Item | Value |
---|---|
geneid | 10392 |
ensemblid | ENSG00000106100.11 |
hgncid | 16390 |
symbol | NOD1 |
name | nucleotide binding oligomerization domain containing 1 |
refseq_nuc | NM_006092.4 |
refseq_prot | NP_006083.1 |
ensembl_nuc | ENST00000222823.9 |
ensembl_prot | ENSP00000222823.4 |
mane_status | MANE Select |
chr | chr7 |
start | 30424527 |
end | 30478784 |
strand | - |
ver | v1.2 |
region | chr7:30424527-30478784 |
region5000 | chr7:30419527-30483784 |
regionname0 | NOD1_chr7_30424527_30478784 |
regionname5000 | NOD1_chr7_30419527_30483784 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 953 | 197 | 36 | 42 | 82 | 10 | 25 | 62 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0002 | 0/0 | 953 | 134 | 36 | 11 | 68 | 2 | 17 | 55 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0003 | 0/0 | 953 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0004 | 0/0 | 953 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0005 | 0/0 | 953 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0006 | 0/0 | 953 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0007 | 0/0 | 953 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0008 | 0/0 | 953 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0009 | 0/0 | 953 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0010 | 0/0 | 953 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
a0011 | 0/0 | 953 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | MEEQG others(948): Show |
chr7 | 30419527 | 30483784 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2859 | 173 | 21 | 39 | 79 | 9 | 23 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0003 | 0/0 | 2859 | 18 | 15 | 2 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0010 | 0/0 | 2859 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0014 | 0/0 | 2859 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0016 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0017 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0001c0018 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0002c0002 | 0/0 | 2859 | 115 | 21 | 10 | 66 | 2 | 16 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0002c0004 | 0/0 | 2859 | 16 | 14 | 1 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0002c0013 | 0/0 | 2859 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0002c0021 | 0/0 | 2859 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0002c0022 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0003c0005 | 0/0 | 2859 | 6 | 6 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0003c0007 | 0/0 | 2859 | 4 | 4 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0003c0011 | 0/0 | 2859 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0004c0006 | 0/0 | 2859 | 5 | 4 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0005c0008 | 0/0 | 2859 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0006c0009 | 0/0 | 2859 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0007c0020 | 0/0 | 2859 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0008c0012 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0009c0019 | 0/0 | 2859 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0010c0023 | 0/0 | 2859 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 | ||
a0011c0015 | 0/0 | 2859 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | ATGGA others(2854): Show |
chr7 | 30419527 | 30483784 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4503 | 135 | 7 | 25 | 77 | 8 | 16 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0002 | 0/0 | 4503 | 15 | 1 | 11 | 0 | 1 | 2 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0006 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0007 | 0/0 | 4503 | 3 | 2 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0009 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0012 | 0/0 | 4501 | 4 | 0 | 1 | 0 | 0 | 3 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4496): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0015 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0016 | 0/0 | 4503 | 2 | 1 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0018 | 0/0 | 4503 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0022 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0023 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0024 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0001t0028 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0003t0002 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0003t0004 | 0/0 | 4503 | 13 | 11 | 2 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0003t0014 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0003t0021 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0010t0001 | 0/0 | 4503 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0014t0001 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0016t0001 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0017t0001 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0001c0018t0001 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0001 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0002 | 0/0 | 4503 | 85 | 7 | 7 | 58 | 2 | 11 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0003 | 0/0 | 4503 | 16 | 11 | 2 | 3 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0005 | 0/0 | 4504 | 3 | 2 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4499): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0009 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0011 | 0/0 | 4503 | 4 | 0 | 0 | 4 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0013 | 0/0 | 4503 | 3 | 0 | 0 | 0 | 0 | 3 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0026 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0002t0027 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0004t0002 | 0/0 | 4503 | 8 | 7 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0004t0005 | 0/0 | 4504 | 6 | 5 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4499): Show |
chr7 | 30419527 | 30483784 |
a0002c0004t0015 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0004t0020 | 0/0 | 4504 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4499): Show |
chr7 | 30419527 | 30483784 |
a0002c0013t0025 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0021t0002 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0002c0022t0002 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0005t0002 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0005t0008 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0005t0010 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0007t0008 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0007t0017 | 0/0 | 4504 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4499): Show |
chr7 | 30419527 | 30483784 |
a0003c0011t0008 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0003c0011t0010 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0004c0006t0001 | 0/0 | 4503 | 2 | 1 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0004c0006t0006 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0005c0008t0001 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0006c0009t0007 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0007c0020t0002 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0008c0012t0001 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0009c0019t0002 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0010c0023t0019 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
a0011c0015t0001 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | AGTTC others(4498): Show |
chr7 | 30419527 | 30483784 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0004 | 1/0 | 8 | 0 | 3 | 3 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0002g0001 | 0/0 | 10 | 0 | 7 | 0 | 1 | 2 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0015g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0016g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0018g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0018g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0022g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0024g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0001t0028g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0014g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0003t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0010t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0010t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0014t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0016t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0017t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0001c0018t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0011g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0011g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0013g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0026g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0002t0027g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0004t0020g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0013t0025g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0021t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0002c0022t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0005t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0007t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0007t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0007t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0007t0017g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0011t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0003c0011t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0004c0006t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0004c0006t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0004c0006t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0004c0006t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0004c0006t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0005c0008t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0005c0008t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0005c0008t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0006c0009t0007g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0007c0020t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0008c0012t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0009c0019t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0010c0023t0019g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
