C | T | 97 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.971-1342C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999313 | |||||||
| chr16:4999326 | C | T | 1 | a0001c0001t0004g0303 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.971-1329C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999326 | |||||||
| chr16:4999354 | G | C | 365 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(362): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.971-1301G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999354 | |||||||
| chr16:4999433 | C | T | 1 | a0001c0008t0009g0283 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.971-1222C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999433 | |||||||
| chr16:4999447 | A | T | 1 | a0001c0002t0035g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.971-1208A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999447 | |||||||
| chr16:4999790 | C | T | 1 | a0001c0003t0003g0269 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.971-865C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999790 | |||||||
| chr16:4999815 | C | T | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.971-840C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 4999815 | |||||||
| chr16:5000020 | G | C | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.971-635G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000020 | |||||||
| chr16:5000085 | G | A | 4 | a0001c0001t0023g0218 a0001c0001t0023g0222 a0001c0005t0001g0223 others(1): Show |
4 | HG02015.hp2 HG02040.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-570G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000085 | |||||||
| chr16:5000210 | G | A | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.971-445G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000210 | |||||||
| chr16:5000213 | C | T | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-442C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000213 | |||||||
| chr16:5000220 | G | T | 70 | a0001c0001t0001g0150 a0001c0001t0001g0278 a0001c0001t0001g0281 others(67): Show |
70 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.971-435G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000220 | |||||||
| chr16:5000330 | T | A | 11 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(8): Show |
11 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.971-325T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000330 | |||||||
| chr16:5000339 | G | A | 1 | a0001c0002t0002g0164 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.971-316G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000339 | |||||||
| chr16:5000396 | C | A | 2 | a0001c0002t0026g0356 a0001c0018t0002g0244 |
2 | HG01516.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.971-259C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000396 | |||||||
| chr16:5000408 | G | A | 4 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0015t0025g0095 others(1): Show |
4 | HG01243.hp1 HG02109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-247G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000408 | |||||||
| chr16:5000425 | A | C | 2 | a0001c0001t0047g0231 a0001c0022t0044g0239 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.971-230A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000425 | |||||||
| chr16:5000462 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0002g0023 |
2 | HG00609.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.971-193T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000462 | |||||||
| chr16:5000553 | C | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.971-102C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000553 | |||||||
| chr16:5000555 | G | C | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(1): Show |
4 | HG02723.hp2 HG02809.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.971-100G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000555 | |||||||
| chr16:5000573 | C | T | 1 | a0001c0004t0012g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.971-82C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000573 | |||||||
| chr16:5000620 | C | T | 2 | a0001c0001t0001g0294 a0010c0031t0003g0267 |
2 | HG03017.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.971-35C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 8/15 | chr16 | 5000620 | |||||||
| chr16:5000780 | G | C | 1 | a0001c0002t0004g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1059+37G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/15 | chr16 | 5000780 | |||||||
| chr16:5000826 | C | G | 1 | a0001c0010t0046g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1060-29C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 9/15 | chr16 | 5000826 | |||||||
| chr16:5000999 | A | G | 1 | a0001c0002t0002g0197 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1130+74A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5000999 | |||||||
| chr16:5001154 | G | A | 2 | a0001c0002t0004g0143 a0001c0002t0036g0156 |
2 | HG00741.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1130+229G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001154 | |||||||
| chr16:5001184 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0249 |
2 | HG00280.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1130+259G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001184 | |||||||
| chr16:5001250 | C | CT | 119 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
119 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1130+344dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5001250 | ||||||
| chr16:5001250 | CT | C | 15 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(12): Show |
15 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1130+344delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5001250 | ||||||
| chr16:5001270 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1130+345C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001270 | |||||||
| chr16:5001271 | T | C | 1 | a0001c0001t0002g0138 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1130+346T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001271 | |||||||
| chr16:5001330 | T | C | 372 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(369): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1130+405T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001330 | |||||||
| chr16:5001352 | G | A | 1 | a0001c0001t0003g0340 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1130+427G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001352 | |||||||
| chr16:5001420 | G | C | 1 | a0001c0003t0003g0290 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1130+495G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001420 | |||||||
| chr16:5001491 | C | G | 1 | a0001c0002t0004g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1130+566C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001491 | |||||||
| chr16:5001500 | C | G | 1 | a0001c0004t0007g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1130+575C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001500 | |||||||
| chr16:5001503 | C | T | 3 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0016t0053g0233 |
3 | HG01243.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1130+578C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001503 | |||||||
| chr16:5001539 | G | A | 3 | a0001c0002t0002g0093 a0001c0002t0002g0094 a0001c0016t0053g0233 |
3 | HG01243.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1130+614G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001539 | |||||||
| chr16:5001541 | G | C | 3 | a0001c0001t0021g0120 a0001c0001t0047g0231 a0005c0025t0029g0121 |
3 | HG01891.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1130+616G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001541 | |||||||
| chr16:5001562 | C | G | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1130+637C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001562 | |||||||
| chr16:5001591 | C | G | 1 | a0001c0001t0001g0321 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1130+666C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001591 | |||||||
