Item | Value |
---|---|
geneid | 6397 |
ensemblid | ENSG00000129657.16 |
hgncid | 10698 |
symbol | SEC14L1 |
name | SEC14 like lipid binding 1 |
refseq_nuc | NM_001143998.2 |
refseq_prot | NP_001137470.2 |
ensembl_nuc | ENST00000436233.9 |
ensembl_prot | ENSP00000390392.3 |
mane_status | MANE Select |
chr | chr17 |
start | 77140969 |
end | 77217101 |
strand | + |
ver | v1.2 |
region | chr17:77140969-77217101 |
region5000 | chr17:77135969-77222101 |
regionname0 | SEC14L1_chr17_77140969_77217101 |
regionname5000 | SEC14L1_chr17_77135969_77222101 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 715 | 413 | 78 | 77 | 198 | 14 | 45 | 157 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0002 | 1/0 | 715 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0003 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0004 | 0/0 | 715 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0005 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0006 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0007 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0008 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
a0009 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | MVQKY others(710): Show |
chr17 | 77135969 | 77222101 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2145 | 249 | 50 | 52 | 122 | 6 | 18 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0001c0002 | 0/0 | 2145 | 127 | 21 | 25 | 55 | 7 | 19 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0001c0003 | 0/0 | 2145 | 30 | 1 | 0 | 21 | 1 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0001c0005 | 0/0 | 2145 | 6 | 6 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0001c0009 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0002c0004 | 1/0 | 2145 | 8 | 7 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0003c0007 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0004c0006 | 0/0 | 2145 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0005c0008 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0006c0010 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0007c0011 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0008c0013 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 | ||
a0009c0012 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | ATGGT others(2140): Show |
chr17 | 77135969 | 77222101 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5487 | 66 | 19 | 14 | 26 | 3 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0002 | 0/0 | 5457 | 31 | 6 | 12 | 9 | 0 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0003 | 0/0 | 5500 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0004 | 0/0 | 5565 | 51 | 4 | 1 | 45 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0005 | 0/0 | 5500 | 2 | 0 | 1 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0006 | 0/0 | 5500 | 37 | 3 | 10 | 19 | 0 | 5 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0007 | 0/0 | 5500 | 17 | 0 | 0 | 14 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0008 | 0/0 | 5474 | 7 | 6 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5469): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0009 | 0/0 | 5448 | 6 | 0 | 5 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5443): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0013 | 0/0 | 5448 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5443): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0015 | 0/0 | 5396 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5391): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0020 | 0/0 | 5435 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5430): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0021 | 0/0 | 5565 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0022 | 0/0 | 5500 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0023 | 0/0 | 5457 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0025 | 0/0 | 5457 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0028 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0030 | 0/0 | 5470 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5465): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0032 | 0/1 | 5448 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5443): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0033 | 0/0 | 5444 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5439): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0034 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5443): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0036 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5443): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0045 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5534): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0046 | 0/0 | 5513 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5508): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0047 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0049 | 0/0 | 5500 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0050 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0052 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0053 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0056 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0001t0058 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0003 | 0/0 | 5500 | 48 | 1 | 12 | 22 | 3 | 10 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0004 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0005 | 0/0 | 5500 | 48 | 17 | 7 | 13 | 4 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0006 | 0/0 | 5500 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0010 | 0/0 | 5500 | 6 | 0 | 0 | 6 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0012 | 0/0 | 5500 | 3 | 1 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0014 | 0/0 | 5487 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0016 | 0/0 | 5500 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0019 | 0/0 | 5422 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5417): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0029 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0031 | 0/0 | 5500 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0038 | 0/0 | 5487 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0039 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0040 | 0/0 | 5513 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5508): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0042 | 0/0 | 5383 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5378): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0043 | 0/0 | 5513 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5508): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0044 | 0/0 | 5513 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5508): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0051 | 0/0 | 5500 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0054 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0055 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0001c0002t0057 | 0/0 | 5500 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0001c0003t0002 | 0/0 | 5457 | 25 | 1 | 0 | 16 | 1 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0003t0018 | 0/0 | 5496 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5491): Show |
chr17 | 77135969 | 77222101 |
a0001c0003t0024 | 0/0 | 5483 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5478): Show |
chr17 | 77135969 | 77222101 |
a0001c0003t0027 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5452): Show |
chr17 | 77135969 | 77222101 |
a0001c0005t0011 | 0/0 | 5435 | 5 | 5 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5430): Show |
chr17 | 77135969 | 77222101 |
a0001c0005t0026 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5430): Show |
chr17 | 77135969 | 77222101 |
a0001c0009t0017 | 0/0 | 5511 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5506): Show |
chr17 | 77135969 | 77222101 |
a0002c0004t0003 | 1/0 | 5500 | 5 | 4 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0002c0004t0037 | 0/0 | 5409 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5404): Show |
chr17 | 77135969 | 77222101 |
a0002c0004t0041 | 0/0 | 5513 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5508): Show |
chr17 | 77135969 | 77222101 |
a0002c0004t0048 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0003c0007t0001 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5482): Show |
chr17 | 77135969 | 77222101 |
a0003c0007t0035 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5430): Show |
chr17 | 77135969 | 77222101 |
a0004c0006t0017 | 0/0 | 5511 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5506): Show |
chr17 | 77135969 | 77222101 |
a0005c0008t0004 | 0/0 | 5565 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0006c0010t0004 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5560): Show |
chr17 | 77135969 | 77222101 |
a0007c0011t0011 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5430): Show |
chr17 | 77135969 | 77222101 |
a0008c0013t0005 | 0/0 | 5500 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
a0009c0012t0005 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | CCCGC others(5495): Show |
chr17 | 77135969 | 77222101 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0006g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0399 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0007g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0009g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0009g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0015g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0015g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0020g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0020g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0021g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0021g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0022g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0023g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0023g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0025g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0028g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0030g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0032g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0033g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0034g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0036g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0045g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0046g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0047g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0049g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0050g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0052g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0053g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0056g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0001t0058g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0003g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0005g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0010g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0010g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0010g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0010g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0010g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0012g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0012g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0012g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0014g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0014g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0016g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0016g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0016g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0019g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0029g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0031g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0038g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0039g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0040g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0042g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0043g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0044g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0051g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0054g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0055g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0002t0057g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0018g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0024g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0003t0027g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0005t0011g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0005t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0005t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0005t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0005t0026g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0001c0009t0017g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0003g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0037g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0041g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0002c0004t0048g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0003c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0003c0007t0035g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0004c0006t0017g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0004c0006t0017g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0005c0008t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0006c0010t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0007c0011t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0008c0013t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
a0009c0012t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0390 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0041 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00140 | hp1 | a0001 | c0003 | t0002 | g0180 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0353 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0316 | EUR | FIN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00408 | hp1 | a0001 | c0003 | t0002 | g0235 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00408 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0131 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00423 | hp2 | a0001 | c0003 | t0024 | g0258 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00438 | hp1 | a0001 | c0002 | t0010 | g0015 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00544 | hp1 | a0001 | c0002 | t0005 | g0292 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00558 | hp1 | a0001 | c0002 | t0043 | g0350 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00597 | hp1 | a0001 | c0002 | t0029 | g0304 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0213 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0345 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0009 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0123 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00673 | hp2 | a0001 | c0002 | t0054 | g0303 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0308 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00735 | hp2 | a0001 | c0001 | t0053 | g0249 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0363 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0125 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0313 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01071 | hp1 | a0001 | c0002 | t0012 | g0329 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0383 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01081 | hp2 | a0001 | c0002 | t0005 | g0314 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0036 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0352 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0321 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01192 | hp2 | a0001 | c0002 | t0005 | g0295 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01243 | hp1 | a0001 | c0002 | t0057 | g0312 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0053 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0347 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01256 | hp2 | a0001 | c0001 | t0025 | g0013 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01257 | hp1 | a0001 | c0002 | t0005 | g0386 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01258 | hp1 | a0001 | c0002 | t0005 | g0377 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01258 | hp2 | a0001 | c0001 | t0025 | g0013 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01346 | hp2 | a0001 | c0002 | t0055 | g0370 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01358 | hp1 | a0001 | c0002 | t0005 | g0309 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01358 | hp2 | a0001 | c0001 | t0009 | g0006 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01361 | hp2 | a0001 | c0002 | t0012 | g0327 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01496 | hp1 | a0001 | c0001 | t0006 | g0214 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0373 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0358 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0328 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0124 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0362 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0325 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01884 | hp1 | a0001 | c0002 | t0005 | g0369 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01891 | hp1 | a0001 | c0005 | t0026 | g0018 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01891 | hp2 | a0002 | c0004 | t0003 | g0174 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0376 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01934 | hp1 | a0001 | c0001 | t0050 | g0047 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0198 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01943 | hp2 | a0005 | c0008 | t0004 | g0076 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02004 | hp1 | a0001 | c0001 | t0046 | g0081 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0210 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02015 | hp1 | a0001 | c0001 | t0058 | g0089 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0359 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02040 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02040 | hp2 | a0006 | c0010 | t0004 | g0196 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0241 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02056 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0243 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02071 | hp2 | a0001 | c0003 | t0024 | g0255 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02074 | hp1 | a0001 | c0002 | t0003 | g0294 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02074 | hp2 | a0001 | c0003 | t0002 | g0234 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02080 | hp2 | a0001 | c0003 | t0002 | g0264 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0285 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0240 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02132 | hp2 | a0001 | c0002 | t0005 | g0284 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02135 | hp2 | a0001 | c0002 | t0010 | g0015 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02145 | hp1 | a0001 | c0001 | t0036 | g0388 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02155 | hp1 | a0001 | c0003 | t0002 | g0238 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02155 | hp2 | a0001 | c0003 | t0002 | g0012 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02165 | hp1 | a0001 | c0002 | t0005 | g0324 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02258 | hp1 | a0001 | c0002 | t0005 | g0315 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0165 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02273 | hp2 | a0001 | c0001 | t0020 | g0392 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02280 | hp1 | a0001 | c0002 | t0005 | g0200 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02293 | hp1 | a0001 | c0002 | t0044 | g0346 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0208 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02300 | hp2 | a0001 | c0002 | t0006 | g0222 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02451 | hp2 | a0001 | c0001 | t0056 | g0194 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02602 | hp1 | a0001 | c0002 | t0038 | g0361 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02615 | hp1 | a0001 | c0002 | t0005 | g0334 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02615 | hp2 | a0002 | c0004 | t0003 | g0173 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0336 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0375 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02698 | hp1 | a0001 | c0001 | t0007 | g0402 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02698 | hp2 | a0001 | c0002 | t0005 | g0332 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02717 | hp1 | a0001 | c0005 | t0011 | g0008 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02723 | hp2 | a0001 | c0002 | t0005 | g0296 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02735 | hp1 | a0001 | c0003 | t0002 | g0280 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02735 | hp2 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0030 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02886 | hp1 | a0002 | c0004 | t0048 | g0188 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02886 | hp2 | a0001 | c0002 | t0005 | g0342 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02895 | hp2 | a0001 | c0002 | t0005 | g0378 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02896 | hp2 | a0001 | c0001 | t0034 | g0118 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0322 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02965 | hp1 | a0001 | c0005 | t0011 | g0008 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02965 | hp2 | a0001 | c0001 | t0015 | g0110 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02970 | hp1 | a0001 | c0005 | t0011 | g0179 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0339 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0218 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0381 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03098 | hp1 | a0003 | c0007 | t0001 | g0026 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0058 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0368 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03139 | hp1 | a0001 | c0001 | t0015 | g0109 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03139 | hp2 | a0001 | c0002 | t0005 | g0338 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03195 | hp1 | a0002 | c0004 | t0041 | g0177 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0166 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0297 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0380 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0265 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03453 | hp1 | a0002 | c0004 | t0003 | g0176 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0164 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03486 | hp1 | a0001 | c0005 | t0011 | g0178 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03486 | hp2 | a0001 | c0002 | t0005 | g0337 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03490 | hp2 | a0001 | c0002 | t0005 | g0319 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03491 | hp1 | a0004 | c0006 | t0017 | g0192 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03491 | hp2 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03492 | hp1 | a0004 | c0006 | t0017 | g0191 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03492 | hp2 | a0001 | c0002 | t0005 | g0320 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03516 | hp1 | a0001 | c0002 | t0012 | g0330 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03540 | hp2 | a0002 | c0004 | t0037 | g0189 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0340 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0209 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0038 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0254 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0360 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03710 | hp2 | a0001 | c0001 | t0020 | g0394 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0399 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03834 | hp1 | a0001 | c0002 | t0005 | g0318 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03834 | hp2 | a0001 | c0003 | t0002 | g0181 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0032 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0403 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03942 | hp1 | a0008 | c0013 | t0005 | g0291 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03942 | hp2 | a0001 | c0002 | t0031 | g0364 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0252 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0199 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0389 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0379 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0317 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0382 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04204 | hp1 | a0001 | c0002 | t0005 | g0326 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0211 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04228 | hp1 | a0001 | c0009 | t0017 | g0193 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0384 | EAS | CHB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0183 | EAS | CHB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18906 | hp1 | a0002 | c0004 | t0003 | g0175 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18906 | hp2 | a0001 | c0002 | t0005 | g0341 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18939 | hp2 | a0001 | c0002 | t0016 | g0374 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18940 | hp1 | a0001 | c0001 | t0007 | g0391 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18943 | hp1 | a0001 | c0002 | t0042 | g0305 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0387 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18945 | hp2 | a0001 | c0001 | t0021 | g0090 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0400 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0365 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18947 | hp1 | a0001 | c0001 | t0052 | g0253 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18949 | hp1 | a0001 | c0002 | t0005 | g0372 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18949 | hp2 | a0001 | c0002 | t0016 | g0298 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0395 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18954 | hp2 | a0001 | c0002 | t0016 | g0307 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18959 | hp1 | a0009 | c0012 | t0005 | g0331 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18959 | hp2 | a0001 | c0001 | t0023 | g0278 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18960 | hp1 | a0001 | c0003 | t0002 | g0262 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18960 | hp2 | a0001 | c0002 | t0014 | g0300 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18963 | hp1 | a0001 | c0002 | t0005 | g0293 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18963 | hp2 | a0001 | c0002 | t0014 | g0302 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18967 | hp2 | a0001 | c0002 | t0005 | g0283 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0367 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0408 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18971 | hp1 | a0001 | c0003 | t0018 | g0012 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18972 | hp1 | a0001 | c0002 | t0040 | g0371 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18974 | hp1 | a0001 | c0002 | t0005 | g0288 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18975 | hp2 | a0001 | c0002 | t0010 | g0301 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0385 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0401 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18979 | hp2 | a0001 | c0001 | t0045 | g0094 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18981 | hp1 | a0001 | c0001 | t0007 | g0404 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18981 | hp2 | a0001 | c0003 | t0018 | g0031 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18982 | hp1 | a0001 | c0002 | t0019 | g0354 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18984 | hp1 | a0001 | c0001 | t0047 | g0075 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18985 | hp2 | a0001 | c0002 | t0005 | g0282 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18990 | hp1 | a0001 | c0001 | t0007 | g0407 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18992 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18993 | hp2 | a0001 | c0003 | t0002 | g0267 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0366 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0410 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0397 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19007 | hp1 | a0001 | c0002 | t0039 | g0286 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19010 | hp1 | a0001 | c0001 | t0023 | g0271 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19010 | hp2 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19011 | hp1 | a0001 | c0002 | t0005 | g0287 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19012 | hp2 | a0001 | c0001 | t0007 | g0409 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19043 | hp2 | a0001 | c0001 | t0030 | g0111 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19054 | hp2 | a0001 | c0002 | t0005 | g0289 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19055 | hp1 | a0001 | c0002 | t0005 | g0034 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19055 | hp2 | a0001 | c0001 | t0021 | g0098 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19056 | hp1 | a0001 | c0002 | t0010 | g0355 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19058 | hp1 | a0001 | c0002 | t0019 | g0002 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19058 | hp2 | a0001 | c0001 | t0007 | g0406 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0398 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0215 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0349 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19068 | hp1 | a0001 | c0001 | t0028 | g0405 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19076 | hp1 | a0001 | c0003 | t0027 | g0230 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19076 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0263 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19081 | hp1 | a0001 | c0002 | t0010 | g0356 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19082 | hp1 | a0001 | c0003 | t0002 | g0260 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19082 | hp2 | a0001 | c0002 | t0010 | g0290 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19083 | hp1 | a0001 | c0002 | t0014 | g0299 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19083 | hp2 | a0001 | c0001 | t0007 | g0393 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19085 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19086 | hp1 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19088 | hp2 | a0001 | c0001 | t0007 | g0396 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19089 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19090 | hp2 | a0001 | c0002 | t0005 | g0035 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19091 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0333 | EUR | TSI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20752 | hp2 | a0001 | c0001 | t0033 | g0048 | EUR | TSI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0357 | SAS | GIH | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | GIH | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02109 | hp1 | a0007 | c0011 | t0011 | g0020 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0055 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02486 | hp1 | a0001 | c0005 | t0011 | g0019 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0310 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02559 | hp1 | a0001 | c0001 | t0022 | g0009 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03471 | hp1 | a0001 | c0001 | t0049 | g0057 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG03471 | hp2 | a0001 | c0002 | t0051 | g0311 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG06807 | hp1 | a0001 | c0002 | t0005 | g0323 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0060 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA20300 | hp2 | a0003 | c0007 | t0035 | g0148 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