a0011c0015t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0091 | EUR | FIN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00558 | hp2 | a0001 | c0010 | t0001 | g0265 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00597 | hp2 | a0007 | c0020 | t0002 | g0102 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00609 | hp2 | a0002 | c0002 | t0003 | g0161 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00735 | hp1 | a0001 | c0001 | t0012 | g0057 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0144 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01081 | hp1 | a0001 | c0003 | t0004 | g0238 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0152 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01109 | hp1 | a0001 | c0003 | t0004 | g0246 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01167 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0009 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01243 | hp1 | a0002 | c0002 | t0005 | g0140 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01255 | hp2 | a0002 | c0004 | t0005 | g0086 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01884 | hp1 | a0001 | c0003 | t0004 | g0240 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01884 | hp2 | a0002 | c0004 | t0005 | g0015 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01891 | hp2 | a0003 | c0005 | t0010 | g0065 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01978 | hp1 | a0004 | c0006 | t0001 | g0176 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01981 | hp1 | a0001 | c0001 | t0028 | g0058 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02027 | hp1 | a0001 | c0010 | t0001 | g0258 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0038 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02055 | hp2 | a0001 | c0003 | t0004 | g0236 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0244 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | CDX | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02257 | hp1 | a0001 | c0003 | t0004 | g0237 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02257 | hp2 | a0003 | c0011 | t0010 | g0075 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0138 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02258 | hp2 | a0002 | c0004 | t0002 | g0048 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02273 | hp2 | a0001 | c0014 | t0001 | g0276 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02451 | hp1 | a0002 | c0004 | t0002 | g0050 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02451 | hp2 | a0002 | c0004 | t0005 | g0049 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02572 | hp1 | a0003 | c0007 | t0008 | g0069 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0151 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02615 | hp2 | a0001 | c0001 | t0015 | g0037 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02622 | hp1 | a0003 | c0007 | t0008 | g0067 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02630 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0146 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02647 | hp1 | a0004 | c0006 | t0001 | g0175 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0130 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02723 | hp1 | a0002 | c0004 | t0005 | g0088 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0118 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02735 | hp2 | a0002 | c0002 | t0027 | g0123 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02809 | hp1 | a0002 | c0004 | t0002 | g0062 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02809 | hp2 | a0001 | c0001 | t0023 | g0247 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02818 | hp2 | a0002 | c0004 | t0002 | g0052 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02886 | hp1 | a0002 | c0004 | t0015 | g0042 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02886 | hp2 | a0002 | c0004 | t0005 | g0015 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02895 | hp1 | a0006 | c0009 | t0007 | g0012 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0131 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02896 | hp2 | a0002 | c0004 | t0002 | g0060 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02897 | hp1 | a0006 | c0009 | t0007 | g0012 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02897 | hp2 | a0002 | c0004 | t0002 | g0061 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02922 | hp2 | a0001 | c0003 | t0004 | g0239 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02965 | hp1 | a0003 | c0005 | t0008 | g0073 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02965 | hp2 | a0003 | c0011 | t0008 | g0076 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0135 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02976 | hp1 | a0005 | c0008 | t0001 | g0078 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02976 | hp2 | a0004 | c0006 | t0006 | g0174 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0235 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0093 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0166 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03098 | hp2 | a0003 | c0005 | t0010 | g0071 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03130 | hp1 | a0002 | c0013 | t0025 | g0068 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03130 | hp2 | a0001 | c0003 | t0004 | g0243 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03139 | hp1 | a0001 | c0003 | t0004 | g0245 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03139 | hp2 | a0001 | c0003 | t0004 | g0171 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03195 | hp1 | a0002 | c0002 | t0003 | g0145 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03195 | hp2 | a0005 | c0008 | t0001 | g0080 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03209 | hp1 | a0001 | c0003 | t0014 | g0013 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03225 | hp1 | a0001 | c0003 | t0004 | g0242 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03225 | hp2 | a0005 | c0008 | t0001 | g0079 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03453 | hp1 | a0003 | c0005 | t0010 | g0072 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03486 | hp1 | a0001 | c0001 | t0015 | g0040 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03486 | hp2 | a0002 | c0002 | t0005 | g0142 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03490 | hp1 | a0002 | c0002 | t0013 | g0008 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03492 | hp2 | a0002 | c0002 | t0013 | g0008 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03516 | hp2 | a0001 | c0003 | t0014 | g0013 | AFR | ESN | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03540 | hp1 | a0002 | c0002 | t0005 | g0143 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03540 | hp2 | a0002 | c0004 | t0002 | g0051 | AFR | GWD | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03579 | hp1 | a0001 | c0003 | t0021 | g0234 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03654 | hp1 | a0001 | c0017 | t0001 | g0046 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03654 | hp2 | a0001 | c0001 | t0022 | g0177 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03688 | hp1 | a0001 | c0018 | t0001 | g0168 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03710 | hp2 | a0001 | c0001 | t0012 | g0056 | SAS | PJL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0137 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03942 | hp1 | a0002 | c0002 | t0013 | g0008 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0116 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0225 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04184 | hp1 | a0008 | c0012 | t0001 | g0203 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0159 | SAS | BEB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04199 | hp1 | a0001 | c0001 | t0012 | g0054 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04204 | hp1 | a0009 | c0019 | t0002 | g0125 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG04228 | hp2 | a0002 | c0022 | t0002 | g0111 | SAS | STU | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0241 | AFR | YRI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18522 | hp2 | a0001 | c0001 | t0024 | g0074 | AFR | YRI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18941 | hp1 | a0001 | c0001 | t0018 | g0259 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18944 | hp2 | a0002 | c0002 | t0011 | g0021 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18949 | hp2 | a0002 | c0002 | t0011 | g0155 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18977 | hp2 | a0001 | c0001 | t0018 | g0287 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18988 | hp1 | a0002 | c0002 | t0026 | g0107 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18995 | hp1 | a0002 | c0004 | t0002 | g0122 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0084 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19011 | hp2 | a0002 | c0002 | t0011 | g0021 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19030 | hp1 | a0003 | c0007 | t0017 | g0066 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19030 | hp2 | a0010 | c0023 | t0019 | g0031 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19043 | hp2 | a0002 | c0004 | t0020 | g0034 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19055 | hp2 | a0011 | c0015 | t0001 | g0212 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19065 | hp2 | a0002 | c0002 | t0011 | g0153 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19077 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19090 | hp1 | a0002 | c0021 | t0002 | g0160 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19240 | hp1 | a0003 | c0005 | t0002 | g0133 | AFR | YRI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20129 | hp1 | a0003 | c0007 | t0017 | g0070 | AFR | ASW | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | TSI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20805 | hp2 | a0001 | c0016 | t0001 | g0220 | EUR | TSI | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20905 | hp1 | a0001 | c0001 | t0012 | g0055 | SAS | GIH | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | GIH | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | CLM | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02109 | hp1 | a0002 | c0002 | t0009 | g0041 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG02559 | hp2 | a0003 | c0005 | t0008 | g0064 | AFR | ACB | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03471 | hp1 | a0004 | c0006 | t0006 | g0250 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG03471 | hp2 | a0004 | c0006 | t0006 | g0173 | AFR | MSL | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG06807 | hp1 | a0002 | c0002 | t0003 | g0085 | AFR | USA | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
HG06807 | hp2 | a0002 | c0004 | t0005 | g0087 | AFR | USA | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA20300 | hp2 | a0001 | c0003 | t0014 | g0032 | AFR | USA | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
NA21309 | hp2 | a0002 | c0002 | t0003 | g0141 | AFR | LWK | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0254 | REF | REF | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | NOD1_chr7_30419527_30483784 | NOD1 | chr7 | 30419527 | 30483784 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30446976 | G | A | 1 | a0006 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.2360C>T | p.Thr787Met | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 8/14 | 2890/4503 | 2360/2862 | 787/953 | chr7 | 30446976 | |||
chr7:30448356 | C | T | 1 | a0007 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.2227G>A | p.Gly743Ser | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/14 | 2757/4503 | 2227/2862 | 743/953 | chr7 | 30448356 | |||
chr7:30451358 | C | T | 1 | a0011 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.2059G>A | p.Ala687Thr | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2589/4503 | 2059/2862 | 687/953 | chr7 | 30451358 | |||
chr7:30452077 | C | T | 1 | a0003 | 12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
missense_variant | MODERATE | c.1340G>A | p.Arg447His | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1870/4503 | 1340/2862 | 447/953 | chr7 | 30452077 | |||
chr7:30452303 | C | T | 1 | a0004 | 5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1114G>A | p.Asp372Asn | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1644/4503 | 1114/2862 | 372/953 | chr7 | 30452303 | |||
chr7:30452401 | G | A | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1016C>T | p.Pro339Leu | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1546/4503 | 1016/2862 | 339/953 | chr7 | 30452401 | |||
chr7:30452621 | C | T | 4 | a0002 a0007 a0009 others(1): Show |
137 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
missense_variant | MODERATE | c.796G>A | p.Glu266Lys | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1326/4503 | 796/2862 | 266/953 | chr7 | 30452621 | |||
chr7:30452741 | C | T | 1 | a0009 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.676G>A | p.Ala226Thr | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1206/4503 | 676/2862 | 226/953 | chr7 | 30452741 | |||
