Item | Value |
---|---|
geneid | 4739 |
ensemblid | ENSG00000111859.17 |
hgncid | 7733 |
symbol | NEDD9 |
name | neural precursor cell expressed, developmentally down-regulated 9 |
refseq_nuc | NM_006403.4 |
refseq_prot | NP_006394.1 |
ensembl_nuc | ENST00000379446.10 |
ensembl_prot | ENSP00000368759.5 |
mane_status | MANE Select |
chr | chr6 |
start | 11183298 |
end | 11232668 |
strand | - |
ver | v1.2 |
region | chr6:11183298-11232668 |
region5000 | chr6:11178298-11237668 |
regionname0 | NEDD9_chr6_11183298_11232668 |
regionname5000 | NEDD9_chr6_11178298_11237668 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 834 | 379 | 89 | 72 | 157 | 18 | 41 | 121 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0002 | 0/0 | 834 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0003 | 0/0 | 834 | 6 | 3 | 2 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0004 | 0/0 | 834 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0005 | 0/0 | 834 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0006 | 0/0 | 834 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0007 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
a0008 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | MKYKN others(829): Show |
chr6 | 11178298 | 11237668 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2502 | 125 | 13 | 25 | 64 | 5 | 18 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0002 | 0/0 | 2502 | 57 | 9 | 13 | 27 | 2 | 6 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0003 | 0/0 | 2502 | 55 | 18 | 5 | 31 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0004 | 0/0 | 2502 | 47 | 10 | 11 | 17 | 2 | 7 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0005 | 0/0 | 2502 | 40 | 22 | 6 | 7 | 2 | 3 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0006 | 1/0 | 2502 | 16 | 0 | 6 | 0 | 6 | 3 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0007 | 0/1 | 2502 | 12 | 2 | 3 | 3 | 1 | 2 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0008 | 0/0 | 2502 | 6 | 5 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0011 | 0/0 | 2502 | 4 | 4 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0012 | 0/0 | 2502 | 2 | 1 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0013 | 0/0 | 2502 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0015 | 0/0 | 2502 | 2 | 1 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0016 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0017 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0019 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0020 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0021 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0022 | 0/0 | 2502 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0023 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0024 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0029 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0030 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0001c0033 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0002c0009 | 0/0 | 2502 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0002c0025 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0002c0031 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0003c0010 | 0/0 | 2502 | 5 | 2 | 2 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0003c0027 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0004c0014 | 0/0 | 2502 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0005c0018 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0006c0028 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0007c0026 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 | ||
a0008c0032 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | ATGAA others(2497): Show |
chr6 | 11178298 | 11237668 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4522 | 111 | 3 | 25 | 64 | 5 | 14 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0003 | 0/0 | 4522 | 8 | 5 | 0 | 0 | 0 | 3 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0012 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0024 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0026 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0029 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0030 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0001t0031 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0002 | 0/0 | 4523 | 49 | 7 | 10 | 25 | 2 | 5 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0005 | 0/0 | 4522 | 3 | 0 | 3 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0006 | 0/0 | 4522 | 2 | 0 | 0 | 1 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0008 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0009 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0002t0019 | 0/0 | 4523 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0001 | 0/0 | 4522 | 21 | 9 | 3 | 8 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0003 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0004 | 0/0 | 4522 | 24 | 0 | 2 | 22 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0012 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0013 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0016 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0017 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0021 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0025 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0003t0028 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0002 | 0/0 | 4523 | 18 | 4 | 2 | 10 | 0 | 2 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0005 | 0/0 | 4522 | 15 | 1 | 4 | 4 | 2 | 4 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0006 | 0/0 | 4522 | 2 | 0 | 1 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0009 | 0/0 | 4522 | 4 | 4 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0010 | 0/0 | 4522 | 4 | 0 | 4 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0015 | 0/0 | 4522 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0023 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0004t0027 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0001 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0002 | 0/0 | 4523 | 15 | 7 | 1 | 6 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0005 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0006 | 0/0 | 4522 | 7 | 0 | 4 | 0 | 2 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0007 | 0/0 | 4522 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0008 | 0/0 | 4522 | 4 | 4 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0009 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0011 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0014 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0020 | 0/0 | 4523 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0005t0022 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0006t0003 | 1/0 | 4522 | 16 | 0 | 6 | 0 | 6 | 3 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0007t0001 | 0/1 | 4522 | 9 | 1 | 3 | 3 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0007t0003 | 0/0 | 4522 | 2 | 1 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0007t0004 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0008t0002 | 0/0 | 4523 | 3 | 2 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0008t0007 | 0/0 | 4522 | 3 | 3 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0011t0007 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0011t0008 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0011t0032 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0012t0003 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0012t0004 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0013t0003 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0015t0003 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0015t0013 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0016t0002 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0017t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0019t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0020t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0021t0005 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0022t0001 | 0/0 | 4522 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0023t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0024t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0029t0001 | 0/0 | 4522 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0001c0030t0002 | 0/0 | 4523 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0001c0033t0002 | 0/0 | 4523 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0002c0009t0002 | 0/0 | 4523 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0002c0009t0008 | 0/0 | 4522 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0002c0009t0011 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0002c0025t0003 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0002c0031t0011 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0003c0010t0003 | 0/0 | 4522 | 5 | 2 | 2 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0003c0027t0018 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0004c0014t0002 | 0/0 | 4523 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0005c0018t0003 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0006c0028t0002 | 0/0 | 4523 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
a0007c0026t0014 | 0/0 | 4522 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4517): Show |
chr6 | 11178298 | 11237668 |
a0008c0032t0002 | 0/0 | 4523 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | AGAGA others(4518): Show |
chr6 | 11178298 | 11237668 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0024g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0026g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0029g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0001t0031g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0002t0019g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0013g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0003t0028g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0010g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0023g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0004t0027g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0011g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0014g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0020g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0005t0022g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0006t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0336 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0007t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0008t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0008t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0008t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0008t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0008t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0011t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0011t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0011t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0011t0032g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0012t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0012t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0013t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0013t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0015t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0015t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0016t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0017t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0019t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0020t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0021t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0022t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0023t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0024t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0029t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0030t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0001c0033t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0009t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0009t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0009t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0009t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0025t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0002c0031t0011g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0010t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0010t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0010t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0010t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0010t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0003c0027t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0004c0014t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0004c0014t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0005c0018t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0006c0028t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0007c0026t0014g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
a0008c0032t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0005 | g0044 | EUR | GBR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00099 | hp2 | a0001 | c0006 | t0003 | g0057 | EUR | GBR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00140 | hp1 | a0001 | c0004 | t0005 | g0059 | EUR | GBR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00280 | hp1 | a0001 | c0006 | t0003 | g0095 | EUR | FIN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00280 | hp2 | a0001 | c0006 | t0003 | g0118 | EUR | FIN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00323 | hp1 | a0001 | c0005 | t0006 | g0169 | EUR | FIN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00323 | hp2 | a0001 | c0006 | t0003 | g0006 | EUR | FIN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00423 | hp1 | a0001 | c0003 | t0004 | g0355 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00423 | hp2 | a0001 | c0004 | t0002 | g0065 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00438 | hp2 | a0001 | c0019 | t0001 | g0200 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00544 | hp1 | a0001 | c0003 | t0004 | g0143 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00544 | hp2 | a0001 | c0004 | t0005 | g0198 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00597 | hp1 | a0001 | c0007 | t0001 | g0229 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00597 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00621 | hp2 | a0001 | c0023 | t0001 | g0152 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00642 | hp1 | a0003 | c0010 | t0003 | g0175 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0128 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00733 | hp2 | a0001 | c0006 | t0003 | g0094 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00735 | hp1 | a0001 | c0015 | t0003 | g0099 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00735 | hp2 | a0001 | c0004 | t0005 | g0241 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00738 | hp2 | a0001 | c0004 | t0010 | g0122 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0013 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG00741 | hp2 | a0001 | c0005 | t0006 | g0244 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01070 | hp1 | a0001 | c0006 | t0003 | g0004 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01071 | hp1 | a0001 | c0006 | t0003 | g0004 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01074 | hp1 | a0001 | c0004 | t0010 | g0066 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01074 | hp2 | a0005 | c0018 | t0003 | g0119 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01081 | hp1 | a0001 | c0004 | t0006 | g0207 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01106 | hp2 | a0001 | c0004 | t0010 | g0064 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01109 | hp1 | a0001 | c0005 | t0014 | g0100 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01167 | hp1 | a0003 | c0010 | t0003 | g0176 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01167 | hp2 | a0001 | c0006 | t0003 | g0006 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01168 | hp1 | a0001 | c0002 | t0005 | g0013 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01168 | hp2 | a0001 | c0006 | t0003 | g0096 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0346 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01243 | hp1 | a0001 | c0005 | t0002 | g0136 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01243 | hp2 | a0001 | c0004 | t0002 | g0243 | AMR | PUR | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01256 | hp1 | a0001 | c0005 | t0006 | g0137 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01256 | hp2 | a0001 | c0005 | t0006 | g0103 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01258 | hp2 | a0001 | c0005 | t0006 | g0102 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01261 | hp2 | a0001 | c0007 | t0001 | g0326 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01358 | hp2 | a0001 | c0004 | t0010 | g0134 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01361 | hp1 | a0001 | c0021 | t0005 | g0332 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01361 | hp2 | a0001 | c0007 | t0001 | g0092 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01433 | hp1 | a0001 | c0006 | t0003 | g0006 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01496 | hp2 | a0001 | c0012 | t0003 | g0277 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01515 | hp1 | a0001 | c0005 | t0006 | g0048 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01516 | hp1 | a0001 | c0007 | t0001 | g0331 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01516 | hp2 | a0001 | c0006 | t0003 | g0004 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01517 | hp2 | a0001 | c0006 | t0003 | g0004 | EUR | IBS | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01884 | hp1 | a0002 | c0009 | t0011 | g0090 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01884 | hp2 | a0001 | c0008 | t0007 | g0021 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01891 | hp1 | a0002 | c0025 | t0003 | g0091 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0180 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01928 | hp1 | a0006 | c0028 | t0002 | g0320 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01943 | hp1 | a0001 | c0004 | t0005 | g0062 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01952 | hp1 | a0001 | c0004 | t0002 | g0233 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01952 | hp2 | a0001 | c0003 | t0004 | g0257 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01975 | hp1 | a0001 | c0004 | t0005 | g0161 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0248 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01978 | hp2 | a0001 | c0004 | t0005 | g0333 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0327 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02015 | hp2 | a0001 | c0003 | t0004 | g0295 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02055 | hp1 | a0001 | c0011 | t0007 | g0146 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02055 | hp2 | a0001 | c0005 | t0007 | g0031 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02056 | hp2 | a0001 | c0003 | t0004 | g0302 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0292 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02129 | hp2 | a0001 | c0003 | t0004 | g0298 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02145 | hp1 | a0001 | c0004 | t0009 | g0079 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0296 | EAS | CDX | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02165 | hp1 | a0001 | c0030 | t0002 | g0328 | EAS | CDX | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02257 | hp1 | a0001 | c0005 | t0022 | g0072 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0354 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02258 | hp1 | a0001 | c0004 | t0002 | g0190 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0256 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02280 | hp1 | a0001 | c0004 | t0009 | g0076 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02280 | hp2 | a0001 | c0005 | t0002 | g0028 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0345 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02300 | hp2 | a0001 | c0003 | t0004 | g0259 | AMR | PEL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02451 | hp1 | a0001 | c0002 | t0009 | g0310 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02523 | hp1 | a0001 | c0004 | t0005 | g0232 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02572 | hp1 | a0001 | c0013 | t0003 | g0132 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02572 | hp2 | a0001 | c0005 | t0007 | g0084 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0324 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0183 