NA21309 | hp2 | a0001 | c0002 | t0005 | g0335 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0119 | REF | REF | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
homoSapiens | grch38p0 | a0002 | c0004 | t0003 | g0172 | REF | REF | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:77191224 | T | G | 1 | a0004 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.257T>G | p.Leu86Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/17 | 531/5500 | 257/2148 | 86/715 | chr17 | 77191224 | |||
chr17:77193467 | G | A | 1 | a0005 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.392G>A | p.Ser131Asn | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/17 | 666/5500 | 392/2148 | 131/715 | chr17 | 77193467 | |||
chr17:77194758 | A | G | 1 | a0004 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.556A>G | p.Ile186Val | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 830/5500 | 556/2148 | 186/715 | chr17 | 77194758 | |||
chr17:77194764 | A | C | 8 | a0001 a0003 a0004 others(5): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
missense_variant | MODERATE | c.562A>C | p.Thr188Pro | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 836/5500 | 562/2148 | 188/715 | chr17 | 77194764 | |||
chr17:77200626 | A | C | 1 | a0008 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.962A>C | p.Gln321Pro | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/17 | 1236/5500 | 962/2148 | 321/715 | chr17 | 77200626 | |||
chr17:77212016 | A | G | 1 | a0009 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1678A>G | p.Ile560Val | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 1952/5500 | 1678/2148 | 560/715 | chr17 | 77212016 | |||
chr17:77212079 | G | T | 1 | a0003 | 2 | HG03098.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1741G>T | p.Ala581Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 2015/5500 | 1741/2148 | 581/715 | chr17 | 77212079 | |||
chr17:77212145 | C | T | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1807C>T | p.Arg603Cys | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 2081/5500 | 1807/2148 | 603/715 | chr17 | 77212145 | |||
chr17:77213398 | C | T | 1 | a0007 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1948C>T | p.Pro650Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/17 | 2222/5500 | 1948/2148 | 650/715 | chr17 | 77213398 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:77194880 | C | T | 3 | a0001c0002 a0008c0013 a0009c0012 |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
synonymous_variant | LOW | c.678C>T | p.Ser226Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 952/5500 | 678/2148 | 226/715 | chr17 | 77194880 | |||
chr17:77196230 | A | G | 2 | a0001c0005 a0007c0011 |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.738A>G | p.Arg246Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/17 | 1012/5500 | 738/2148 | 246/715 | chr17 | 77196230 | |||
chr17:77206305 | C | A | 1 | a0001c0003 | 30 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
synonymous_variant | LOW | c.1246C>A | p.Arg416Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/17 | 1520/5500 | 1246/2148 | 416/715 | chr17 | 77206305 | |||
chr17:77213972 | C | T | 2 | a0001c0009 a0004c0006 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.2097C>T | p.Ala699Ala | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371/5500 | 2097/2148 | 699/715 | chr17 | 77213972 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:77140982 | C | T | 1 | a0001c0001t0058 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-261C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2615 | chr17 | 77140982 | ||||||
chr17:77140995 | A | G | 1 | a0001c0002t0057 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-248A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2602 | chr17 | 77140995 | ||||||
chr17:77141074 | C | G | 1 | a0001c0001t0056 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2523 | chr17 | 77141074 | ||||||
chr17:77214030 | G | A | 1 | a0001c0005t0026 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 7 | chr17 | 77214030 | ||||||
chr17:77214094 | C | T | 1 | a0001c0002t0055 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 71 | chr17 | 77214094 | ||||||
chr17:77214140 | A | G | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 117 | chr17 | 77214140 | ||||||
chr17:77214358 | G | A | 1 | a0001c0003t0027 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 335 | chr17 | 77214358 | ||||||
chr17:77214360 | A | G | 2 | a0001c0002t0016 a0001c0002t0054 |
4 | HG00673.hp2 NA18939.hp2 NA18949.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 337 | chr17 | 77214360 | ||||||
chr17:77214461 | C | T | 5 | a0001c0005t0011 a0001c0005t0026 a0001c0009t0017 others(2): Show |
10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 438 | chr17 | 77214461 | ||||||
chr17:77214492 | A | C | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0023 others(7): Show |
103 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*469A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 469 | chr17 | 77214492 | ||||||
chr17:77214571 | C | T | 1 | a0001c0001t0053 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 548 | chr17 | 77214571 | ||||||
chr17:77214936 | A | G | 1 | a0001c0002t0051 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 913 | chr17 | 77214936 | ||||||
chr17:77214945 | T | G | 1 | a0001c0001t0028 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 922 | chr17 | 77214945 | ||||||
chr17:77215018 | T | G | 1 | a0001c0002t0029 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 995 | chr17 | 77215018 | ||||||
chr17:77215062 | CGTGT | C | 10 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0025 others(7): Show |
68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1052delTGTG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1049 | INFO_REALIGN_3_PRIME | chr17 | 77215062 | |||||
chr17:77215066 | T | C | 1 | a0001c0001t0004 | 3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1043T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1043 | chr17 | 77215066 | ||||||
chr17:77215126 | C | T | 3 | a0001c0001t0050 a0001c0009t0017 a0004c0006t0017 |
4 | HG01934.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1103C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1103 | chr17 | 77215126 | ||||||
chr17:77215202 | T | C | 1 | a0001c0002t0031 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1179T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1179 | chr17 | 77215202 | ||||||
chr17:77215461 | C | A | 1 | a0001c0002t0012 | 3 | HG01071.hp1 HG01361.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1438C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1438 | chr17 | 77215461 | ||||||
chr17:77215526 | G | A | 9 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(6): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1503G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1503 | chr17 | 77215526 | ||||||
chr17:77215714 | G | A | 1 | a0001c0001t0052 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1691 | chr17 | 77215714 | ||||||
chr17:77215747 | T | C | 1 | a0001c0001t0023 | 2 | NA18959.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1724T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1724 | chr17 | 77215747 | ||||||
chr17:77215760 | CTAGTAGG others(58): Show |
C | 5 | a0001c0001t0036 a0001c0005t0011 a0001c0005t0026 others(2): Show |
9 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1765_*1829delCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | INFO_REALIGN_3_PRIME | chr17 | 77215760 | |||||
chr17:77215762 | AGTAGGTA others(19): Show |
A | 1 | a0001c0001t0023 | 2 | NA18959.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1750_*1775delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1750 | INFO_REALIGN_3_PRIME | chr17 | 77215762 | |||||
chr17:77215773 | CTAGTAGG others(71): Show |
C | 1 | a0001c0001t0030 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1789_*1866delCTGG others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215773 | |||||
chr17:77215775 | AGTAGGTA others(6): Show |
A | 1 | a0001c0003t0002 | 3 | HG02738.hp2 HG03927.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1776_*1788delTTCG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1776 | INFO_REALIGN_3_PRIME | chr17 | 77215775 | |||||
chr17:77215786 | T | C | 8 | a0001c0001t0002 a0001c0001t0025 a0001c0001t0052 others(5): Show |
62 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1763T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1763 | chr17 | 77215786 | ||||||
chr17:77215786 | TTCGTAGG others(45): Show |
T | 1 | a0001c0001t0022 | 2 | HG00639.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1765_*1816delCGTA others(48): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | INFO_REALIGN_3_PRIME | chr17 | 77215786 | |||||
chr17:77215788 | C | A | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(51): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*1765C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | chr17 | 77215788 | ||||||
chr17:77215788 | CGTAGGTA others(58): Show |
C | 1 | a0001c0001t0008 | 7 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1789_*1853delCTGG others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215788 | |||||
chr17:77215801 | CGTAGGTA others(523): Show |
C | 3 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0006 |
37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1789_*2318del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215801 | |||||
chr17:77215801 | CGTAGGTA others(536): Show |
C | 1 | a0001c0001t0006 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791_*2333del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1791 | INFO_REALIGN_3_PRIME | chr17 | 77215801 | |||||
chr17:77215805 | G | T | 1 | a0001c0001t0045 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1782 | chr17 | 77215805 | ||||||
chr17:77215812 | C | T | 3 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0049 |
5 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1789C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | chr17 | 77215812 | ||||||
chr17:77215814 | G | C | 3 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0049 |
5 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1791G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1791 | chr17 | 77215814 | ||||||
chr17:77215825 | T | C | 9 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0033 others(6): Show |
76 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1802T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1802 | chr17 | 77215825 | ||||||
chr17:77215825 | TTAGTAGG others(536): Show |
T | 1 | a0001c0001t0006 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1828_*2370del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1828 | INFO_REALIGN_3_PRIME | chr17 | 77215825 | |||||
chr17:77215827 | A | AGTAGGTA others(58): Show |
7 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0047 others(4): Show |
58 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1869_*1933dupCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215827 | |||||
chr17:77215827 | A | C | 2 | a0001c0001t0015 a0001c0001t0049 |
4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1804A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1804 | chr17 | 77215827 | ||||||
chr17:77215827 | AGTAGGTA others(32): Show |
A | 1 | a0001c0001t0009 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1815_*1853delCTAG others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1815 | INFO_REALIGN_3_PRIME | chr17 | 77215827 | |||||
chr17:77215853 | A | C | 13 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0015 others(10): Show |
84 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1830A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1830 | chr17 | 77215853 | ||||||
chr17:77215890 | TTCGTAGG others(71): Show |
T | 1 | a0001c0001t0015 | 3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1869_*1946delCGTA others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1869 | INFO_REALIGN_3_PRIME | chr17 | 77215890 | |||||
chr17:77215892 | CGTAGGTA others(6): Show |
C | 1 | a0001c0001t0025 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1880_*1892delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | INFO_REALIGN_3_PRIME | chr17 | 77215892 | |||||
chr17:77215902 | GCTA | G | 1 | a0001c0001t0009 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1880_*1882delCTA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | chr17 | 77215902 | ||||||
chr17:77215903 | C | CTAGTAGG others(6): Show |
2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1895_*1907dupAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1908 | INFO_REALIGN_3_PRIME | chr17 | 77215903 | |||||
chr17:77215903 | C | T | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | chr17 | 77215903 | ||||||
chr17:77215903 | CTAGTAGG others(6): Show |
C | 1 | a0001c0002t0012 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1895_*1907delAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1895 | INFO_REALIGN_3_PRIME | chr17 | 77215903 | |||||
chr17:77215905 | A | C | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1882A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1882 | chr17 | 77215905 | ||||||
chr17:77215906 | G | T | 1 | a0001c0001t0009 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1883G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1883 | chr17 | 77215906 | ||||||
chr17:77215918 | A | AGTAGGTA others(58): Show |
1 | a0001c0001t0005 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1933_*1934insCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215918 | |||||
chr17:77215918 | A | C | 3 | a0001c0001t0008 a0001c0001t0022 a0001c0001t0030 |
10 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1895A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1895 | chr17 | 77215918 | ||||||
chr17:77215929 | T | C | 2 | a0001c0001t0009 a0001c0001t0049 |
7 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1906T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1906 | chr17 | 77215929 | ||||||
chr17:77215931 | C | A | 2 | a0001c0001t0009 a0001c0001t0049 |
7 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1908C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1908 | chr17 | 77215931 | ||||||
chr17:77215944 | C | A | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1921C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1921 | chr17 | 77215944 | ||||||
chr17:77215955 | T | TTCGTAGG others(22): Show |
1 | a0001c0001t0046 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1933_*1934insCGTA others(25): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | |||||
chr17:77215955 | TTAGGTAG others(6): Show |
T | 1 | a0001c0001t0030 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1944_*1956delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1944 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | |||||
chr17:77215955 | TTAGGTAG others(136): Show |
T | 3 | a0001c0005t0011 a0001c0005t0026 a0007c0011t0011 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2061_*2203del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2061 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | |||||
chr17:77215965 | T | C | 2 | a0001c0001t0045 a0001c0001t0049 |
2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1942T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1942 | chr17 | 77215965 | ||||||
chr17:77215967 | C | A | 2 | a0001c0001t0045 a0001c0001t0049 |
2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1944C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1944 | chr17 | 77215967 | ||||||
chr17:77215967 | CGTAGGTA others(6): Show |
C | 8 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0025 others(5): Show |
65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1955_*1967delTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1955 | INFO_REALIGN_3_PRIME | chr17 | 77215967 | |||||
chr17:77215978 | T | C | 2 | a0001c0002t0038 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1955 | chr17 | 77215978 | ||||||
chr17:77215980 | A | C | 1 | a0001c0001t0046 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1957 | chr17 | 77215980 | ||||||
chr17:77215991 | C | T | 2 | a0001c0001t0045 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1968C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1968 | chr17 | 77215991 | ||||||
chr17:77215993 | A | C | 2 | a0001c0001t0045 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1970A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1970 | chr17 | 77215993 | ||||||
chr17:77215993 | AGTAGGTA others(140): Show |
A | 1 | a0001c0005t0011 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1976_*2122del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1976 | INFO_REALIGN_3_PRIME | chr17 | 77215993 | |||||
chr17:77215994 | G | T | 1 | a0001c0001t0046 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1971G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1971 | chr17 | 77215994 | ||||||
chr17:77215999 | T | C | 1 | a0001c0002t0039 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1976 | chr17 | 77215999 | ||||||
chr17:77216004 | T | C | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1981 | chr17 | 77216004 | ||||||
chr17:77216006 | C | A | 8 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0030 others(5): Show |
17 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1983C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1983 | chr17 | 77216006 | ||||||
chr17:77216008 | T | TA | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1986dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1987 | INFO_REALIGN_3_PRIME | chr17 | 77216008 | |||||
chr17:77216017 | T | C | 1 | a0001c0003t0024 | 2 | HG00423.hp2 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1994T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1994 | chr17 | 77216017 | ||||||
chr17:77216019 | C | A | 3 | a0001c0001t0046 a0001c0001t0049 a0001c0003t0024 |
4 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1996C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1996 | chr17 | 77216019 | ||||||
chr17:77216019 | C | CGTAGGTA others(6): Show |
1 | a0001c0002t0040 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2007_*2019dupCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2020 | INFO_REALIGN_3_PRIME | chr17 | 77216019 | |||||
chr17:77216030 | C | T | 3 | a0001c0001t0045 a0001c0001t0049 a0001c0003t0024 |
4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2007C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2007 | chr17 | 77216030 | ||||||
chr17:77216032 | A | C | 2 | a0001c0001t0045 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2009A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2009 | chr17 | 77216032 | ||||||
chr17:77216043 | T | C | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2020 | chr17 | 77216043 | ||||||
chr17:77216045 | A | C | 2 | a0001c0001t0046 a0001c0003t0024 |
3 | HG00423.hp2 HG02004.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2022 | chr17 | 77216045 | ||||||
chr17:77216056 | C | T | 5 | a0001c0001t0045 a0001c0001t0046 a0001c0001t0049 others(2): Show |
6 | HG02004.hp1 HG03471.hp1 HG03491.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2033C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2033 | chr17 | 77216056 | ||||||
chr17:77216058 | A | C | 4 | a0001c0001t0046 a0001c0001t0049 a0001c0009t0017 others(1): Show |
5 | HG02004.hp1 HG03471.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2035A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2035 | chr17 | 77216058 | ||||||
chr17:77216069 | C | CTAGTAGG others(6): Show |
2 | a0001c0001t0036 a0001c0002t0044 |
2 | HG02145.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059_*2071dupTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | INFO_REALIGN_3_PRIME | chr17 | 77216069 | |||||
chr17:77216069 | C | T | 5 | a0001c0001t0045 a0001c0001t0049 a0001c0003t0024 others(2): Show |
7 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2046C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2046 | chr17 | 77216069 | ||||||
chr17:77216071 | A | C | 4 | a0001c0001t0045 a0001c0001t0049 a0001c0009t0017 others(1): Show |
5 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2048A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2048 | chr17 | 77216071 | ||||||
chr17:77216082 | T | C | 2 | a0001c0001t0049 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2059 | chr17 | 77216082 | ||||||
chr17:77216084 | A | AGGTAGGG others(3): Show |
2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2062_*2063insGTAG others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2063 | INFO_REALIGN_3_PRIME | chr17 | 77216084 | |||||
chr17:77216084 | A | C | 1 | a0001c0001t0045 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2061A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2061 | chr17 | 77216084 | ||||||
chr17:77216084 | AGTAGGTA others(19): Show |
A | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0030 others(1): Show |
12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2072_*2097delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | INFO_REALIGN_3_PRIME | chr17 | 77216084 | |||||
chr17:77216095 | C | T | 3 | a0001c0001t0049 a0001c0009t0017 a0004c0006t0017 |
4 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2072C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | chr17 | 77216095 | ||||||
chr17:77216108 | T | C | 5 | a0001c0001t0036 a0001c0001t0046 a0001c0001t0049 others(2): Show |
6 | HG02004.hp1 HG02145.hp1 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2085 | chr17 | 77216108 | ||||||
chr17:77216110 | C | A | 7 | a0001c0001t0036 a0001c0001t0045 a0001c0001t0046 others(4): Show |
9 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2087C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2087 | chr17 | 77216110 | ||||||
chr17:77216121 | T | C | 2 | a0001c0001t0049 a0001c0003t0024 |
3 | HG00423.hp2 HG02071.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2098T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2098 | chr17 | 77216121 | ||||||
chr17:77216123 | A | C | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2100A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2100 | chr17 | 77216123 | ||||||
chr17:77216134 | C | T | 4 | a0001c0001t0049 a0001c0003t0024 a0001c0009t0017 others(1): Show |
6 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2111C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2111 | chr17 | 77216134 | ||||||
chr17:77216136 | A | C | 4 | a0001c0001t0049 a0001c0003t0024 a0001c0009t0017 others(1): Show |
6 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2113A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2113 | chr17 | 77216136 | ||||||
chr17:77216147 | T | C | 3 | a0001c0001t0045 a0001c0009t0017 a0004c0006t0017 |
4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2124T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2124 | chr17 | 77216147 | ||||||
chr17:77216147 | TTCGTAGG others(19): Show |
T | 7 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0025 others(4): Show |
63 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2151delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | INFO_REALIGN_3_PRIME | chr17 | 77216147 | |||||
chr17:77216149 | C | A | 5 | a0001c0001t0045 a0001c0001t0049 a0001c0003t0024 others(2): Show |
7 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2126C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | chr17 | 77216149 | ||||||
chr17:77216149 | C | T | 1 | a0001c0003t0018 | 2 | NA18971.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2126C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | chr17 | 77216149 | ||||||
chr17:77216149 | CGTAGGTA others(19): Show |
C | 1 | a0001c0001t0028 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2139_*2164delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | INFO_REALIGN_3_PRIME | chr17 | 77216149 | |||||
chr17:77216150 | G | A | 1 | a0001c0001t0036 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2127G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2127 | chr17 | 77216150 | ||||||
chr17:77216160 | T | C | 3 | a0001c0001t0045 a0001c0001t0049 a0001c0003t0024 |
4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2137T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2137 | chr17 | 77216160 | ||||||
chr17:77216160 | TTCGTAGG others(32): Show |
T | 8 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(5): Show |
95 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2139_*2177delCGTA others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | INFO_REALIGN_3_PRIME | chr17 | 77216160 | |||||
chr17:77216162 | C | A | 11 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0033 others(8): Show |
16 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2139C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | chr17 | 77216162 | ||||||
chr17:77216173 | C | T | 3 | a0001c0001t0045 a0001c0001t0049 a0001c0003t0024 |
4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2150C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2150 | chr17 | 77216173 | ||||||
chr17:77216175 | A | AGTAGGTA others(6): Show |
1 | a0001c0001t0046 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2164_*2165insCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | |||||
chr17:77216175 | A | C | 2 | a0001c0001t0045 a0001c0001t0049 |
2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2152A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2152 | chr17 | 77216175 | ||||||
chr17:77216175 | A | T | 8 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0025 others(5): Show |
65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2152A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2152 | chr17 | 77216175 | ||||||
chr17:77216175 | AGTAGGTA others(36): Show |
A | 1 | a0001c0001t0033 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2158_*2200delTAGG others(39): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2158 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | |||||
chr17:77216175 | AGTAGGTA others(45): Show |
A | 2 | a0001c0001t0013 a0001c0001t0034 |
4 | HG02258.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2165_*2216delAGTA others(48): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | |||||
chr17:77216175 | AGTAGGTA others(58): Show |
A | 2 | a0001c0001t0020 a0003c0007t0035 |
3 | HG02273.hp2 HG03710.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2165_*2229delAGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | |||||
chr17:77216186 | T | C | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2163T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2163 | chr17 | 77216186 | ||||||
chr17:77216186 | T | TTAGTAGG others(6): Show |
1 | a0002c0004t0041 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2189_*2201dupCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2202 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | |||||
chr17:77216186 | TTAGTAGG others(6): Show |
T | 8 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0025 others(5): Show |
65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2189_*2201delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | |||||
chr17:77216186 | TTAGTAGG others(110): Show |
T | 1 | a0001c0002t0042 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2204_*2320del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2204 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | |||||
chr17:77216188 | A | C | 1 | a0001c0001t0046 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | chr17 | 77216188 | ||||||
chr17:77216199 | C | T | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2176C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2176 | chr17 | 77216199 | ||||||
chr17:77216212 | C | A | 1 | a0001c0002t0029 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2189C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | chr17 | 77216212 | ||||||
chr17:77216212 | C | T | 3 | a0001c0001t0028 a0001c0001t0045 a0001c0001t0049 |
3 | HG03471.hp1 NA18979.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2189C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | chr17 | 77216212 | ||||||
chr17:77216214 | A | C | 2 | a0001c0001t0028 a0001c0001t0045 |
2 | NA18979.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2191A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2191 | chr17 | 77216214 | ||||||
chr17:77216214 | AGTAGGTA others(6): Show |
A | 1 | a0001c0002t0038 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243_*2255delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2243 | INFO_REALIGN_3_PRIME | chr17 | 77216214 | |||||
chr17:77216219 | G | A | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2196G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2196 | chr17 | 77216219 | ||||||
chr17:77216238 | T | C | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2215T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2215 | chr17 | 77216238 | ||||||
chr17:77216240 | C | A | 3 | a0001c0001t0028 a0001c0009t0017 a0004c0006t0017 |
4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2217C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2217 | chr17 | 77216240 | ||||||
chr17:77216240 | C | CGTAGGTA others(32): Show |
1 | a0001c0001t0045 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2227_*2228insCTAG others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2228 | INFO_REALIGN_3_PRIME | chr17 | 77216240 | |||||
chr17:77216242 | T | C | 1 | a0001c0001t0028 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2219T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2219 | chr17 | 77216242 | ||||||
chr17:77216253 | C | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(40): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*2230C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2230 | chr17 | 77216253 | ||||||
chr17:77216255 | T | C | 1 | a0001c0001t0007 | 17 | HG02698.hp1 HG03831.hp2 HG03927.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2232T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2232 | chr17 | 77216255 | ||||||
chr17:77216266 | C | A | 4 | a0001c0001t0028 a0001c0001t0034 a0001c0009t0017 others(1): Show |