chr7:30452776 | C | T | 1 | a0005 | 3 | HG02976.hp1 HG03195.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.641G>A | p.Arg214Gln | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1171/4503 | 641/2862 | 214/953 | chr7 | 30452776 | |||
chr7:30455259 | A | T | 1 | a0008 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.254T>A | p.Phe85Tyr | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/14 | 784/4503 | 254/2862 | 85/953 | chr7 | 30455259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30429400 | C | T | 1 | a0002c0021 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.2763G>A | p.Gln921Gln | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/14 | 3293/4503 | 2763/2862 | 921/953 | chr7 | 30429400 | |||
chr7:30451230 | G | A | 1 | a0001c0010 | 2 | HG00558.hp2 HG02027.hp1 |
synonymous_variant | LOW | c.2187C>T | p.Arg729Arg | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2717/4503 | 2187/2862 | 729/953 | chr7 | 30451230 | |||
chr7:30451373 | G | A | 1 | a0001c0018 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.2044C>T | p.Leu682Leu | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2574/4503 | 2044/2862 | 682/953 | chr7 | 30451373 | |||
chr7:30451695 | C | T | 9 | a0002c0002 a0002c0013 a0002c0021 others(6): Show |
127 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(124): Show |
synonymous_variant | LOW | c.1722G>A | p.Ala574Ala | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2252/4503 | 1722/2862 | 574/953 | chr7 | 30451695 | |||
chr7:30451698 | C | T | 1 | a0001c0014 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.1719G>A | p.Pro573Pro | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2249/4503 | 1719/2862 | 573/953 | chr7 | 30451698 | |||
chr7:30451899 | G | A | 1 | a0002c0022 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.1518C>T | p.Pro506Pro | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 2048/4503 | 1518/2862 | 506/953 | chr7 | 30451899 | |||
chr7:30452487 | G | C | 1 | a0001c0016 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.930C>G | p.Pro310Pro | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1460/4503 | 930/2862 | 310/953 | chr7 | 30452487 | |||
chr7:30452526 | G | A | 3 | a0003c0005 a0003c0007 a0003c0011 |
12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
synonymous_variant | LOW | c.891C>T | p.Arg297Arg | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1421/4503 | 891/2862 | 297/953 | chr7 | 30452526 | |||
chr7:30452586 | G | A | 1 | a0003c0011 | 2 | HG02257.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.831C>T | p.His277His | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1361/4503 | 831/2862 | 277/953 | chr7 | 30452586 | |||
chr7:30452934 | G | A | 8 | a0001c0017 a0002c0002 a0002c0004 others(5): Show |
137 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
synonymous_variant | LOW | c.483C>T | p.Asp161Asp | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/14 | 1013/4503 | 483/2862 | 161/953 | chr7 | 30452934 | |||
chr7:30455276 | G | A | 1 | a0001c0018 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.237C>T | p.Gly79Gly | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/14 | 767/4503 | 237/2862 | 79/953 | chr7 | 30455276 | |||
chr7:30456766 | G | C | 8 | a0001c0003 a0002c0002 a0002c0004 others(5): Show |
154 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(151): Show |
synonymous_variant | LOW | c.156C>G | p.Ala52Ala | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/14 | 686/4503 | 156/2862 | 52/953 | chr7 | 30456766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30424599 | C | T | 1 | a0002c0002t0026 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1039G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 1039 | chr7 | 30424599 | ||||||
chr7:30424616 | C | T | 1 | a0002c0002t0011 | 4 | NA18944.hp2 NA18949.hp2 NA19011.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1022G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 1022 | chr7 | 30424616 | ||||||
chr7:30424633 | T | TG | 4 | a0002c0002t0005 a0002c0004t0005 a0002c0004t0020 others(1): Show |
12 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1004dupC | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 1004 | chr7 | 30424633 | ||||||
chr7:30424946 | T | G | 1 | a0002c0002t0027 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*692A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 692 | chr7 | 30424946 | ||||||
chr7:30425086 | GCA | G | 1 | a0001c0001t0012 | 4 | HG00735.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*550_*551delTG | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 550 | chr7 | 30425086 | ||||||
chr7:30425193 | G | A | 1 | a0001c0001t0023 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 445 | chr7 | 30425193 | ||||||
chr7:30425256 | G | A | 1 | a0001c0001t0016 | 2 | HG03209.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*382C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 382 | chr7 | 30425256 | ||||||
chr7:30425316 | T | G | 2 | a0001c0003t0021 a0002c0013t0025 |
2 | HG03130.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 322 | chr7 | 30425316 | ||||||
chr7:30425345 | T | C | 13 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0024 others(10): Show |
36 | HG00609.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*293A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 293 | chr7 | 30425345 | ||||||
chr7:30425419 | G | A | 11 | a0001c0001t0006 a0001c0001t0009 a0001c0003t0021 others(8): Show |
34 | HG00609.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*219C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 219 | chr7 | 30425419 | ||||||
chr7:30425548 | C | T | 1 | a0001c0001t0022 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 14/14 | 90 | chr7 | 30425548 | ||||||
chr7:30459190 | A | G | 10 | a0001c0003t0004 a0001c0003t0014 a0001c0003t0021 others(7): Show |
29 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-160T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/14 | 2269 | chr7 | 30459190 | ||||||
chr7:30459213 | T | A | 2 | a0001c0001t0012 a0001c0001t0028 |
5 | HG00735.hp1 HG01981.hp1 HG03710.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-183A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/14 | 2292 | chr7 | 30459213 | ||||||
chr7:30459959 | T | C | 31 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(28): Show |
174 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-269A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 2/14 | 3038 | chr7 | 30459959 | ||||||
chr7:30459966 | T | C | 1 | a0001c0001t0018 | 2 | NA18941.hp1 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-276A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 2/14 | 3045 | chr7 | 30459966 | ||||||
chr7:30478750 | C | T | 8 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0015 others(5): Show |
16 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-496G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/14 | 21829 | chr7 | 30478750 | ||||||
chr7:30478751 | G | T | 1 | a0010c0023t0019 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-497C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/14 | 21830 | chr7 | 30478751 | ||||||
chr7:30478772 | C | T | 1 | a0002c0002t0013 | 3 | HG03490.hp1 HG03492.hp2 HG03942.hp1 |
5_prime_UTR_variant | MODIFIER | c.-518G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/14 | 21851 | chr7 | 30478772 | ||||||
chr7:30478778 | G | T | 1 | a0002c0002t0013 | 3 | HG03490.hp1 HG03492.hp2 HG03942.hp1 |
5_prime_UTR_variant | MODIFIER | c.-524C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/14 | 21857 | chr7 | 30478778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:30425758 | T | C | 31 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0009g0038 others(28): Show |
36 | HG00609.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.2790-48A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30425758 | |||||||
chr7:30425808 | A | C | 10 | a0002c0002t0005g0140 a0002c0002t0005g0142 a0002c0002t0005g0143 others(7): Show |
11 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2790-98T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30425808 | |||||||
chr7:30425880 | C | T | 24 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0002c0002t0003g0009 others(21): Show |
29 | HG00609.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.2790-170G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30425880 | |||||||
chr7:30426567 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2790-857G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426567 | |||||||
chr7:30426605 | G | T | 44 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0007g0033 others(41): Show |
50 | HG00609.hp2 HG01109.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.2790-895C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426605 | |||||||
chr7:30426606 | C | G | 44 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0007g0033 others(41): Show |
50 | HG00609.hp2 HG01109.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.2790-896G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426606 | |||||||
chr7:30426784 | A | T | 1 | a0002c0002t0002g0116 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2790-1074T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426784 | |||||||
chr7:30426835 | C | T | 14 | a0001c0001t0001g0211 a0001c0017t0001g0046 a0002c0002t0002g0016 others(11): Show |
18 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2790-1125G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426835 | |||||||
chr7:30426999 | G | A | 1 | a0002c0002t0002g0106 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2790-1289C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30426999 | |||||||
chr7:30427024 | T | A | 45 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0007g0033 others(42): Show |
51 | HG00609.hp2 HG01109.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.2790-1314A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427024 | |||||||
chr7:30427042 | T | C | 2 | a0002c0004t0005g0088 a0003c0007t0017g0066 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2790-1332A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427042 | |||||||
chr7:30427312 | C | G | 28 | a0001c0001t0006g0024 a0001c0001t0006g0047 a0001c0001t0007g0033 others(25): Show |
33 | HG00609.hp2 HG01109.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.2790-1602G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427312 | |||||||
chr7:30427424 | C | T | 1 | a0002c0002t0002g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2790-1714G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427424 | |||||||
chr7:30427442 | G | A | 5 | a0001c0001t0001g0181 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG01192.hp1 HG01255.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.2790-1732C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427442 | |||||||
chr7:30427586 | G | C | 11 | a0002c0002t0005g0140 a0002c0002t0005g0142 a0002c0002t0005g0143 others(8): Show |
12 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2789+1788C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427586 | |||||||
chr7:30427770 | T | C | 8 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2789+1604A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427770 | |||||||
chr7:30427793 | G | C | 15 | a0001c0001t0028g0058 a0001c0017t0001g0046 a0002c0002t0001g0209 others(12): Show |
19 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.2789+1581C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427793 | |||||||
chr7:30427948 | C | G | 63 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(60): Show |
73 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2789+1426G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30427948 | |||||||
chr7:30428074 | C | T | 1 | a0001c0001t0028g0058 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2789+1300G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428074 | |||||||