| chr16:5001622 | C | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00140.hp2 HG00280.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130+697C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001622 | |||||||
| chr16:5001801 | C | G | 11 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(8): Show |
11 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1130+876C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001801 | |||||||
| chr16:5001819 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1130+894C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001819 | |||||||
| chr16:5001851 | C | T | 2 | a0001c0001t0051g0238 a0001c0001t0056g0236 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1130+926C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001851 | |||||||
| chr16:5001893 | C | G | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1130+968C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001893 | |||||||
| chr16:5001904 | C | T | 2 | a0001c0002t0004g0175 a0001c0002t0004g0178 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1130+979C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5001904 | |||||||
| chr16:5001939 | A | AT | 7 | a0001c0001t0001g0088 a0001c0001t0017g0116 a0001c0001t0017g0117 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1130+1025dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5001939 | ||||||
| chr16:5002041 | A | T | 1 | a0001c0003t0003g0299 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1130+1116A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002041 | |||||||
| chr16:5002050 | G | A | 1 | a0001c0006t0003g0130 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1130+1125G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002050 | |||||||
| chr16:5002173 | C | T | 1 | a0001c0004t0033g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1131-1229C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002173 | |||||||
| chr16:5002213 | C | T | 2 | a0001c0002t0002g0329 a0001c0002t0004g0328 |
2 | HG01167.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1131-1189C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002213 | |||||||
| chr16:5002260 | G | A | 1 | a0001c0003t0003g0299 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1131-1142G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002260 | |||||||
| chr16:5002298 | A | AT | 19 | a0001c0001t0001g0249 a0001c0001t0001g0351 a0001c0001t0006g0086 others(16): Show |
19 | HG00280.hp1 HG00323.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1131-1086dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5002298 | ||||||
| chr16:5002298 | A | ATT | 135 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0049 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1131-1087_1131-108 others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5002298 | ||||||
| chr16:5002298 | A | ATTT | 178 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
178 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1131-1088_1131-108 others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5002298 | ||||||
| chr16:5002298 | A | ATTTT | 7 | a0001c0001t0001g0268 a0001c0001t0004g0277 a0001c0003t0003g0286 others(4): Show |
7 | HG01981.hp2 HG02083.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131-1089_1131-108 others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 5002298 | ||||||
| chr16:5002338 | C | A | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131-1064C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002338 | |||||||
| chr16:5002360 | A | G | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1131-1042A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002360 | |||||||
| chr16:5002374 | C | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131-1028C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002374 | |||||||
| chr16:5002382 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1131-1020C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002382 | |||||||
| chr16:5002395 | C | T | 3 | a0001c0002t0002g0350 a0001c0002t0002g0357 a0001c0002t0002g0360 |
3 | HG01258.hp2 HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1131-1007C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002395 | |||||||
| chr16:5002404 | C | G | 1 | a0001c0002t0002g0370 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1131-998C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002404 | |||||||
| chr16:5002407 | G | A | 7 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0051g0238 others(4): Show |
7 | HG01243.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131-995G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002407 | |||||||
| chr16:5002453 | C | T | 1 | a0001c0002t0004g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1131-949C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002453 | |||||||
| chr16:5002485 | T | C | 1 | a0001c0003t0003g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1131-917T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002485 | |||||||
| chr16:5002662 | C | T | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1131-740C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002662 | |||||||
| chr16:5002678 | G | A | 3 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0016t0053g0233 |
3 | HG01243.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1131-724G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002678 | |||||||
| chr16:5002700 | C | T | 2 | a0001c0002t0004g0148 a0001c0002t0030g0169 |
2 | NA18957.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1131-702C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002700 | |||||||
| chr16:5002767 | G | A | 2 | a0001c0001t0051g0238 a0001c0001t0056g0236 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1131-635G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002767 | |||||||
| chr16:5002888 | T | G | 75 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(72): Show |
75 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1131-514T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002888 | |||||||
| chr16:5002934 | A | G | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1131-468A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5002934 | |||||||
| chr16:5003160 | T | G | 238 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1131-242T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003160 | |||||||
| chr16:5003187 | C | G | 1 | a0001c0001t0017g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131-215C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003187 | |||||||
| chr16:5003240 | A | T | 7 | a0001c0001t0001g0351 a0001c0004t0010g0202 a0001c0004t0010g0207 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1131-162A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003240 | |||||||
| chr16:5003266 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1131-136T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003266 | |||||||
| chr16:5003312 | G | A | 7 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1131-90G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003312 | |||||||
| chr16:5003330 | C | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1131-72C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 10/15 | chr16 | 5003330 | |||||||
| chr16:5003829 | C | T | 1 | a0001c0008t0009g0283 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1302+256C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5003829 | |||||||
| chr16:5003994 | A | G | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1302+421A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5003994 | |||||||
| chr16:5004001 | C | G | 8 | a0001c0001t0006g0086 a0001c0001t0020g0096 a0001c0001t0021g0098 others(5): Show |
8 | HG02809.hp2 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1302+428C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004001 | |||||||
| chr16:5004122 | TGAGCAAA others(3): Show |
T | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1302+558_1302+567d others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5004122 | ||||||