5 | HG02896.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2243C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2243 | chr17 | 77216266 | ||||||
chr17:77216266 | C | CGTAGGTA others(6): Show |
1 | a0001c0002t0043 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2256_*2268dupAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2269 | INFO_REALIGN_3_PRIME | chr17 | 77216266 | |||||
chr17:77216266 | CGTAGGTA others(6): Show |
C | 1 | a0001c0002t0014 | 3 | NA18960.hp2 NA18963.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2256_*2268delAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2256 | INFO_REALIGN_3_PRIME | chr17 | 77216266 | |||||
chr17:77216277 | T | C | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2254T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2254 | chr17 | 77216277 | ||||||
chr17:77216279 | A | C | 5 | a0001c0001t0028 a0001c0002t0010 a0001c0002t0016 others(2): Show |
12 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2256A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2256 | chr17 | 77216279 | ||||||
chr17:77216281 | T | C | 1 | a0001c0001t0020 | 2 | HG02273.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2258T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2258 | chr17 | 77216281 | ||||||
chr17:77216290 | T | C | 1 | a0001c0001t0028 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2267T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2267 | chr17 | 77216290 | ||||||
chr17:77216292 | C | A | 2 | a0001c0001t0028 a0001c0001t0034 |
2 | HG02896.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2269C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2269 | chr17 | 77216292 | ||||||
chr17:77216292 | CGTAGGTA others(6): Show |
C | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0033 others(4): Show |
77 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2306_*2318delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2306 | INFO_REALIGN_3_PRIME | chr17 | 77216292 | |||||
chr17:77216303 | C | T | 7 | a0001c0001t0020 a0001c0001t0034 a0001c0001t0045 others(4): Show |
9 | HG01361.hp2 HG02273.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2280C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2280 | chr17 | 77216303 | ||||||
chr17:77216305 | A | C | 4 | a0001c0001t0034 a0001c0002t0012 a0001c0009t0017 others(1): Show |
5 | HG01361.hp2 HG02896.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2282A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2282 | chr17 | 77216305 | ||||||
chr17:77216312 | A | C | 1 | a0001c0001t0047 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2289 | chr17 | 77216312 | ||||||
chr17:77216316 | C | T | 5 | a0001c0001t0020 a0001c0001t0045 a0001c0009t0017 others(2): Show |
7 | HG02273.hp2 HG03491.hp1 HG03492.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2293C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2293 | chr17 | 77216316 | ||||||
chr17:77216318 | A | C | 2 | a0001c0001t0020 a0003c0007t0035 |
3 | HG02273.hp2 HG03710.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2295A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2295 | chr17 | 77216318 | ||||||
chr17:77216329 | C | T | 2 | a0001c0009t0017 a0004c0006t0017 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2306C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2306 | chr17 | 77216329 | ||||||
chr17:77216329 | CTAGTAGG others(6): Show |
C | 1 | a0001c0002t0055 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319_*2331delTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2319 | INFO_REALIGN_3_PRIME | chr17 | 77216329 | |||||
chr17:77216331 | AGTAGGTA others(71): Show |
A | 1 | a0001c0002t0019 | 2 | NA18982.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2321_*2398delAGTA others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2321 | INFO_REALIGN_3_PRIME | chr17 | 77216331 | |||||
chr17:77216342 | T | C | 4 | a0001c0001t0002 a0001c0001t0045 a0001c0002t0003 others(1): Show |
5 | HG01346.hp1 HG01433.hp2 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2319 | chr17 | 77216342 | ||||||
chr17:77216342 | TTAGTAGG others(6): Show |
T | 4 | a0001c0001t0004 a0001c0001t0007 a0001c0002t0003 others(1): Show |
11 | HG00558.hp2 HG02074.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2371_*2383delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | INFO_REALIGN_3_PRIME | chr17 | 77216342 | |||||
chr17:77216344 | A | C | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(5): Show |
58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2321A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2321 | chr17 | 77216344 | ||||||
chr17:77216355 | C | T | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(4): Show |
57 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2332C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2332 | chr17 | 77216355 | ||||||
chr17:77216357 | A | C | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(3): Show |
58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2334A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2334 | chr17 | 77216357 | ||||||
chr17:77216368 | C | T | 3 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0028 |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2345C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2345 | chr17 | 77216368 | ||||||
chr17:77216370 | A | C | 3 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0020 |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2347A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2347 | chr17 | 77216370 | ||||||
chr17:77216381 | C | T | 3 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0028 |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2358C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2358 | chr17 | 77216381 | ||||||
chr17:77216383 | A | C | 2 | a0001c0001t0007 a0001c0001t0028 |
3 | HG02698.hp1 NA19068.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2360A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2360 | chr17 | 77216383 | ||||||
chr17:77216383 | AGTAGGTA others(19): Show |
A | 16 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0015 others(13): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2371_*2396delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | INFO_REALIGN_3_PRIME | chr17 | 77216383 | |||||
chr17:77216393 | G | T | 9 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(6): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2370G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2370 | chr17 | 77216393 | ||||||
chr17:77216394 | C | T | 3 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0028 |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2371C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | chr17 | 77216394 | ||||||
chr17:77216396 | A | AGTAGGTA others(6): Show |
2 | a0001c0001t0007 a0001c0002t0003 |
2 | HG01928.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2412_*2424dupCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2425 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | |||||
chr17:77216396 | A | C | 3 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0028 |
18 | HG02273.hp2 HG03710.hp2 HG03831.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2373A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2373 | chr17 | 77216396 | ||||||
chr17:77216396 | AGTAGGTA others(6): Show |
A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(8): Show |
67 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2424delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2412 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | |||||
chr17:77216396 | AGTAGGTA others(19): Show |
A | 1 | a0001c0001t0001 | 2 | HG00099.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2399_*2424delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2399 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | |||||
chr17:77216406 | G | T | 1 | a0003c0007t0035 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2383G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2383 | chr17 | 77216406 | ||||||
chr17:77216407 | T | C | 1 | a0003c0007t0035 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2384T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2384 | chr17 | 77216407 | ||||||
chr17:77216409 | C | A | 1 | a0003c0007t0035 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2386C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2386 | chr17 | 77216409 | ||||||
chr17:77216890 | G | A | 1 | a0001c0001t0021 | 2 | NA18945.hp2 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2867G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2867 | chr17 | 77216890 | ||||||
chr17:77217072 | C | T | 1 | a0001c0002t0054 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3049C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 3049 | chr17 | 77217072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:77141199 | C | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+92C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141199 | |||||||
chr17:77141227 | C | T | 1 | a0001c0001t0001g0390 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-136+120C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141227 | |||||||
chr17:77141234 | C | G | 1 | a0001c0001t0006g0389 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-136+127C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141234 | |||||||
chr17:77141238 | C | G | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-136+131C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141238 | |||||||
chr17:77141259 | A | G | 1 | a0001c0001t0006g0387 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-136+152A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141259 | |||||||
chr17:77141333 | C | A | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-136+226C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141333 | |||||||
chr17:77141336 | T | TC | 18 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(15): Show |
18 | HG01109.hp1 HG01261.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.-136+234dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77141336 | ||||||
chr17:77141369 | C | T | 115 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(112): Show |
119 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-136+262C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141369 | |||||||
chr17:77141496 | C | T | 1 | a0001c0001t0004g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-136+389C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141496 | |||||||
chr17:77141534 | C | T | 1 | a0001c0003t0002g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136+427C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141534 | |||||||
chr17:77141560 | C | T | 60 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(57): Show |
63 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.-136+453C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141560 | |||||||
chr17:77141569 | C | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+462C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141569 | |||||||
chr17:77141596 | C | T | 1 | a0001c0001t0006g0229 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-136+489C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141596 | |||||||
chr17:77141722 | G | A | 10 | a0001c0002t0005g0034 a0001c0002t0005g0035 a0001c0002t0005g0282 others(7): Show |
10 | HG02129.hp2 HG02132.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+615G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141722 | |||||||
chr17:77141738 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136+631C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141738 | |||||||
chr17:77141800 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-136+693G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141800 | |||||||
chr17:77141812 | A | C | 155 | a0001c0001t0001g0201 a0001c0001t0002g0216 a0001c0001t0003g0001 others(152): Show |
162 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-136+705A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141812 | |||||||
chr17:77141873 | C | T | 1 | a0001c0002t0003g0195 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-136+766C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141873 | |||||||
chr17:77142060 | A | C | 1 | a0001c0001t0056g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-135-586A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142060 | |||||||
chr17:77142296 | C | T | 1 | a0001c0001t0001g0390 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-135-350C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142296 | |||||||
chr17:77142300 | C | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-135-346C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142300 | |||||||
chr17:77142324 | T | A | 1 | a0001c0003t0002g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-135-322T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142324 | |||||||
chr17:77142557 | C | CA | 65 | a0001c0001t0001g0023 a0001c0001t0001g0108 a0001c0001t0001g0112 others(62): Show |
67 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-135-68dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | ||||||
chr17:77142557 | C | CAA | 12 | a0001c0001t0004g0050 a0001c0001t0004g0051 a0001c0001t0004g0052 others(9): Show |
13 | HG01255.hp1 HG01884.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-135-69_-135-68dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | ||||||
chr17:77142557 | CA | C | 50 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0231 others(47): Show |
50 | HG00408.hp1 HG01074.hp1 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.-135-68delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | ||||||
chr17:77142557 | CAA | C | 45 | a0001c0001t0002g0011 a0001c0001t0002g0237 a0001c0001t0002g0239 others(42): Show |
47 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-135-69_-135-68del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | ||||||
chr17:77142557 | CAAA | C | 9 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0273 others(6): Show |
10 | NA18952.hp2 NA18957.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-70_-135-68del others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | ||||||
chr17:77142630 | CT | C | 23 | a0001c0001t0006g0198 a0001c0001t0007g0391 a0001c0001t0007g0393 others(20): Show |
23 | HG01943.hp1 HG02273.hp2 HG02698.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.-135-6delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142630 | ||||||
chr17:77142632 | T | C | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142632 | |||||||
chr17:77142634 | T | C | 1 | a0001c0001t0004g0050 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-135-12T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142634 | |||||||
chr17:77142641 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.-135-5A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142641 | |||||||
chr17:77142870 | A | G | 4 | a0001c0003t0002g0190 a0001c0009t0017g0193 a0004c0006t0017g0191 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+120A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77142870 | |||||||
chr17:77142918 | C | A | 2 | a0001c0001t0008g0053 a0001c0001t0008g0054 |
2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+168C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77142918 | |||||||
chr17:77143037 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-31+287T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143037 | |||||||
chr17:77143104 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-31+354A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143104 | |||||||
chr17:77143104 | AT | A | 117 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(114): Show |
121 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-31+361delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr17 | 77143104 | ||||||
chr17:77143248 | G | C | 1 | a0001c0001t0009g0116 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-30-319G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143248 | |||||||
chr17:77143347 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30-220C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143347 | |||||||
chr17:77143423 | A | C | 1 | a0001c0002t0055g0370 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30-144A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143423 | |||||||
chr17:77143531 | T | C | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-30-36T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143531 | |||||||
chr17:77143757 | C | T | 1 | a0001c0001t0006g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+98C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143757 | |||||||
chr17:77143881 | G | T | 1 | a0001c0001t0006g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+222G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143881 | |||||||
chr17:77143915 | C | T | 1 | a0001c0003t0002g0272 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+256C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143915 | |||||||
chr17:77143942 | C | G | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+283C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143942 | |||||||
chr17:77143948 | G | T | 3 | a0001c0002t0003g0182 a0001c0002t0003g0183 a0001c0002t0003g0184 |
3 | NA18612.hp2 NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.63+289G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143948 | |||||||
chr17:77143956 | CT | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(83): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+304delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77143956 | ||||||
chr17:77144206 | C | T | 1 | a0001c0001t0004g0107 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.63+547C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144206 | |||||||
chr17:77144229 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144229 | |||||||
chr17:77144241 | T | A | 2 | a0001c0002t0005g0293 a0001c0002t0005g0372 |
2 | NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.63+582T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144241 | |||||||
chr17:77144325 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+666C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144325 | |||||||
chr17:77144344 | A | G | 1 | a0001c0002t0005g0369 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+685A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144344 | |||||||
chr17:77144416 | G | C | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+757G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144416 | |||||||
chr17:77144827 | G | A | 1 | a0001c0002t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+1168G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144827 | |||||||
chr17:77145002 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+1343C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145002 | |||||||
chr17:77145012 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+1353A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145012 | |||||||
chr17:77145063 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+1404C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145063 | |||||||
chr17:77145077 | TTGTGTGT others(15): Show |
T | 90 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(87): Show |
93 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.63+1436_63+1457del others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | ||||||
chr17:77145077 | TTGTGTGT others(17): Show |
T | 4 | a0001c0002t0003g0310 a0001c0002t0003g0376 a0001c0002t0005g0284 others(1): Show |
4 | HG01928.hp1 HG02129.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1436_63+1459del others(24): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | ||||||
chr17:77145077 | TTGTGTGT others(21): Show |
T | 1 | a0001c0002t0005g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.63+1436_63+1463del others(28): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | ||||||
chr17:77145079 | GTGTGTGT others(13): Show |
G | 21 | a0001c0002t0003g0036 a0001c0002t0003g0195 a0001c0002t0003g0306 others(18): Show |
22 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+1436_63+1455del others(20): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145079 | ||||||
chr17:77145081 | GTGTGTGT others(11): Show |
G | 1 | a0001c0002t0003g0308 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.63+1436_63+1453del others(18): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145081 | ||||||
chr17:77145095 | A | ATG | 4 | a0001c0003t0002g0190 a0001c0003t0002g0265 a0001c0003t0018g0012 others(1): Show |
4 | HG03239.hp2 NA18941.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1438_63+1439dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145095 | ||||||
chr17:77145095 | A | ATGTG | 6 | a0001c0003t0002g0012 a0001c0003t0002g0234 a0001c0003t0002g0235 others(3): Show |
6 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+1439_63+1440ins others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145095 | ||||||
chr17:77145099 | A | ATG | 11 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0236 others(8): Show |
11 | HG01070.hp2 HG01106.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+1476_63+1477dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | A | ATGTG | 28 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0231 others(25): Show |
30 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+1474_63+1477dup others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | A | ATGTGTG | 10 | a0001c0001t0002g0239 a0001c0001t0002g0266 a0001c0003t0002g0030 others(7): Show |
10 | HG00140.hp1 HG02155.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+1472_63+1477dup others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | A | ATGTGTGT others(1): Show |
3 | a0001c0003t0002g0252 a0001c0003t0002g0260 a0001c0003t0002g0262 |
3 | HG04115.hp1 NA18960.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.63+1470_63+1477dup others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | A | G | 10 | a0001c0003t0002g0012 a0001c0003t0002g0190 a0001c0003t0002g0234 others(7): Show |
10 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+1440A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145099 | |||||||
chr17:77145099 | ATG | A | 15 | a0001c0001t0006g0198 a0001c0001t0006g0226 a0001c0001t0006g0227 others(12): Show |
16 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+1476_63+1477del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | ATGTG | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0006g0389 others(8): Show |
12 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+1474_63+1477del others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145099 | ATGTGTG | A | 102 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(99): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.63+1472_63+1477del others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | ||||||
chr17:77145125 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0004g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.63+1468_63+1479del others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145125 | ||||||
chr17:77145127 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0004g0069 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.63+1470_63+1479del others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145127 | ||||||
chr17:77145129 | GTGTGTGT others(1): Show |
G | 52 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(49): Show |
54 | HG00558.hp2 HG00673.hp1 HG01943.hp2 others(51): Show |
intron_variant | MODIFIER | c.63+1472_63+1479del others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145129 | ||||||
chr17:77145131 | G | A | 1 | a0001c0001t0006g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+1472G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145131 | |||||||
chr17:77145131 | GTGTGTA | G | 4 | a0001c0001t0004g0063 a0001c0001t0004g0084 a0001c0001t0004g0102 others(1): Show |
4 | HG00544.hp2 NA18967.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1474_63+1479del others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145131 | ||||||
chr17:77145133 | G | A | 41 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0002g0216 others(38): Show |
46 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.63+1474G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145133 | |||||||
chr17:77145135 | G | A | 246 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(243): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.63+1476G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145135 | |||||||
chr17:77145137 | A | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0237 a0001c0001t0002g0245 |
4 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1478A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145137 | |||||||
chr17:77145153 | ATTTGT | A | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+1508_63+1512del others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145153 | ||||||
chr17:77145239 | C | T | 1 | a0006c0010t0004g0196 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+1580C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145239 | |||||||
chr17:77145322 | G | T | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+1663G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145322 | |||||||
chr17:77145561 | T | C | 37 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(34): Show |
40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+1902T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145561 | |||||||
chr17:77145596 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+1937C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145596 | |||||||
chr17:77145723 | G | A | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+2064G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145723 | |||||||
chr17:77145828 | G | T | 35 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+2169G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145828 | |||||||
chr17:77145831 | G | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0237 |
3 | HG00642.hp2 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.63+2172G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145831 | |||||||
chr17:77145832 | G | T | 1 | a0001c0001t0030g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+2173G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145832 | |||||||
chr17:77145869 | C | T | 2 | a0001c0001t0004g0103 a0001c0001t0004g0104 |
2 | NA18944.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.63+2210C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145869 | |||||||
chr17:77146022 | A | C | 1 | a0001c0002t0005g0368 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+2363A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146022 | |||||||
chr17:77146039 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+2380C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146039 | |||||||
chr17:77146237 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+2578G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146237 | |||||||
chr17:77146278 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0009g0006 others(4): Show |
8 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+2619G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146278 | |||||||
chr17:77146713 | A | C | 1 | a0001c0002t0055g0370 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.63+3054A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146713 | |||||||
chr17:77146713 | A | G | 11 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(8): Show |
12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3054A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146713 | |||||||
chr17:77146728 | A | G | 406 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(403): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.63+3069A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146728 | |||||||
chr17:77146734 | G | A | 1 | a0001c0001t0004g0061 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.63+3075G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146734 | |||||||
chr17:77146993 | A | G | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+3334A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146993 | |||||||
chr17:77146999 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+3340G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146999 | |||||||
chr17:77147050 | C | T | 60 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(57): Show |
64 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.63+3391C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147050 | |||||||
chr17:77147079 | C | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+3420C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147079 | |||||||
chr17:77147139 | A | G | 11 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(8): Show |
12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3480A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147139 | |||||||
chr17:77147230 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+3571G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147230 | |||||||
chr17:77147279 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.63+3620C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147279 | |||||||
chr17:77147312 | T | C | 4 | a0001c0003t0002g0190 a0001c0009t0017g0193 a0004c0006t0017g0191 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+3653T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147312 | |||||||
chr17:77147373 | T | TA | 48 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(45): Show |
48 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.63+3724dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77147373 | ||||||
chr17:77147538 | G | A | 12 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0343 others(9): Show |
12 | HG00558.hp1 HG00639.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+3879G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147538 | |||||||
chr17:77147601 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+3942G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147601 | |||||||
chr17:77147680 | A | C | 2 | a0001c0002t0003g0366 a0001c0002t0003g0367 |
2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.63+4021A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147680 | |||||||
chr17:77147770 | G | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4111G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147770 | |||||||
chr17:77147949 | C | G | 5 | a0001c0002t0005g0035 a0001c0002t0005g0282 a0001c0002t0005g0283 others(2): Show |
5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+4290C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147949 | |||||||
chr17:77147984 | C | T | 1 | a0001c0002t0005g0333 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.63+4325C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147984 | |||||||
chr17:77148004 | C | T | 1 | a0001c0001t0007g0410 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.63+4345C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148004 | |||||||
chr17:77148047 | G | A | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.63+4388G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148047 | |||||||
chr17:77148058 | AGT | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+4402_63+4403del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77148058 | ||||||
chr17:77148065 | C | G | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+4406C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148065 | |||||||