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02622 | hp1 | a0001 | c0005 | t0009 | g0051 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02630 | hp2 | a0001 | c0005 | t0002 | g0266 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02647 | hp1 | a0002 | c0009 | t0002 | g0089 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02647 | hp2 | a0001 | c0005 | t0008 | g0177 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02717 | hp1 | a0001 | c0004 | t0009 | g0078 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02717 | hp2 | a0001 | c0016 | t0002 | g0170 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02723 | hp2 | a0001 | c0003 | t0013 | g0025 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02738 | hp1 | a0001 | c0004 | t0002 | g0145 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02738 | hp2 | a0001 | c0006 | t0003 | g0140 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02809 | hp1 | a0001 | c0007 | t0001 | g0311 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0179 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02818 | hp1 | a0002 | c0031 | t0011 | g0340 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02818 | hp2 | a0003 | c0010 | t0003 | g0037 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02886 | hp1 | a0001 | c0008 | t0007 | g0276 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02886 | hp2 | a0001 | c0005 | t0008 | g0086 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02895 | hp2 | a0003 | c0010 | t0003 | g0036 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02896 | hp1 | a0001 | c0005 | t0011 | g0267 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02896 | hp2 | a0001 | c0003 | t0012 | g0032 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02897 | hp2 | a0001 | c0003 | t0012 | g0029 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02922 | hp1 | a0001 | c0004 | t0002 | g0171 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02922 | hp2 | a0001 | c0005 | t0002 | g0083 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02965 | hp1 | a0001 | c0008 | t0002 | g0313 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02965 | hp2 | a0001 | c0015 | t0013 | g0026 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0281 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02970 | hp2 | a0001 | c0005 | t0002 | g0082 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02976 | hp1 | a0001 | c0005 | t0008 | g0181 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02976 | hp2 | a0001 | c0005 | t0007 | g0012 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03017 | hp1 | a0001 | c0006 | t0003 | g0213 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0282 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03041 | hp2 | a0001 | c0011 | t0007 | g0172 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03098 | hp1 | a0001 | c0004 | t0009 | g0053 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03098 | hp2 | a0001 | c0003 | t0016 | g0030 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03130 | hp1 | a0001 | c0002 | t0008 | g0049 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03130 | hp2 | a0001 | c0005 | t0002 | g0081 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03139 | hp1 | a0001 | c0033 | t0002 | g0312 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03139 | hp2 | a0001 | c0008 | t0002 | g0309 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03195 | hp1 | a0001 | c0005 | t0007 | g0035 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03195 | hp2 | a0001 | c0001 | t0029 | g0316 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0073 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03225 | hp1 | a0001 | c0004 | t0023 | g0315 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03225 | hp2 | a0001 | c0007 | t0003 | g0342 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03239 | hp1 | a0001 | c0007 | t0003 | g0335 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0265 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03453 | hp2 | a0001 | c0003 | t0028 | g0046 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03486 | hp1 | a0001 | c0005 | t0002 | g0085 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03486 | hp2 | a0001 | c0003 | t0017 | g0027 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03490 | hp1 | a0001 | c0004 | t0005 | g0069 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03516 | hp1 | a0002 | c0009 | t0002 | g0088 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03516 | hp2 | a0001 | c0001 | t0030 | g0077 | AFR | ESN | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03540 | hp1 | a0001 | c0003 | t0016 | g0098 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03540 | hp2 | a0001 | c0005 | t0008 | g0184 | AFR | GWD | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03579 | hp1 | a0001 | c0005 | t0002 | g0280 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03579 | hp2 | a0001 | c0003 | t0025 | g0173 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03654 | hp1 | a0001 | c0007 | t0004 | g0275 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03654 | hp2 | a0003 | c0010 | t0003 | g0237 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03704 | hp1 | a0001 | c0002 | t0006 | g0286 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03704 | hp2 | a0001 | c0001 | t0024 | g0038 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03710 | hp1 | a0001 | c0022 | t0001 | g0273 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03710 | hp2 | a0001 | c0004 | t0027 | g0045 | SAS | PJL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03834 | hp1 | a0001 | c0005 | t0005 | g0135 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03927 | hp2 | a0001 | c0004 | t0005 | g0070 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04115 | hp1 | a0001 | c0005 | t0002 | g0288 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0155 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04184 | hp1 | a0001 | c0006 | t0003 | g0108 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04184 | hp2 | a0001 | c0004 | t0005 | g0080 | SAS | BEB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04199 | hp1 | a0001 | c0004 | t0002 | g0185 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04199 | hp2 | a0001 | c0004 | t0005 | g0061 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0123 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04228 | hp1 | a0001 | c0005 | t0006 | g0138 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | STU | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18522 | hp2 | a0002 | c0009 | t0008 | g0010 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18612 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | CHB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18612 | hp2 | a0001 | c0003 | t0004 | g0165 | EAS | CHB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | CHB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18906 | hp1 | a0001 | c0004 | t0002 | g0317 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0194 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18943 | hp1 | a0001 | c0003 | t0004 | g0299 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18945 | hp1 | a0001 | c0004 | t0005 | g0067 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18945 | hp2 | a0008 | c0032 | t0002 | g0218 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18954 | hp2 | a0001 | c0004 | t0002 | g0216 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18956 | hp1 | a0001 | c0002 | t0019 | g0343 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18956 | hp2 | a0001 | c0017 | t0001 | g0158 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18959 | hp2 | a0001 | c0005 | t0002 | g0289 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18961 | hp1 | a0001 | c0003 | t0004 | g0220 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18963 | hp1 | a0001 | c0007 | t0001 | g0285 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18963 | hp2 | a0001 | c0004 | t0002 | g0121 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18965 | hp2 | a0001 | c0003 | t0004 | g0293 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18967 | hp1 | a0004 | c0014 | t0002 | g0154 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18967 | hp2 | a0001 | c0020 | t0001 | g0201 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18968 | hp1 | a0001 | c0002 | t0006 | g0325 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18970 | hp1 | a0001 | c0007 | t0001 | g0251 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18971 | hp1 | a0001 | c0024 | t0001 | g0300 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18975 | hp2 | a0004 | c0014 | t0002 | g0228 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18977 | hp2 | a0001 | c0004 | t0002 | g0250 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18980 | hp1 | a0001 | c0005 | t0002 | g0187 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18980 | hp2 | a0001 | c0004 | t0002 | g0117 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18984 | hp1 | a0001 | c0004 | t0015 | g0166 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18985 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18987 | hp1 | a0001 | c0003 | t0004 | g0258 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18990 | hp2 | a0001 | c0005 | t0002 | g0283 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18992 | hp2 | a0001 | c0003 | t0004 | g0353 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18997 | hp1 | a0001 | c0003 | t0004 | g0347 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18997 | hp2 | a0001 | c0004 | t0002 | g0191 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19000 | hp2 | a0001 | c0004 | t0002 | g0124 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19002 | hp1 | a0001 | c0003 | t0004 | g0348 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19004 | hp1 | a0001 | c0004 | t0002 | g0206 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19004 | hp2 | a0001 | c0004 | t0006 | g0113 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19005 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0301 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19012 | hp2 | a0001 | c0003 | t0004 | g0356 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19030 | hp1 | a0001 | c0005 | t0011 | g0268 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19030 | hp2 | a0001 | c0001 | t0026 | g0269 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0055 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19043 | hp2 | a0001 | c0004 | t0002 | g0054 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19054 | hp2 | a0001 | c0003 | t0004 | g0297 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19060 | hp1 | a0001 | c0029 | t0001 | g0221 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19064 | hp1 | a0001 | c0003 | t0004 | g0022 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19068 | hp2 | a0001 | c0004 | t0015 | g0060 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19070 | hp1 | a0001 | c0005 | t0002 | g0186 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19070 | hp2 | a0001 | c0005 | t0002 | g0284 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19076 | hp1 | a0001 | c0004 | t0002 | g0193 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19084 | hp1 | a0001 | c0008 | t0002 | g0287 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19084 | hp2 | a0001 | c0003 | t0021 | g0231 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19087 | hp1 | a0001 | c0005 | t0002 | g0290 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19088 | hp2 | a0001 | c0003 | t0004 | g0319 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19090 | hp1 | a0001 | c0005 | t0020 | g0142 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19091 | hp1 | a0001 | c0004 | t0005 | g0068 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19091 | hp2 | a0001 | c0003 | t0004 | g0022 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA19240 | hp2 | a0001 | c0005 | t0007 | g0012 | AFR | YRI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ASW | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0321 | EUR | TSI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0023 | EUR | TSI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0131 | EUR | TSI | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02109 | hp1 | a0001 | c0005 | t0007 | g0033 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02109 | hp2 | a0001 | c0011 | t0032 | g0358 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02486 | hp1 | a0001 | c0013 | t0003 | g0174 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG02559 | hp2 | a0001 | c0008 | t0007 | g0021 | AFR | ACB | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG03471 | hp2 | a0001 | c0011 | t0008 | g0147 | AFR | MSL | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG06807 | hp1 | a0007 | c0026 | t0014 | g0318 | AFR | USA | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
HG06807 | hp2 | a0002 | c0009 | t0008 | g0010 | AFR | USA | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA18955 | hp2 | a0001 | c0003 | t0004 | g0349 | EAS | JPT | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20300 | hp1 | a0001 | c0012 | t0004 | g0254 | AFR | USA | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0262 | AFR | USA | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA21309 | hp1 | a0001 | c0004 | t0005 | g0058 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
NA21309 | hp2 | a0003 | c0027 | t0018 | g0087 | AFR | LWK | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
homoSapiens | chm13v2 | a0001 | c0007 | t0001 | g0336 | REF | REF | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
homoSapiens | grch38p0 | a0001 | c0006 | t0003 | g0120 | REF | REF | NEDD9_chr6_11178298_11237668 | NEDD9 | chr6 | 11178298 | 11237668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:11190139 | G | A | 1 | a0004 | 2 | NA18967.hp1 NA18975.hp2 |
missense_variant | MODERATE | c.1730C>T | p.Thr577Met | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1883/4522 | 1730/2505 | 577/834 | chr6 | 11190139 | |||
chr6:11190245 | C | T | 1 | a0006 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1624G>A | p.Ala542Thr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1777/4522 | 1624/2505 | 542/834 | chr6 | 11190245 | |||
chr6:11190409 | C | T | 1 | a0006 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1460G>A | p.Arg487Gln | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1613/4522 | 1460/2505 | 487/834 | chr6 | 11190409 | |||
chr6:11190626 | G | A | 1 | a0002 | 7 | HG01884.hp1 HG01891.hp1 HG02647.hp1 others(4): Show |
missense_variant | MODERATE | c.1243C>T | p.Arg415Trp | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1396/4522 | 1243/2505 | 415/834 | chr6 | 11190626 | |||
chr6:11190749 | C | T | 1 | a0005 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1120G>A | p.Gly374Ser | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1273/4522 | 1120/2505 | 374/834 | chr6 | 11190749 | |||
chr6:11190958 | G | A | 1 | a0007 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.911C>T | p.Pro304Leu | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1064/4522 | 911/2505 | 304/834 | chr6 | 11190958 | |||
chr6:11191201 | T | C | 1 | a0003 | 6 | HG00642.hp1 HG01167.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.668A>G | p.Tyr223Cys | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 821/4522 | 668/2505 | 223/834 | chr6 | 11191201 | |||
chr6:11193630 | C | A | 1 | a0008 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.522G>T | p.Lys174Asn | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/7 | 675/4522 | 522/2505 | 174/834 | chr6 | 11193630 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:11185276 | G | T | 2 | a0001c0020 a0001c0029 |
2 | NA18967.hp2 NA19060.hp1 |
synonymous_variant | LOW | c.2391C>A | p.Ala797Ala | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 2544/4522 | 2391/2505 | 797/834 | chr6 | 11185276 | |||
chr6:11185300 | G | A | 16 | a0001c0002 a0001c0004 a0001c0005 others(13): Show |
170 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(167): Show |
synonymous_variant | LOW | c.2367C>T | p.Thr789Thr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 2520/4522 | 2367/2505 | 789/834 | chr6 | 11185300 | |||
chr6:11189970 | G | A | 1 | a0001c0021 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.1899C>T | p.His633His | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 2052/4522 | 1899/2505 | 633/834 | chr6 | 11189970 | |||
chr6:11189982 | G | A | 1 | a0001c0022 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.1887C>T | p.Tyr629Tyr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 2040/4522 | 1887/2505 | 629/834 | chr6 | 11189982 | |||
chr6:11190213 | G | A | 1 | a0001c0030 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1656C>T | p.Asn552Asn | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1809/4522 | 1656/2505 | 552/834 | chr6 | 11190213 | |||
chr6:11190393 | A | G | 29 | a0001c0001 a0001c0002 a0001c0003 others(26): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
synonymous_variant | LOW | c.1476T>C | p.Val492Val | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1629/4522 | 1476/2505 | 492/834 | chr6 | 11190393 | |||
chr6:11190570 | G | A | 1 | a0001c0023 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1299C>T | p.Thr433Thr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1452/4522 | 1299/2505 | 433/834 | chr6 | 11190570 | |||
chr6:11190723 | C | T | 1 | a0001c0019 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.1146G>A | p.Thr382Thr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1299/4522 | 1146/2505 | 382/834 | chr6 | 11190723 | |||
chr6:11190891 | A | C | 1 | a0001c0024 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.978T>G | p.Leu326Leu | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/7 | 1131/4522 | 978/2505 | 326/834 | chr6 | 11190891 | |||
chr6:11192357 | C | T | 1 | a0001c0017 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.651G>A | p.Pro217Pro | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/7 | 804/4522 | 651/2505 | 217/834 | chr6 | 11192357 | |||
chr6:11193627 | G | A | 10 | a0001c0002 a0001c0007 a0001c0008 others(7): Show |
83 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
synonymous_variant | LOW | c.525C>T | p.Asp175Asp | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/7 | 678/4522 | 525/2505 | 175/834 | chr6 | 11193627 | |||
chr6:11213422 | G | A | 2 | a0001c0015 a0001c0033 |
3 | HG00735.hp1 HG02965.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.318C>T | p.Tyr106Tyr | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/7 | 471/4522 | 318/2505 | 106/834 | chr6 | 11213422 | |||
chr6:11213599 | T | C | 20 | a0001c0002 a0001c0003 a0001c0005 others(17): Show |
190 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
synonymous_variant | LOW | c.141A>G | p.Ser47Ser | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/7 | 294/4522 | 141/2505 | 47/834 | chr6 | 11213599 | |||
chr6:11213620 | C | T | 1 | a0001c0016 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.120G>A | p.Leu40Leu | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/7 | 273/4522 | 120/2505 | 40/834 | chr6 | 11213620 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:11183354 | C | T | 46 | a0001c0001t0012 a0001c0001t0031 a0001c0002t0002 others(43): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1808G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1808 | chr6 | 11183354 | ||||||
chr6:11183368 | A | G | 1 | a0001c0001t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1794T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1794 | chr6 | 11183368 | ||||||
chr6:11183576 | A | G | 1 | a0001c0003t0016 | 2 | HG03098.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1586T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1586 | chr6 | 11183576 | ||||||
chr6:11183647 | A | AT | 15 | a0001c0002t0002 a0001c0002t0019 a0001c0003t0025 others(12): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1514dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1514 | chr6 | 11183647 | ||||||
chr6:11183651 | T | C | 1 | a0001c0001t0024 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1511A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1511 | chr6 | 11183651 | ||||||
chr6:11183663 | T | G | 64 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0024 others(61): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1499A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1499 | chr6 | 11183663 | ||||||
chr6:11183670 | T | A | 18 | a0001c0001t0001 a0001c0001t0024 a0001c0001t0026 others(15): Show |
178 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*1492A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1492 | chr6 | 11183670 | ||||||
chr6:11183679 | C | T | 18 | a0001c0001t0001 a0001c0001t0024 a0001c0001t0026 others(15): Show |
178 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*1483G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1483 | chr6 | 11183679 | ||||||