| chr16:5004153 | C | T | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1302+580C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004153 | |||||||
| chr16:5004214 | G | A | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1302+641G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004214 | |||||||
| chr16:5004215 | A | G | 1 | a0001c0003t0003g0344 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1302+642A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004215 | |||||||
| chr16:5004401 | C | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1302+828C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004401 | |||||||
| chr16:5004540 | G | A | 1 | a0001c0001t0032g0044 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1302+967G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004540 | |||||||
| chr16:5004697 | C | G | 2 | a0001c0001t0023g0218 a0001c0001t0023g0222 |
2 | NA19083.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1302+1124C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004697 | |||||||
| chr16:5004697 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1302+1124C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004697 | |||||||
| chr16:5004724 | C | T | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1302+1151C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004724 | |||||||
| chr16:5004757 | A | G | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1303-1157A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004757 | |||||||
| chr16:5004980 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1303-934G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5004980 | |||||||
| chr16:5005019 | T | G | 2 | a0001c0001t0051g0238 a0001c0001t0056g0236 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1303-895T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005019 | |||||||
| chr16:5005049 | G | A | 2 | a0001c0002t0004g0001 a0001c0022t0044g0239 |
2 | HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1303-865G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005049 | |||||||
| chr16:5005071 | G | C | 4 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 others(1): Show |
4 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-843G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005071 | |||||||
| chr16:5005085 | T | C | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1303-829T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005085 | |||||||
| chr16:5005140 | A | G | 2 | a0001c0002t0014g0367 a0001c0002t0014g0368 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1303-774A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005140 | |||||||
| chr16:5005163 | A | G | 11 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0002g0118 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1303-751A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005163 | |||||||
| chr16:5005225 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1303-689G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005225 | |||||||
| chr16:5005245 | G | T | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1303-669G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005245 | |||||||
| chr16:5005248 | C | T | 1 | a0001c0002t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1303-666C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005248 | |||||||
| chr16:5005294 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1303-620G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005294 | |||||||
| chr16:5005398 | G | A | 1 | a0001c0010t0013g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1303-516G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005398 | |||||||
| chr16:5005448 | G | T | 70 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(67): Show |
70 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1303-466G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005448 | |||||||
| chr16:5005468 | G | A | 29 | a0001c0001t0006g0086 a0001c0001t0047g0231 a0001c0002t0004g0001 others(26): Show |
29 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1303-446G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005468 | |||||||
| chr16:5005495 | T | C | 1 | a0001c0002t0004g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1303-419T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005495 | |||||||
| chr16:5005519 | C | T | 1 | a0001c0002t0014g0367 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1303-395C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005519 | |||||||
| chr16:5005524 | T | C | 2 | a0001c0007t0024g0055 a0001c0007t0024g0056 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1303-390T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005524 | |||||||
| chr16:5005549 | A | G | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1303-365A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005549 | |||||||
| chr16:5005563 | TA | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1303-344delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005563 | ||||||
| chr16:5005623 | A | T | 3 | a0001c0002t0002g0292 a0001c0002t0002g0325 a0001c0002t0040g0289 |
3 | HG01106.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1303-291A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005623 | |||||||
| chr16:5005652 | G | C | 4 | a0001c0001t0017g0116 a0001c0001t0025g0260 a0001c0008t0028g0119 others(1): Show |
4 | HG02109.hp2 HG02622.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-262G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005652 | |||||||
| chr16:5005657 | C | A | 71 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(68): Show |
71 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1303-257C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005657 | |||||||
| chr16:5005666 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1303-248C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005666 | |||||||
| chr16:5005731 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1303-183G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005731 | |||||||
| chr16:5005811 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1303-103C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005811 | |||||||
| chr16:5005812 | C | A | 1 | a0010c0031t0003g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1303-102C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005812 | |||||||
| chr16:5005842 | C | T | 1 | a0001c0020t0052g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1303-72C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005842 | |||||||
| chr16:5005857 | C | G | 9 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0009g0362 others(6): Show |
9 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1303-57C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005857 | |||||||
| chr16:5005863 | C | CAAA | 31 | a0001c0001t0001g0351 a0001c0001t0003g0341 a0001c0001t0009g0115 others(28): Show |
31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1303-34_1303-32dup others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005863 | ||||||
| chr16:5005863 | C | CAAAA | 65 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0330 others(62): Show |
65 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1303-35_1303-32dup others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005863 | ||||||
| chr16:5005863 | C | CAAAAA | 15 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0003g0333 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1303-36_1303-32dup others(5): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005863 | ||||||
| chr16:5005863 | CA | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0027 others(205): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1303-32delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005863 | ||||||
| chr16:5005872 | A | AAAC | 17 | a0001c0001t0017g0117 a0001c0002t0005g0006 a0001c0002t0005g0011 others(14): Show |
17 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1303-40_1303-39ins others(3): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 5005872 | ||||||