chr17:77148140 | A | G | 1 | a0001c0002t0005g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+4481A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148140 | |||||||
chr17:77148190 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.63+4531G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148190 | |||||||
chr17:77148311 | A | G | 61 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(58): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+4652A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148311 | |||||||
chr17:77148522 | C | T | 118 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(115): Show |
122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+4863C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148522 | |||||||
chr17:77148676 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+5017G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148676 | |||||||
chr17:77148753 | C | T | 61 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(58): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+5094C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148753 | |||||||
chr17:77148774 | C | T | 1 | a0001c0001t0004g0101 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.63+5115C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148774 | |||||||
chr17:77149015 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5356T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149015 | |||||||
chr17:77149139 | C | T | 1 | a0001c0001t0007g0409 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.63+5480C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149139 | |||||||
chr17:77149163 | T | G | 1 | a0001c0001t0004g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5504T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149163 | |||||||
chr17:77149216 | T | A | 1 | a0001c0001t0004g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5557T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149216 | |||||||
chr17:77149610 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+5951G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149610 | |||||||
chr17:77149660 | C | A | 1 | a0001c0001t0004g0062 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+6001C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149660 | |||||||
chr17:77149856 | GT | G | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0231 others(9): Show |
12 | HG01167.hp1 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+6215delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77149856 | ||||||
chr17:77149864 | T | G | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6205T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149864 | |||||||
chr17:77150184 | T | C | 35 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+6525T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150184 | |||||||
chr17:77150287 | G | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+6628G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150287 | |||||||
chr17:77150351 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+6692G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150351 | |||||||
chr17:77150594 | AG | A | 5 | a0001c0002t0005g0035 a0001c0002t0005g0282 a0001c0002t0005g0283 others(2): Show |
5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6938delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77150594 | ||||||
chr17:77150719 | T | C | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+7060T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150719 | |||||||
chr17:77150808 | C | T | 5 | a0001c0001t0006g0197 a0001c0001t0006g0221 a0001c0001t0006g0223 others(2): Show |
5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+7149C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150808 | |||||||
chr17:77150827 | C | G | 68 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(65): Show |
72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.63+7168C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150827 | |||||||
chr17:77151159 | C | T | 2 | a0001c0003t0002g0240 a0001c0003t0002g0241 |
2 | HG02055.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.63+7500C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151159 | |||||||
chr17:77151238 | C | CAATCAGT others(3): Show |
1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+7581_63+7590dup others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77151238 | ||||||
chr17:77151242 | C | G | 1 | a0002c0004t0041g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+7583C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151242 | |||||||
chr17:77151264 | C | T | 1 | a0006c0010t0004g0196 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+7605C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151264 | |||||||
chr17:77151419 | G | C | 1 | a0001c0001t0006g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.63+7760G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151419 | |||||||
chr17:77151572 | C | T | 1 | a0001c0002t0005g0342 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+7913C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151572 | |||||||
chr17:77151591 | GT | G | 405 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(402): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.63+7937delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77151591 | ||||||
chr17:77151592 | T | A | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+7933T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151592 | |||||||
chr17:77151701 | A | G | 18 | a0001c0001t0004g0005 a0001c0001t0004g0022 a0001c0001t0004g0087 others(15): Show |
19 | HG00558.hp2 HG02015.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+8042A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151701 | |||||||
chr17:77152074 | C | T | 11 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(8): Show |
12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+8415C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152074 | |||||||
chr17:77152147 | T | C | 1 | a0001c0002t0003g0376 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.63+8488T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152147 | |||||||
chr17:77152264 | G | A | 4 | a0001c0002t0003g0379 a0001c0002t0003g0380 a0001c0002t0003g0381 others(1): Show |
4 | HG03017.hp2 HG03239.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8605G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152264 | |||||||
chr17:77152307 | G | A | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+8648G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152307 | |||||||
chr17:77152315 | C | T | 1 | a0001c0001t0034g0118 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+8656C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152315 | |||||||
chr17:77152436 | T | C | 273 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(270): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+8777T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152436 | |||||||
chr17:77152535 | CA | C | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(361): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.63+8895delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77152535 | ||||||
chr17:77152535 | CAA | C | 9 | a0001c0001t0001g0170 a0001c0001t0002g0279 a0001c0001t0004g0107 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8894_63+8895del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77152535 | ||||||
chr17:77152551 | A | C | 1 | a0001c0002t0010g0290 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+8892A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152551 | |||||||
chr17:77152659 | G | A | 67 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(64): Show |
71 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+9000G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152659 | |||||||
chr17:77152731 | A | G | 36 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+9072A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152731 | |||||||
chr17:77152913 | C | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(9): Show |
12 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+9254C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152913 | |||||||
chr17:77152964 | C | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+9305C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152964 | |||||||
chr17:77153072 | T | C | 1 | a0001c0002t0014g0299 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63+9413T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153072 | |||||||
chr17:77153199 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0127 |
2 | NA19000.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.63+9540C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153199 | |||||||
chr17:77153385 | T | C | 1 | a0001c0001t0034g0118 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+9726T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153385 | |||||||
chr17:77153420 | A | G | 1 | a0001c0002t0003g0308 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.63+9761A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153420 | |||||||
chr17:77153515 | T | C | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+9856T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153515 | |||||||
chr17:77153741 | C | T | 1 | a0001c0001t0004g0086 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.63+10082C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153741 | |||||||
chr17:77153951 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+10292C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153951 | |||||||
chr17:77154057 | C | A | 1 | a0001c0002t0003g0344 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.63+10398C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154057 | |||||||
chr17:77154094 | A | G | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+10435A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154094 | |||||||
chr17:77154115 | A | T | 1 | a0001c0001t0002g0239 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.63+10456A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154115 | |||||||
chr17:77154241 | C | T | 1 | a0001c0002t0043g0350 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+10582C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154241 | |||||||
chr17:77154350 | C | T | 7 | a0001c0001t0036g0388 a0001c0005t0011g0008 a0001c0005t0011g0019 others(4): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+10691C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154350 | |||||||
chr17:77154369 | G | A | 86 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(83): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+10710G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154369 | |||||||
chr17:77154405 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+10746G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154405 | |||||||
chr17:77154475 | A | G | 13 | a0001c0001t0004g0004 a0001c0001t0004g0077 a0001c0001t0004g0078 others(10): Show |
14 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+10816A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154475 | |||||||
chr17:77154567 | A | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+10908A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154567 | |||||||
chr17:77154601 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+10942G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154601 | |||||||
chr17:77154637 | G | GT | 201 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.63+10987dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77154637 | ||||||
chr17:77154637 | G | T | 2 | a0001c0001t0033g0048 a0009c0012t0005g0331 |
2 | NA18959.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.63+10978G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154637 | |||||||
chr17:77154647 | G | T | 404 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(401): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.63+10988G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154647 | |||||||
chr17:77154648 | G | T | 5 | a0001c0001t0006g0389 a0001c0009t0017g0193 a0004c0006t0017g0191 others(2): Show |
5 | HG03491.hp1 HG03492.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+10989G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154648 | |||||||
chr17:77154675 | A | G | 57 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(54): Show |
60 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+11016A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154675 | |||||||
chr17:77154946 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+11287G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154946 | |||||||
chr17:77154963 | C | G | 2 | a0001c0001t0004g0072 a0001c0001t0004g0106 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+11304C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154963 | |||||||
chr17:77155277 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0237 |
3 | HG00642.hp2 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.63+11618T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155277 | |||||||
chr17:77155357 | A | G | 37 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(34): Show |
40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+11698A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155357 | |||||||
chr17:77155361 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+11702A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155361 | |||||||
chr17:77155390 | C | T | 118 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(115): Show |
122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11731C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155390 | |||||||
chr17:77155422 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+11763G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155422 | |||||||
chr17:77155499 | C | G | 1 | a0001c0003t0002g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.63+11840C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155499 | |||||||
chr17:77155504 | A | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+11845A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155504 | |||||||
chr17:77155635 | G | T | 266 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(263): Show |
276 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.63+11976G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155635 | |||||||
chr17:77155719 | C | T | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+12060C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155719 | |||||||
chr17:77155766 | C | T | 3 | a0001c0001t0007g0406 a0001c0001t0007g0407 a0001c0001t0007g0408 |
3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.63+12107C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155766 | |||||||
chr17:77155828 | C | G | 37 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(34): Show |
40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+12169C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155828 | |||||||
chr17:77155935 | T | G | 118 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(115): Show |
122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+12276T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155935 | |||||||
chr17:77156116 | G | A | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+12457G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156116 | |||||||
chr17:77156132 | A | G | 2 | a0001c0001t0023g0271 a0001c0001t0023g0278 |
2 | NA18959.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+12473A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156132 | |||||||
chr17:77156156 | C | A | 117 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(114): Show |
121 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+12497C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156156 | |||||||
chr17:77156175 | C | A | 1 | a0001c0001t0004g0063 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.63+12516C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156175 | |||||||
chr17:77156180 | G | T | 1 | a0001c0001t0007g0408 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.63+12521G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156180 | |||||||
chr17:77156298 | G | A | 35 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+12639G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156298 | |||||||
chr17:77156329 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+12670C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156329 | |||||||
chr17:77156337 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+12678A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156337 | |||||||
chr17:77156349 | C | T | 144 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(141): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.63+12690C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156349 | |||||||
chr17:77156431 | T | C | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+12772T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156431 | |||||||
chr17:77156561 | C | T | 4 | a0001c0001t0001g0390 a0001c0009t0017g0193 a0004c0006t0017g0191 others(1): Show |
4 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12902C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156561 | |||||||
chr17:77156574 | TA | T | 15 | a0001c0001t0002g0236 a0001c0001t0002g0279 a0001c0001t0004g0071 others(12): Show |
15 | HG01891.hp1 HG02109.hp1 HG03041.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+12931delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77156574 | ||||||
chr17:77156668 | T | G | 1 | a0001c0002t0003g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.63+13009T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156668 | |||||||
chr17:77156669 | G | T | 1 | a0001c0002t0003g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.63+13010G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156669 | |||||||
chr17:77156851 | C | T | 1 | a0001c0001t0050g0047 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.63+13192C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156851 | |||||||
chr17:77156995 | T | C | 1 | a0001c0001t0006g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.63+13336T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156995 | |||||||
chr17:77157118 | T | C | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+13459T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157118 | |||||||
chr17:77157169 | T | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+13510T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157169 | |||||||
chr17:77157340 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.63+13681C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157340 | |||||||
chr17:77157389 | G | A | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+13730G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157389 | |||||||
chr17:77157530 | C | CT | 71 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(68): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+13886dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77157530 | ||||||
chr17:77157546 | G | A | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+13887G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157546 | |||||||
chr17:77157559 | G | A | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+13900G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157559 | |||||||
chr17:77157731 | T | C | 2 | a0001c0001t0004g0005 a0001c0001t0004g0107 |
3 | NA18961.hp2 NA18973.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.63+14072T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157731 | |||||||
chr17:77157762 | G | A | 61 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(58): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+14103G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157762 | |||||||
chr17:77157767 | G | C | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+14108G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157767 | |||||||
chr17:77157812 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.63+14153C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157812 | |||||||
chr17:77157833 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.63+14174T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157833 | |||||||
chr17:77157843 | G | A | 2 | a0001c0001t0006g0221 a0001c0002t0006g0222 |
2 | HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.63+14184G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157843 | |||||||
chr17:77157893 | T | C | 1 | a0001c0002t0005g0314 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.63+14234T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157893 | |||||||
chr17:77157907 | C | A | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.63+14248C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157907 | |||||||
chr17:77158032 | C | T | 2 | a0001c0002t0012g0329 a0001c0002t0012g0330 |
2 | HG01071.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.63+14373C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158032 | |||||||
chr17:77158056 | A | G | 3 | a0001c0001t0006g0197 a0001c0001t0006g0223 a0001c0001t0006g0224 |
3 | NA19000.hp2 NA19002.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.63+14397A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158056 | |||||||
chr17:77158090 | A | G | 1 | a0001c0001t0006g0389 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+14431A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158090 | |||||||
chr17:77158119 | A | G | 3 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0236 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+14460A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158119 | |||||||
chr17:77158149 | A | T | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0166 |
3 | HG02258.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+14490A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158149 | |||||||
chr17:77158469 | T | TTAA | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+14810_63+14811i others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158469 | |||||||
chr17:77158565 | T | G | 124 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(121): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.63+14906T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158565 | |||||||
chr17:77158619 | CA | C | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+14961delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158619 | |||||||
chr17:77158674 | A | G | 1 | a0001c0002t0005g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+15015A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158674 | |||||||
chr17:77158691 | C | T | 4 | a0001c0001t0004g0072 a0001c0001t0004g0105 a0001c0001t0004g0106 others(1): Show |
4 | HG02717.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+15032C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158691 | |||||||
chr17:77158714 | T | C | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15055T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158714 | |||||||
chr17:77158765 | T | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+15106T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158765 | |||||||
chr17:77158774 | A | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+15115A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158774 | |||||||
chr17:77158798 | C | CT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0127 a0001c0001t0001g0133 others(11): Show |
15 | HG00544.hp1 HG01516.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+15172dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | C | CTT | 25 | a0001c0001t0001g0023 a0001c0001t0001g0108 a0001c0001t0001g0126 others(22): Show |
25 | HG00438.hp2 HG01168.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+15171_63+15172d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | C | CTTT | 25 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(22): Show |
25 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+15170_63+15172d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | C | CTTTT | 10 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
10 | HG00738.hp2 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+15169_63+15172d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CT | C | 30 | a0001c0001t0002g0011 a0001c0001t0002g0237 a0001c0001t0036g0388 others(27): Show |
31 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.63+15172delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTT | C | 49 | a0001c0001t0002g0033 a0001c0001t0002g0231 a0001c0001t0002g0232 others(46): Show |
51 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.63+15171_63+15172d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTTT | C | 148 | a0001c0001t0001g0201 a0001c0001t0002g0014 a0001c0001t0002g0233 others(145): Show |
154 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.63+15170_63+15172d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTTTT | C | 40 | a0001c0001t0002g0274 a0001c0001t0004g0004 a0001c0001t0004g0024 others(37): Show |
42 | HG01074.hp1 HG01167.hp2 HG01943.hp2 others(39): Show |
intron_variant | MODIFIER | c.63+15169_63+15172d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTTTTTTT others(1): Show |
C | 39 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(36): Show |
42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15165_63+15172d others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0005g0377 a0001c0002t0005g0386 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.63+15161_63+15172d others(14): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158798 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+15154_63+15172d others(21): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | ||||||
chr17:77158826 | T | A | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15167T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158826 | |||||||
chr17:77158827 | T | C | 39 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(36): Show |
42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15168T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158827 | |||||||
chr17:77158889 | G | T | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15230G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158889 | |||||||
chr17:77158890 | C | G | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15231C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158890 | |||||||
chr17:77158916 | A | C | 1 | a0001c0001t0008g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63+15257A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158916 | |||||||
chr17:77159030 | G | A | 1 | a0001c0001t0004g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63+15371G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159030 | |||||||
chr17:77159096 | T | A | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+15437T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159096 | |||||||
chr17:77159098 | A | T | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+15439A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159098 | |||||||
chr17:77159264 | G | T | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+15605G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159264 | |||||||
chr17:77159338 | G | A | 39 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(36): Show |
42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15679G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159338 | |||||||
chr17:77159363 | G | A | 7 | a0001c0003t0002g0012 a0001c0003t0002g0235 a0001c0003t0002g0243 others(4): Show |
7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+15704G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159363 | |||||||
chr17:77159382 | C | CT | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+15739dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159382 | ||||||
chr17:77159385 | T | C | 2 | a0001c0002t0003g0310 a0001c0002t0003g0353 |
2 | HG00140.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.63+15726T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159385 | |||||||
chr17:77159483 | C | T | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+15824C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159483 | |||||||
chr17:77159642 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.63+15983G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159642 | |||||||
chr17:77159694 | T | C | 39 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(36): Show |
42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+16035T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159694 | |||||||
chr17:77159868 | G | GACCC | 62 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(59): Show |
65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.63+16212_63+16215d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159868 | ||||||
chr17:77159899 | G | T | 1 | a0001c0001t0002g0276 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.63+16240G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159899 | |||||||
chr17:77159929 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0162 |
2 | HG01099.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.63+16270G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159929 | |||||||
chr17:77159956 | T | C | 406 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(403): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.63+16297T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159956 | |||||||
chr17:77160131 | T | C | 3 | a0001c0001t0015g0055 a0001c0001t0015g0109 a0001c0001t0015g0110 |
3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+16472T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160131 | |||||||
chr17:77160323 | C | T | 119 | a0001c0001t0002g0268 a0001c0002t0003g0002 a0001c0002t0003g0016 others(116): Show |
123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.63+16664C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160323 | |||||||
chr17:77160331 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+16672G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160331 | |||||||
chr17:77160362 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.63+16703A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160362 | |||||||
chr17:77160531 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.63+16872C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160531 | |||||||
chr17:77160532 | G | A | 406 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(403): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.63+16873G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160532 | |||||||
chr17:77160539 | T | C | 12 | a0001c0002t0005g0334 a0001c0002t0005g0335 a0001c0002t0005g0336 others(9): Show |
12 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+16880T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160539 | |||||||
chr17:77160663 | C | G | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.63+17004C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160663 | |||||||
chr17:77160721 | T | C | 1 | a0001c0002t0003g0195 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.63+17062T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160721 | |||||||
chr17:77160802 | C | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+17143C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160802 | |||||||
chr17:77160810 | T | TTTTTTTT others(3): Show |
3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17151_63+17152i others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160810 | |||||||
chr17:77160811 | A | G | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17152A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160811 | |||||||