chr6:11183857 | G | A | 46 | a0001c0001t0012 a0001c0001t0031 a0001c0002t0002 others(43): Show |
174 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1305C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1305 | chr6 | 11183857 | ||||||
chr6:11183894 | C | A | 5 | a0001c0004t0023 a0001c0005t0011 a0001c0005t0022 others(2): Show |
6 | HG01884.hp1 HG02257.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1268G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1268 | chr6 | 11183894 | ||||||
chr6:11184061 | C | A | 1 | a0001c0001t0026 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1101G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1101 | chr6 | 11184061 | ||||||
chr6:11184079 | T | C | 2 | a0001c0001t0012 a0001c0003t0012 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1083A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 1083 | chr6 | 11184079 | ||||||
chr6:11184248 | T | A | 23 | a0001c0001t0030 a0001c0001t0031 a0001c0002t0008 others(20): Show |
63 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*914A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 914 | chr6 | 11184248 | ||||||
chr6:11184290 | A | T | 1 | a0001c0005t0020 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*872T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 872 | chr6 | 11184290 | ||||||
chr6:11184460 | C | G | 1 | a0001c0004t0010 | 4 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*702G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 702 | chr6 | 11184460 | ||||||
chr6:11184568 | C | T | 4 | a0001c0002t0006 a0001c0004t0006 a0001c0004t0015 others(1): Show |
13 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*594G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 594 | chr6 | 11184568 | ||||||
chr6:11184569 | G | A | 1 | a0001c0004t0027 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 593 | chr6 | 11184569 | ||||||
chr6:11184634 | C | A | 61 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0024 others(58): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 528 | chr6 | 11184634 | ||||||
chr6:11184801 | A | G | 2 | a0001c0005t0014 a0007c0026t0014 |
2 | HG01109.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*361T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 361 | chr6 | 11184801 | ||||||
chr6:11184887 | A | T | 1 | a0001c0002t0019 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 275 | chr6 | 11184887 | ||||||
chr6:11184928 | C | T | 5 | a0001c0002t0006 a0001c0004t0006 a0001c0004t0015 others(2): Show |
14 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*234G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 234 | chr6 | 11184928 | ||||||
chr6:11184951 | A | G | 21 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0019 others(18): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*211T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 211 | chr6 | 11184951 | ||||||
chr6:11184978 | A | G | 4 | a0001c0002t0009 a0001c0004t0009 a0001c0005t0009 others(1): Show |
7 | HG02145.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*184T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 184 | chr6 | 11184978 | ||||||
chr6:11185024 | A | T | 63 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0024 others(60): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*138T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 7/7 | 138 | chr6 | 11185024 | ||||||
chr6:11232598 | C | T | 3 | a0001c0003t0013 a0001c0003t0017 a0001c0015t0013 |
3 | HG02723.hp2 HG02965.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-83G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/7 | 83 | chr6 | 11232598 | ||||||
chr6:11232608 | T | C | 1 | a0001c0011t0032 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-93A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/7 | 93 | chr6 | 11232608 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:11185734 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1996-63A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185734 | |||||||
chr6:11185757 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1996-86C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185757 | |||||||
chr6:11185811 | A | G | 13 | a0001c0002t0006g0286 a0001c0002t0006g0325 a0001c0004t0006g0113 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1996-140T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185811 | |||||||
chr6:11185816 | C | T | 23 | a0001c0002t0005g0013 a0001c0002t0005g0128 a0001c0004t0005g0044 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1996-145G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185816 | |||||||
chr6:11185898 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
171 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1996-227A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185898 | |||||||
chr6:11185939 | G | A | 3 | a0001c0001t0012g0073 a0001c0003t0012g0029 a0001c0003t0012g0032 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1996-268C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185939 | |||||||
chr6:11185988 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0001g0106 others(17): Show |
22 | HG00609.hp1 HG00673.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1996-317G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185988 | |||||||
chr6:11185992 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1996-321T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11185992 | |||||||
chr6:11186198 | C | G | 160 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(157): Show |
171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1996-527G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186198 | |||||||
chr6:11186314 | A | G | 1 | a0001c0002t0006g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1996-643T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186314 | |||||||
chr6:11186389 | C | A | 1 | a0001c0004t0005g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1996-718G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186389 | |||||||
chr6:11186474 | A | C | 1 | a0001c0004t0002g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1996-803T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186474 | |||||||
chr6:11186506 | C | T | 1 | a0001c0003t0004g0220 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1996-835G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186506 | |||||||
chr6:11186517 | G | C | 2 | a0003c0010t0003g0175 a0003c0010t0003g0176 |
2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1996-846C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186517 | |||||||
chr6:11186612 | T | G | 36 | a0001c0002t0005g0013 a0001c0002t0005g0128 a0001c0004t0005g0044 others(33): Show |
39 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1996-941A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186612 | |||||||
chr6:11186686 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.1996-1015A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186686 | |||||||
chr6:11186703 | C | T | 23 | a0001c0002t0005g0013 a0001c0002t0005g0128 a0001c0004t0005g0044 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1996-1032G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186703 | |||||||
chr6:11186713 | G | C | 23 | a0001c0002t0005g0013 a0001c0002t0005g0128 a0001c0004t0005g0044 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1996-1042C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186713 | |||||||
chr6:11186725 | C | G | 160 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(157): Show |
171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1996-1054G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186725 | |||||||
chr6:11186806 | C | T | 1 | a0001c0003t0016g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1996-1135G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11186806 | |||||||
chr6:11187019 | C | G | 13 | a0001c0002t0006g0286 a0001c0002t0006g0325 a0001c0004t0006g0113 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1995+1199G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187019 | |||||||
chr6:11187131 | TG | T | 151 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(148): Show |
162 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1995+1086delC | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187131 | |||||||
chr6:11187241 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.1995+977A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187241 | |||||||
chr6:11187547 | A | AAGAG | 4 | a0001c0004t0005g0061 a0001c0004t0005g0062 a0001c0004t0005g0080 others(1): Show |
4 | HG00735.hp2 HG01943.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+667_1995+670d others(6): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187547 | |||||||
chr6:11187563 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1995+655C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187563 | |||||||
chr6:11187677 | A | G | 1 | a0001c0003t0004g0220 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1995+541T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187677 | |||||||
chr6:11187692 | G | A | 36 | a0001c0002t0005g0013 a0001c0002t0005g0128 a0001c0004t0005g0044 others(33): Show |
39 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1995+526C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187692 | |||||||
chr6:11187696 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1995+522T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187696 | |||||||
chr6:11187764 | T | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
361 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.1995+454A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187764 | |||||||
chr6:11187779 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.1995+439G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187779 | |||||||
chr6:11187838 | C | A | 7 | a0001c0004t0009g0053 a0001c0004t0009g0076 a0001c0004t0009g0078 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995+380G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187838 | |||||||
chr6:11187868 | T | C | 2 | a0001c0005t0001g0262 a0001c0005t0009g0051 |
2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1995+350A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187868 | |||||||
chr6:11187920 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
174 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1995+298A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11187920 | |||||||
chr6:11188011 | G | GTTTAGAT others(41): Show |
1 | a0001c0004t0002g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1995+206_1995+207i others(50): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 6/6 | chr6 | 11188011 | |||||||
chr6:11188456 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1906-149C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188456 | |||||||
chr6:11188564 | T | TA | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1906-258dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188564 | |||||||
chr6:11188706 | G | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1906-399C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188706 | |||||||
chr6:11188740 | T | A | 9 | a0001c0002t0008g0049 a0001c0005t0008g0086 a0001c0005t0008g0177 others(6): Show |
10 | HG01109.hp1 HG02647.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1906-433A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188740 | |||||||
chr6:11188854 | C | T | 13 | a0001c0002t0006g0286 a0001c0002t0006g0325 a0001c0004t0006g0113 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1906-547G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188854 | |||||||
chr6:11188947 | A | AT | 104 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0001t0031g0055 others(101): Show |
111 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1906-641dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188947 | |||||||
chr6:11188947 | A | ATT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
188 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1906-642_1906-641d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188947 | |||||||
chr6:11188985 | C | T | 13 | a0001c0002t0006g0286 a0001c0002t0006g0325 a0001c0004t0006g0113 others(10): Show |
13 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1906-678G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11188985 | |||||||
chr6:11189029 | C | T | 9 | a0001c0001t0003g0052 a0001c0001t0031g0055 a0001c0002t0008g0049 others(6): Show |
9 | HG01109.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1906-722G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189029 | |||||||
chr6:11189063 | C | T | 4 | a0001c0001t0003g0126 a0001c0005t0002g0266 a0001c0005t0011g0267 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-756G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189063 | |||||||
chr6:11189118 | C | T | 56 | a0001c0001t0030g0077 a0001c0003t0001g0139 a0001c0003t0001g0256 others(53): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1906-811G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189118 | |||||||
chr6:11189127 | A | T | 12 | a0001c0002t0006g0325 a0001c0004t0006g0113 a0001c0004t0006g0207 others(9): Show |
12 | HG00323.hp1 HG00741.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1906-820T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189127 | |||||||
chr6:11189155 | C | G | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1905+809G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189155 | |||||||
chr6:11189178 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1905+786G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189178 | |||||||
chr6:11189192 | G | A | 7 | a0001c0001t0001g0314 a0001c0003t0001g0034 a0001c0003t0001g0179 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1905+772C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189192 | |||||||
chr6:11189253 | GT | G | 42 | a0001c0001t0001g0314 a0001c0003t0001g0034 a0001c0003t0001g0139 others(39): Show |
45 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1905+710delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189253 | |||||||
chr6:11189286 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1905+678G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189286 | |||||||
chr6:11189338 | A | C | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1905+626T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189338 | |||||||
chr6:11189385 | G | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1905+579C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189385 | |||||||
chr6:11189628 | T | C | 6 | a0001c0001t0031g0055 a0001c0003t0016g0098 a0001c0005t0007g0012 others(3): Show |
7 | HG01361.hp2 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1905+336A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189628 | |||||||
chr6:11189744 | A | G | 1 | a0001c0001t0031g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1905+220T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189744 | |||||||
chr6:11189842 | T | C | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1905+122A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189842 | |||||||
chr6:11189896 | A | G | 1 | a0001c0003t0016g0030 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1905+68T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 5/6 | chr6 | 11189896 | |||||||
chr6:11191276 | C | T | 13 | a0001c0003t0001g0256 a0001c0003t0004g0165 a0001c0003t0004g0220 others(10): Show |
13 | HG00423.hp1 HG01952.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.664-71G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191276 | |||||||
chr6:11191292 | C | T | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664-87G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191292 | |||||||
chr6:11191299 | T | A | 1 | a0001c0003t0001g0219 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.664-94A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191299 | |||||||
chr6:11191420 | A | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
369 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.664-215T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191420 | |||||||
chr6:11191470 | T | C | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664-265A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191470 | |||||||
chr6:11191490 | T | C | 1 | a0001c0004t0002g0243 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.664-285A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191490 | |||||||
chr6:11191541 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.664-336C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191541 | |||||||
chr6:11191549 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(333): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.664-344A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191549 | |||||||
chr6:11191551 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.664-346C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191551 | |||||||
chr6:11191873 | C | T | 8 | a0001c0001t0031g0055 a0001c0005t0002g0028 a0001c0005t0002g0081 others(5): Show |
8 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.663+472G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191873 | |||||||
chr6:11191874 | G | A | 1 | a0001c0006t0003g0213 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.663+471C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11191874 | |||||||
chr6:11192128 | G | T | 2 | a0001c0015t0013g0026 a0001c0033t0002g0312 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.663+217C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11192128 | |||||||
chr6:11192289 | C | CT | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(331): Show |
369 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(366): Show |
intron_variant | MODIFIER | c.663+55_663+56insA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11192289 | |||||||
chr6:11192342 | C | T | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(326): Show |
364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
splice_region_variant&intron_variant | LOW | c.663+3G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 4/6 | chr6 | 11192342 | |||||||
chr6:11192458 | C | T | 2 | a0001c0008t0002g0309 a0001c0008t0002g0313 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.562-12G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192458 | |||||||
chr6:11192596 | C | CT | 48 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0001g0314 others(45): Show |
49 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.562-151dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192596 | |||||||
chr6:11192596 | C | CTT | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(162): Show |
186 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.562-152_562-151dup others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192596 | |||||||
chr6:11192596 | C | CTTT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(120): Show |
136 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.562-153_562-151dup others(3): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192596 | |||||||
chr6:11192605 | T | A | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.562-159A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192605 | |||||||
chr6:11192632 | A | G | 2 | a0001c0001t0026g0269 a0001c0003t0013g0025 |
2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.562-186T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192632 | |||||||
chr6:11192648 | A | G | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.562-202T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192648 | |||||||
chr6:11192672 | C | T | 69 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(66): Show |
77 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.562-226G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192672 | |||||||
chr6:11192794 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
5 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-348C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192794 | |||||||
chr6:11192932 | C | CA | 94 | a0001c0001t0001g0242 a0001c0001t0001g0271 a0001c0001t0012g0073 others(91): Show |
101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.562-487dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192932 | |||||||
chr6:11192932 | C | CAA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
130 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.562-488_562-487dup others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192932 | |||||||
chr6:11192932 | C | CAAA | 30 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0106 others(27): Show |
30 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.562-489_562-487dup others(3): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192932 | |||||||
chr6:11192967 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
46 | HG00621.hp1 HG01069.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.562-521A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11192967 | |||||||