chr7:30428233 | G | T | 16 | a0001c0001t0001g0211 a0001c0001t0028g0058 a0001c0017t0001g0046 others(13): Show |
20 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.2789+1141C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428233 | |||||||
chr7:30428373 | T | TA | 4 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2789+1000_2789+100 others(5): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428373 | |||||||
chr7:30428374 | T | A | 4 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2789+1000A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428374 | |||||||
chr7:30428374 | T | TA | 42 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(39): Show |
50 | HG00323.hp2 HG00609.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.2789+999_2789+1000 others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428374 | |||||||
chr7:30428374 | T | TAA | 6 | a0002c0002t0002g0016 a0002c0002t0002g0100 a0002c0002t0002g0106 others(3): Show |
7 | HG00597.hp2 HG03490.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.2789+999_2789+1000 others(5): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428374 | |||||||
chr7:30428375 | T | A | 52 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(49): Show |
61 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2789+999A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428375 | |||||||
chr7:30428375 | T | TA | 13 | a0001c0001t0001g0261 a0001c0001t0023g0247 a0002c0002t0002g0104 others(10): Show |
14 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2789+998dupT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428375 | |||||||
chr7:30428568 | T | C | 64 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(61): Show |
74 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2789+806A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428568 | |||||||
chr7:30428600 | C | T | 64 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(61): Show |
74 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.2789+774G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428600 | |||||||
chr7:30428762 | G | A | 48 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(45): Show |
57 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2789+612C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428762 | |||||||
chr7:30428852 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2789+522T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428852 | |||||||
chr7:30428996 | C | T | 1 | a0001c0001t0023g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2789+378G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30428996 | |||||||
chr7:30429130 | G | A | 1 | a0002c0004t0002g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2789+244C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30429130 | |||||||
chr7:30429154 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.2789+220G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30429154 | |||||||
chr7:30429236 | A | T | 1 | a0001c0001t0023g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2789+138T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30429236 | |||||||
chr7:30429237 | A | T | 1 | a0001c0001t0023g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2789+137T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30429237 | |||||||
chr7:30429238 | A | T | 1 | a0001c0001t0023g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2789+136T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 13/13 | chr7 | 30429238 | |||||||
chr7:30429471 | A | G | 1 | a0002c0002t0002g0117 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2706-14T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429471 | |||||||
chr7:30429487 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2706-30G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429487 | |||||||
chr7:30429516 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0228 |
2 | HG02135.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2706-59G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429516 | |||||||
chr7:30429654 | T | C | 34 | a0001c0001t0001g0188 a0001c0001t0001g0211 a0001c0001t0009g0038 others(31): Show |
39 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.2706-197A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429654 | |||||||
chr7:30429813 | C | T | 1 | a0002c0002t0002g0165 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2706-356G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429813 | |||||||
chr7:30429903 | C | G | 2 | a0001c0001t0001g0211 a0001c0003t0021g0234 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2706-446G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429903 | |||||||
chr7:30429927 | A | G | 13 | a0001c0001t0028g0058 a0002c0002t0005g0140 a0002c0002t0005g0142 others(10): Show |
14 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2706-470T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429927 | |||||||
chr7:30429984 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2706-527G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30429984 | |||||||
chr7:30430160 | G | C | 1 | a0002c0002t0002g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2706-703C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430160 | |||||||
chr7:30430274 | T | C | 29 | a0001c0001t0023g0247 a0001c0003t0004g0171 a0001c0003t0004g0235 others(26): Show |
31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.2706-817A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430274 | |||||||
chr7:30430466 | T | C | 1 | a0002c0002t0013g0008 | 3 | HG03490.hp1 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2706-1009A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430466 | |||||||
chr7:30430537 | T | C | 64 | a0001c0001t0001g0196 a0001c0001t0001g0248 a0001c0001t0001g0253 others(61): Show |
68 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.2706-1080A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430537 | |||||||
chr7:30430599 | C | T | 1 | a0002c0002t0003g0161 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2706-1142G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430599 | |||||||
chr7:30430645 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2706-1188T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430645 | |||||||
chr7:30430654 | C | T | 42 | a0001c0001t0001g0216 a0001c0001t0002g0139 a0001c0001t0009g0039 others(39): Show |
43 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2706-1197G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430654 | |||||||
chr7:30430685 | A | G | 2 | a0002c0002t0002g0166 a0004c0006t0006g0174 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2706-1228T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430685 | |||||||
chr7:30430707 | T | G | 74 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0268 others(71): Show |
85 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2706-1250A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430707 | |||||||
chr7:30430779 | T | G | 30 | a0001c0001t0001g0226 a0001c0001t0001g0268 a0001c0001t0001g0274 others(27): Show |
39 | HG00609.hp1 HG00673.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.2706-1322A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430779 | |||||||
chr7:30430807 | A | G | 16 | a0001c0001t0002g0139 a0001c0001t0009g0038 a0001c0001t0009g0039 others(13): Show |
16 | HG00735.hp1 HG01099.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2706-1350T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430807 | |||||||
chr7:30430927 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2706-1470A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30430927 | |||||||
chr7:30431085 | T | C | 1 | a0002c0004t0015g0042 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2706-1628A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431085 | |||||||
chr7:30431229 | C | CAAAT | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(73): Show |
91 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.2706-1776_2706-177 others(8): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431229 | |||||||
chr7:30431253 | G | C | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(93): Show |
111 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2706-1796C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431253 | |||||||
chr7:30431495 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(76): Show |
95 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2705+1601T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431495 | |||||||
chr7:30431524 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2705+1572A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431524 | |||||||
chr7:30431576 | G | A | 1 | a0009c0019t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2705+1520C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431576 | |||||||
chr7:30431617 | C | T | 1 | a0002c0002t0002g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2705+1479G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431617 | |||||||
chr7:30431702 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2705+1394G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431702 | |||||||
chr7:30431753 | G | A | 5 | a0002c0002t0003g0093 a0002c0002t0003g0138 a0002c0002t0003g0145 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2705+1343C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431753 | |||||||
chr7:30431961 | C | A | 12 | a0001c0003t0004g0171 a0001c0003t0004g0235 a0001c0003t0004g0236 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2705+1135G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431961 | |||||||
chr7:30431983 | T | C | 14 | a0001c0001t0002g0139 a0001c0001t0007g0033 a0001c0001t0007g0035 others(11): Show |
15 | HG00735.hp1 HG01109.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.2705+1113A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30431983 | |||||||
chr7:30432156 | AAG | A | 3 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0127 |
4 | NA18951.hp2 NA18956.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2705+938_2705+939d others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432156 | |||||||
chr7:30432233 | T | C | 1 | a0002c0002t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2705+863A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432233 | |||||||
chr7:30432475 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(70): Show |
89 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.2705+621A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432475 | |||||||
chr7:30432659 | C | T | 1 | a0004c0006t0006g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2705+437G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432659 | |||||||
chr7:30432705 | G | C | 1 | a0002c0002t0003g0131 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2705+391C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432705 | |||||||
chr7:30432798 | A | G | 2 | a0005c0008t0001g0079 a0005c0008t0001g0080 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2705+298T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30432798 | |||||||
chr7:30433081 | G | C | 1 | a0002c0002t0002g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2705+15C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 12/13 | chr7 | 30433081 | |||||||
chr7:30433186 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.2622-7T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433186 | |||||||
chr7:30433381 | T | C | 9 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(6): Show |
9 | HG00735.hp1 HG01981.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2622-202A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433381 | |||||||
chr7:30433382 | G | A | 1 | a0001c0001t0028g0058 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2622-203C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433382 | |||||||