chr17:77160812 | G | A | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17153G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160812 | |||||||
chr17:77160830 | C | A | 14 | a0001c0001t0006g0202 a0001c0001t0006g0203 a0001c0001t0006g0204 others(11): Show |
14 | HG02145.hp2 HG02630.hp2 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+17171C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160830 | |||||||
chr17:77160855 | T | C | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+17196T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160855 | |||||||
chr17:77161037 | C | T | 1 | a0001c0001t0004g0096 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.63+17378C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161037 | |||||||
chr17:77161272 | G | T | 60 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(57): Show |
63 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.63+17613G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161272 | |||||||
chr17:77161301 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+17642A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161301 | |||||||
chr17:77161318 | C | G | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0166 |
3 | HG02258.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+17659C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161318 | |||||||
chr17:77161334 | A | G | 5 | a0001c0001t0006g0197 a0001c0001t0006g0221 a0001c0001t0006g0223 others(2): Show |
5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17675A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161334 | |||||||
chr17:77161458 | A | G | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+17799A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161458 | |||||||
chr17:77161475 | G | A | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+17816G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161475 | |||||||
chr17:77161557 | G | C | 35 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+17898G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161557 | |||||||
chr17:77161558 | G | A | 15 | a0001c0001t0006g0060 a0001c0001t0006g0202 a0001c0001t0006g0203 others(12): Show |
15 | HG02145.hp2 HG02630.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+17899G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161558 | |||||||
chr17:77161624 | A | G | 2 | a0002c0004t0003g0174 a0002c0004t0003g0175 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.63+17965A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161624 | |||||||
chr17:77161656 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+17997A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161656 | |||||||
chr17:77161707 | T | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+18048T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161707 | |||||||
chr17:77161712 | C | CT | 114 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0242 others(111): Show |
120 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.63+18077dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161712 | C | CTT | 18 | a0001c0001t0004g0050 a0001c0001t0004g0069 a0001c0001t0004g0071 others(15): Show |
19 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+18076_63+18077d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161712 | C | CTTT | 10 | a0001c0001t0006g0204 a0001c0001t0006g0209 a0001c0001t0006g0210 others(7): Show |
10 | HG02004.hp2 HG02109.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+18075_63+18077d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161712 | C | CTTTT | 28 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(25): Show |
31 | HG00597.hp2 HG00741.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+18074_63+18077d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161712 | CT | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.63+18077delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161712 | CTT | C | 9 | a0001c0001t0001g0039 a0001c0001t0001g0129 a0001c0001t0001g0153 others(6): Show |
10 | HG00323.hp2 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+18076_63+18077d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | ||||||
chr17:77161736 | T | A | 1 | a0001c0002t0014g0300 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.63+18077T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161736 | |||||||
chr17:77161743 | C | T | 1 | a0001c0002t0005g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+18084C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161743 | |||||||
chr17:77161784 | T | A | 40 | a0001c0001t0002g0216 a0001c0001t0003g0001 a0001c0001t0006g0001 others(37): Show |
43 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.63+18125T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161784 | |||||||
chr17:77161818 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.63+18159C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161818 | |||||||
chr17:77161852 | C | T | 1 | a0001c0001t0006g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.63+18193C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161852 | |||||||
chr17:77161915 | TTTCTTCT others(6): Show |
T | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+18266_63+18278d others(15): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161915 | ||||||
chr17:77161937 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+18278T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161937 | |||||||
chr17:77161978 | C | T | 1 | a0001c0001t0033g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.63+18319C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161978 | |||||||
chr17:77161980 | A | G | 1 | a0001c0001t0006g0217 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.63+18321A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161980 | |||||||
chr17:77162022 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+18363C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162022 | |||||||
chr17:77162036 | G | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.63+18377G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162036 | |||||||
chr17:77162131 | T | G | 185 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(182): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.63+18472T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162131 | |||||||
chr17:77162174 | C | T | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+18515C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162174 | |||||||
chr17:77162179 | C | G | 288 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(285): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.63+18520C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162179 | |||||||
chr17:77162189 | A | G | 1 | a0001c0002t0003g0375 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+18530A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162189 | |||||||
chr17:77162259 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+18600C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162259 | |||||||
chr17:77162260 | G | A | 1 | a0001c0001t0004g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+18601G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162260 | |||||||
chr17:77162437 | A | G | 147 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.63+18778A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162437 | |||||||
chr17:77162625 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.63+18966G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162625 | |||||||
chr17:77162631 | G | A | 1 | a0001c0002t0003g0384 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.63+18972G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162631 | |||||||
chr17:77162644 | C | T | 44 | a0001c0002t0003g0313 a0001c0002t0005g0034 a0001c0002t0005g0035 others(41): Show |
44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+18985C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162644 | |||||||
chr17:77162729 | T | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+19070T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162729 | |||||||
chr17:77162761 | T | C | 392 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(389): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.63+19102T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162761 | |||||||
chr17:77162765 | G | C | 1 | a0001c0002t0010g0290 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+19106G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162765 | |||||||
chr17:77162825 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(9): Show |
12 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+19166T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162825 | |||||||
chr17:77162830 | C | CAA | 157 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0027 others(154): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.63+19182_63+19183d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | ||||||
chr17:77162830 | C | CAAA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0154 a0001c0001t0001g0201 others(7): Show |
10 | HG00408.hp2 HG00423.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+19181_63+19183d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | ||||||
chr17:77162830 | CA | C | 118 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(115): Show |
122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+19183delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | ||||||
chr17:77162999 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+19340C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162999 | |||||||
chr17:77163017 | G | A | 1 | a0001c0001t0006g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.63+19358G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163017 | |||||||
chr17:77163203 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+19544C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163203 | |||||||
chr17:77163281 | G | A | 1 | a0001c0001t0058g0089 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+19622G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163281 | |||||||
chr17:77163391 | T | TTTTTCTC others(18): Show |
404 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(401): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.63+19733_63+19734i others(27): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77163391 | ||||||
chr17:77163459 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+19800C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163459 | |||||||
chr17:77163632 | T | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG02622.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+19973T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163632 | |||||||
chr17:77163859 | T | C | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+20200T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163859 | |||||||
chr17:77164028 | T | G | 2 | a0001c0002t0005g0316 a0001c0002t0057g0312 |
2 | HG00323.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.63+20369T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164028 | |||||||
chr17:77164138 | G | A | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+20479G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164138 | |||||||
chr17:77164158 | G | A | 1 | a0001c0002t0005g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+20499G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164158 | |||||||
chr17:77164175 | C | T | 1 | a0001c0002t0005g0378 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.63+20516C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164175 | |||||||
chr17:77164555 | G | A | 1 | a0001c0002t0057g0312 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+20896G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164555 | |||||||
chr17:77164778 | C | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+21119C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164778 | |||||||
chr17:77164994 | C | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+21335C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164994 | |||||||
chr17:77165070 | A | AC | 5 | a0001c0001t0001g0049 a0001c0001t0001g0121 a0001c0002t0003g0037 others(2): Show |
5 | HG01123.hp1 HG02602.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21415dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77165070 | ||||||
chr17:77165096 | A | T | 45 | a0001c0002t0003g0313 a0001c0002t0005g0034 a0001c0002t0005g0035 others(42): Show |
45 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+21437A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165096 | |||||||
chr17:77165208 | A | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+21549A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165208 | |||||||
chr17:77165403 | A | G | 4 | a0001c0001t0015g0055 a0001c0001t0015g0109 a0001c0001t0015g0110 others(1): Show |
4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+21744A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165403 | |||||||
chr17:77165476 | A | T | 1 | a0001c0002t0005g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.63+21817A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165476 | |||||||
chr17:77165621 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+21962T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165621 | |||||||
chr17:77165873 | A | G | 1 | a0001c0001t0008g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63+22214A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165873 | |||||||
chr17:77165965 | G | T | 3 | a0001c0002t0003g0313 a0001c0002t0005g0333 a0001c0002t0005g0373 |
3 | HG00741.hp2 HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.63+22306G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165965 | |||||||
chr17:77166076 | A | G | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+22417A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166076 | |||||||
chr17:77166124 | T | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+22465T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166124 | |||||||
chr17:77166140 | T | G | 79 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(76): Show |
81 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.63+22481T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166140 | |||||||
chr17:77166189 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.63+22530C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166189 | |||||||
chr17:77166254 | G | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.63+22595G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166254 | |||||||
chr17:77166304 | A | G | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+22645A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166304 | |||||||
chr17:77166469 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+22810A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166469 | |||||||
chr17:77166696 | A | T | 1 | a0001c0001t0033g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.63+23037A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166696 | |||||||
chr17:77166710 | A | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+23051A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166710 | |||||||
chr17:77166799 | A | G | 5 | a0001c0002t0005g0200 a0001c0002t0005g0319 a0001c0002t0005g0320 others(2): Show |
5 | HG01175.hp1 HG02280.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+23140A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166799 | |||||||
chr17:77166882 | A | C | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+23223A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166882 | |||||||
chr17:77167146 | C | CT | 14 | a0001c0001t0002g0033 a0001c0001t0002g0242 a0001c0001t0006g0226 others(11): Show |
15 | HG01070.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+23506dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | ||||||
chr17:77167146 | CT | C | 73 | a0001c0001t0002g0231 a0001c0001t0002g0275 a0001c0001t0004g0004 others(70): Show |
76 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+23506delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | ||||||
chr17:77167146 | CTT | C | 17 | a0001c0001t0004g0022 a0001c0001t0008g0053 a0001c0001t0008g0054 others(14): Show |
17 | HG01255.hp1 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+23505_63+23506d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | ||||||
chr17:77167146 | CTTTTT | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(74): Show |
79 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.63+23502_63+23506d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | ||||||
chr17:77167283 | C | T | 152 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(149): Show |
158 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.64-23520C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167283 | |||||||
chr17:77167885 | T | G | 3 | a0001c0002t0003g0016 a0001c0002t0003g0352 a0001c0002t0003g0363 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22918T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167885 | |||||||
chr17:77167932 | G | T | 68 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(65): Show |
72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-22871G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167932 | |||||||
chr17:77167947 | G | A | 284 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(281): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.64-22856G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167947 | |||||||
chr17:77168345 | G | T | 66 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(63): Show |
70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-22458G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168345 | |||||||
chr17:77168386 | G | T | 62 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(59): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-22417G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168386 | |||||||
chr17:77168395 | G | A | 14 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-22408G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168395 | |||||||
chr17:77168730 | G | T | 1 | a0001c0002t0003g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.64-22073G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168730 | |||||||
chr17:77168737 | C | G | 1 | a0001c0001t0006g0227 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-22066C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168737 | |||||||
chr17:77168804 | A | G | 284 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(281): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.64-21999A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168804 | |||||||
chr17:77168879 | G | T | 14 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-21924G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168879 | |||||||
chr17:77168996 | G | A | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-21807G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168996 | |||||||
chr17:77169007 | C | CTTTTT | 8 | a0001c0001t0007g0393 a0001c0001t0007g0400 a0001c0001t0007g0406 others(5): Show |
8 | NA18946.hp1 NA18970.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-21770_64-21766d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CT | C | 103 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(100): Show |
107 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-21766delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTT | C | 20 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(17): Show |
21 | HG00323.hp1 HG00423.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-21767_64-21766d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTT | C | 7 | a0001c0001t0006g0197 a0001c0001t0006g0202 a0001c0001t0006g0220 others(4): Show |
7 | HG02145.hp2 NA18994.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-21768_64-21766d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTT | C | 30 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(27): Show |
33 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.64-21769_64-21766d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTT | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0117 a0001c0001t0001g0127 others(4): Show |
7 | HG01175.hp2 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-21771_64-21766d others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTTT | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.64-21772_64-21766d others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0004g0050 a0001c0001t0004g0099 a0001c0005t0011g0008 others(2): Show |
6 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-21774_64-21766d others(11): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTTT others(3): Show |
C | 56 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(53): Show |
58 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-21775_64-21766d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTTT others(4): Show |
C | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-21776_64-21766d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169007 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0237 a0001c0001t0023g0278 |
2 | HG01192.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.64-21777_64-21766d others(14): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | ||||||
chr17:77169205 | G | C | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-21598G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169205 | |||||||
chr17:77169317 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-21486G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169317 | |||||||
chr17:77169370 | A | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-21433A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169370 | |||||||
chr17:77169452 | C | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-21351C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169452 | |||||||
chr17:77169553 | C | T | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-21250C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169553 | |||||||
chr17:77169574 | T | C | 3 | a0001c0001t0001g0161 a0001c0003t0002g0180 a0001c0003t0002g0181 |
3 | HG00140.hp1 HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.64-21229T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169574 | |||||||
chr17:77169696 | G | T | 1 | a0001c0001t0033g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64-21107G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169696 | |||||||
chr17:77169705 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-21098G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169705 | |||||||
chr17:77169760 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-21043A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169760 | |||||||
chr17:77169823 | A | C | 1 | a0001c0001t0002g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.64-20980A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169823 | |||||||
chr17:77169848 | T | G | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-20955T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169848 | |||||||
chr17:77170015 | A | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.64-20788A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170015 | |||||||
chr17:77170268 | C | T | 50 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(47): Show |
55 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.64-20535C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170268 | |||||||
chr17:77170314 | G | T | 33 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(30): Show |
36 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.64-20489G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170314 | |||||||
chr17:77170405 | TC | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-20397delC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170405 | |||||||
chr17:77170430 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-20373C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170430 | |||||||
chr17:77170647 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
5 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-20156C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170647 | |||||||
chr17:77170795 | T | C | 1 | a0001c0001t0053g0249 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64-20008T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170795 | |||||||
chr17:77170860 | A | G | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-19943A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170860 | |||||||
chr17:77170882 | A | G | 2 | a0001c0001t0002g0233 a0001c0001t0002g0239 |
2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.64-19921A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170882 | |||||||
chr17:77171079 | T | C | 2 | a0001c0001t0006g0209 a0001c0001t0006g0211 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.64-19724T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171079 | |||||||
chr17:77171117 | T | G | 1 | a0001c0002t0005g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-19686T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171117 | |||||||
chr17:77171182 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.64-19621A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171182 | |||||||
chr17:77171185 | A | T | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-19618A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171185 | |||||||
chr17:77171191 | G | A | 5 | a0001c0001t0004g0024 a0001c0001t0004g0050 a0001c0001t0004g0052 others(2): Show |
5 | NA18972.hp2 NA18985.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-19612G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171191 | |||||||
chr17:77171222 | C | T | 1 | a0001c0002t0012g0329 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.64-19581C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171222 | |||||||
chr17:77171233 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-19570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171233 | |||||||
chr17:77171360 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-19443T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171360 | |||||||
chr17:77171371 | G | A | 1 | a0001c0002t0003g0313 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-19432G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171371 | |||||||
chr17:77171525 | A | G | 62 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(59): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-19278A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171525 | |||||||
chr17:77171590 | G | A | 14 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-19213G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171590 | |||||||
chr17:77171725 | G | A | 3 | a0001c0002t0005g0293 a0001c0002t0005g0324 a0001c0002t0005g0372 |
3 | HG02165.hp1 NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.64-19078G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171725 | |||||||
chr17:77171760 | A | G | 41 | a0001c0002t0005g0034 a0001c0002t0005g0035 a0001c0002t0005g0199 others(38): Show |
41 | HG00323.hp1 HG00544.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-19043A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171760 | |||||||
chr17:77171768 | C | T | 404 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(401): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.64-19035C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171768 | |||||||
chr17:77171778 | T | C | 1 | a0001c0002t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-19025T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171778 | |||||||
chr17:77171919 | G | A | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-18884G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171919 | |||||||
chr17:77171947 | T | A | 14 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-18856T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171947 | |||||||
chr17:77172030 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.64-18773C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172030 | |||||||
chr17:77172041 | T | C | 4 | a0001c0001t0009g0116 a0001c0001t0009g0123 a0001c0001t0009g0124 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-18762T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172041 | |||||||
chr17:77172078 | C | A | 12 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(9): Show |
13 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-18725C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172078 | |||||||
chr17:77172082 | C | G | 1 | a0001c0002t0042g0305 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.64-18721C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172082 | |||||||
chr17:77172241 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.64-18562T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172241 | |||||||
chr17:77172547 | C | T | 1 | a0001c0001t0004g0066 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64-18256C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172547 | |||||||
chr17:77172548 | G | A | 5 | a0001c0002t0005g0334 a0001c0002t0005g0335 a0001c0002t0005g0336 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-18255G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172548 | |||||||
chr17:77172622 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-18181T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172622 | |||||||
chr17:77172815 | G | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(78): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.64-17988G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172815 | |||||||
chr17:77172818 | A | G | 279 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(276): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.64-17985A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172818 | |||||||
chr17:77172846 | C | G | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-17957C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172846 | |||||||
chr17:77172919 | A | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-17884A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172919 | |||||||
chr17:77173039 | A | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0073 a0001c0001t0004g0074 |
3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64-17764A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173039 | |||||||
chr17:77173283 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0186 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-17520G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173283 | |||||||
chr17:77173287 | C | T | 1 | a0001c0003t0002g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-17516C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173287 | |||||||
chr17:77173288 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-17515G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173288 | |||||||
chr17:77173368 | G | A | 1 | a0001c0001t0006g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.64-17435G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173368 | |||||||
chr17:77173430 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0163 |
2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-17373G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173430 | |||||||
chr17:77173477 | G | A | 1 | a0001c0002t0003g0308 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-17326G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173477 | |||||||
chr17:77173577 | C | T | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-17226C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173577 | |||||||
chr17:77173674 | G | C | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-17129G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173674 | |||||||