chr6:11193034 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.561+557C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193034 | |||||||
chr6:11193120 | C | G | 2 | a0001c0003t0012g0029 a0001c0003t0012g0032 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.561+471G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193120 | |||||||
chr6:11193177 | TGC | T | 31 | a0001c0001t0029g0316 a0001c0003t0001g0123 a0001c0003t0001g0178 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.561+412_561+413del others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193177 | |||||||
chr6:11193193 | T | C | 1 | a0002c0009t0011g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.561+398A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193193 | |||||||
chr6:11193264 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG02735.hp1 HG03710.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+327A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193264 | |||||||
chr6:11193310 | TA | T | 7 | a0001c0001t0001g0163 a0001c0002t0002g0005 a0001c0002t0002g0223 others(4): Show |
10 | HG01943.hp2 HG02293.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+280delT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193310 | |||||||
chr6:11193311 | A | T | 1 | a0001c0002t0002g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.561+280T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193311 | |||||||
chr6:11193312 | AAAAAAAA others(26): Show |
A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0097 |
3 | HG03017.hp2 HG03491.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.561+246_561+278del others(33): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193312 | |||||||
chr6:11193359 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.561+232C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193359 | |||||||
chr6:11193364 | AG | A | 35 | a0001c0001t0029g0316 a0001c0003t0001g0123 a0001c0003t0001g0178 others(32): Show |
35 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.561+226delC | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193364 | |||||||
chr6:11193497 | A | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(34): Show |
47 | HG00621.hp1 HG01069.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.561+94T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193497 | |||||||
chr6:11193532 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.561+59G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193532 | |||||||
chr6:11193587 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19066.hp2 | splice_region_variant&intron_variant | LOW | c.561+4C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 3/6 | chr6 | 11193587 | |||||||
chr6:11193749 | T | G | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-57A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11193749 | |||||||
chr6:11193795 | G | A | 3 | a0001c0007t0001g0326 a0001c0007t0001g0331 a0001c0007t0001g0346 |
3 | HG01175.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.460-103C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11193795 | |||||||
chr6:11193797 | T | C | 1 | a0001c0002t0002g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.460-105A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11193797 | |||||||
chr6:11193868 | T | C | 1 | a0001c0003t0004g0349 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.460-176A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11193868 | |||||||
chr6:11194009 | G | A | 29 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(26): Show |
29 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-317C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194009 | |||||||
chr6:11194021 | A | G | 49 | a0001c0003t0001g0034 a0001c0003t0001g0139 a0001c0003t0001g0219 others(46): Show |
53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.460-329T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194021 | |||||||
chr6:11194231 | A | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.460-539T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194231 | |||||||
chr6:11194278 | C | T | 104 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(101): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.460-586G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194278 | |||||||
chr6:11194359 | G | A | 1 | a0001c0003t0013g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.460-667C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194359 | |||||||
chr6:11194395 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(132): Show |
146 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.460-703A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194395 | |||||||
chr6:11194583 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.460-891C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194583 | |||||||
chr6:11194734 | G | A | 1 | a0001c0003t0013g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.460-1042C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194734 | |||||||
chr6:11194743 | G | T | 77 | a0001c0001t0003g0052 a0001c0002t0002g0005 a0001c0002t0002g0016 others(74): Show |
86 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.460-1051C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194743 | |||||||
chr6:11194765 | G | C | 5 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0002g0131 others(2): Show |
6 | HG00642.hp2 HG00741.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-1073C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194765 | |||||||
chr6:11194828 | C | G | 69 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(66): Show |
77 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.460-1136G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194828 | |||||||
chr6:11194970 | C | T | 7 | a0001c0005t0002g0028 a0001c0005t0002g0081 a0001c0005t0002g0082 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-1278G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11194970 | |||||||
chr6:11195146 | G | A | 5 | a0001c0004t0005g0061 a0001c0004t0005g0062 a0001c0004t0005g0080 others(2): Show |
5 | HG00735.hp2 HG01361.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1454C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195146 | |||||||
chr6:11195344 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.460-1652G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195344 | |||||||
chr6:11195392 | C | A | 1 | a0001c0007t0001g0311 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.460-1700G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195392 | |||||||
chr6:11195458 | GT | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
187 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.460-1767delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195458 | |||||||
chr6:11195470 | T | G | 8 | a0001c0003t0001g0034 a0001c0003t0001g0270 a0001c0003t0012g0029 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-1778A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195470 | |||||||
chr6:11195523 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(35): Show |
48 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.460-1831G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195523 | |||||||
chr6:11195719 | G | T | 1 | a0001c0002t0002g0264 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.460-2027C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195719 | |||||||
chr6:11195853 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(114): Show |
128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.460-2161C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195853 | |||||||
chr6:11195902 | G | A | 7 | a0001c0005t0002g0028 a0001c0005t0002g0081 a0001c0005t0002g0082 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-2210C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11195902 | |||||||
chr6:11196077 | C | T | 1 | a0002c0025t0003g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.460-2385G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196077 | |||||||
chr6:11196079 | C | A | 2 | a0001c0007t0001g0092 a0001c0007t0001g0311 |
2 | HG01361.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.460-2387G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196079 | |||||||
chr6:11196192 | T | C | 107 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.460-2500A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196192 | |||||||
chr6:11196297 | C | G | 1 | a0001c0001t0003g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.460-2605G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196297 | |||||||
chr6:11196489 | G | A | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.460-2797C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196489 | |||||||
chr6:11196517 | A | C | 2 | a0001c0001t0001g0314 a0001c0004t0023g0315 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.460-2825T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196517 | |||||||
chr6:11196584 | T | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(320): Show |
358 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.460-2892A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196584 | |||||||
chr6:11196690 | G | A | 4 | a0001c0001t0003g0052 a0001c0004t0002g0054 a0001c0004t0002g0171 others(1): Show |
4 | HG02486.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-2998C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196690 | |||||||
chr6:11196827 | C | T | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-3135G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196827 | |||||||
chr6:11196999 | G | C | 8 | a0001c0001t0012g0073 a0001c0005t0002g0028 a0001c0005t0002g0081 others(5): Show |
8 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-3307C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11196999 | |||||||
chr6:11197192 | T | A | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-3500A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197192 | |||||||
chr6:11197252 | C | CT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(71): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.460-3561dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197252 | |||||||
chr6:11197252 | CT | C | 53 | a0001c0003t0001g0034 a0001c0003t0001g0139 a0001c0003t0001g0219 others(50): Show |
57 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.460-3561delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197252 | |||||||
chr6:11197307 | G | T | 3 | a0001c0005t0006g0102 a0001c0005t0006g0103 a0001c0005t0006g0244 |
3 | HG00741.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.460-3615C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197307 | |||||||
chr6:11197422 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.460-3730C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197422 | |||||||
chr6:11197667 | G | A | 4 | a0001c0001t0030g0077 a0001c0004t0009g0076 a0001c0004t0009g0078 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-3975C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197667 | |||||||
chr6:11197970 | G | T | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-4278C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197970 | |||||||
chr6:11197971 | C | T | 1 | a0001c0001t0012g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-4279G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11197971 | |||||||
chr6:11198103 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0004t0002g0233 |
7 | HG01257.hp1 HG01258.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-4411G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198103 | |||||||
chr6:11198119 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.460-4427A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198119 | |||||||
chr6:11198181 | A | C | 1 | a0001c0007t0001g0311 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.460-4489T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198181 | |||||||
chr6:11198241 | G | A | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-4549C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198241 | |||||||
chr6:11198265 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
171 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.460-4573G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198265 | |||||||
chr6:11198333 | C | A | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.460-4641G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198333 | |||||||
chr6:11198428 | C | A | 1 | a0001c0006t0003g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.460-4736G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198428 | |||||||
chr6:11198445 | T | C | 52 | a0001c0003t0001g0034 a0001c0003t0001g0139 a0001c0003t0001g0219 others(49): Show |
56 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.460-4753A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198445 | |||||||
chr6:11198530 | T | C | 114 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(111): Show |
124 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.460-4838A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198530 | |||||||
chr6:11198581 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
137 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.460-4889C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198581 | |||||||
chr6:11198784 | G | A | 1 | a0001c0004t0002g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.460-5092C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198784 | |||||||
chr6:11198908 | A | G | 2 | a0001c0003t0004g0022 a0001c0003t0004g0297 |
3 | NA19054.hp2 NA19064.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.460-5216T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198908 | |||||||
chr6:11198992 | A | C | 1 | a0001c0004t0005g0241 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.460-5300T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11198992 | |||||||
chr6:11199001 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
149 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.460-5309T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199001 | |||||||
chr6:11199246 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.460-5554A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199246 | |||||||
chr6:11199502 | T | C | 3 | a0001c0004t0002g0191 a0001c0004t0002g0206 a0001c0004t0002g0216 |
3 | NA18954.hp2 NA18997.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.460-5810A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199502 | |||||||
chr6:11199637 | C | CTT | 6 | a0001c0006t0003g0108 a0001c0006t0003g0118 a0001c0006t0003g0140 others(3): Show |
6 | HG00280.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-5947_460-5946d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | C | CTTTTTTT others(3): Show |
1 | a0001c0005t0002g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.460-5955_460-5946d others(12): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CT | C | 24 | a0001c0001t0001g0063 a0001c0001t0001g0314 a0001c0001t0003g0075 others(21): Show |
26 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.460-5946delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTT | C | 45 | a0001c0001t0003g0009 a0001c0001t0003g0097 a0001c0001t0026g0269 others(42): Show |
52 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.460-5947_460-5946d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTT | C | 28 | a0001c0002t0002g0017 a0001c0002t0002g0043 a0001c0002t0002g0131 others(25): Show |
29 | HG00408.hp1 HG01081.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-5948_460-5946d others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0234 others(5): Show |
8 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-5953_460-5946d others(10): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(2): Show |
C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0071 others(27): Show |
35 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(32): Show |
intron_variant | MODIFIER | c.460-5954_460-5946d others(11): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(3): Show |
C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.460-5955_460-5946d others(12): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(4): Show |
C | 38 | a0001c0001t0001g0203 a0001c0001t0001g0212 a0001c0001t0001g0291 others(35): Show |
40 | HG00544.hp1 HG00642.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.460-5956_460-5946d others(13): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(5): Show |
C | 7 | a0001c0003t0001g0047 a0001c0003t0001g0219 a0001c0003t0004g0258 others(4): Show |
7 | HG01167.hp1 HG01258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-5957_460-5946d others(14): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(6): Show |
C | 24 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(21): Show |
24 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.460-5958_460-5946d others(15): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(7): Show |
C | 8 | a0001c0003t0013g0025 a0001c0003t0016g0098 a0001c0005t0007g0012 others(5): Show |
9 | HG02717.hp2 HG02723.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-5959_460-5946d others(16): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0030g0077 a0001c0004t0009g0076 a0001c0004t0009g0078 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-5961_460-5946d others(18): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0247 a0001c0001t0001g0304 others(4): Show |
7 | HG00621.hp1 HG02273.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-5962_460-5946d others(19): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(11): Show |
C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(23): Show |
32 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.460-5963_460-5946d others(20): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0153 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.460-5964_460-5946d others(21): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(20): Show |
C | 1 | a0001c0007t0001g0229 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.460-5972_460-5946d others(29): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199637 | CTTTTTTT others(22): Show |
C | 1 | a0001c0002t0002g0240 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.460-5974_460-5946d others(31): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199637 | |||||||
chr6:11199676 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.460-5984A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199676 | |||||||
chr6:11199723 | A | C | 1 | a0001c0002t0002g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.460-6031T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199723 | |||||||
chr6:11199729 | C | T | 23 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(20): Show |
24 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.460-6037G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199729 | |||||||
chr6:11199922 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.460-6230G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199922 | |||||||
chr6:11199931 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(82): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.460-6239G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11199931 | |||||||
chr6:11200090 | T | G | 1 | a0001c0001t0001g0351 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.460-6398A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200090 | |||||||
chr6:11200160 | GAAC | G | 25 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(22): Show |
26 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.460-6471_460-6469d others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200160 | |||||||
chr6:11200188 | C | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(334): Show |
372 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.460-6496G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200188 | |||||||
chr6:11200341 | A | C | 102 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(99): Show |
107 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.460-6649T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200341 | |||||||
chr6:11200623 | A | C | 102 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(99): Show |
107 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.460-6931T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200623 | |||||||
chr6:11200693 | G | A | 1 | a0001c0005t0008g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460-7001C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200693 | |||||||
chr6:11200699 | G | A | 1 | a0001c0005t0008g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460-7007C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200699 | |||||||
chr6:11200744 | C | T | 1 | a0001c0003t0001g0292 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.460-7052G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200744 | |||||||
chr6:11200810 | T | C | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0005t0007g0035 |