chr7:30433407 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2622-228G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433407 | |||||||
chr7:30433435 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2622-256G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433435 | |||||||
chr7:30433440 | C | T | 1 | a0002c0002t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2622-261G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433440 | |||||||
chr7:30433483 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2622-304G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433483 | |||||||
chr7:30433811 | T | A | 7 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2622-632A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30433811 | |||||||
chr7:30434047 | G | C | 7 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2622-868C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434047 | |||||||
chr7:30434203 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2622-1024C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434203 | |||||||
chr7:30434222 | T | C | 2 | a0005c0008t0001g0079 a0005c0008t0001g0080 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2622-1043A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434222 | |||||||
chr7:30434342 | T | A | 2 | a0003c0005t0002g0133 a0003c0005t0008g0073 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2622-1163A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434342 | |||||||
chr7:30434542 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2622-1363A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434542 | |||||||
chr7:30434595 | A | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0001g0185 others(2): Show |
5 | HG02027.hp2 HG02523.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.2621+1403T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434595 | |||||||
chr7:30434692 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2621+1306G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434692 | |||||||
chr7:30434939 | G | GT | 15 | a0001c0001t0001g0232 a0001c0001t0002g0139 a0001c0001t0007g0033 others(12): Show |
16 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2621+1058dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434939 | |||||||
chr7:30434990 | C | T | 1 | a0002c0002t0026g0107 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2621+1008G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30434990 | |||||||
chr7:30435020 | C | T | 8 | a0003c0007t0008g0067 a0003c0007t0008g0069 a0003c0007t0017g0066 others(5): Show |
8 | HG01978.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2621+978G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30435020 | |||||||
chr7:30435518 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2621+480G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30435518 | |||||||
chr7:30435639 | G | C | 1 | a0006c0009t0007g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2621+359C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 11/13 | chr7 | 30435639 | |||||||
chr7:30436117 | A | G | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2538-36T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30436117 | |||||||
chr7:30436246 | C | T | 1 | a0002c0002t0002g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2538-165G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30436246 | |||||||
chr7:30436550 | C | CTAAG | 3 | a0001c0001t0001g0025 a0001c0001t0001g0195 a0001c0001t0001g0214 |
4 | HG01099.hp1 HG02683.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2538-473_2538-470d others(6): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30436550 | |||||||
chr7:30436752 | G | A | 1 | a0002c0002t0002g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2538-671C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30436752 | |||||||
chr7:30436934 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2537+639A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30436934 | |||||||
chr7:30437166 | T | A | 1 | a0002c0002t0002g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2537+407A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30437166 | |||||||
chr7:30437365 | A | G | 1 | a0001c0001t0016g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2537+208T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 10/13 | chr7 | 30437365 | |||||||
chr7:30437826 | G | T | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2454-170C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30437826 | |||||||
chr7:30437954 | A | G | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(74): Show |
93 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2454-298T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30437954 | |||||||
chr7:30438008 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2454-352G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438008 | |||||||
chr7:30438418 | G | A | 2 | a0005c0008t0001g0079 a0005c0008t0001g0080 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2454-762C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438418 | |||||||
chr7:30438440 | C | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(75): Show |
94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.2454-784G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438440 | |||||||
chr7:30438559 | C | T | 12 | a0001c0003t0004g0171 a0001c0003t0004g0235 a0001c0003t0004g0236 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2454-903G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438559 | |||||||
chr7:30438607 | T | G | 2 | a0005c0008t0001g0079 a0005c0008t0001g0080 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2454-951A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438607 | |||||||
chr7:30438694 | C | T | 3 | a0002c0004t0002g0060 a0002c0004t0002g0061 a0002c0004t0002g0062 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2454-1038G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438694 | |||||||
chr7:30438768 | A | G | 16 | a0001c0003t0004g0238 a0002c0002t0003g0093 a0002c0002t0003g0138 others(13): Show |
17 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2454-1112T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438768 | |||||||
chr7:30438805 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2454-1149A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438805 | |||||||
chr7:30438831 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2454-1175T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438831 | |||||||
chr7:30438869 | G | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2454-1213C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438869 | |||||||
chr7:30438900 | T | G | 6 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454-1244A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30438900 | |||||||
chr7:30439037 | C | G | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2454-1381G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439037 | |||||||
chr7:30439138 | A | G | 1 | a0002c0002t0002g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2454-1482T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439138 | |||||||
chr7:30439232 | CAAAAGAA others(6059): Show |
C | 17 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(14): Show |
18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2453+843_2454-1577 others(3): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439232 | |||||||
chr7:30439279 | C | T | 8 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2454-1623G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439279 | |||||||
chr7:30439334 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2454-1678T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439334 | |||||||
chr7:30439366 | C | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
234 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.2454-1710G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439366 | |||||||
chr7:30439386 | C | T | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(55): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2454-1730G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439386 | |||||||
chr7:30439392 | T | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(55): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2454-1736A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439392 | |||||||
chr7:30439394 | T | C | 1 | a0007c0020t0002g0102 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2454-1738A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439394 | |||||||
chr7:30439397 | G | A | 8 | a0003c0007t0008g0067 a0003c0007t0008g0069 a0003c0007t0017g0066 others(5): Show |
8 | HG01978.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2454-1741C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439397 | |||||||
chr7:30439404 | G | A | 4 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 others(1): Show |
5 | HG01891.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2454-1748C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439404 | |||||||
chr7:30439407 | C | A | 1 | a0001c0003t0004g0238 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2454-1751G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439407 | |||||||
chr7:30439407 | C | T | 6 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454-1751G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439407 | |||||||
chr7:30439456 | A | G | 4 | a0001c0001t0001g0207 a0002c0004t0002g0060 a0002c0004t0002g0061 others(1): Show |
4 | HG01070.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454-1800T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439456 | |||||||
chr7:30439471 | T | C | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2454-1815A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439471 | |||||||
chr7:30439495 | G | A | 2 | a0003c0007t0017g0070 a0003c0011t0010g0075 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2454-1839C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439495 | |||||||
chr7:30439507 | A | C | 8 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2454-1851T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439507 | |||||||
chr7:30439528 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2454-1872C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439528 | |||||||
chr7:30439570 | C | G | 11 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(8): Show |
12 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2454-1914G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439570 | |||||||
chr7:30439584 | A | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0063 a0001c0001t0002g0139 |
7 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2454-1928T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439584 | |||||||
chr7:30439595 | A | G | 3 | a0001c0001t0001g0223 a0001c0001t0002g0001 a0001c0001t0002g0063 |
7 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2454-1939T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439595 | |||||||
chr7:30439615 | A | T | 1 | a0002c0002t0011g0153 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2454-1959T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439615 | |||||||
chr7:30439616 | A | G | 4 | a0001c0001t0001g0182 a0002c0002t0011g0153 a0005c0008t0001g0079 others(1): Show |
4 | HG01167.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454-1960T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439616 | |||||||
chr7:30439625 | A | G | 10 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(7): Show |
10 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2454-1969T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439625 | |||||||
chr7:30439666 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0223 a0002c0002t0001g0209 others(5): Show |