| chr16:5005872 | A | C | 1 | a0001c0004t0012g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1303-42A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 11/15 | chr16 | 5005872 | |||||||
| chr16:5006102 | G | C | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1437+54G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006102 | |||||||
| chr16:5006121 | C | T | 118 | a0001c0001t0004g0076 a0001c0001t0004g0099 a0001c0001t0004g0319 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1437+73C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006121 | |||||||
| chr16:5006147 | G | C | 6 | a0001c0004t0007g0226 a0001c0004t0007g0227 a0001c0004t0007g0228 others(3): Show |
6 | HG02109.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1437+99G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006147 | |||||||
| chr16:5006152 | G | T | 119 | a0001c0001t0004g0076 a0001c0001t0004g0099 a0001c0001t0004g0319 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1437+104G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006152 | |||||||
| chr16:5006239 | T | C | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1437+191T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006239 | |||||||
| chr16:5006272 | T | A | 1 | a0005c0025t0029g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1437+224T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006272 | |||||||
| chr16:5006294 | A | C | 126 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(123): Show |
126 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1437+246A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006294 | |||||||
| chr16:5006298 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1437+250A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006298 | |||||||
| chr16:5006416 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1437+368C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006416 | |||||||
| chr16:5006433 | C | G | 2 | a0001c0001t0023g0218 a0001c0001t0023g0222 |
2 | NA19083.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1437+385C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006433 | |||||||
| chr16:5006448 | G | A | 3 | a0001c0004t0012g0113 a0001c0004t0012g0114 a0001c0004t0012g0258 |
3 | HG01099.hp2 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1437+400G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006448 | |||||||
| chr16:5006481 | G | A | 1 | a0005c0025t0029g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1437+433G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006481 | |||||||
| chr16:5006497 | C | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1437+449C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006497 | |||||||
| chr16:5006522 | C | A | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1437+474C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006522 | |||||||
| chr16:5006619 | T | G | 40 | a0001c0001t0002g0023 a0001c0002t0001g0122 a0001c0002t0001g0132 others(37): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1437+571T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006619 | |||||||
| chr16:5006638 | C | G | 9 | a0001c0001t0006g0086 a0001c0001t0047g0231 a0001c0002t0006g0208 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1437+590C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006638 | |||||||
| chr16:5006640 | A | G | 1 | a0001c0001t0031g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1437+592A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006640 | |||||||
| chr16:5006655 | G | A | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1437+607G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006655 | |||||||
| chr16:5006896 | C | G | 1 | a0001c0001t0001g0351 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1438-456C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006896 | |||||||
| chr16:5006935 | C | T | 80 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(77): Show |
80 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1438-417C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006935 | |||||||
| chr16:5006980 | C | G | 2 | a0001c0001t0051g0238 a0001c0001t0056g0236 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1438-372C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5006980 | |||||||
| chr16:5007066 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1438-286C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5007066 | |||||||
| chr16:5007145 | A | G | 1 | a0001c0002t0002g0167 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1438-207A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5007145 | |||||||
| chr16:5007263 | C | T | 1 | a0001c0008t0028g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1438-89C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5007263 | |||||||
| chr16:5007314 | C | T | 9 | a0001c0001t0006g0086 a0001c0001t0047g0231 a0001c0002t0006g0208 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1438-38C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 12/15 | chr16 | 5007314 | |||||||
| chr16:5007586 | T | TTTTC | 5 | a0001c0002t0002g0003 a0001c0002t0002g0090 a0001c0002t0002g0103 others(2): Show |
5 | HG02280.hp1 HG02818.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572+120_1572+123d others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 5007586 | ||||||
| chr16:5007606 | C | CT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0063 others(16): Show |
19 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1572+137dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 5007606 | ||||||
| chr16:5007606 | CT | C | 121 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(118): Show |
121 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1572+137delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 5007606 | ||||||
| chr16:5007611 | T | C | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572+125T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007611 | |||||||
| chr16:5007720 | C | T | 9 | a0001c0001t0006g0086 a0001c0001t0047g0231 a0001c0002t0006g0208 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1572+234C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007720 | |||||||
| chr16:5007831 | C | G | 1 | a0001c0001t0020g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572+345C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007831 | |||||||
| chr16:5007837 | G | C | 1 | a0001c0001t0006g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1572+351G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007837 | |||||||
| chr16:5007849 | G | A | 2 | a0001c0001t0051g0238 a0001c0001t0056g0236 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1572+363G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007849 | |||||||
| chr16:5007869 | G | A | 1 | a0001c0003t0003g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1572+383G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007869 | |||||||
| chr16:5007885 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0002g0023 |
2 | HG00609.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1572+399C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007885 | |||||||
| chr16:5007897 | C | G | 1 | a0001c0004t0012g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1572+411C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007897 | |||||||
| chr16:5007907 | C | CT | 86 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0150 others(83): Show |
86 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1572+439dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 5007907 | ||||||
| chr16:5007907 | CT | C | 8 | a0001c0001t0006g0086 a0001c0001t0047g0231 a0001c0002t0006g0208 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1572+439delT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 5007907 | ||||||
| chr16:5007983 | C | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG00140.hp2 HG00280.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1573-438C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5007983 | |||||||