4 | HG02976.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-7118A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200810 | |||||||
chr6:11200829 | A | G | 1 | a0001c0003t0004g0297 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.460-7137T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200829 | |||||||
chr6:11200902 | C | G | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-7210G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200902 | |||||||
chr6:11200924 | C | T | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-7232G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11200924 | |||||||
chr6:11201204 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
379 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(376): Show |
intron_variant | MODIFIER | c.460-7512G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201204 | |||||||
chr6:11201234 | A | G | 1 | a0001c0002t0006g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.460-7542T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201234 | |||||||
chr6:11201235 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(83): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.460-7543T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201235 | |||||||
chr6:11201294 | A | G | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-7602T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201294 | |||||||
chr6:11201546 | G | A | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-7854C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201546 | |||||||
chr6:11201576 | T | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(28): Show |
37 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.460-7884A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201576 | |||||||
chr6:11201576 | T | C | 1 | a0001c0003t0001g0034 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.460-7884A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201576 | |||||||
chr6:11201669 | C | T | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-7977G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201669 | |||||||
chr6:11201704 | A | AAT | 93 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(90): Show |
98 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.460-8014_460-8013d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201704 | |||||||
chr6:11201820 | C | T | 1 | a0001c0004t0005g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.460-8128G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201820 | |||||||
chr6:11201828 | CTCTGAG | C | 41 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(38): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.460-8142_460-8137d others(8): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11201828 | |||||||
chr6:11202015 | T | C | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-8323A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202015 | |||||||
chr6:11202044 | TG | T | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-8353delC | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202044 | |||||||
chr6:11202124 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(82): Show |
99 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.460-8432G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202124 | |||||||
chr6:11202325 | GGCT | G | 41 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(38): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.460-8636_460-8634d others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202325 | |||||||
chr6:11202326 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
196 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.460-8634C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202326 | |||||||
chr6:11202329 | T | A | 41 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(38): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.460-8637A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202329 | |||||||
chr6:11202371 | A | G | 95 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(92): Show |
100 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.460-8679T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202371 | |||||||
chr6:11202401 | T | G | 1 | a0001c0004t0002g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.460-8709A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202401 | |||||||
chr6:11202484 | T | C | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.460-8792A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202484 | |||||||
chr6:11202589 | G | T | 1 | a0001c0004t0005g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.460-8897C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202589 | |||||||
chr6:11202711 | A | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(28): Show |
37 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.460-9019T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202711 | |||||||
chr6:11202792 | T | C | 102 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(99): Show |
107 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.460-9100A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202792 | |||||||
chr6:11202971 | G | A | 36 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(33): Show |
36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.460-9279C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202971 | |||||||
chr6:11202986 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.460-9294G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11202986 | |||||||
chr6:11203109 | G | C | 45 | a0001c0003t0001g0047 a0001c0003t0001g0123 a0001c0003t0001g0178 others(42): Show |
46 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.460-9417C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203109 | |||||||
chr6:11203172 | G | A | 1 | a0001c0001t0031g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460-9480C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203172 | |||||||
chr6:11203301 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.460-9609C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203301 | |||||||
chr6:11203453 | C | T | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-9761G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203453 | |||||||
chr6:11203673 | T | G | 107 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(104): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.459+9608A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203673 | |||||||
chr6:11203745 | C | T | 1 | a0001c0006t0003g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.459+9536G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203745 | |||||||
chr6:11203823 | T | C | 2 | a0001c0005t0001g0262 a0001c0005t0009g0051 |
2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.459+9458A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203823 | |||||||
chr6:11203975 | T | TA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(35): Show |
45 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.459+9305dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203975 | |||||||
chr6:11203975 | T | TAA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(83): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.459+9304_459+9305d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203975 | |||||||
chr6:11203975 | TAA | T | 45 | a0001c0003t0001g0047 a0001c0003t0001g0123 a0001c0003t0001g0178 others(42): Show |
46 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.459+9304_459+9305d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11203975 | |||||||
chr6:11204238 | C | T | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.459+9043G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204238 | |||||||
chr6:11204283 | A | C | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.459+8998T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204283 | |||||||
chr6:11204339 | A | G | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+8942T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204339 | |||||||
chr6:11204372 | T | G | 2 | a0001c0004t0005g0061 a0001c0004t0005g0062 |
2 | HG01943.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.459+8909A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204372 | |||||||
chr6:11204447 | C | T | 41 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(38): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.459+8834G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204447 | |||||||
chr6:11204517 | T | C | 52 | a0001c0003t0001g0047 a0001c0003t0001g0123 a0001c0003t0001g0178 others(49): Show |
53 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.459+8764A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204517 | |||||||
chr6:11204522 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459+8759G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204522 | |||||||
chr6:11204652 | G | A | 1 | a0001c0021t0005g0332 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.459+8629C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204652 | |||||||
chr6:11204669 | G | A | 40 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(37): Show |
41 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.459+8612C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204669 | |||||||
chr6:11204681 | C | T | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.459+8600G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204681 | |||||||
chr6:11204719 | C | A | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+8562G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204719 | |||||||
chr6:11204719 | C | CA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(77): Show |
88 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.459+8561dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204719 | |||||||
chr6:11204719 | C | CAA | 78 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0017 others(75): Show |
86 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.459+8560_459+8561d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204719 | |||||||
chr6:11204719 | C | CAAA | 46 | a0001c0001t0003g0052 a0001c0001t0026g0269 a0001c0002t0002g0156 others(43): Show |
50 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.459+8559_459+8561d others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204719 | |||||||
chr6:11204719 | CA | C | 6 | a0001c0003t0016g0098 a0001c0005t0006g0138 a0001c0005t0007g0012 others(3): Show |
7 | HG02717.hp2 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+8561delT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204719 | |||||||
chr6:11204737 | AG | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0071 others(9): Show |
13 | HG00733.hp1 HG00738.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+8543delC | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204737 | |||||||
chr6:11204738 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.459+8543C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204738 | |||||||
chr6:11204742 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0255 |
2 | NA18942.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.459+8539C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204742 | |||||||
chr6:11204769 | A | C | 2 | a0001c0001t0001g0314 a0001c0004t0023g0315 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459+8512T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204769 | |||||||
chr6:11204778 | T | C | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+8503A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204778 | |||||||
chr6:11204779 | G | A | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+8502C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204779 | |||||||
chr6:11204807 | A | G | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+8474T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204807 | |||||||
chr6:11204911 | C | G | 1 | a0001c0001t0003g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459+8370G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11204911 | |||||||
chr6:11205039 | G | A | 1 | a0001c0005t0005g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.459+8242C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205039 | |||||||
chr6:11205111 | A | G | 7 | a0001c0005t0002g0028 a0001c0005t0002g0081 a0001c0005t0002g0082 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+8170T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205111 | |||||||
chr6:11205112 | T | C | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.459+8169A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205112 | |||||||
chr6:11205202 | C | A | 1 | a0001c0004t0005g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459+8079G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205202 | |||||||
chr6:11205249 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.459+8032C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205249 | |||||||
chr6:11205318 | C | A | 1 | a0001c0004t0002g0117 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.459+7963G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205318 | |||||||
chr6:11205351 | A | G | 1 | a0002c0031t0011g0340 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459+7930T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205351 | |||||||
chr6:11205352 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.459+7929A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205352 | |||||||
chr6:11205378 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.459+7903C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205378 | |||||||
chr6:11205631 | T | C | 2 | a0001c0001t0012g0073 a0001c0001t0026g0269 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.459+7650A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205631 | |||||||
chr6:11205880 | G | A | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+7401C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205880 | |||||||
chr6:11205953 | A | G | 2 | a0001c0001t0012g0073 a0001c0001t0026g0269 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.459+7328T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205953 | |||||||
chr6:11205981 | C | T | 1 | a0001c0005t0002g0280 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.459+7300G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11205981 | |||||||
chr6:11206037 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.459+7244T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206037 | |||||||
chr6:11206068 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0144 others(10): Show |
15 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.459+7213C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206068 | |||||||
chr6:11206124 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(30): Show |
39 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.459+7157T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206124 | |||||||
chr6:11206141 | G | A | 1 | a0001c0005t0002g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.459+7140C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206141 | |||||||
chr6:11206375 | C | T | 1 | a0001c0002t0002g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.459+6906G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206375 | |||||||
chr6:11206379 | A | G | 1 | a0001c0003t0001g0222 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.459+6902T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206379 | |||||||
chr6:11206566 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0093 |
3 | NA18975.hp1 NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.459+6715C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206566 | |||||||
chr6:11206691 | G | A | 1 | a0001c0015t0013g0026 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.459+6590C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206691 | |||||||
chr6:11206810 | TA | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
375 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.459+6470delT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11206810 | |||||||
chr6:11207076 | C | G | 1 | a0001c0004t0002g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.459+6205G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207076 | |||||||
chr6:11207147 | A | T | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+6134T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207147 | |||||||
chr6:11207218 | A | T | 1 | a0001c0004t0002g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.459+6063T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207218 | |||||||
chr6:11207231 | A | G | 7 | a0001c0005t0002g0028 a0001c0005t0002g0081 a0001c0005t0002g0082 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+6050T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207231 | |||||||
chr6:11207454 | C | T | 35 | a0001c0003t0001g0139 a0001c0003t0001g0219 a0001c0003t0001g0256 others(32): Show |
38 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.459+5827G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207454 | |||||||
chr6:11207923 | A | T | 7 | a0001c0001t0001g0314 a0001c0001t0029g0316 a0001c0004t0002g0317 others(4): Show |
8 | HG01496.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+5358T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11207923 | |||||||
chr6:11208007 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(29): Show |
38 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+5274C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208007 | |||||||
chr6:11208007 | G | T | 1 | a0001c0005t0006g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.459+5274C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208007 | |||||||
chr6:11208124 | G | C | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+5157C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208124 | |||||||
chr6:11208177 | C | CA | 12 | a0001c0001t0001g0110 a0001c0001t0001g0215 a0001c0002t0002g0130 others(9): Show |
12 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+5103dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208177 | |||||||
chr6:11208218 | C | A | 1 | a0001c0008t0007g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.459+5063G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208218 | |||||||
chr6:11208457 | C | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(29): Show |
38 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+4824G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208457 | |||||||
chr6:11208582 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(83): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.459+4699T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208582 | |||||||
chr6:11208647 | T | C | 46 | a0001c0003t0001g0047 a0001c0003t0001g0123 a0001c0003t0001g0178 others(43): Show |
47 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.459+4634A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208647 | |||||||
chr6:11208970 | A | G | 1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.459+4311T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11208970 | |||||||
chr6:11209096 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.459+4185G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209096 | |||||||
chr6:11209398 | C | T | 1 | a0001c0003t0001g0219 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.459+3883G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209398 | |||||||
chr6:11209436 | C | G | 4 | a0001c0007t0001g0326 a0001c0007t0001g0331 a0001c0007t0001g0346 others(1): Show |
4 | HG01175.hp2 HG01261.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3845G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209436 | |||||||
chr6:11209729 | T | C | 3 | a0001c0002t0002g0164 a0001c0002t0002g0196 a0001c0002t0002g0197 |
3 | HG00438.hp1 NA18973.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.459+3552A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209729 | |||||||
chr6:11209921 | G | C | 1 | a0003c0010t0003g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.459+3360C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209921 | |||||||
chr6:11209970 | C | CTTTTTTT others(4): Show |
2 | a0001c0005t0008g0181 a0001c0015t0003g0099 |
2 | HG00735.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.459+3310_459+3311i others(13): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209970 | C | CTTTTTTT others(5): Show |
40 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(37): Show |
41 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.459+3310_459+3311i others(14): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209970 | C | CTTTTTTT others(6): Show |
50 | a0001c0003t0001g0034 a0001c0003t0001g0139 a0001c0003t0001g0219 others(47): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.459+3310_459+3311i others(15): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209970 | C | CTTTTTTT others(7): Show |
78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(75): Show |