8 | HG03017.hp1 HG03195.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.2454-2010T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439666 | |||||||
chr7:30439685 | G | A | 1 | a0002c0002t0027g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2454-2029C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439685 | |||||||
chr7:30439694 | A | T | 23 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0001g0248 others(20): Show |
28 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.2454-2038T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439694 | |||||||
chr7:30439706 | C | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0206 others(13): Show |
21 | HG00609.hp1 HG00673.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2454-2050G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439706 | |||||||
chr7:30439725 | C | T | 4 | a0001c0001t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0128 others(1): Show |
4 | HG02129.hp1 HG03669.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454-2069G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439725 | |||||||
chr7:30439734 | C | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0208 a0001c0001t0001g0219 |
3 | NA18999.hp2 NA19066.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2454-2078G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439734 | |||||||
chr7:30439758 | C | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0128 a0009c0019t0002g0125 |
3 | HG02129.hp1 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2454-2102G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439758 | |||||||
chr7:30439806 | CACAG | C | 3 | a0002c0002t0002g0005 a0002c0002t0002g0128 a0009c0019t0002g0125 |
3 | HG02129.hp1 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2454-2154_2454-215 others(8): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439806 | |||||||
chr7:30439812 | C | G | 2 | a0005c0008t0001g0079 a0005c0008t0001g0080 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2454-2156G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439812 | |||||||
chr7:30439828 | A | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2454-2172T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439828 | |||||||
chr7:30439892 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2454-2236G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439892 | |||||||
chr7:30439908 | T | C | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2454-2252A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439908 | |||||||
chr7:30439957 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
63 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.2454-2301G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439957 | |||||||
chr7:30439964 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0252 |
2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2454-2308G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439964 | |||||||
chr7:30439982 | C | T | 1 | a0002c0002t0002g0005 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2454-2326G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439982 | |||||||
chr7:30439986 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0252 |
2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2454-2330C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439986 | |||||||
chr7:30439990 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0206 others(10): Show |
15 | HG00735.hp1 HG01070.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454-2334T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439990 | |||||||
chr7:30439991 | G | A | 1 | a0002c0002t0002g0005 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2454-2335C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30439991 | |||||||
chr7:30440011 | G | T | 2 | a0002c0002t0002g0005 a0002c0013t0025g0068 |
2 | HG03130.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2454-2355C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440011 | |||||||
chr7:30440013 | C | T | 1 | a0002c0002t0002g0005 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2454-2357G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440013 | |||||||
chr7:30440020 | T | C | 4 | a0001c0001t0001g0077 a0002c0002t0002g0017 a0002c0002t0002g0103 others(1): Show |
6 | HG01081.hp2 HG01106.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.2454-2364A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440020 | |||||||
chr7:30440032 | T | C | 1 | a0004c0006t0006g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2454-2376A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440032 | |||||||
chr7:30440048 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2454-2392C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440048 | |||||||
chr7:30440070 | A | G | 2 | a0001c0001t0001g0077 a0006c0009t0007g0012 |
3 | HG01106.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2454-2414T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440070 | |||||||
chr7:30440091 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(265): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.2454-2435A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440091 | |||||||
chr7:30440246 | G | A | 1 | a0001c0018t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2454-2590C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440246 | |||||||
chr7:30440249 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2454-2593C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440249 | |||||||
chr7:30440279 | A | C | 1 | a0001c0001t0022g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2454-2623T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440279 | |||||||
chr7:30440294 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2454-2638C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440294 | |||||||
chr7:30440305 | T | C | 6 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454-2649A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440305 | |||||||
chr7:30440361 | A | C | 1 | a0001c0003t0021g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2454-2705T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440361 | |||||||
chr7:30440364 | T | C | 1 | a0001c0003t0021g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2454-2708A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440364 | |||||||
chr7:30440396 | C | T | 2 | a0002c0004t0002g0060 a0002c0004t0002g0061 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2454-2740G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440396 | |||||||
chr7:30440450 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2454-2794C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440450 | |||||||
chr7:30440477 | G | A | 3 | a0002c0004t0002g0062 a0005c0008t0001g0079 a0005c0008t0001g0080 |
3 | HG02809.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2454-2821C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440477 | |||||||
chr7:30440508 | A | G | 2 | a0002c0002t0002g0005 a0002c0002t0002g0100 |
2 | NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2454-2852T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440508 | |||||||
chr7:30440594 | T | C | 1 | a0002c0002t0002g0081 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2454-2938A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440594 | |||||||
chr7:30440663 | C | T | 2 | a0001c0001t0001g0218 a0002c0002t0002g0117 |
2 | HG00099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2454-3007G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440663 | |||||||
chr7:30440681 | T | G | 1 | a0001c0001t0001g0002 | 2 | HG02074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2454-3025A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440681 | |||||||
chr7:30440682 | G | T | 1 | a0001c0001t0001g0002 | 2 | HG02074.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2454-3026C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440682 | |||||||
chr7:30440730 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0024g0074 a0006c0009t0007g0012 |
4 | HG01106.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2454-3074G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440730 | |||||||
chr7:30440745 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2454-3089T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440745 | |||||||
chr7:30440791 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2454-3135T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440791 | |||||||
chr7:30440901 | G | A | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2454-3245C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30440901 | |||||||
chr7:30441096 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2454-3440G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441096 | |||||||
chr7:30441130 | C | T | 1 | a0002c0002t0002g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2454-3474G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441130 | |||||||
chr7:30441326 | G | C | 1 | a0004c0006t0006g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2454-3670C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441326 | |||||||
chr7:30441334 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2454-3678G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441334 | |||||||
chr7:30441448 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2454-3792C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441448 | |||||||
chr7:30441615 | C | G | 6 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(3): Show |
6 | HG02559.hp2 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2454-3959G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441615 | |||||||
chr7:30441698 | T | C | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(83): Show |
102 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.2454-4042A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441698 | |||||||
chr7:30441753 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2454-4097T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441753 | |||||||
chr7:30441759 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2454-4103T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30441759 | |||||||
chr7:30442015 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2453+4126G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442015 | |||||||
chr7:30442387 | A | G | 1 | a0002c0013t0025g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2453+3754T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442387 | |||||||
chr7:30442433 | C | T | 1 | a0002c0002t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2453+3708G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442433 | |||||||
chr7:30442435 | G | A | 1 | a0002c0002t0002g0154 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2453+3706C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442435 | |||||||
chr7:30442470 | C | G | 1 | a0002c0002t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2453+3671G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442470 | |||||||
chr7:30442527 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2453+3614G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442527 | |||||||
chr7:30442527 | C | T | 1 | a0002c0004t0002g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2453+3614G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442527 | |||||||
chr7:30442592 | G | C | 10 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(7): Show |
10 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2453+3549C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442592 | |||||||
chr7:30442620 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2453+3521A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442620 | |||||||
chr7:30442662 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2453+3479G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442662 | |||||||