| chr16:5008065 | G | A | 2 | a0001c0002t0002g0118 a0001c0002t0002g0235 |
2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1573-356G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008065 | |||||||
| chr16:5008168 | G | T | 1 | a0001c0002t0004g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1573-253G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008168 | |||||||
| chr16:5008232 | T | C | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1573-189T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008232 | |||||||
| chr16:5008242 | C | G | 72 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(69): Show |
72 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1573-179C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008242 | |||||||
| chr16:5008270 | C | G | 98 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(95): Show |
98 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1573-151C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008270 | |||||||
| chr16:5008285 | C | T | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1573-136C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008285 | |||||||
| chr16:5008326 | C | G | 18 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0001t0017g0116 others(15): Show |
18 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1573-95C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 13/15 | chr16 | 5008326 | |||||||
| chr16:5008730 | G | C | 5 | a0001c0001t0001g0078 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+82G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008730 | |||||||
| chr16:5008786 | G | A | 1 | a0010c0031t0003g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1800+138G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008786 | |||||||
| chr16:5008790 | A | C | 79 | a0001c0001t0004g0076 a0001c0001t0004g0099 a0001c0001t0004g0319 others(76): Show |
79 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1800+142A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008790 | |||||||
| chr16:5008790 | A | G | 71 | a0001c0001t0001g0150 a0001c0001t0001g0288 a0001c0001t0001g0296 others(68): Show |
71 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1800+142A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008790 | |||||||
| chr16:5008823 | C | G | 5 | a0001c0002t0001g0105 a0001c0002t0001g0255 a0001c0002t0001g0256 others(2): Show |
5 | HG00642.hp1 HG01192.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+175C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008823 | |||||||
| chr16:5008886 | G | A | 1 | a0001c0008t0009g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1800+238G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008886 | |||||||
| chr16:5008927 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0041 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1800+279C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5008927 | |||||||
| chr16:5009035 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1800+387C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009035 | |||||||
| chr16:5009112 | G | A | 2 | a0001c0001t0025g0260 a0001c0015t0025g0095 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1800+464G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009112 | |||||||
| chr16:5009161 | G | T | 5 | a0001c0001t0009g0115 a0001c0002t0009g0362 a0001c0008t0009g0111 others(2): Show |
5 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1800+513G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009161 | |||||||
| chr16:5009257 | C | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1800+609C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009257 | |||||||
| chr16:5009292 | G | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1800+644G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009292 | |||||||
| chr16:5009340 | C | G | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1800+692C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009340 | |||||||
| chr16:5009446 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1800+798T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009446 | |||||||
| chr16:5009455 | C | T | 8 | a0001c0001t0006g0086 a0001c0002t0006g0208 a0001c0002t0006g0210 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1800+807C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009455 | |||||||
| chr16:5009461 | C | A | 2 | a0001c0008t0028g0119 a0005c0025t0029g0121 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1800+813C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009461 | |||||||
| chr16:5009480 | T | C | 28 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(25): Show |
28 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1800+832T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009480 | |||||||
| chr16:5009514 | G | A | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1800+866G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009514 | |||||||
| chr16:5009524 | A | G | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1800+876A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009524 | |||||||
| chr16:5009627 | C | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1800+979C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009627 | |||||||
| chr16:5009661 | G | A | 268 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1800+1013G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009661 | |||||||
| chr16:5009664 | A | G | 1 | a0010c0031t0003g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1800+1016A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009664 | |||||||
| chr16:5009718 | A | T | 7 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(4): Show |
7 | HG02630.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1800+1070A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009718 | |||||||
| chr16:5009740 | G | A | 6 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0009g0362 others(3): Show |
6 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1800+1092G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5009740 | |||||||
| chr16:5010017 | G | A | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-1078G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010017 | |||||||
| chr16:5010022 | G | A | 1 | a0005c0025t0029g0121 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1801-1073G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010022 | |||||||
| chr16:5010023 | T | C | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-1072T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010023 | |||||||
| chr16:5010024 | G | A | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-1071G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010024 | |||||||
| chr16:5010034 | C | G | 1 | a0001c0002t0004g0001 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1801-1061C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010034 | |||||||
| chr16:5010042 | A | G | 1 | a0001c0001t0034g0214 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1801-1053A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010042 | |||||||
| chr16:5010065 | G | A | 3 | a0001c0002t0005g0347 a0001c0002t0005g0353 a0001c0002t0041g0354 |
3 | HG02886.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1801-1030G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010065 | |||||||
| chr16:5010085 | A | G | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-1010A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010085 | |||||||
| chr16:5010150 | C | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-945C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010150 | |||||||
| chr16:5010169 | T | C | 256 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(253): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1801-926T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010169 | |||||||
| chr16:5010188 | C | CA | 11 | a0001c0001t0001g0066 a0001c0001t0004g0076 a0001c0001t0006g0092 others(8): Show |