92 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.459+3310_459+3311i others(16): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209970 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0236 a0001c0001t0001g0278 a0001c0004t0002g0185 others(3): Show |
6 | HG00438.hp2 HG04199.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+3310_459+3311i others(17): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209970 | C | CTTTTTTT others(9): Show |
1 | a0001c0004t0027g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.459+3310_459+3311i others(18): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209970 | |||||||
chr6:11209975 | T | TTTTTTTG others(6): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0303 a0001c0001t0001g0357 |
3 | HG02523.hp2 NA18942.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.459+3305_459+3306i others(15): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209975 | |||||||
chr6:11209975 | T | TTTTTTTT others(5): Show |
1 | a0001c0004t0002g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.459+3305_459+3306i others(14): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209975 | |||||||
chr6:11209975 | T | TTTTTTTT others(6): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(24): Show |
33 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.459+3305_459+3306i others(15): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11209975 | |||||||
chr6:11210101 | G | A | 42 | a0001c0003t0001g0123 a0001c0003t0001g0178 a0001c0003t0001g0179 others(39): Show |
43 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.459+3180C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210101 | |||||||
chr6:11210263 | C | T | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0005t0007g0035 |
4 | HG02976.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3018G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210263 | |||||||
chr6:11210335 | C | G | 102 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(99): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.459+2946G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210335 | |||||||
chr6:11210473 | G | A | 50 | a0001c0003t0001g0034 a0001c0003t0001g0139 a0001c0003t0001g0219 others(47): Show |
54 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.459+2808C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210473 | |||||||
chr6:11210526 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.459+2755T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210526 | |||||||
chr6:11210545 | A | C | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0005t0007g0035 |
4 | HG02976.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+2736T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210545 | |||||||
chr6:11210766 | G | GAGAGAGA others(8): Show |
1 | a0001c0004t0002g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.459+2514_459+2515i others(17): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGA | 12 | a0001c0001t0001g0104 a0001c0002t0002g0131 a0001c0002t0002g0156 others(9): Show |
13 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+2513_459+2514d others(4): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGA | 97 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0003g0009 others(94): Show |
106 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.459+2511_459+2514d others(6): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGA | 52 | a0001c0001t0003g0075 a0001c0001t0012g0073 a0001c0003t0001g0139 others(49): Show |
56 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.459+2509_459+2514d others(8): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGAG others(1): Show |
122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(119): Show |
136 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.459+2507_459+2514d others(10): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGAG others(3): Show |
17 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0304 others(14): Show |
18 | HG00323.hp1 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.459+2505_459+2514d others(12): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGAG others(5): Show |
4 | a0001c0001t0003g0125 a0001c0001t0029g0316 a0001c0004t0002g0317 others(1): Show |
4 | HG03195.hp2 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+2503_459+2514d others(14): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGAG others(7): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(18): Show |
27 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+2501_459+2514d others(16): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGAGAGAG others(9): Show |
2 | a0001c0001t0001g0042 a0001c0002t0002g0164 |
2 | HG01978.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.459+2499_459+2514d others(18): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210766 | G | GGGAGAGA others(8): Show |
1 | a0001c0004t0002g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.459+2514_459+2515i others(17): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210766 | |||||||
chr6:11210789 | G | GAGAGAGA others(5): Show |
1 | a0001c0003t0025g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459+2491_459+2492i others(14): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210789 | |||||||
chr6:11210793 | T | A | 1 | a0001c0003t0025g0173 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459+2488A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210793 | |||||||
chr6:11210820 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(83): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.459+2461T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210820 | |||||||
chr6:11210827 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.459+2454T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210827 | |||||||
chr6:11210842 | C | T | 1 | a0001c0002t0006g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.459+2439G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210842 | |||||||
chr6:11210850 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(83): Show |
100 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.459+2431A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210850 | |||||||
chr6:11210866 | C | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.459+2415G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11210866 | |||||||
chr6:11211018 | T | G | 1 | a0001c0003t0001g0248 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.459+2263A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211018 | |||||||
chr6:11211161 | G | C | 1 | a0001c0015t0003g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.459+2120C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211161 | |||||||
chr6:11211182 | G | A | 2 | a0001c0003t0001g0281 a0001c0003t0003g0282 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+2099C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211182 | |||||||
chr6:11211191 | A | T | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0005t0007g0035 |
4 | HG02976.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+2090T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211191 | |||||||
chr6:11211245 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459+2036C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211245 | |||||||
chr6:11211515 | A | G | 2 | a0001c0008t0002g0309 a0001c0008t0002g0313 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.459+1766T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211515 | |||||||
chr6:11211581 | C | G | 1 | a0001c0001t0031g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459+1700G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211581 | |||||||
chr6:11211661 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(84): Show |
101 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.459+1620A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211661 | |||||||
chr6:11211746 | C | T | 1 | a0001c0033t0002g0312 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+1535G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211746 | |||||||
chr6:11211774 | C | T | 1 | a0001c0002t0006g0325 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.459+1507G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211774 | |||||||
chr6:11211839 | G | A | 1 | a0001c0005t0008g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.459+1442C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211839 | |||||||
chr6:11211964 | A | AGTATCCT others(6): Show |
354 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(351): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.459+1316_459+1317i others(15): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11211964 | |||||||
chr6:11212102 | C | G | 1 | a0001c0001t0003g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.459+1179G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212102 | |||||||
chr6:11212102 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.459+1179G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212102 | |||||||
chr6:11212145 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.459+1136A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212145 | |||||||
chr6:11212292 | G | A | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0005t0007g0035 |
4 | HG02976.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+989C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212292 | |||||||
chr6:11212369 | T | C | 12 | a0001c0001t0001g0314 a0001c0001t0003g0125 a0001c0001t0029g0316 others(9): Show |
13 | HG01496.hp2 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+912A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212369 | |||||||
chr6:11212521 | G | A | 96 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(93): Show |
101 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.459+760C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212521 | |||||||
chr6:11212726 | G | A | 96 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(93): Show |
101 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.459+555C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212726 | |||||||
chr6:11212791 | C | A | 3 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+490G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11212791 | |||||||
chr6:11213088 | G | A | 4 | a0001c0003t0001g0047 a0001c0003t0001g0183 a0001c0003t0001g0265 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+193C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11213088 | |||||||
chr6:11213114 | A | G | 92 | a0001c0003t0001g0034 a0001c0003t0001g0123 a0001c0003t0001g0139 others(89): Show |
97 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.459+167T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11213114 | |||||||
chr6:11213235 | A | G | 96 | a0001c0003t0001g0034 a0001c0003t0001g0047 a0001c0003t0001g0123 others(93): Show |
101 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.459+46T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 2/6 | chr6 | 11213235 | |||||||
chr6:11213850 | A | T | 2 | a0001c0002t0002g0159 a0008c0032t0002g0218 |
2 | NA18945.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.13-123T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11213850 | |||||||
chr6:11213859 | A | T | 167 | a0001c0001t0001g0101 a0001c0001t0001g0321 a0001c0001t0001g0322 others(164): Show |
180 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.13-132T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11213859 | |||||||
chr6:11213983 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(303): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.13-256A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11213983 | |||||||
chr6:11214038 | C | T | 1 | a0001c0004t0002g0194 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.13-311G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214038 | |||||||
chr6:11214170 | C | T | 1 | a0001c0005t0006g0137 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.13-443G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214170 | |||||||
chr6:11214335 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG00609.hp1 HG00673.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-608G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214335 | |||||||
chr6:11214469 | T | C | 1 | a0001c0001t0003g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.13-742A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214469 | |||||||
chr6:11214472 | G | A | 211 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0063 others(208): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.13-745C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214472 | |||||||
chr6:11214699 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0234 a0001c0004t0002g0233 |
7 | HG01257.hp1 HG01258.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-972A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214699 | |||||||
chr6:11214764 | C | T | 5 | a0001c0001t0003g0052 a0001c0001t0012g0073 a0001c0004t0002g0054 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-1037G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214764 | |||||||
chr6:11214979 | C | T | 11 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0001t0012g0073 others(8): Show |
11 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.13-1252G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11214979 | |||||||
chr6:11215050 | G | C | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13-1323C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215050 | |||||||
chr6:11215076 | C | T | 1 | a0001c0004t0002g0193 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-1349G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215076 | |||||||
chr6:11215145 | G | A | 1 | a0002c0025t0003g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.13-1418C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215145 | |||||||
chr6:11215148 | C | T | 4 | a0001c0002t0002g0129 a0001c0002t0002g0130 a0001c0002t0005g0013 others(1): Show |
5 | HG00642.hp2 HG00741.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-1421G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215148 | |||||||
chr6:11215321 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.13-1594G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215321 | |||||||
chr6:11215333 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.13-1606G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215333 | |||||||
chr6:11215440 | A | G | 11 | a0001c0001t0003g0125 a0001c0001t0026g0269 a0001c0001t0030g0077 others(8): Show |
11 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.13-1713T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215440 | |||||||
chr6:11215467 | G | C | 2 | a0001c0001t0001g0334 a0001c0001t0001g0344 |
2 | HG00140.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.13-1740C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215467 | |||||||
chr6:11215509 | G | T | 1 | a0001c0001t0001g0278 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.13-1782C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215509 | |||||||
chr6:11215565 | T | C | 4 | a0001c0003t0013g0025 a0001c0003t0017g0027 a0001c0003t0028g0046 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-1838A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215565 | |||||||
chr6:11215688 | C | T | 3 | a0001c0003t0016g0098 a0001c0005t0007g0012 a0001c0015t0003g0099 |
4 | HG00735.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-1961G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215688 | |||||||
chr6:11215716 | G | T | 1 | a0001c0002t0002g0345 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.13-1989C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215716 | |||||||
chr6:11215809 | A | C | 12 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 others(9): Show |
14 | HG00735.hp1 HG02622.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-2082T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215809 | |||||||
chr6:11215841 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0001t0001g0235 |
3 | HG02056.hp1 NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.13-2114C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215841 | |||||||
chr6:11215870 | A | C | 24 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0167 others(21): Show |
25 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.13-2143T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215870 | |||||||
chr6:11215945 | A | G | 4 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0004t0002g0054 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-2218T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11215945 | |||||||
chr6:11216046 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(298): Show |
330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.13-2319A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216046 | |||||||
chr6:11216064 | T | C | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13-2337A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216064 | |||||||
chr6:11216196 | G | A | 1 | a0001c0001t0003g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.13-2469C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216196 | |||||||
chr6:11216214 | T | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.13-2487A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216214 | |||||||
chr6:11216262 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.13-2535C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216262 | |||||||
chr6:11216285 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.13-2558C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216285 | |||||||
chr6:11216315 | G | T | 3 | a0001c0003t0013g0025 a0001c0003t0017g0027 a0001c0015t0013g0026 |
3 | HG02723.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.13-2588C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216315 | |||||||
chr6:11216371 | G | T | 2 | a0001c0004t0005g0044 a0001c0004t0027g0045 |
2 | HG00099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.13-2644C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216371 | |||||||
chr6:11216429 | AAT | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0238 a0001c0001t0001g0239 others(3): Show |
7 | HG00735.hp2 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.13-2704_13-2703del others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216429 | |||||||
chr6:11216467 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(293): Show |
325 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.13-2740T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216467 | |||||||
chr6:11216476 | G | A | 1 | a0007c0026t0014g0318 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13-2749C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216476 | |||||||
chr6:11216493 | G | A | 42 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-2766C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216493 | |||||||
chr6:11216549 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(29): Show |
38 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.13-2822T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216549 | |||||||
chr6:11216552 | A | G | 5 | a0001c0001t0003g0125 a0001c0001t0030g0077 a0001c0004t0009g0076 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-2825T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216552 | |||||||
chr6:11216693 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(28): Show |
37 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.13-2966C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216693 | |||||||
chr6:11216744 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(112): Show |
134 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.13-3017A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216744 | |||||||
chr6:11216772 | C | T | 3 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-3045G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216772 | |||||||
chr6:11216788 | C | G | 42 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-3061G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216788 | |||||||
chr6:11216840 | T | C | 27 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0167 others(24): Show |
28 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.13-3113A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216840 | |||||||
chr6:11216863 | A | T | 6 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0003t0001g0047 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-3136T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216863 | |||||||
chr6:11216952 | T | G | 10 | a0001c0001t0003g0125 a0001c0001t0030g0077 a0001c0004t0009g0076 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-3225A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11216952 | |||||||
chr6:11217031 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0109 a0001c0001t0001g0110 |
5 | HG00733.hp1 HG01070.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-3304T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217031 | |||||||
chr6:11217166 | C | G | 12 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 others(9): Show |