chr7:30442663 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2453+3478C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442663 | |||||||
chr7:30442852 | A | G | 2 | a0002c0002t0002g0017 a0002c0002t0002g0116 |
3 | HG01081.hp2 HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2453+3289T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442852 | |||||||
chr7:30442875 | C | A | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2453+3266G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442875 | |||||||
chr7:30442958 | G | A | 2 | a0002c0002t0002g0099 a0002c0002t0027g0123 |
2 | HG02735.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2453+3183C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442958 | |||||||
chr7:30442969 | A | C | 1 | a0002c0002t0002g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2453+3172T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30442969 | |||||||
chr7:30443060 | C | G | 8 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2453+3081G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443060 | |||||||
chr7:30443102 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2453+3039G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443102 | |||||||
chr7:30443123 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2453+3018G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443123 | |||||||
chr7:30443223 | G | A | 2 | a0002c0004t0002g0060 a0002c0004t0002g0061 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2453+2918C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443223 | |||||||
chr7:30443283 | A | T | 1 | a0002c0002t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2453+2858T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443283 | |||||||
chr7:30443284 | A | C | 3 | a0002c0004t0002g0060 a0002c0004t0002g0061 a0002c0004t0002g0062 |
3 | HG02809.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2453+2857T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443284 | |||||||
chr7:30443294 | A | G | 11 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(8): Show |
12 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2453+2847T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443294 | |||||||
chr7:30443311 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2453+2830C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443311 | |||||||
chr7:30443346 | T | A | 1 | a0001c0001t0022g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2453+2795A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443346 | |||||||
chr7:30443364 | C | T | 8 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2453+2777G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443364 | |||||||
chr7:30443698 | A | G | 11 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(8): Show |
12 | HG01081.hp1 HG01255.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2453+2443T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443698 | |||||||
chr7:30443803 | T | G | 1 | a0002c0002t0002g0005 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2453+2338A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443803 | |||||||
chr7:30443942 | C | T | 12 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(9): Show |
12 | HG01081.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2453+2199G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443942 | |||||||
chr7:30443955 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0204 others(30): Show |
43 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(40): Show |
intron_variant | MODIFIER | c.2453+2186C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30443955 | |||||||
chr7:30444006 | G | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0284 |
3 | NA18967.hp2 NA18974.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2453+2135C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444006 | |||||||
chr7:30444132 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2453+2009G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444132 | |||||||
chr7:30444168 | C | T | 1 | a0002c0004t0020g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2453+1973G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444168 | |||||||
chr7:30444187 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2453+1954C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444187 | |||||||
chr7:30444297 | A | G | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2453+1844T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444297 | |||||||
chr7:30444310 | A | T | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2453+1831T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444310 | |||||||
chr7:30444337 | G | T | 12 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(9): Show |
12 | HG01081.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2453+1804C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444337 | |||||||
chr7:30444348 | C | T | 1 | a0002c0002t0003g0019 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2453+1793G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444348 | |||||||
chr7:30444446 | C | T | 5 | a0002c0004t0005g0015 a0002c0004t0005g0086 a0002c0004t0005g0087 others(2): Show |
6 | HG01255.hp2 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2453+1695G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444446 | |||||||
chr7:30444450 | G | A | 1 | a0002c0002t0002g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2453+1691C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444450 | |||||||
chr7:30444593 | T | G | 3 | a0002c0002t0002g0010 a0002c0002t0002g0147 a0002c0002t0002g0148 |
5 | NA18946.hp2 NA18965.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.2453+1548A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444593 | |||||||
chr7:30444611 | G | A | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2453+1530C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444611 | |||||||
chr7:30444677 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2453+1464A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444677 | |||||||
chr7:30444811 | C | T | 1 | a0002c0002t0003g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2453+1330G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444811 | |||||||
chr7:30444824 | T | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(59): Show |
77 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2453+1317A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30444824 | |||||||
chr7:30445027 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(47): Show |
65 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2453+1114G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445027 | |||||||
chr7:30445075 | C | G | 6 | a0001c0003t0004g0238 a0002c0004t0002g0048 a0002c0004t0002g0050 others(3): Show |
6 | HG01081.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2453+1066G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445075 | |||||||
chr7:30445111 | T | C | 2 | a0001c0001t0001g0077 a0006c0009t0007g0012 |
3 | HG01106.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2453+1030A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445111 | |||||||
chr7:30445129 | G | T | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2453+1012C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445129 | |||||||
chr7:30445235 | C | T | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2453+906G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445235 | |||||||
chr7:30445261 | TA | T | 7 | a0002c0002t0002g0023 a0002c0002t0002g0158 a0002c0002t0002g0159 others(4): Show |
9 | HG00609.hp2 HG02155.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.2453+879delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445261 | |||||||
chr7:30445278 | T | TA | 56 | a0001c0001t0001g0200 a0001c0001t0001g0208 a0001c0001t0001g0211 others(53): Show |
64 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2453+862dupT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445278 | |||||||
chr7:30445278 | TA | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0059 others(37): Show |
44 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.2453+862delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445278 | |||||||
chr7:30445278 | TAA | T | 12 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2453+861_2453+862d others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445278 | |||||||
chr7:30445278 | TAAA | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(45): Show |
60 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2453+860_2453+862d others(5): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445278 | |||||||
chr7:30445377 | T | C | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2453+764A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445377 | |||||||
chr7:30445409 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2453+732A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445409 | |||||||
chr7:30445480 | G | A | 5 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(2): Show |
5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2453+661C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445480 | |||||||
chr7:30445756 | C | CA | 49 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0170 others(46): Show |
50 | HG00438.hp1 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.2453+384dupT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445756 | |||||||
chr7:30445756 | C | CAAA | 9 | a0001c0001t0007g0033 a0001c0001t0007g0036 a0001c0003t0014g0032 others(6): Show |
9 | HG01109.hp2 HG02622.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2453+382_2453+384d others(5): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445756 | |||||||
chr7:30445756 | CA | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(44): Show |
58 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.2453+384delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445756 | |||||||
chr7:30445756 | CAA | C | 10 | a0001c0001t0001g0077 a0001c0001t0001g0268 a0001c0001t0009g0038 others(7): Show |
11 | HG01106.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2453+383_2453+384d others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445756 | |||||||
chr7:30445799 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2453+342A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445799 | |||||||
chr7:30445814 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2453+327C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445814 | |||||||
chr7:30445909 | G | C | 1 | a0002c0002t0002g0101 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2453+232C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445909 | |||||||
chr7:30445960 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2453+181C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30445960 | |||||||
chr7:30446018 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2453+123T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30446018 | |||||||
chr7:30446034 | G | A | 1 | a0001c0003t0002g0084 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2453+107C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30446034 | |||||||
chr7:30446087 | G | GC | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(44): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.2453+53dupG | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30446087 | |||||||
chr7:30446094 | A | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(62): Show |
81 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2453+47T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30446094 | |||||||
chr7:30446125 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(102): Show |
123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2453+16T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 9/13 | chr7 | 30446125 | |||||||
chr7:30446362 | GGCCTGGG others(267): Show |