11 | HG00438.hp1 HG00621.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1801-878dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CA | C | 162 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(159): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1801-878delA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CAA | C | 38 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0101 others(35): Show |
38 | HG01099.hp2 HG01255.hp1 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.1801-879_1801-878d others(4): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0006g0086 a0001c0001t0031g0224 a0001c0002t0006g0208 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1801-885_1801-878d others(10): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0003g0054 a0001c0001t0003g0310 a0001c0001t0003g0336 others(6): Show |
9 | HG00438.hp2 HG01361.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1801-886_1801-878d others(11): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CAAAAAAA others(3): Show |
C | 56 | a0001c0001t0003g0219 a0001c0001t0003g0307 a0001c0001t0003g0311 others(53): Show |
56 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1801-887_1801-878d others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010188 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1801-889_1801-878d others(14): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 5010188 | ||||||
| chr16:5010208 | AAAAAAAA others(3): Show |
A | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-886_1801-877d others(12): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010208 | |||||||
| chr16:5010223 | G | T | 1 | a0001c0005t0001g0015 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1801-872G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010223 | |||||||
| chr16:5010233 | G | A | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1801-862G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010233 | |||||||
| chr16:5010234 | G | C | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1801-861G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010234 | |||||||
| chr16:5010359 | G | A | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1801-736G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010359 | |||||||
| chr16:5010371 | A | C | 1 | a0001c0002t0018g0253 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1801-724A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010371 | |||||||
| chr16:5010429 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1801-666C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010429 | |||||||
| chr16:5010497 | A | T | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1801-598A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010497 | |||||||
| chr16:5010513 | C | T | 1 | a0001c0001t0001g0376 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1801-582C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010513 | |||||||
| chr16:5010567 | C | T | 67 | a0001c0001t0003g0054 a0001c0001t0003g0219 a0001c0001t0003g0307 others(64): Show |
67 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1801-528C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010567 | |||||||
| chr16:5010740 | C | T | 13 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0001t0017g0116 others(10): Show |
13 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1801-355C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010740 | |||||||
| chr16:5010819 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1801-276T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010819 | |||||||
| chr16:5010846 | A | G | 258 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1801-249A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010846 | |||||||
| chr16:5010847 | C | T | 7 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0001t0047g0231 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1801-248C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010847 | |||||||
| chr16:5010915 | A | T | 6 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0001t0025g0260 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1801-180A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5010915 | |||||||
| chr16:5011010 | G | A | 1 | a0001c0001t0051g0238 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1801-85G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5011010 | |||||||
| chr16:5011084 | A | C | 362 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(359): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1801-11A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 14/15 | chr16 | 5011084 | |||||||
| chr16:5011286 | C | G | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1979+13C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011286 | |||||||
| chr16:5011286 | C | T | 2 | a0001c0001t0017g0116 a0001c0001t0017g0117 |
2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1979+13C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011286 | |||||||
| chr16:5011458 | C | T | 6 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0009g0362 others(3): Show |
6 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1979+185C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011458 | |||||||
| chr16:5011486 | A | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(197): Show |
200 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1979+213A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011486 | |||||||
| chr16:5011497 | A | G | 2 | a0001c0002t0004g0075 a0001c0002t0004g0148 |
2 | HG02074.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1979+224A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011497 | |||||||
| chr16:5011497 | A | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1979+224A>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011497 | |||||||
| chr16:5011554 | G | A | 6 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1979+281G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011554 | |||||||
| chr16:5011579 | T | C | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1979+306T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011579 | |||||||
| chr16:5011642 | C | A | 1 | a0001c0004t0033g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1979+369C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011642 | |||||||
| chr16:5011647 | C | T | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1979+374C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011647 | |||||||
| chr16:5011670 | G | T | 1 | a0001c0001t0020g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1979+397G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011670 | |||||||
| chr16:5011762 | C | T | 2 | a0001c0001t0025g0260 a0001c0015t0025g0095 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1979+489C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011762 | |||||||
| chr16:5011843 | G | A | 1 | a0001c0015t0025g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1979+570G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011843 | |||||||
| chr16:5011857 | C | T | 1 | a0001c0004t0007g0234 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1979+584C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011857 | |||||||
| chr16:5011882 | A | C | 157 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0079 others(154): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1979+609A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011882 | |||||||
| chr16:5011947 | T | C | 164 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0079 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1979+674T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011947 | |||||||
| chr16:5011958 | C | T | 1 | a0001c0022t0044g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1979+685C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011958 | |||||||
| chr16:5011970 | T | C | 164 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0079 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1979+697T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5011970 | |||||||
| chr16:5012018 | C | T | 167 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0079 others(164): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1979+745C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012018 | |||||||