14 | HG00735.hp1 HG02622.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-3439G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217166 | |||||||
chr6:11217495 | C | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.13-3768G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217495 | |||||||
chr6:11217610 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(214): Show |
243 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.13-3883C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217610 | |||||||
chr6:11217643 | G | A | 14 | a0001c0001t0001g0101 a0001c0002t0002g0188 a0001c0002t0002g0189 others(11): Show |
14 | HG00323.hp1 HG00741.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.13-3916C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217643 | |||||||
chr6:11217656 | T | C | 1 | a0001c0002t0002g0157 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.13-3929A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217656 | |||||||
chr6:11217664 | T | C | 40 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 others(37): Show |
42 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.13-3937A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217664 | |||||||
chr6:11217679 | G | A | 1 | a0001c0007t0001g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.13-3952C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217679 | |||||||
chr6:11217738 | A | G | 3 | a0001c0002t0009g0310 a0001c0007t0001g0092 a0001c0007t0001g0311 |
3 | HG01361.hp2 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.13-4011T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217738 | |||||||
chr6:11217891 | C | T | 42 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-4164G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217891 | |||||||
chr6:11217928 | T | C | 42 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-4201A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217928 | |||||||
chr6:11217933 | G | C | 42 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(39): Show |
42 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.13-4206C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11217933 | |||||||
chr6:11218006 | G | A | 3 | a0001c0011t0007g0146 a0001c0011t0008g0147 a0001c0011t0032g0358 |
3 | HG02055.hp1 HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.13-4279C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218006 | |||||||
chr6:11218006 | G | C | 12 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0001t0012g0073 others(9): Show |
12 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-4279C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218006 | |||||||
chr6:11218014 | G | A | 1 | a0001c0007t0001g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.13-4287C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218014 | |||||||
chr6:11218051 | T | C | 1 | a0001c0003t0001g0123 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.13-4324A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218051 | |||||||
chr6:11218188 | A | C | 2 | a0001c0005t0001g0262 a0001c0005t0009g0051 |
2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.13-4461T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218188 | |||||||
chr6:11218308 | C | T | 47 | a0001c0001t0001g0101 a0001c0001t0003g0052 a0001c0001t0003g0075 others(44): Show |
47 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.13-4581G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218308 | |||||||
chr6:11218345 | CT | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(215): Show |
244 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.13-4619delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218345 | |||||||
chr6:11218345 | CTT | C | 8 | a0001c0001t0001g0337 a0001c0002t0002g0240 a0001c0003t0001g0281 others(5): Show |
8 | HG00738.hp1 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.13-4620_13-4619del others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218345 | |||||||
chr6:11218474 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0242 a0001c0004t0005g0241 |
4 | HG00735.hp2 HG01123.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-4747A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218474 | |||||||
chr6:11218499 | C | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.13-4772G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218499 | |||||||
chr6:11218621 | A | C | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13-4894T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218621 | |||||||
chr6:11218794 | T | C | 2 | a0001c0004t0005g0044 a0001c0004t0027g0045 |
2 | HG00099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.13-5067A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218794 | |||||||
chr6:11218797 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(198): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.13-5070G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218797 | |||||||
chr6:11218837 | G | C | 7 | a0001c0003t0001g0034 a0001c0003t0012g0029 a0001c0003t0012g0032 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-5110C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218837 | |||||||
chr6:11218930 | A | G | 2 | a0001c0005t0008g0086 a0003c0027t0018g0087 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.13-5203T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11218930 | |||||||
chr6:11219187 | A | G | 29 | a0001c0001t0001g0101 a0001c0002t0002g0182 a0001c0002t0002g0188 others(26): Show |
29 | HG00323.hp1 HG00642.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.13-5460T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219187 | |||||||
chr6:11219321 | C | T | 12 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 others(9): Show |
14 | HG00735.hp1 HG02622.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-5594G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219321 | |||||||
chr6:11219452 | A | G | 1 | a0001c0002t0002g0324 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.13-5725T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219452 | |||||||
chr6:11219503 | C | G | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13-5776G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219503 | |||||||
chr6:11219543 | C | G | 1 | a0001c0003t0001g0292 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.13-5816G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219543 | |||||||
chr6:11219591 | C | T | 12 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0008g0049 others(9): Show |
14 | HG00735.hp1 HG02622.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-5864G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219591 | |||||||
chr6:11219676 | G | A | 5 | a0001c0001t0003g0125 a0001c0001t0030g0077 a0001c0004t0009g0076 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-5949C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219676 | |||||||
chr6:11219803 | T | C | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-6076A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219803 | |||||||
chr6:11219939 | C | T | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.13-6212G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11219939 | |||||||
chr6:11220184 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
373 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.13-6457T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220184 | |||||||
chr6:11220314 | C | T | 1 | a0001c0002t0002g0345 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.13-6587G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220314 | |||||||
chr6:11220320 | C | T | 2 | a0001c0002t0005g0013 a0001c0002t0005g0128 |
3 | HG00642.hp2 HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.13-6593G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220320 | |||||||
chr6:11220324 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(26): Show |
35 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.13-6597C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220324 | |||||||
chr6:11220350 | C | T | 7 | a0001c0002t0002g0050 a0001c0002t0008g0049 a0001c0003t0016g0098 others(4): Show |
8 | HG00735.hp1 HG02622.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-6623G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220350 | |||||||
chr6:11220591 | A | G | 7 | a0001c0003t0001g0034 a0001c0003t0012g0029 a0001c0003t0012g0032 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.13-6864T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220591 | |||||||
chr6:11220715 | T | G | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13-6988A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220715 | |||||||
chr6:11220932 | A | G | 1 | a0001c0005t0006g0169 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13-7205T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220932 | |||||||
chr6:11220934 | T | A | 24 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0167 others(21): Show |
25 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.13-7207A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11220934 | |||||||
chr6:11221060 | G | A | 2 | a0001c0005t0008g0086 a0003c0027t0018g0087 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.13-7333C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221060 | |||||||
chr6:11221106 | C | T | 24 | a0001c0001t0001g0063 a0001c0001t0001g0071 a0001c0001t0001g0167 others(21): Show |
25 | HG00140.hp1 HG00423.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.13-7379G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221106 | |||||||
chr6:11221160 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.13-7433T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221160 | |||||||
chr6:11221208 | C | A | 3 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0002t0002g0043 |
3 | HG03239.hp2 HG03491.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.13-7481G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221208 | |||||||
chr6:11221244 | A | G | 1 | a0001c0008t0002g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.13-7517T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221244 | |||||||
chr6:11221382 | T | TA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.13-7656dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221382 | |||||||
chr6:11221622 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0104 others(21): Show |
26 | HG00609.hp1 HG00673.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.13-7895G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221622 | |||||||
chr6:11221631 | A | T | 2 | a0001c0004t0005g0044 a0001c0004t0027g0045 |
2 | HG00099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.13-7904T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221631 | |||||||
chr6:11221697 | G | A | 2 | a0001c0004t0002g0243 a0001c0004t0005g0161 |
2 | HG01243.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.13-7970C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221697 | |||||||
chr6:11221732 | T | C | 17 | a0001c0001t0001g0314 a0001c0001t0029g0316 a0001c0002t0009g0310 others(14): Show |
18 | HG01361.hp2 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.13-8005A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221732 | |||||||
chr6:11221744 | A | G | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-8017T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221744 | |||||||
chr6:11221841 | T | C | 1 | a0001c0006t0003g0004 | 4 | HG01070.hp1 HG01071.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-8114A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221841 | |||||||
chr6:11221907 | A | G | 2 | a0001c0005t0008g0086 a0003c0027t0018g0087 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.13-8180T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11221907 | |||||||
chr6:11222071 | C | A | 4 | a0001c0001t0030g0077 a0001c0004t0009g0076 a0001c0004t0009g0078 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-8344G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11222071 | |||||||
chr6:11222107 | G | C | 10 | a0001c0001t0003g0125 a0001c0001t0030g0077 a0001c0004t0009g0076 others(7): Show |
10 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-8380C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11222107 | |||||||
chr6:11222293 | T | C | 4 | a0001c0003t0013g0025 a0001c0003t0017g0027 a0001c0003t0028g0046 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-8566A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11222293 | |||||||
chr6:11222975 | C | T | 52 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(49): Show |
59 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.13-9248G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11222975 | |||||||
chr6:11223150 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(126): Show |
146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.12+9354T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223150 | |||||||
chr6:11223487 | G | GA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
204 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.12+9016dupT | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223487 | |||||||
chr6:11223497 | C | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(213): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.12+9007G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223497 | |||||||
chr6:11223527 | T | C | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.12+8977A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223527 | |||||||
chr6:11223671 | G | A | 4 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0004t0002g0054 others(1): Show |
4 | HG02486.hp2 HG02559.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+8833C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223671 | |||||||
chr6:11223682 | G | A | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+8822C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223682 | |||||||
chr6:11223844 | C | T | 6 | a0001c0001t0003g0052 a0001c0001t0003g0075 a0001c0003t0001g0047 others(3): Show |
6 | HG02486.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+8660G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223844 | |||||||
chr6:11223849 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(115): Show |
135 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.12+8655G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223849 | |||||||
chr6:11223878 | C | T | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
375 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.12+8626G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223878 | |||||||
chr6:11223909 | A | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(27): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.12+8595T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11223909 | |||||||
chr6:11224192 | C | T | 17 | a0001c0001t0001g0314 a0001c0001t0029g0316 a0001c0002t0009g0310 others(14): Show |
18 | HG01361.hp2 HG01496.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.12+8312G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224192 | |||||||
chr6:11224224 | A | G | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+8280T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224224 | |||||||
chr6:11224233 | C | G | 5 | a0001c0005t0002g0283 a0001c0005t0002g0284 a0001c0005t0002g0288 others(2): Show |
5 | HG04115.hp1 NA18959.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+8271G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224233 | |||||||
chr6:11224354 | C | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(26): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.12+8150G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224354 | |||||||
chr6:11224444 | G | C | 13 | a0001c0002t0002g0074 a0001c0002t0002g0129 a0001c0002t0002g0130 others(10): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.12+8060C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224444 | |||||||
chr6:11224480 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
253 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.12+8024A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224480 | |||||||
chr6:11224515 | A | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(147): Show |
168 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.12+7989T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224515 | |||||||
chr6:11224635 | AT | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(60): Show |
71 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.12+7868delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224635 | |||||||
chr6:11224636 | T | A | 1 | a0001c0001t0001g0351 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.12+7868A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224636 | |||||||
chr6:11224780 | A | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.12+7724T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224780 | |||||||
chr6:11224972 | A | G | 12 | a0001c0003t0001g0034 a0001c0003t0012g0029 a0001c0003t0012g0032 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.12+7532T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11224972 | |||||||
chr6:11225041 | A | T | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+7463T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225041 | |||||||
chr6:11225283 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.12+7221T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225283 | |||||||
chr6:11225562 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(168): Show |
184 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.12+6942A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225562 | |||||||
chr6:11225722 | G | C | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.12+6782C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225722 | |||||||
chr6:11225753 | G | A | 33 | a0001c0001t0001g0291 a0001c0001t0001g0350 a0001c0003t0001g0256 others(30): Show |
36 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.12+6751C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225753 | |||||||
chr6:11225776 | C | T | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+6728G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225776 | |||||||
chr6:11225796 | C | T | 88 | a0001c0001t0001g0291 a0001c0001t0001g0321 a0001c0001t0001g0322 others(85): Show |
93 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.12+6708G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225796 | |||||||
chr6:11225800 | C | CT | 12 | a0001c0005t0008g0086 a0001c0006t0003g0006 a0001c0006t0003g0094 others(9): Show |
15 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.12+6703dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225800 | |||||||
chr6:11225800 | CT | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(153): Show |
176 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.12+6703delA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225800 | |||||||
chr6:11225819 | T | A | 7 | a0001c0001t0003g0125 a0001c0001t0030g0077 a0001c0004t0009g0076 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+6685A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225819 | |||||||
chr6:11225820 | A | G | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0323 |
3 | HG03688.hp1 HG03834.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.12+6684T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225820 | |||||||
chr6:11225872 | G | A | 2 | a0001c0002t0002g0345 a0001c0007t0001g0346 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.12+6632C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11225872 | |||||||
chr6:11226067 | C | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(143): Show |
158 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.12+6437G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226067 | |||||||
chr6:11226207 | C | T | 1 | a0006c0028t0002g0320 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.12+6297G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226207 | |||||||
chr6:11226263 | T | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(102): Show |
115 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.12+6241A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226263 | |||||||
chr6:11226267 | G | A | 6 | a0001c0002t0002g0050 a0001c0002t0008g0049 a0001c0003t0016g0098 others(3): Show |
7 | HG00735.hp1 HG02976.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+6237C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226267 | |||||||
chr6:11226405 | G | T | 2 | a0001c0005t0001g0262 a0001c0005t0009g0051 |
2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.12+6099C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226405 | |||||||
chr6:11226421 | C | G | 1 | a0001c0003t0004g0319 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.12+6083G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226421 | |||||||
chr6:11226591 | A | T | 6 | a0001c0002t0002g0050 a0001c0002t0008g0049 a0001c0003t0016g0098 others(3): Show |
7 | HG00735.hp1 HG02976.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+5913T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226591 | |||||||