chr17:77173793 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-17010G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173793 | |||||||
chr17:77173905 | C | CT | 21 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(18): Show |
21 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-16885dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77173905 | ||||||
chr17:77173971 | G | A | 1 | a0001c0002t0012g0330 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.64-16832G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173971 | |||||||
chr17:77174005 | A | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16798A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174005 | |||||||
chr17:77174040 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16763A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174040 | |||||||
chr17:77174095 | T | G | 11 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(8): Show |
11 | NA18940.hp1 NA18946.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-16708T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174095 | |||||||
chr17:77174194 | C | T | 163 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.64-16609C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174194 | |||||||
chr17:77174199 | A | G | 94 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(91): Show |
98 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.64-16604A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174199 | |||||||
chr17:77174210 | C | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16593C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174210 | |||||||
chr17:77174225 | A | G | 1 | a0001c0003t0002g0264 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-16578A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174225 | |||||||
chr17:77174291 | CCTT | C | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-16509_64-16507d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77174291 | ||||||
chr17:77174392 | T | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16411T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174392 | |||||||
chr17:77174421 | C | T | 1 | a0001c0002t0005g0378 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-16382C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174421 | |||||||
chr17:77174591 | C | T | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-16212C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174591 | |||||||
chr17:77174625 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16178G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174625 | |||||||
chr17:77174652 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16151C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174652 | |||||||
chr17:77174677 | C | T | 1 | a0001c0002t0012g0327 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-16126C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174677 | |||||||
chr17:77174728 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-16075G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174728 | |||||||
chr17:77174894 | C | T | 1 | a0002c0004t0037g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64-15909C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174894 | |||||||
chr17:77174906 | C | T | 1 | a0001c0001t0004g0074 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64-15897C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174906 | |||||||
chr17:77174947 | T | G | 55 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(52): Show |
58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-15856T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174947 | |||||||
chr17:77174987 | A | G | 2 | a0001c0002t0005g0199 a0001c0002t0005g0200 |
2 | HG02280.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.64-15816A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174987 | |||||||
chr17:77175069 | G | A | 1 | a0001c0002t0005g0283 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64-15734G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175069 | |||||||
chr17:77175096 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64-15707A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175096 | |||||||
chr17:77175142 | G | C | 1 | a0001c0002t0005g0283 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64-15661G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175142 | |||||||
chr17:77175194 | A | G | 1 | a0001c0001t0004g0065 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-15609A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175194 | |||||||
chr17:77175253 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-15550G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175253 | |||||||
chr17:77175351 | C | T | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-15452C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175351 | |||||||
chr17:77175354 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.64-15449A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175354 | |||||||
chr17:77175548 | G | A | 406 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(403): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.64-15255G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175548 | |||||||
chr17:77175572 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0006g0226 a0001c0001t0006g0227 |
3 | HG02135.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-15231C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175572 | |||||||
chr17:77175631 | G | A | 3 | a0001c0001t0036g0388 a0002c0004t0037g0189 a0002c0004t0048g0188 |
3 | HG02145.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-15172G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175631 | |||||||
chr17:77175867 | G | A | 1 | a0001c0002t0003g0379 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-14936G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175867 | |||||||
chr17:77175870 | C | T | 1 | a0001c0002t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-14933C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175870 | |||||||
chr17:77176006 | G | A | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-14797G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176006 | |||||||
chr17:77176056 | A | G | 405 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(402): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.64-14747A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176056 | |||||||
chr17:77176152 | T | C | 65 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(62): Show |
68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.64-14651T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176152 | |||||||
chr17:77176191 | G | A | 1 | a0001c0001t0007g0402 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-14612G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176191 | |||||||
chr17:77176234 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.64-14569G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176234 | |||||||
chr17:77176321 | G | C | 32 | a0001c0001t0001g0135 a0001c0001t0003g0001 a0001c0001t0006g0001 others(29): Show |
35 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.64-14482G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176321 | |||||||
chr17:77176393 | C | T | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-14410C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176393 | |||||||
chr17:77176402 | G | C | 38 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(35): Show |
43 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-14401G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176402 | |||||||
chr17:77176404 | G | A | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-14399G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176404 | |||||||
chr17:77176411 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0163 |
2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-14392T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176411 | |||||||
chr17:77176550 | C | T | 15 | a0001c0003t0002g0012 a0001c0003t0002g0190 a0001c0003t0002g0234 others(12): Show |
15 | HG00408.hp1 HG02040.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-14253C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176550 | |||||||
chr17:77176769 | TA | T | 18 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(15): Show |
21 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-14033delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176769 | |||||||
chr17:77176829 | C | T | 1 | a0001c0003t0002g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.64-13974C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176829 | |||||||
chr17:77176866 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0056g0194 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.64-13937C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176866 | |||||||
chr17:77177100 | A | G | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-13703A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177100 | |||||||
chr17:77177138 | C | T | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-13665C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177138 | |||||||
chr17:77177142 | A | G | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13661A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177142 | |||||||
chr17:77177167 | CAT | C | 7 | a0001c0003t0002g0012 a0001c0003t0002g0235 a0001c0003t0002g0243 others(4): Show |
7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-13635_64-13634d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177167 | |||||||
chr17:77177270 | G | A | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13533G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177270 | |||||||
chr17:77177395 | A | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-13408A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177395 | |||||||
chr17:77177480 | G | T | 1 | a0001c0002t0003g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64-13323G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177480 | |||||||
chr17:77177766 | T | G | 283 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.64-13037T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177766 | |||||||
chr17:77177816 | C | G | 5 | a0001c0001t0006g0202 a0001c0001t0006g0204 a0001c0001t0006g0205 others(2): Show |
5 | NA18945.hp1 NA18969.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-12987C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177816 | |||||||
chr17:77177833 | A | G | 1 | a0001c0002t0010g0356 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.64-12970A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177833 | |||||||
chr17:77178055 | T | TC | 37 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0122 others(34): Show |
37 | HG00438.hp2 HG00735.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.64-12738dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178055 | ||||||
chr17:77178055 | TC | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0134 a0001c0001t0001g0150 others(12): Show |
16 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-12738delC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178055 | ||||||
chr17:77178065 | C | CT | 6 | a0001c0001t0002g0266 a0001c0001t0007g0398 a0001c0002t0005g0334 others(3): Show |
6 | HG02615.hp1 HG02622.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12728dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178065 | ||||||
chr17:77178065 | C | T | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-12738C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178065 | |||||||
chr17:77178093 | A | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-12710A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178093 | |||||||
chr17:77178207 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-12596G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178207 | |||||||
chr17:77178258 | C | T | 1 | a0001c0002t0003g0379 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-12545C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178258 | |||||||
chr17:77178525 | AGCAGTGG others(4): Show |
A | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64-12277_64-12267d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178525 | |||||||
chr17:77178613 | C | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-12190C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178613 | |||||||
chr17:77178661 | C | T | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-12142C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178661 | |||||||
chr17:77179084 | C | T | 1 | a0001c0001t0006g0224 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.64-11719C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179084 | |||||||
chr17:77179135 | G | GCAGA | 3 | a0001c0001t0004g0062 a0001c0001t0004g0073 a0001c0001t0004g0074 |
3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64-11667_64-11664d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77179135 | ||||||
chr17:77179481 | C | T | 1 | a0001c0001t0004g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-11322C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179481 | |||||||
chr17:77179497 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.64-11306C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179497 | |||||||
chr17:77179519 | A | C | 5 | a0001c0002t0005g0035 a0001c0002t0005g0282 a0001c0002t0005g0283 others(2): Show |
5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11284A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179519 | |||||||
chr17:77179719 | G | A | 1 | a0002c0004t0048g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-11084G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179719 | |||||||
chr17:77179735 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-11068C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179735 | |||||||
chr17:77179810 | G | A | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-10993G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179810 | |||||||
chr17:77179877 | C | G | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-10926C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179877 | |||||||
chr17:77179931 | C | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-10872C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179931 | |||||||
chr17:77179965 | C | G | 1 | a0001c0002t0005g0282 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.64-10838C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179965 | |||||||
chr17:77179966 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0163 |
2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-10837C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179966 | |||||||
chr17:77179968 | C | T | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-10835C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179968 | |||||||
chr17:77180036 | ATGTTT | A | 10 | a0001c0001t0002g0273 a0001c0001t0007g0395 a0001c0001t0007g0404 others(7): Show |
10 | HG01891.hp1 HG02273.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10757_64-10753d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180036 | ||||||
chr17:77180041 | TTGTTTTG others(3): Show |
T | 17 | a0001c0001t0002g0011 a0001c0001t0002g0237 a0001c0001t0002g0266 others(14): Show |
18 | HG00642.hp2 HG01099.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-10757_64-10748d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | ||||||
chr17:77180041 | TTGTTTTG others(8): Show |
T | 54 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0216 others(51): Show |
56 | HG00423.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.64-10757_64-10743d others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | ||||||
chr17:77180041 | TTGTTTTG others(13): Show |
T | 39 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0236 others(36): Show |
42 | HG00408.hp1 HG00597.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.64-10757_64-10738d others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | ||||||
chr17:77180041 | TTGTTTTG others(18): Show |
T | 6 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0022g0009 others(3): Show |
8 | HG00639.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-10757_64-10733d others(27): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | ||||||
chr17:77180041 | TTGTTTTG others(28): Show |
T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-10757_64-10723d others(37): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | ||||||
chr17:77180046 | T | TTGTTA | 22 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0112 others(19): Show |
22 | HG00423.hp1 HG01123.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-10706_64-10702d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180046 | TTGTTA | T | 113 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0027 others(110): Show |
118 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.64-10706_64-10702d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180046 | TTGTTATG others(3): Show |
T | 59 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0042 others(56): Show |
60 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-10711_64-10702d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180046 | TTGTTATG others(8): Show |
T | 5 | a0001c0001t0004g0050 a0001c0001t0004g0052 a0001c0001t0004g0071 others(2): Show |
5 | NA18972.hp2 NA18994.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-10716_64-10702d others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180046 | TTGTTATG others(13): Show |
T | 1 | a0001c0001t0004g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-10721_64-10702d others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180046 | TTGTTATG others(23): Show |
T | 1 | a0001c0002t0003g0347 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.64-10731_64-10702d others(32): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | ||||||
chr17:77180051 | A | T | 1 | a0001c0001t0004g0066 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64-10752A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180051 | |||||||
chr17:77180056 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0149 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-10747A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180056 | |||||||
chr17:77180096 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-10707A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180096 | |||||||
chr17:77180463 | G | A | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-10340G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180463 | |||||||
chr17:77180718 | T | C | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-10085T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180718 | |||||||
chr17:77180760 | C | T | 8 | a0001c0001t0002g0011 a0001c0001t0002g0233 a0001c0001t0002g0237 others(5): Show |
9 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-10043C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180760 | |||||||
chr17:77180840 | C | T | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-9963C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180840 | |||||||
chr17:77181002 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-9801C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181002 | |||||||
chr17:77181179 | A | G | 103 | a0001c0001t0003g0001 a0001c0001t0004g0004 a0001c0001t0004g0005 others(100): Show |
109 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.64-9624A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181179 | |||||||
chr17:77181233 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(80): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-9570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181233 | |||||||
chr17:77181297 | A | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(80): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-9506A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181297 | |||||||
chr17:77181356 | G | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-9447G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181356 | |||||||
chr17:77181453 | T | C | 405 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(402): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.64-9350T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181453 | |||||||
chr17:77181488 | C | G | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9315C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181488 | |||||||
chr17:77181815 | T | G | 1 | a0001c0005t0026g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-8988T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181815 | |||||||
chr17:77181897 | C | T | 1 | a0001c0001t0021g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.64-8906C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181897 | |||||||
chr17:77181932 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0201 a0001c0003t0002g0180 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8871A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181932 | |||||||
chr17:77182502 | G | A | 1 | a0001c0001t0008g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-8301G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182502 | |||||||
chr17:77182632 | T | C | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8171T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182632 | |||||||
chr17:77182647 | C | G | 9 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0028 others(6): Show |
11 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-8156C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182647 | |||||||
chr17:77182732 | G | A | 1 | a0001c0002t0005g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-8071G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182732 | |||||||
chr17:77183310 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64-7493G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183310 | |||||||
chr17:77183328 | T | C | 1 | a0001c0002t0003g0375 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-7475T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183328 | |||||||
chr17:77183334 | TTC | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-7465_64-7464del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77183334 | ||||||
chr17:77183412 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-7391A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183412 | |||||||
chr17:77183560 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-7243G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183560 | |||||||
chr17:77183669 | T | G | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-7134T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183669 | |||||||
chr17:77183708 | G | A | 1 | a0001c0001t0025g0013 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-7095G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183708 | |||||||
chr17:77183805 | G | T | 283 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.64-6998G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183805 | |||||||
chr17:77183833 | A | AT | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.64-6960dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77183833 | ||||||
chr17:77183853 | G | A | 1 | a0001c0001t0004g0103 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.64-6950G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183853 | |||||||
chr17:77183887 | G | A | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-6916G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183887 | |||||||
chr17:77184185 | T | C | 1 | a0001c0001t0052g0253 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.64-6618T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184185 | |||||||
chr17:77184189 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.64-6614G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184189 | |||||||
chr17:77184193 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-6610T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184193 | |||||||
chr17:77184350 | A | G | 270 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(267): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.64-6453A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184350 | |||||||
chr17:77184505 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0201 a0001c0003t0002g0180 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-6298G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184505 | |||||||
chr17:77184745 | C | A | 44 | a0001c0002t0003g0313 a0001c0002t0005g0034 a0001c0002t0005g0035 others(41): Show |
44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.64-6058C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184745 | |||||||
chr17:77184751 | C | T | 1 | a0001c0002t0005g0378 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-6052C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184751 | |||||||
chr17:77184805 | A | G | 1 | a0006c0010t0004g0196 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.64-5998A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184805 | |||||||
chr17:77184907 | C | G | 1 | a0001c0005t0011g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64-5896C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184907 | |||||||
chr17:77184935 | G | A | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-5868G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184935 | |||||||
chr17:77185016 | A | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-5787A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185016 | |||||||
chr17:77185052 | G | A | 6 | a0001c0002t0005g0338 a0001c0002t0005g0339 a0001c0002t0005g0341 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5751G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185052 | |||||||
chr17:77185271 | C | T | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-5532C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185271 | |||||||
chr17:77185416 | C | T | 1 | a0001c0001t0004g0086 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.64-5387C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185416 | |||||||
chr17:77185447 | G | A | 5 | a0001c0002t0005g0309 a0001c0002t0005g0317 a0001c0002t0005g0318 others(2): Show |
5 | HG01358.hp1 HG03834.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-5356G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185447 | |||||||
chr17:77185459 | G | C | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-5344G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185459 | |||||||
chr17:77185661 | G | A | 1 | a0001c0001t0004g0079 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64-5142G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185661 | |||||||
chr17:77185799 | G | C | 6 | a0001c0002t0005g0338 a0001c0002t0005g0339 a0001c0002t0005g0341 others(3): Show |
6 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5004G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185799 | |||||||
chr17:77186086 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-4717T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186086 | |||||||
chr17:77186140 | T | C | 405 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(402): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.64-4663T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186140 | |||||||
chr17:77186169 | A | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-4634A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186169 | |||||||
chr17:77186195 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64-4608G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186195 | |||||||
chr17:77186195 | G | T | 1 | a0001c0001t0020g0394 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64-4608G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186195 | |||||||
chr17:77186339 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.64-4464C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186339 | |||||||
chr17:77186341 | C | G | 11 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(8): Show |
12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-4462C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186341 | |||||||
chr17:77186496 | A | C | 3 | a0001c0001t0004g0072 a0001c0001t0004g0106 a0001c0001t0004g0113 |
3 | HG02818.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-4307A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186496 | |||||||
chr17:77186591 | A | G | 2 | a0001c0002t0003g0344 a0001c0002t0003g0348 |
2 | NA18948.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.64-4212A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186591 | |||||||
chr17:77186605 | C | T | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-4198C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186605 | |||||||
chr17:77186649 | A | G | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-4154A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186649 | |||||||
chr17:77186729 | T | C | 56 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(53): Show |
59 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.64-4074T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186729 | |||||||
chr17:77186737 | C | G | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-4066C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186737 | |||||||
chr17:77187040 | A | G | 27 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-3763A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187040 | |||||||
chr17:77187109 | T | C | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-3694T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187109 | |||||||
chr17:77187128 | C | T | 1 | a0001c0001t0004g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.64-3675C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187128 | |||||||
chr17:77187379 | C | A | 77 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(74): Show |
81 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-3424C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187379 | |||||||
chr17:77187437 | G | A | 1 | a0001c0001t0006g0028 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64-3366G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187437 | |||||||
chr17:77187456 | C | T | 1 | a0001c0001t0004g0022 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.64-3347C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187456 | |||||||
chr17:77187696 | A | G | 1 | a0001c0002t0016g0307 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.64-3107A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187696 | |||||||
chr17:77187737 | A | AT | 115 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(112): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-3048dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77187737 | ||||||
chr17:77187737 | AT | A | 18 | a0001c0001t0002g0248 a0001c0001t0004g0022 a0001c0001t0004g0080 others(15): Show |
19 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-3048delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77187737 | ||||||
chr17:77187830 | C | T | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-2973C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187830 | |||||||
chr17:77187870 | G | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-2933G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187870 | |||||||
chr17:77188299 | T | C | 37 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(34): Show |
41 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-2504T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188299 | |||||||