| chr16:5012100 | T | A | 1 | a0001c0001t0001g0004 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1979+827T>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012100 | |||||||
| chr16:5012117 | G | C | 5 | a0001c0001t0025g0260 a0001c0009t0011g0221 a0001c0009t0011g0305 others(2): Show |
5 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.1979+844G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012117 | |||||||
| chr16:5012193 | G | T | 8 | a0001c0002t0002g0021 a0001c0002t0002g0124 a0001c0002t0002g0140 others(5): Show |
8 | HG00558.hp2 NA18966.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1979+920G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012193 | |||||||
| chr16:5012253 | C | T | 2 | a0001c0008t0028g0119 a0005c0025t0029g0121 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1979+980C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012253 | |||||||
| chr16:5012300 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(12): Show |
15 | HG00408.hp2 HG00558.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1979+1027T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012300 | |||||||
| chr16:5012358 | A | G | 1 | a0001c0006t0003g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1979+1085A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012358 | |||||||
| chr16:5012401 | C | G | 3 | a0001c0009t0011g0221 a0001c0009t0011g0305 a0001c0009t0011g0312 |
3 | HG00544.hp2 HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1979+1128C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012401 | |||||||
| chr16:5012473 | C | T | 7 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(4): Show |
7 | HG01884.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1979+1200C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012473 | |||||||
| chr16:5012508 | A | G | 5 | a0001c0001t0025g0260 a0001c0009t0011g0221 a0001c0009t0011g0305 others(2): Show |
5 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.1979+1235A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012508 | |||||||
| chr16:5012538 | C | G | 1 | a0001c0002t0008g0273 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1979+1265C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012538 | |||||||
| chr16:5012585 | G | C | 3 | a0001c0004t0012g0113 a0001c0004t0012g0114 a0001c0004t0012g0258 |
3 | HG01099.hp2 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1979+1312G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012585 | |||||||
| chr16:5012605 | T | C | 361 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(358): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1979+1332T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012605 | |||||||
| chr16:5012684 | C | T | 1 | a0001c0002t0014g0367 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1979+1411C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012684 | |||||||
| chr16:5012686 | T | C | 2 | a0001c0016t0053g0233 a0001c0020t0052g0216 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1979+1413T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012686 | |||||||
| chr16:5012686 | T | G | 23 | a0001c0002t0005g0006 a0001c0002t0005g0011 a0001c0002t0005g0012 others(20): Show |
23 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1979+1413T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012686 | |||||||
| chr16:5012730 | C | T | 6 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0009g0362 others(3): Show |
6 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1979+1457C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012730 | |||||||
| chr16:5012763 | G | GGTGTGGT others(3): Show |
74 | a0001c0001t0031g0224 a0001c0002t0005g0006 a0001c0002t0005g0011 others(71): Show |
74 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1979+1491_1979+149 others(14): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5012763 | ||||||
| chr16:5012822 | G | A | 1 | a0001c0001t0003g0326 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1979+1549G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012822 | |||||||
| chr16:5012890 | CTCAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0004 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1979+1618_1979+163 others(23): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012890 | |||||||
| chr16:5012905 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1979+1632G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012905 | |||||||
| chr16:5012905 | G | GA | 271 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0027 others(268): Show |
271 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1979+1644dupA | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5012905 | ||||||
| chr16:5012905 | G | GAA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0061 others(7): Show |
10 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1979+1643_1979+164 others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5012905 | ||||||
| chr16:5012905 | G | GAAAA | 68 | a0001c0001t0031g0224 a0001c0002t0005g0006 a0001c0002t0005g0011 others(65): Show |
68 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1979+1641_1979+164 others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5012905 | ||||||
| chr16:5012938 | T | G | 7 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0002g0259 others(4): Show |
7 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1979+1665T>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012938 | |||||||
| chr16:5012947 | AAGG | A | 70 | a0001c0001t0031g0224 a0001c0002t0005g0006 a0001c0002t0005g0011 others(67): Show |
70 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1979+1678_1979+168 others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5012947 | ||||||
| chr16:5012968 | G | A | 7 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(4): Show |
7 | HG02630.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1979+1695G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012968 | |||||||
| chr16:5012999 | C | T | 49 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1979+1726C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5012999 | |||||||
| chr16:5013021 | A | C | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1979+1748A>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013021 | |||||||
| chr16:5013098 | C | G | 8 | a0001c0002t0005g0006 a0001c0002t0005g0011 a0001c0002t0005g0012 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1980-1761C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013098 | |||||||
| chr16:5013099 | G | A | 49 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1980-1760G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013099 | |||||||
| chr16:5013100 | C | T | 50 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1980-1759C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013100 | |||||||
| chr16:5013101 | A | G | 372 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(369): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1980-1758A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013101 | |||||||
| chr16:5013106 | G | C | 49 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(46): Show |
49 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1980-1753G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013106 | |||||||
| chr16:5013151 | A | G | 209 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0067 others(206): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1980-1708A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013151 | |||||||
| chr16:5013210 | C | T | 3 | a0001c0004t0010g0202 a0001c0004t0010g0207 a0001c0029t0010g0237 |
3 | HG02486.hp2 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1980-1649C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013210 | |||||||
| chr16:5013225 | C | A | 64 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(61): Show |
64 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1980-1634C>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013225 | |||||||