chr6:11226600 | G | A | 1 | a0001c0007t0001g0251 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.12+5904C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226600 | |||||||
chr6:11226615 | A | AT | 101 | a0001c0001t0001g0278 a0001c0001t0001g0291 a0001c0001t0001g0321 others(98): Show |
107 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.12+5888dupA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226615 | |||||||
chr6:11226759 | T | A | 2 | a0001c0004t0005g0044 a0001c0004t0027g0045 |
2 | HG00099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.12+5745A>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226759 | |||||||
chr6:11226778 | A | G | 1 | a0001c0017t0001g0158 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.12+5726T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226778 | |||||||
chr6:11226800 | A | G | 2 | a0001c0002t0002g0156 a0001c0002t0002g0157 |
2 | HG02040.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.12+5704T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226800 | |||||||
chr6:11226922 | A | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0022t0001g0273 |
3 | HG02735.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.12+5582T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226922 | |||||||
chr6:11226931 | C | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.12+5573G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11226931 | |||||||
chr6:11227000 | T | G | 20 | a0001c0001t0001g0314 a0001c0001t0029g0316 a0001c0002t0009g0310 others(17): Show |
21 | HG00099.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+5504A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227000 | |||||||
chr6:11227013 | A | G | 106 | a0001c0001t0001g0278 a0001c0001t0001g0291 a0001c0001t0001g0321 others(103): Show |
111 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.12+5491T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227013 | |||||||
chr6:11227036 | A | T | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+5468T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227036 | |||||||
chr6:11227095 | C | T | 100 | a0001c0001t0001g0278 a0001c0001t0001g0291 a0001c0001t0001g0321 others(97): Show |
105 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.12+5409G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227095 | |||||||
chr6:11227152 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.12+5352A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227152 | |||||||
chr6:11227172 | A | G | 2 | a0001c0004t0005g0058 a0004c0014t0002g0154 |
2 | NA18967.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.12+5332T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227172 | |||||||
chr6:11227297 | A | G | 1 | a0001c0006t0003g0057 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.12+5207T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227297 | |||||||
chr6:11227488 | C | CA | 32 | a0001c0001t0001g0314 a0001c0001t0003g0125 a0001c0001t0029g0316 others(29): Show |
33 | HG00099.hp1 HG01496.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.12+5015_12+5016ins others(1): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227488 | |||||||
chr6:11227504 | T | C | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+5000A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227504 | |||||||
chr6:11227599 | C | T | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+4905G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227599 | |||||||
chr6:11227736 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(276): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.12+4768T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227736 | |||||||
chr6:11227754 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(164): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.12+4750C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227754 | |||||||
chr6:11227767 | G | A | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+4737C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227767 | |||||||
chr6:11227804 | A | AGAGGT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(169): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.12+4695_12+4699dup others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227804 | |||||||
chr6:11227875 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.12+4629T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227875 | |||||||
chr6:11227895 | G | A | 1 | a0001c0012t0004g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.12+4609C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227895 | |||||||
chr6:11227911 | C | G | 1 | a0001c0001t0003g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.12+4593G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227911 | |||||||
chr6:11227930 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.12+4574T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227930 | |||||||
chr6:11227952 | C | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.12+4552G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11227952 | |||||||
chr6:11228066 | G | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.12+4438C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228066 | |||||||
chr6:11228068 | G | A | 2 | a0003c0010t0003g0036 a0003c0010t0003g0037 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.12+4436C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228068 | |||||||
chr6:11228069 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.12+4435T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228069 | |||||||
chr6:11228106 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(199): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.12+4398C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228106 | |||||||
chr6:11228106 | G | GC | 13 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
17 | HG01175.hp1 HG01346.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.12+4397dupG | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228106 | |||||||
chr6:11228106 | G | T | 45 | a0001c0001t0001g0291 a0001c0001t0001g0303 a0001c0001t0001g0304 others(42): Show |
49 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.12+4398C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228106 | |||||||
chr6:11228113 | A | G | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+4391T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228113 | |||||||
chr6:11228121 | G | T | 1 | a0001c0006t0003g0140 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.12+4383C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228121 | |||||||
chr6:11228160 | G | A | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+4344C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228160 | |||||||
chr6:11228181 | G | A | 2 | a0001c0004t0005g0044 a0001c0004t0027g0045 |
2 | HG00099.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.12+4323C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228181 | |||||||
chr6:11228256 | T | C | 9 | a0001c0003t0001g0034 a0001c0003t0001g0265 a0001c0003t0012g0029 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.12+4248A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228256 | |||||||
chr6:11228257 | G | C | 2 | a0001c0003t0001g0265 a0001c0003t0028g0046 |
2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.12+4247C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228257 | |||||||
chr6:11228311 | A | T | 1 | a0001c0002t0006g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.12+4193T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228311 | |||||||
chr6:11228313 | C | T | 1 | a0001c0003t0001g0139 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.12+4191G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228313 | |||||||
chr6:11228412 | C | A | 1 | a0001c0002t0002g0354 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.12+4092G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228412 | |||||||
chr6:11228422 | C | T | 3 | a0001c0004t0010g0122 a0001c0005t0006g0137 a0001c0005t0006g0138 |
3 | HG00738.hp2 HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.12+4082G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228422 | |||||||
chr6:11228423 | A | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.12+4081T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228423 | |||||||
chr6:11228423 | A | T | 5 | a0001c0005t0002g0081 a0001c0005t0002g0082 a0001c0005t0002g0083 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+4081T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228423 | |||||||
chr6:11228424 | G | C | 34 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0071 others(31): Show |
35 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(32): Show |
intron_variant | MODIFIER | c.12+4080C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228424 | |||||||
chr6:11228430 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(168): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.12+4074G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228430 | |||||||
chr6:11228499 | C | CT | 4 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0005t0006g0102 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+4004_12+4005ins others(1): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228499 | |||||||
chr6:11228508 | C | T | 1 | a0001c0007t0001g0285 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.12+3996G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228508 | |||||||
chr6:11228529 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
9 | HG01175.hp1 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+3967_12+3974del others(8): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228529 | |||||||
chr6:11228564 | G | GTT | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.12+3938_12+3939dup others(2): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228564 | |||||||
chr6:11228622 | AG | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(319): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.12+3881delC | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228622 | |||||||
chr6:11228631 | C | T | 1 | a0001c0005t0002g0136 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.12+3873G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228631 | |||||||
chr6:11228648 | A | G | 8 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0127 others(5): Show |
8 | HG02451.hp2 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+3856T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228648 | |||||||
chr6:11228715 | C | G | 1 | a0001c0005t0014g0100 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.12+3789G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228715 | |||||||
chr6:11228750 | A | G | 42 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0071 others(39): Show |
43 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.12+3754T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228750 | |||||||
chr6:11228760 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(151): Show |
175 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.12+3744A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228760 | |||||||
chr6:11228781 | A | G | 4 | a0001c0001t0003g0125 a0001c0001t0003g0126 a0001c0001t0003g0127 others(1): Show |
4 | HG02451.hp2 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3723T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11228781 | |||||||
chr6:11229069 | C | T | 2 | a0001c0005t0002g0283 a0001c0005t0002g0284 |
2 | NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.12+3435G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229069 | |||||||
chr6:11229166 | C | G | 3 | a0001c0002t0002g0043 a0001c0004t0005g0044 a0001c0004t0027g0045 |
3 | HG00099.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.12+3338G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229166 | |||||||
chr6:11229173 | C | T | 3 | a0001c0003t0001g0281 a0001c0003t0003g0282 a0001c0005t0002g0280 |
3 | HG02970.hp1 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.12+3331G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229173 | |||||||
chr6:11229264 | A | G | 30 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0071 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.12+3240T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229264 | |||||||
chr6:11229311 | A | G | 1 | a0001c0004t0002g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.12+3193T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229311 | |||||||
chr6:11229335 | A | C | 1 | a0001c0003t0001g0123 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.12+3169T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229335 | |||||||
chr6:11229336 | G | T | 1 | a0001c0003t0001g0123 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.12+3168C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229336 | |||||||
chr6:11229340 | T | C | 3 | a0001c0003t0001g0047 a0001c0005t0001g0262 a0001c0005t0009g0051 |
3 | HG02622.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.12+3164A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229340 | |||||||
chr6:11229372 | C | G | 3 | a0001c0001t0003g0052 a0001c0004t0002g0054 a0001c0004t0009g0053 |
3 | HG02486.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.12+3132G>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229372 | |||||||
chr6:11229424 | G | C | 3 | a0001c0003t0001g0047 a0001c0005t0001g0262 a0001c0005t0009g0051 |
3 | HG02622.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.12+3080C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229424 | |||||||
chr6:11229720 | G | A | 87 | a0001c0001t0001g0291 a0001c0001t0001g0303 a0001c0001t0001g0304 others(84): Show |
93 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.12+2784C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229720 | |||||||
chr6:11229752 | A | C | 1 | a0001c0005t0002g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.12+2752T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229752 | |||||||
chr6:11229863 | C | T | 3 | a0001c0003t0013g0025 a0001c0003t0017g0027 a0001c0015t0013g0026 |
3 | HG02723.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.12+2641G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229863 | |||||||
chr6:11229972 | A | G | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+2532T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11229972 | |||||||
chr6:11230081 | A | G | 1 | a0001c0011t0032g0358 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12+2423T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230081 | |||||||
chr6:11230169 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.12+2335C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230169 | |||||||
chr6:11230190 | G | T | 4 | a0001c0003t0001g0270 a0001c0003t0016g0098 a0001c0005t0007g0012 others(1): Show |
5 | HG00735.hp1 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+2314C>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230190 | |||||||
chr6:11230243 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.12+2261T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230243 | |||||||
chr6:11230306 | G | C | 3 | a0001c0003t0013g0025 a0001c0003t0017g0027 a0001c0015t0013g0026 |
3 | HG02723.hp2 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.12+2198C>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230306 | |||||||
chr6:11230532 | C | T | 4 | a0001c0006t0003g0006 a0001c0006t0003g0094 a0001c0006t0003g0095 others(1): Show |
6 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.12+1972G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230532 | |||||||
chr6:11230573 | C | T | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+1931G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230573 | |||||||
chr6:11230649 | CATCAT | C | 83 | a0001c0001t0001g0291 a0001c0001t0001g0303 a0001c0001t0001g0304 others(80): Show |
88 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.12+1850_12+1854del others(5): Show |
NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230649 | |||||||
chr6:11230765 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0093 |
3 | NA18975.hp1 NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.12+1739T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230765 | |||||||
chr6:11230777 | T | C | 2 | a0001c0002t0002g0263 a0001c0002t0002g0264 |
2 | NA18964.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.12+1727A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230777 | |||||||
chr6:11230782 | A | G | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+1722T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230782 | |||||||
chr6:11230879 | C | T | 44 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0071 others(41): Show |
46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.12+1625G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11230879 | |||||||
chr6:11231069 | C | A | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+1435G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231069 | |||||||
chr6:11231141 | T | G | 1 | a0001c0001t0026g0269 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12+1363A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231141 | |||||||
chr6:11231549 | A | T | 3 | a0001c0008t0007g0021 a0001c0008t0007g0276 a0001c0012t0003g0277 |
4 | HG01496.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+955T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231549 | |||||||
chr6:11231589 | T | C | 1 | a0001c0003t0001g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.12+915A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231589 | |||||||
chr6:11231830 | CTG | C | 4 | a0001c0001t0026g0269 a0001c0005t0002g0266 a0001c0005t0011g0267 others(1): Show |
4 | HG02630.hp2 HG02896.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+672_12+673delCA | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231830 | |||||||
chr6:11231891 | C | T | 3 | a0001c0002t0002g0050 a0001c0002t0008g0049 a0001c0005t0009g0051 |
3 | HG02622.hp1 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.12+613G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231891 | |||||||
chr6:11231968 | T | C | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+536A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11231968 | |||||||
chr6:11232019 | A | C | 1 | a0001c0005t0006g0048 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.12+485T>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232019 | |||||||
chr6:11232019 | A | T | 1 | a0001c0007t0004g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.12+485T>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232019 | |||||||
chr6:11232031 | C | A | 1 | a0001c0003t0004g0356 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.12+473G>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232031 | |||||||
chr6:11232229 | T | G | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0022t0001g0273 |
3 | HG02735.hp1 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.12+275A>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232229 | |||||||
chr6:11232237 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.12+267G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232237 | |||||||
chr6:11232276 | A | G | 1 | a0001c0003t0028g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.12+228T>C | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232276 | |||||||
chr6:11232317 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.12+187C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232317 | |||||||
chr6:11232334 | C | T | 3 | a0001c0002t0002g0043 a0001c0004t0005g0044 a0001c0004t0027g0045 |
3 | HG00099.hp1 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.12+170G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232334 | |||||||
chr6:11232355 | G | GC | 85 | a0001c0001t0001g0278 a0001c0001t0001g0291 a0001c0001t0001g0303 others(82): Show |
90 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.12+148dupG | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232355 | |||||||
chr6:11232373 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.12+131C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232373 | |||||||
chr6:11232451 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
9 | HG01175.hp1 HG01346.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+53G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232451 | |||||||
chr6:11232456 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18961.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.12+48C>T | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232456 | |||||||
chr6:11232471 | T | C | 1 | a0001c0011t0032g0358 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.12+33A>G | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232471 | |||||||
chr6:11232474 | C | T | 11 | a0001c0003t0001g0034 a0001c0003t0012g0029 a0001c0003t0012g0032 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.12+30G>A | NEDD9 | ENSG00000111859.17 | transcript | ENST00000379446.10 | protein_coding | 1/6 | chr6 | 11232474 |