chr17:77188412 | CT | C | 374 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(371): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.64-2377delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188412 | ||||||
chr17:77188494 | T | A | 1 | a0001c0001t0002g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-2309T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188494 | |||||||
chr17:77188494 | T | G | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-2309T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188494 | |||||||
chr17:77188510 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-2293G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188510 | |||||||
chr17:77188533 | A | G | 1 | a0001c0002t0003g0308 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-2270A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188533 | |||||||
chr17:77188550 | A | AAGGACAT others(5): Show |
1 | a0001c0002t0003g0344 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64-2250_64-2239dup others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188550 | ||||||
chr17:77188561 | G | A | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-2242G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188561 | |||||||
chr17:77188591 | C | T | 123 | a0001c0001t0022g0009 a0001c0002t0003g0002 a0001c0002t0003g0016 others(120): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.64-2212C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188591 | |||||||
chr17:77188626 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-2177G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188626 | |||||||
chr17:77188789 | C | T | 392 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(389): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.64-2014C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188789 | |||||||
chr17:77188899 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-1904G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188899 | |||||||
chr17:77188994 | G | GT | 11 | a0001c0001t0001g0122 a0001c0001t0002g0033 a0001c0001t0006g0060 others(8): Show |
11 | HG00423.hp2 HG02738.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-1797dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188994 | ||||||
chr17:77189006 | T | TA | 31 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(28): Show |
34 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.64-1795dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77189006 | ||||||
chr17:77189042 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-1761A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189042 | |||||||
chr17:77189266 | G | C | 1 | a0001c0002t0003g0375 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-1537G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189266 | |||||||
chr17:77189322 | C | T | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.64-1481C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189322 | |||||||
chr17:77189345 | G | T | 1 | a0005c0008t0004g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64-1458G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189345 | |||||||
chr17:77189595 | T | G | 1 | a0001c0002t0012g0329 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.64-1208T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189595 | |||||||
chr17:77189626 | G | GGTTTT | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-1160_64-1156dup others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77189626 | ||||||
chr17:77189690 | G | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-1113G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189690 | |||||||
chr17:77189715 | G | T | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-1088G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189715 | |||||||
chr17:77189764 | A | G | 62 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(59): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-1039A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189764 | |||||||
chr17:77189778 | G | A | 1 | a0001c0002t0003g0375 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-1025G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189778 | |||||||
chr17:77189818 | C | T | 8 | a0001c0001t0001g0128 a0001c0001t0001g0158 a0001c0001t0001g0159 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-985C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189818 | |||||||
chr17:77189919 | C | T | 3 | a0001c0002t0003g0016 a0001c0002t0003g0352 a0001c0002t0003g0363 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-884C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189919 | |||||||
chr17:77189994 | C | G | 1 | a0001c0001t0006g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-809C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189994 | |||||||
chr17:77189998 | T | C | 1 | a0001c0003t0002g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-805T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189998 | |||||||
chr17:77190017 | C | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-786C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190017 | |||||||
chr17:77190072 | C | T | 392 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(389): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.64-731C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190072 | |||||||
chr17:77190271 | C | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-532C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190271 | |||||||
chr17:77190447 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-356G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190447 | |||||||
chr17:77190961 | C | T | 9 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+9C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77190961 | |||||||
chr17:77190962 | G | A | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+10G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77190962 | |||||||
chr17:77190983 | AAGGGCGT others(11): Show |
A | 1 | a0001c0001t0004g0086 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.213+62_213+79delTG others(16): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr17 | 77190983 | ||||||
chr17:77191043 | A | ATCCTGGA others(11): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0163 others(1): Show |
4 | HG01106.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-109_214-92dupA others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr17 | 77191043 | ||||||
chr17:77191155 | C | T | 1 | a0001c0001t0006g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.214-26C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77191155 | |||||||
chr17:77191321 | T | C | 7 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(4): Show |
8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+9T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191321 | |||||||
chr17:77191331 | G | A | 9 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.345+19G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191331 | |||||||
chr17:77191334 | G | A | 1 | a0001c0003t0002g0260 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.345+22G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191334 | |||||||
chr17:77191355 | T | C | 3 | a0001c0002t0003g0036 a0001c0002t0003g0308 a0001c0002t0055g0370 |
3 | HG00735.hp1 HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.345+43T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191355 | |||||||
chr17:77191641 | C | T | 2 | a0001c0003t0002g0240 a0001c0003t0002g0241 |
2 | HG02055.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.345+329C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191641 | |||||||
chr17:77191652 | C | G | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.345+340C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191652 | |||||||
chr17:77191666 | C | T | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.345+354C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191666 | |||||||
chr17:77191763 | G | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.345+451G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191763 | |||||||
chr17:77191774 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(78): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.345+462C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191774 | |||||||
chr17:77191778 | C | T | 1 | a0001c0003t0002g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345+466C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191778 | |||||||
chr17:77191957 | C | T | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.345+645C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191957 | |||||||
chr17:77192158 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.345+846A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192158 | |||||||
chr17:77192247 | A | G | 2 | a0001c0001t0004g0086 a0001c0001t0004g0102 |
2 | NA18956.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.345+935A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192247 | |||||||
chr17:77192269 | A | T | 1 | a0001c0001t0030g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345+957A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192269 | |||||||
chr17:77192291 | G | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.345+979G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192291 | |||||||
chr17:77192538 | G | C | 78 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(75): Show |
80 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.346-883G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192538 | |||||||
chr17:77192600 | A | G | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.346-821A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192600 | |||||||
chr17:77192618 | C | T | 62 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(59): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.346-803C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192618 | |||||||
chr17:77192663 | C | CT | 10 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0158 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.346-746dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr17 | 77192663 | ||||||
chr17:77192777 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.346-644C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192777 | |||||||
chr17:77192970 | T | C | 12 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(9): Show |
12 | NA18940.hp1 NA18946.hp1 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.346-451T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192970 | |||||||
chr17:77193158 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.346-263G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77193158 | |||||||
chr17:77193418 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.346-3C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77193418 | |||||||
chr17:77193995 | A | G | 2 | a0001c0002t0005g0284 a0001c0002t0005g0285 |
2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.474+446A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77193995 | |||||||
chr17:77193999 | G | A | 1 | a0001c0002t0005g0369 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474+450G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77193999 | |||||||
chr17:77194030 | C | T | 34 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(31): Show |
37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.474+481C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194030 | |||||||
chr17:77194176 | G | T | 1 | a0002c0004t0003g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.475-501G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194176 | |||||||
chr17:77194280 | C | T | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-397C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194280 | |||||||
chr17:77194352 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | NA18940.hp2 NA18973.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.475-325C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194352 | |||||||
chr17:77194540 | A | G | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.475-137A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194540 | |||||||
chr17:77194551 | C | CA | 22 | a0001c0001t0004g0071 a0001c0001t0006g0206 a0001c0001t0007g0391 others(19): Show |
22 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(19): Show |
intron_variant | MODIFIER | c.475-113dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr17 | 77194551 | ||||||
chr17:77194937 | G | A | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.709+26G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194937 | |||||||
chr17:77194961 | G | A | 3 | a0001c0003t0002g0030 a0001c0003t0002g0032 a0001c0003t0002g0252 |
3 | HG02738.hp2 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.709+50G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194961 | |||||||
chr17:77194967 | G | T | 1 | a0001c0002t0003g0384 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.709+56G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194967 | |||||||
chr17:77195160 | G | GTGTT | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.709+263_709+266dup others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195160 | ||||||
chr17:77195243 | G | A | 1 | a0001c0001t0006g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.709+332G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195243 | |||||||
chr17:77195304 | G | T | 217 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(214): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.709+393G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195304 | |||||||
chr17:77195306 | G | GT | 67 | a0001c0001t0001g0228 a0001c0001t0004g0004 a0001c0001t0004g0005 others(64): Show |
69 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.709+404dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195306 | ||||||
chr17:77195315 | TG | T | 3 | a0001c0001t0006g0219 a0001c0001t0006g0226 a0001c0001t0006g0227 |
3 | HG02145.hp2 HG02630.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.709+405delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195315 | |||||||
chr17:77195316 | G | T | 383 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0027 others(380): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.709+405G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195316 | |||||||
chr17:77195318 | T | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.709+407T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195318 | |||||||
chr17:77195320 | G | T | 1 | a0001c0001t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.709+409G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195320 | |||||||
chr17:77195475 | C | T | 7 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(4): Show |
8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.709+564C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195475 | |||||||
chr17:77195510 | A | G | 54 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(51): Show |
57 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.709+599A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195510 | |||||||
chr17:77195514 | A | G | 4 | a0001c0001t0006g0203 a0001c0001t0006g0218 a0001c0001t0006g0229 others(1): Show |
4 | HG03017.hp1 HG04184.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+603A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195514 | |||||||
chr17:77195629 | A | G | 4 | a0001c0001t0015g0055 a0001c0001t0015g0109 a0001c0001t0015g0110 others(1): Show |
4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-573A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195629 | |||||||
chr17:77195663 | T | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.710-539T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195663 | |||||||
chr17:77195736 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.710-466C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195736 | |||||||
chr17:77195837 | C | CT | 21 | a0001c0001t0006g0206 a0001c0001t0007g0391 a0001c0001t0007g0393 others(18): Show |
21 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(18): Show |
intron_variant | MODIFIER | c.710-355dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195837 | ||||||
chr17:77195853 | A | G | 1 | a0001c0002t0003g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.710-349A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195853 | |||||||
chr17:77195929 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.710-273A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195929 | |||||||
chr17:77196071 | A | G | 26 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(23): Show |
26 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-131A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196071 | |||||||
chr17:77196082 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(78): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.710-120C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196082 | |||||||
chr17:77196155 | A | G | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-47A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196155 | |||||||
chr17:77196692 | AG | A | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+383delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77196692 | ||||||
chr17:77196816 | T | C | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.819+505T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196816 | |||||||
chr17:77196825 | G | A | 78 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(75): Show |
82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.819+514G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196825 | |||||||
chr17:77196940 | G | C | 1 | a0001c0002t0005g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.819+629G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196940 | |||||||
chr17:77197080 | A | G | 1 | a0001c0009t0017g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.819+769A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197080 | |||||||
chr17:77197162 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.819+851G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197162 | |||||||
chr17:77197193 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0149 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+882G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197193 | |||||||
chr17:77197218 | C | G | 121 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(118): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.819+907C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197218 | |||||||
chr17:77197313 | A | G | 1 | a0001c0001t0004g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.819+1002A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197313 | |||||||
chr17:77197317 | C | T | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+1006C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197317 | |||||||
chr17:77197572 | C | G | 2 | a0002c0004t0037g0189 a0002c0004t0048g0188 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+1261C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197572 | |||||||
chr17:77197637 | G | A | 123 | a0001c0001t0003g0001 a0001c0001t0004g0004 a0001c0001t0004g0005 others(120): Show |
129 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.819+1326G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197637 | |||||||
chr17:77197656 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.819+1345G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197656 | |||||||
chr17:77197714 | A | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.819+1403A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197714 | |||||||
chr17:77197808 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.819+1497G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197808 | |||||||
chr17:77197881 | C | T | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.819+1570C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197881 | |||||||
chr17:77197886 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.819+1575G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197886 | |||||||
chr17:77197907 | C | T | 2 | a0001c0002t0010g0355 a0001c0002t0010g0356 |
2 | NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.819+1596C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197907 | |||||||
chr17:77197956 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.819+1645G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197956 | |||||||
chr17:77198164 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.819+1853G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198164 | |||||||
chr17:77198170 | G | A | 1 | a0001c0002t0005g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819+1859G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198170 | |||||||
chr17:77198197 | C | A | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+1886C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198197 | |||||||
chr17:77198305 | T | C | 268 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(265): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.819+1994T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198305 | |||||||
chr17:77198327 | A | G | 1 | a0001c0001t0004g0104 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.819+2016A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198327 | |||||||
chr17:77198368 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.819+2057C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198368 | |||||||
chr17:77198372 | CT | C | 4 | a0001c0002t0005g0317 a0001c0002t0005g0318 a0001c0002t0005g0326 others(1): Show |
4 | HG03834.hp1 HG03942.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+2064delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77198372 | ||||||
chr17:77198421 | G | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.820-2063G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198421 | |||||||
chr17:77198576 | C | CT | 6 | a0001c0001t0001g0044 a0001c0001t0004g0004 a0001c0001t0006g0212 others(3): Show |
7 | HG00597.hp2 HG00733.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1892dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77198576 | ||||||
chr17:77198598 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.820-1886G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198598 | |||||||
chr17:77198614 | G | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.820-1870G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198614 | |||||||
chr17:77198648 | C | T | 1 | a0001c0001t0004g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.820-1836C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198648 | |||||||
chr17:77198731 | G | T | 1 | a0001c0001t0030g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.820-1753G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198731 | |||||||
chr17:77198785 | G | C | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-1699G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198785 | |||||||
chr17:77198819 | G | A | 34 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(31): Show |
37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.820-1665G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198819 | |||||||
chr17:77198824 | G | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.820-1660G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198824 | |||||||
chr17:77198862 | G | A | 1 | a0009c0012t0005g0331 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.820-1622G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198862 | |||||||
chr17:77198863 | C | T | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-1621C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198863 | |||||||
chr17:77198864 | G | T | 123 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(120): Show |
127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.820-1620G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198864 | |||||||
chr17:77198867 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.820-1617C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198867 | |||||||
chr17:77198879 | C | G | 1 | a0001c0002t0051g0311 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.820-1605C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198879 | |||||||
chr17:77199005 | C | CG | 33 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(30): Show |
36 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.820-1479_820-1478i others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199005 | |||||||
chr17:77199005 | C | CT | 138 | a0001c0001t0001g0046 a0001c0001t0002g0011 a0001c0001t0002g0014 others(135): Show |
143 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.820-1462dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199005 | ||||||
chr17:77199005 | CT | C | 6 | a0001c0001t0015g0110 a0001c0002t0005g0200 a0001c0002t0005g0319 others(3): Show |
6 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-1462delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199005 | ||||||
chr17:77199006 | T | G | 1 | a0001c0001t0006g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.820-1478T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199006 | |||||||
chr17:77199022 | T | G | 1 | a0001c0001t0006g0215 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.820-1462T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199022 | |||||||
chr17:77199147 | G | GGC | 12 | a0001c0002t0003g0037 a0001c0002t0003g0038 a0001c0002t0003g0343 others(9): Show |
12 | HG00558.hp1 HG00639.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.820-1335_820-1334d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199147 | ||||||
chr17:77199161 | C | T | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1323C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199161 | |||||||
chr17:77199185 | G | A | 1 | a0001c0001t0004g0066 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.820-1299G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199185 | |||||||
chr17:77199273 | G | A | 1 | a0001c0002t0005g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.820-1211G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199273 | |||||||
chr17:77199356 | C | G | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1128C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199356 | |||||||
chr17:77199393 | G | A | 282 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(279): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.820-1091G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199393 | |||||||
chr17:77199432 | C | T | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.820-1052C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199432 | |||||||
chr17:77199441 | G | A | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-1043G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199441 | |||||||
chr17:77199445 | G | C | 1 | a0001c0003t0002g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.820-1039G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199445 | |||||||
chr17:77199457 | A | G | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-1027A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199457 | |||||||
chr17:77199552 | C | T | 1 | a0001c0002t0003g0017 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.820-932C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199552 | |||||||
chr17:77199573 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.820-911G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199573 | |||||||
chr17:77199675 | A | G | 1 | a0001c0003t0002g0264 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.820-809A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199675 | |||||||
chr17:77199683 | G | A | 1 | a0001c0001t0004g0088 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.820-801G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199683 | |||||||
chr17:77199695 | G | A | 5 | a0001c0003t0002g0030 a0001c0003t0002g0032 a0001c0003t0002g0252 others(2): Show |
5 | HG02735.hp1 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-789G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199695 | |||||||
chr17:77199781 | G | A | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.820-703G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199781 | |||||||
chr17:77199963 | G | A | 1 | a0001c0002t0038g0361 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.820-521G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199963 | |||||||
chr17:77199971 | C | G | 1 | a0001c0002t0003g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.820-513C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199971 | |||||||
chr17:77200034 | C | T | 124 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(121): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.820-450C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200034 | |||||||
chr17:77200059 | A | T | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-425A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200059 | |||||||
chr17:77200173 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.820-311G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200173 | |||||||
chr17:77200177 | A | G | 1 | a0001c0001t0007g0401 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.820-307A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200177 | |||||||
chr17:77200356 | A | T | 1 | a0001c0002t0005g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820-128A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200356 | |||||||
chr17:77200678 | C | T | 1 | a0001c0001t0006g0218 | 1 | HG03017.hp1 | splice_region_variant&intron_variant | LOW | c.1009+5C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200678 | |||||||
chr17:77200679 | G | A | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
splice_region_variant&intron_variant | LOW | c.1009+6G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200679 | |||||||
chr17:77200753 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1009+80G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200753 | |||||||
chr17:77200920 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1009+247C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200920 | |||||||
chr17:77200969 | C | T | 1 | a0001c0002t0004g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1009+296C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200969 | |||||||
chr17:77200983 | G | A | 1 | a0001c0002t0005g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1009+310G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200983 | |||||||
chr17:77201315 | A | T | 1 | a0001c0002t0005g0318 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1009+642A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201315 | |||||||
chr17:77201376 | C | T | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1009+703C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201376 | |||||||
chr17:77201452 | C | CT | 121 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(118): Show |
127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1009+795dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77201452 | ||||||
chr17:77201550 | A | G | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1009+877A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201550 | |||||||
chr17:77201773 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | NA18940.hp2 NA18973.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1009+1100T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201773 | |||||||
chr17:77201942 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1009+1269C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201942 | |||||||