| chr16:5013232 | C | G | 6 | a0001c0002t0004g0141 a0001c0002t0004g0248 a0001c0002t0004g0251 others(3): Show |
6 | HG00741.hp2 HG01106.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980-1627C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013232 | |||||||
| chr16:5013305 | A | G | 47 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1980-1554A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013305 | |||||||
| chr16:5013331 | G | C | 6 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0002t0009g0362 others(3): Show |
6 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1980-1528G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013331 | |||||||
| chr16:5013335 | C | T | 47 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(44): Show |
47 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1980-1524C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013335 | |||||||
| chr16:5013347 | C | G | 2 | a0001c0001t0022g0005 a0001c0001t0022g0089 |
2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1980-1512C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013347 | |||||||
| chr16:5013386 | TTTTA | T | 50 | a0001c0001t0031g0224 a0001c0003t0003g0029 a0001c0003t0003g0134 others(47): Show |
50 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1980-1461_1980-145 others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013386 | ||||||
| chr16:5013480 | G | A | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0002t0002g0093 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980-1379G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013480 | |||||||
| chr16:5013480 | G | C | 62 | a0001c0001t0031g0224 a0001c0002t0002g0363 a0001c0002t0005g0006 others(59): Show |
62 | HG00323.hp2 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.1980-1379G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013480 | |||||||
| chr16:5013526 | A | G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1980-1333A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013526 | |||||||
| chr16:5013534 | G | A | 24 | a0001c0001t0001g0351 a0001c0001t0009g0115 a0001c0001t0020g0096 others(21): Show |
24 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1980-1325G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013534 | |||||||
| chr16:5013550 | C | CT | 125 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0067 others(122): Show |
125 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1980-1284dupT | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013550 | ||||||
| chr16:5013550 | C | CTT | 39 | a0001c0001t0031g0224 a0001c0002t0002g0003 a0001c0002t0002g0164 others(36): Show |
39 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.1980-1285_1980-128 others(6): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013550 | ||||||
| chr16:5013550 | C | CTTT | 26 | a0001c0001t0004g0099 a0001c0001t0004g0261 a0001c0001t0006g0092 others(23): Show |
26 | HG00140.hp1 HG01081.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1980-1286_1980-128 others(7): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013550 | ||||||
| chr16:5013550 | C | CTTTT | 22 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0082 others(19): Show |
22 | HG00558.hp1 HG00621.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1980-1287_1980-128 others(8): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013550 | ||||||
| chr16:5013550 | C | CTTTTT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0284 others(17): Show |
20 | HG00438.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1980-1288_1980-128 others(9): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 5013550 | ||||||
| chr16:5013577 | G | A | 1 | a0001c0001t0025g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1980-1282G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013577 | |||||||
| chr16:5013621 | C | T | 2 | a0001c0001t0002g0060 a0001c0006t0003g0131 |
2 | HG01975.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1980-1238C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013621 | |||||||
| chr16:5013630 | C | T | 2 | a0001c0008t0028g0119 a0005c0025t0029g0121 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1980-1229C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013630 | |||||||
| chr16:5013715 | C | T | 1 | a0001c0001t0056g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1980-1144C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013715 | |||||||
| chr16:5013910 | C | G | 4 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0002t0002g0093 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980-949C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013910 | |||||||
| chr16:5013916 | C | T | 2 | a0001c0001t0006g0092 a0001c0002t0006g0369 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1980-943C>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013916 | |||||||
| chr16:5013952 | C | G | 86 | a0001c0001t0004g0008 a0001c0001t0004g0065 a0001c0001t0004g0069 others(83): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1980-907C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013952 | |||||||
| chr16:5013973 | G | A | 15 | a0001c0001t0047g0231 a0001c0002t0005g0006 a0001c0002t0005g0011 others(12): Show |
15 | HG01099.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1980-886G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5013973 | |||||||
| chr16:5014018 | G | A | 50 | a0001c0001t0004g0008 a0001c0001t0004g0065 a0001c0001t0004g0069 others(47): Show |
50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1980-841G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014018 | |||||||
| chr16:5014090 | T | C | 7 | a0001c0001t0025g0260 a0001c0001t0051g0238 a0001c0001t0054g0240 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-769T>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014090 | |||||||
| chr16:5014227 | G | T | 48 | a0001c0001t0004g0008 a0001c0001t0004g0065 a0001c0001t0004g0069 others(45): Show |
48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1980-632G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014227 | |||||||
| chr16:5014287 | G | A | 5 | a0001c0001t0009g0115 a0001c0002t0009g0362 a0001c0008t0009g0111 others(2): Show |
5 | HG02258.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-572G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014287 | |||||||
| chr16:5014454 | G | C | 5 | a0001c0001t0017g0116 a0001c0001t0017g0117 a0001c0002t0002g0093 others(2): Show |
5 | HG02622.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980-405G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014454 | |||||||
| chr16:5014491 | G | A | 1 | a0001c0001t0020g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1980-368G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014491 | |||||||
| chr16:5014496 | C | G | 12 | a0001c0002t0005g0006 a0001c0002t0005g0011 a0001c0002t0005g0012 others(9): Show |
12 | HG01099.hp2 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1980-363C>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014496 | |||||||
| chr16:5014571 | A | G | 14 | a0001c0001t0020g0096 a0001c0001t0020g0243 a0001c0001t0021g0098 others(11): Show |
14 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1980-288A>G | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014571 | |||||||
| chr16:5014581 | G | C | 7 | a0001c0001t0025g0260 a0001c0001t0051g0238 a0001c0001t0054g0240 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980-278G>C | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014581 | |||||||
| chr16:5014676 | AGATGGGA others(16): Show |
A | 1 | a0001c0003t0003g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1980-182_1980-160d others(25): Show |
SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014676 | |||||||
| chr16:5014680 | G | T | 1 | a0001c0001t0002g0016 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1980-179G>T | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014680 | |||||||
| chr16:5014744 | G | A | 1 | a0001c0002t0041g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1980-115G>A | SEC14L5 | ENSG00000103184.12 | transcript | ENST00000251170.12 | protein_coding | 15/15 | chr16 | 5014744 |