chr17:77202072 | G | A | 1 | a0001c0001t0030g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1009+1399G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202072 | |||||||
chr17:77202078 | A | G | 1 | a0001c0003t0002g0267 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1009+1405A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202078 | |||||||
chr17:77202141 | T | C | 3 | a0001c0001t0002g0233 a0001c0001t0002g0239 a0001c0001t0002g0247 |
3 | HG01257.hp2 HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1010-1429T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202141 | |||||||
chr17:77202154 | C | T | 1 | a0001c0001t0008g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1010-1416C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202154 | |||||||
chr17:77202164 | G | A | 1 | a0001c0001t0006g0010 | 2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1010-1406G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202164 | |||||||
chr17:77202324 | TAAAA | T | 6 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0273 others(3): Show |
7 | NA18952.hp2 NA18957.hp1 NA19005.hp2 others(4): Show |
intron_variant | MODIFIER | c.1010-1240_1010-123 others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202324 | ||||||
chr17:77202347 | G | A | 3 | a0001c0002t0005g0317 a0001c0002t0005g0318 a0008c0013t0005g0291 |
3 | HG03834.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1010-1223G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202347 | |||||||
chr17:77202447 | C | T | 6 | a0001c0001t0006g0210 a0001c0002t0005g0334 a0001c0002t0005g0335 others(3): Show |
6 | HG02004.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-1123C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202447 | |||||||
chr17:77202658 | G | A | 1 | a0001c0001t0004g0085 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1010-912G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202658 | |||||||
chr17:77202662 | A | G | 1 | a0006c0010t0004g0196 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1010-908A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202662 | |||||||
chr17:77202748 | T | A | 1 | a0001c0003t0002g0190 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1010-822T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202748 | |||||||
chr17:77202781 | A | G | 267 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(264): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1010-789A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202781 | |||||||
chr17:77202849 | G | T | 3 | a0001c0001t0015g0055 a0001c0001t0015g0109 a0001c0001t0015g0110 |
3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1010-721G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202849 | |||||||
chr17:77202858 | G | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1010-712G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202858 | |||||||
chr17:77202863 | G | A | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1010-707G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202863 | |||||||
chr17:77202873 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1010-697C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202873 | |||||||
chr17:77202874 | G | A | 1 | a0001c0002t0005g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1010-696G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202874 | |||||||
chr17:77202928 | T | A | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1010-642T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202928 | |||||||
chr17:77202928 | T | TA | 4 | a0001c0001t0004g0084 a0001c0001t0004g0095 a0001c0001t0004g0100 others(1): Show |
4 | HG03831.hp1 NA18967.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-635dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202928 | ||||||
chr17:77202935 | AT | A | 3 | a0001c0001t0004g0091 a0001c0001t0005g0083 a0006c0010t0004g0196 |
3 | HG02040.hp2 HG02273.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1010-634delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202935 | |||||||
chr17:77202936 | T | A | 58 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(55): Show |
60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1010-634T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202936 | |||||||
chr17:77202936 | T | TA | 14 | a0001c0001t0007g0409 a0001c0001t0008g0003 a0001c0001t0008g0053 others(11): Show |
16 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1010-618dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202936 | ||||||
chr17:77202936 | TA | T | 167 | a0001c0001t0001g0117 a0001c0001t0001g0169 a0001c0001t0001g0228 others(164): Show |
175 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1010-618delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202936 | ||||||
chr17:77202939 | A | T | 3 | a0001c0001t0007g0406 a0001c0001t0007g0407 a0001c0001t0007g0408 |
3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1010-631A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202939 | |||||||
chr17:77202941 | A | T | 1 | a0001c0003t0002g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1010-629A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202941 | |||||||
chr17:77202942 | A | T | 8 | a0001c0001t0002g0011 a0001c0001t0002g0233 a0001c0001t0002g0237 others(5): Show |
9 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1010-628A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202942 | |||||||
chr17:77203267 | T | C | 1 | a0001c0002t0003g0017 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1010-303T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203267 | |||||||
chr17:77203267 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1010-303T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203267 | |||||||
chr17:77203310 | C | T | 34 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(31): Show |
35 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1010-260C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203310 | |||||||
chr17:77203319 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1010-251C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203319 | |||||||
chr17:77203456 | T | A | 1 | a0001c0001t0008g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1010-114T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203456 | |||||||
chr17:77203473 | C | G | 1 | a0001c0002t0003g0384 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1010-97C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203473 | |||||||
chr17:77203494 | G | A | 2 | a0001c0002t0014g0299 a0001c0002t0014g0302 |
2 | NA18963.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1010-76G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203494 | |||||||
chr17:77203498 | A | G | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1010-72A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203498 | |||||||
chr17:77203667 | G | A | 1 | a0001c0001t0007g0409 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1098+9G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203667 | |||||||
chr17:77203787 | T | C | 1 | a0001c0002t0005g0322 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1098+129T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203787 | |||||||
chr17:77203791 | A | C | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1098+133A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203791 | |||||||
chr17:77203796 | C | T | 14 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(11): Show |
14 | HG02145.hp1 HG03540.hp2 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+138C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203796 | |||||||
chr17:77203821 | CAG | C | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+165_1098+166d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77203821 | ||||||
chr17:77203872 | G | T | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+214G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203872 | |||||||
chr17:77203950 | C | T | 44 | a0001c0002t0003g0313 a0001c0002t0005g0034 a0001c0002t0005g0035 others(41): Show |
44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1098+292C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203950 | |||||||
chr17:77203997 | C | T | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1098+339C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203997 | |||||||
chr17:77204074 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1098+416A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204074 | |||||||
chr17:77204199 | T | TA | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1098+542dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204199 | ||||||
chr17:77204300 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+642C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204300 | |||||||
chr17:77204344 | A | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1098+686A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204344 | |||||||
chr17:77204466 | C | T | 9 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+808C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204466 | |||||||
chr17:77204479 | C | T | 65 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(62): Show |
69 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1099-797C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204479 | |||||||
chr17:77204521 | G | GC | 33 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0027 others(30): Show |
35 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1099-754dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204521 | ||||||
chr17:77204522 | C | CA | 24 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(21): Show |
27 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-754_1099-753i others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204522 | |||||||
chr17:77204522 | C | CAT | 6 | a0001c0001t0006g0197 a0001c0001t0006g0203 a0001c0001t0006g0206 others(3): Show |
6 | HG03669.hp1 HG04184.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-754_1099-753i others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204522 | |||||||
chr17:77204522 | C | CT | 126 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(123): Show |
131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1099-727dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | ||||||
chr17:77204522 | C | CTT | 15 | a0001c0001t0004g0064 a0001c0001t0004g0069 a0001c0001t0004g0072 others(12): Show |
16 | HG01256.hp2 HG01258.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-728_1099-727d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | ||||||
chr17:77204522 | CT | C | 65 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0112 others(62): Show |
65 | HG00323.hp1 HG00597.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1099-727delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | ||||||
chr17:77204522 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1099-737_1099-727d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | ||||||
chr17:77204523 | T | A | 2 | a0001c0001t0006g0214 a0001c0001t0006g0225 |
2 | HG01496.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1099-753T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204523 | |||||||
chr17:77204523 | T | C | 32 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0042 others(29): Show |
32 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1099-753T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204523 | |||||||
chr17:77204524 | T | A | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1099-752T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204524 | |||||||
chr17:77204524 | T | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0112 others(11): Show |
14 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-752T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204524 | |||||||
chr17:77204526 | T | A | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1099-750T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204526 | |||||||
chr17:77204527 | T | A | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-749T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204527 | |||||||
chr17:77204529 | T | A | 2 | a0001c0009t0017g0193 a0004c0006t0017g0191 |
2 | HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1099-747T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204529 | |||||||
chr17:77204530 | T | A | 1 | a0004c0006t0017g0192 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099-746T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204530 | |||||||
chr17:77204534 | T | A | 1 | a0001c0001t0006g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1099-742T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204534 | |||||||
chr17:77204662 | C | G | 1 | a0001c0001t0052g0253 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1099-614C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204662 | |||||||
chr17:77204764 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0163 others(1): Show |
4 | HG01106.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-512A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204764 | |||||||
chr17:77204766 | G | A | 13 | a0001c0001t0008g0003 a0001c0001t0008g0053 a0001c0001t0008g0054 others(10): Show |
14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-510G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204766 | |||||||
chr17:77204862 | C | A | 9 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(6): Show |
10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-414C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204862 | |||||||
chr17:77204888 | C | T | 2 | a0001c0001t0006g0209 a0001c0001t0006g0211 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1099-388C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204888 | |||||||
chr17:77204935 | C | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1099-341C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204935 | |||||||
chr17:77205048 | G | A | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1099-228G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205048 | |||||||
chr17:77205070 | G | C | 1 | a0001c0001t0002g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1099-206G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205070 | |||||||
chr17:77205246 | T | C | 3 | a0001c0003t0002g0267 a0001c0003t0024g0255 a0001c0003t0024g0258 |
3 | HG00423.hp2 HG02071.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1099-30T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205246 | |||||||
chr17:77205270 | A | G | 1 | a0001c0001t0004g0066 | 1 | NA18970.hp2 | splice_region_variant&intron_variant | LOW | c.1099-6A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205270 | |||||||
chr17:77205447 | G | C | 34 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(31): Show |
37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1169+101G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205447 | |||||||
chr17:77205560 | C | T | 3 | a0001c0001t0007g0406 a0001c0001t0007g0407 a0001c0001t0007g0408 |
3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1169+214C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205560 | |||||||
chr17:77205668 | A | G | 2 | a0001c0001t0015g0109 a0001c0001t0015g0110 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1169+322A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205668 | |||||||
chr17:77205861 | T | C | 393 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(390): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1170-368T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205861 | |||||||
chr17:77205931 | G | A | 1 | a0001c0003t0002g0190 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1170-298G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205931 | |||||||
chr17:77205963 | A | G | 9 | a0001c0003t0002g0012 a0001c0003t0002g0190 a0001c0003t0002g0234 others(6): Show |
9 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170-266A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205963 | |||||||
chr17:77206146 | A | C | 1 | a0009c0012t0005g0331 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1170-83A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77206146 | |||||||
chr17:77206428 | T | C | 2 | a0001c0003t0002g0259 a0001c0003t0002g0272 |
2 | NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1341+28T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206428 | |||||||
chr17:77206502 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1341+102A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206502 | |||||||
chr17:77206586 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1342-142A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206586 | |||||||
chr17:77206636 | C | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342-92C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206636 | |||||||
chr17:77206895 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1476+33C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206895 | |||||||
chr17:77206925 | G | A | 2 | a0004c0006t0017g0191 a0004c0006t0017g0192 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1476+63G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206925 | |||||||
chr17:77206982 | G | T | 1 | a0001c0002t0003g0344 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1476+120G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206982 | |||||||
chr17:77207010 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1476+148C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207010 | |||||||
chr17:77207088 | C | G | 124 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(121): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1476+226C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207088 | |||||||
chr17:77207089 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1476+227G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207089 | |||||||
chr17:77207256 | CAG | C | 124 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(121): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1476+395_1476+396d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207256 | |||||||
chr17:77207319 | T | TTGG | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1476+461_1476+463d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr17 | 77207319 | ||||||
chr17:77207377 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1476+515T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207377 | |||||||
chr17:77207429 | C | T | 10 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0158 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1476+567C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207429 | |||||||
chr17:77207461 | T | C | 7 | a0001c0002t0005g0338 a0001c0002t0005g0339 a0001c0002t0005g0340 others(4): Show |
7 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+599T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207461 | |||||||
chr17:77207601 | G | A | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1476+739G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207601 | |||||||
chr17:77207628 | T | A | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1476+766T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207628 | |||||||
chr17:77207783 | G | A | 2 | a0001c0001t0020g0392 a0001c0001t0020g0394 |
2 | HG02273.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1476+921G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207783 | |||||||
chr17:77208069 | C | T | 1 | a0001c0001t0004g0066 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1476+1207C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208069 | |||||||
chr17:77208261 | C | T | 1 | a0001c0003t0002g0262 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1477-1081C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208261 | |||||||
chr17:77208466 | C | T | 124 | a0001c0002t0003g0002 a0001c0002t0003g0016 a0001c0002t0003g0017 others(121): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1477-876C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208466 | |||||||
chr17:77208658 | A | G | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1477-684A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208658 | |||||||
chr17:77208805 | T | C | 64 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(61): Show |
67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1477-537T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208805 | |||||||
chr17:77208992 | CTT | C | 13 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.1477-347_1477-346d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr17 | 77208992 | ||||||
chr17:77209063 | A | G | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1477-279A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209063 | |||||||
chr17:77209086 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1477-256G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209086 | |||||||
chr17:77209202 | T | G | 1 | a0001c0002t0005g0316 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1477-140T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209202 | |||||||
chr17:77209480 | C | T | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.1611+4C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209480 | |||||||
chr17:77209536 | C | T | 6 | a0001c0002t0005g0200 a0001c0002t0005g0314 a0001c0002t0005g0319 others(3): Show |
6 | HG01081.hp2 HG01175.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611+60C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209536 | |||||||
chr17:77209577 | C | T | 3 | a0001c0005t0011g0019 a0001c0005t0026g0018 a0007c0011t0011g0020 |
3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1611+101C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209577 | |||||||
chr17:77209641 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1611+165A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209641 | |||||||
chr17:77209848 | C | CT | 65 | a0001c0001t0001g0112 a0001c0001t0002g0011 a0001c0001t0002g0014 others(62): Show |
68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1611+383dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr17 | 77209848 | ||||||
chr17:77209848 | CT | C | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1611+383delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr17 | 77209848 | ||||||
chr17:77209979 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0228 a0001c0001t0034g0118 |
3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1611+503A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209979 | |||||||
chr17:77210000 | G | A | 5 | a0001c0001t0006g0197 a0001c0001t0006g0221 a0001c0001t0006g0223 others(2): Show |
5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+524G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210000 | |||||||
chr17:77210069 | C | G | 35 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(32): Show |
38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1611+593C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210069 | |||||||
chr17:77210097 | C | T | 79 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(76): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1611+621C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210097 | |||||||
chr17:77210142 | C | T | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1611+666C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210142 | |||||||
chr17:77210519 | G | C | 1 | a0001c0001t0022g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1611+1043G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210519 | |||||||
chr17:77210569 | C | T | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1611+1093C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210569 | |||||||
chr17:77211148 | A | G | 281 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(278): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1612-802A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211148 | |||||||
chr17:77211162 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0006g0226 a0001c0001t0006g0227 |
3 | HG02135.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1612-788C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211162 | |||||||
chr17:77211229 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1612-721G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211229 | |||||||
chr17:77211238 | G | A | 1 | a0001c0001t0006g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1612-712G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211238 | |||||||
chr17:77211261 | T | G | 10 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0158 others(7): Show |
10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1612-689T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211261 | |||||||
chr17:77211264 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1612-686C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211264 | |||||||
chr17:77211271 | A | G | 1 | a0001c0002t0003g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1612-679A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211271 | |||||||
chr17:77211341 | C | T | 3 | a0001c0005t0011g0008 a0001c0005t0011g0178 a0001c0005t0011g0179 |
4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612-609C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211341 | |||||||
chr17:77211449 | G | A | 1 | a0001c0001t0004g0085 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1612-501G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211449 | |||||||
chr17:77211463 | G | A | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-487G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211463 | |||||||
chr17:77211500 | C | T | 2 | a0001c0001t0006g0226 a0001c0001t0006g0227 |
2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1612-450C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211500 | |||||||
chr17:77211504 | T | G | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-446T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211504 | |||||||
chr17:77211541 | C | T | 5 | a0001c0003t0002g0012 a0001c0003t0002g0235 a0001c0003t0018g0012 others(2): Show |
5 | HG00408.hp1 HG02155.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1612-409C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211541 | |||||||
chr17:77211771 | A | C | 63 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(60): Show |
66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-179A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211771 | |||||||
chr17:77211866 | G | A | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1612-84G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211866 | |||||||
chr17:77211882 | C | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1612-68C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211882 | |||||||
chr17:77211884 | A | G | 279 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(276): Show |
292 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.1612-66A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211884 | |||||||
chr17:77211891 | C | T | 1 | a0001c0002t0003g0306 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1612-59C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211891 | |||||||
chr17:77212331 | G | A | 20 | a0001c0001t0007g0391 a0001c0001t0007g0393 a0001c0001t0007g0395 others(17): Show |
20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1863+130G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212331 | |||||||
chr17:77212392 | A | G | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1863+191A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212392 | |||||||
chr17:77212440 | A | G | 1 | a0001c0001t0007g0395 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1863+239A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212440 | |||||||
chr17:77212482 | T | A | 10 | a0001c0001t0004g0004 a0001c0001t0004g0077 a0001c0001t0004g0082 others(7): Show |
11 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1863+281T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212482 | |||||||
chr17:77212498 | C | T | 79 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(76): Show |
81 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1863+297C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212498 | |||||||
chr17:77212501 | C | A | 1 | a0001c0001t0004g0281 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1863+300C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212501 | |||||||
chr17:77212519 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(77): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1863+318G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212519 | |||||||
chr17:77212556 | G | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(89): Show |
95 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1863+355G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212556 | |||||||
chr17:77212684 | C | T | 60 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0033 others(57): Show |
63 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1863+483C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212684 | |||||||
chr17:77212716 | T | C | 1 | a0001c0003t0002g0265 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1863+515T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212716 | |||||||
chr17:77212912 | G | A | 7 | a0001c0002t0005g0338 a0001c0002t0005g0339 a0001c0002t0005g0340 others(4): Show |
7 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1864-402G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212912 | |||||||
chr17:77212925 | C | T | 3 | a0001c0002t0005g0293 a0001c0002t0005g0324 a0001c0002t0005g0372 |
3 | HG02165.hp1 NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1864-389C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212925 | |||||||
chr17:77212967 | C | T | 1 | a0001c0002t0003g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1864-347C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212967 | |||||||
chr17:77213307 | G | C | 1 | a0001c0003t0002g0262 | 1 | NA18960.hp1 | splice_region_variant&intron_variant | LOW | c.1864-7G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77213307 | |||||||
chr17:77213496 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.2042+4C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213496 | |||||||
chr17:77213575 | A | T | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2042+83A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213575 | |||||||
chr17:77213621 | G | GA | 36 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(33): Show |
39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.2042+130dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr17 | 77213621 | ||||||
chr17:77213727 | C | T | 1 | a0001c0001t0036g0388 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2043-191C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213727 | |||||||
chr17:77213734 | G | C | 59 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0022 others(56): Show |
61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2043-184G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213734 | |||||||
chr17:77213855 | T | C | 6 | a0001c0005t0011g0008 a0001c0005t0011g0019 a0001c0005t0011g0178 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043-63T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213855 | |||||||
chr17:77213860 | G | A | 4 | a0001c0002t0005g0338 a0001c0002t0005g0339 a0001c0002t0005g0340 others(1): Show |
4 | HG02970.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043-58G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213860 | |||||||
chr17:77213863 | G | A | 3 | a0001c0009t0017g0193 a0004c0006t0017g0191 a0004c0006t0017g0192 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2043-55G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213863 |