G | 1 | a0002c0002t0002g0112 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2369+331_2370-139d others(2): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 8/13 | chr7 | 30446362 | |||||||
chr7:30446383 | A | C | 17 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(14): Show |
18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2370-159T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 8/13 | chr7 | 30446383 | |||||||
chr7:30446612 | A | AC | 7 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0211 others(4): Show |
7 | HG02300.hp1 HG02622.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2369+354dupG | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 8/13 | chr7 | 30446612 | |||||||
chr7:30446655 | C | A | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2369+312G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 8/13 | chr7 | 30446655 | |||||||
chr7:30447293 | T | C | 1 | a0002c0002t0005g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2286-243A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447293 | |||||||
chr7:30447491 | C | T | 8 | a0001c0001t0001g0077 a0001c0001t0009g0038 a0001c0001t0009g0039 others(5): Show |
8 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2286-441G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447491 | |||||||
chr7:30447581 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2286-531C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447581 | |||||||
chr7:30447704 | G | A | 2 | a0003c0005t0002g0133 a0003c0005t0008g0073 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2285+594C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447704 | |||||||
chr7:30447742 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2285+556A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447742 | |||||||
chr7:30447743 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2285+555C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447743 | |||||||
chr7:30447926 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0228 |
2 | HG02135.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2285+372T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447926 | |||||||
chr7:30447965 | G | A | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2285+333C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30447965 | |||||||
chr7:30448278 | T | G | 4 | a0001c0001t0012g0054 a0001c0001t0012g0055 a0001c0001t0012g0056 others(1): Show |
4 | HG00735.hp1 HG03710.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.2285+20A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 7/13 | chr7 | 30448278 | |||||||
chr7:30448416 | G | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 |
3 | HG01109.hp2 HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2202-35C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30448416 | |||||||
chr7:30448521 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2202-140G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30448521 | |||||||
chr7:30448562 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2202-181C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30448562 | |||||||
chr7:30448607 | C | A | 8 | a0002c0002t0002g0146 a0002c0002t0003g0009 a0002c0002t0003g0019 others(5): Show |
11 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2202-226G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30448607 | |||||||
chr7:30448874 | C | G | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2202-493G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30448874 | |||||||
chr7:30449056 | T | C | 3 | a0003c0007t0008g0067 a0003c0007t0008g0069 a0003c0007t0017g0066 |
3 | HG02572.hp1 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2202-675A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449056 | |||||||
chr7:30449169 | A | G | 1 | a0008c0012t0001g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2202-788T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449169 | |||||||
chr7:30449305 | G | A | 9 | a0001c0001t0001g0200 a0001c0001t0001g0208 a0001c0001t0001g0219 others(6): Show |
11 | HG00323.hp2 HG00738.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2202-924C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449305 | |||||||
chr7:30449391 | A | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(60): Show |
78 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2202-1010T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449391 | |||||||
chr7:30449881 | G | A | 1 | a0001c0003t0004g0240 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2201+1335C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449881 | |||||||
chr7:30449949 | T | C | 28 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(25): Show |
30 | HG01081.hp1 HG01109.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2201+1267A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30449949 | |||||||
chr7:30450051 | G | A | 7 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(4): Show |
7 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2201+1165C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450051 | |||||||
chr7:30450181 | G | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2201+1035C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450181 | |||||||
chr7:30450201 | A | G | 7 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2201+1015T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450201 | |||||||
chr7:30450351 | A | G | 1 | a0002c0002t0002g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2201+865T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450351 | |||||||
chr7:30450355 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2201+861T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450355 | |||||||
chr7:30450421 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2201+795A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450421 | |||||||
chr7:30450729 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2201+487C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450729 | |||||||
chr7:30450751 | G | A | 1 | a0007c0020t0002g0102 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2201+465C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450751 | |||||||
chr7:30450980 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2201+236C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30450980 | |||||||
chr7:30451144 | A | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(44): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.2201+72T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 6/13 | chr7 | 30451144 | |||||||
chr7:30453270 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.377-230A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30453270 | |||||||
chr7:30453379 | C | T | 1 | a0009c0019t0002g0125 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.377-339G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30453379 | |||||||
chr7:30453386 | G | C | 1 | a0001c0001t0002g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.377-346C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30453386 | |||||||
chr7:30453789 | T | A | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.377-749A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30453789 | |||||||
chr7:30454021 | T | C | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.377-981A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454021 | |||||||
chr7:30454032 | T | C | 4 | a0001c0001t0001g0077 a0005c0008t0001g0078 a0005c0008t0001g0079 others(1): Show |
4 | HG01106.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-992A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454032 | |||||||
chr7:30454219 | A | G | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.376+918T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454219 | |||||||
chr7:30454406 | T | A | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(203): Show |
249 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.376+731A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454406 | |||||||
chr7:30454521 | T | C | 2 | a0003c0011t0008g0076 a0003c0011t0010g0075 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+616A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454521 | |||||||
chr7:30454538 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.376+599G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454538 | |||||||
chr7:30454692 | G | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(1): Show |
14 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.376+445C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454692 | |||||||
chr7:30454760 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0222 |
2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.376+377C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454760 | |||||||
chr7:30454952 | G | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+185C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454952 | |||||||
chr7:30454969 | C | A | 10 | a0002c0002t0002g0023 a0002c0002t0002g0134 a0002c0002t0002g0158 others(7): Show |
12 | HG00609.hp2 HG02155.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.376+168G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30454969 | |||||||
chr7:30455006 | T | C | 132 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(129): Show |
160 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.376+131A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30455006 | |||||||
chr7:30455029 | C | T | 1 | a0002c0002t0002g0124 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.376+108G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 5/13 | chr7 | 30455029 | |||||||
chr7:30455349 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0092 |
2 | HG02523.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.202-38C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455349 | |||||||
chr7:30455354 | G | A | 1 | a0001c0003t0004g0238 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.202-43C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455354 | |||||||
chr7:30455411 | G | A | 1 | a0002c0004t0005g0049 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.202-100C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455411 | |||||||
chr7:30455469 | C | T | 1 | a0001c0001t0016g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.202-158G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455469 | |||||||
chr7:30455517 | T | C | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.202-206A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455517 | |||||||
chr7:30455590 | C | CT | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0170 others(3): Show |
6 | HG02698.hp2 HG03654.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-280dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455590 | |||||||
chr7:30455590 | C | CTT | 131 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(128): Show |
159 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.202-281_202-280dup others(2): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455590 | |||||||
chr7:30455590 | CT | C | 7 | a0001c0001t0001g0211 a0001c0001t0001g0284 a0001c0001t0006g0024 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-280delA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455590 | |||||||
chr7:30455671 | G | T | 2 | a0002c0002t0002g0023 a0002c0002t0002g0159 |
3 | HG03491.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.202-360C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455671 | |||||||
chr7:30455781 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202-470A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455781 | |||||||
chr7:30455781 | T | G | 1 | a0005c0008t0001g0080 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.202-470A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455781 | |||||||
chr7:30455891 | G | A | 1 | a0002c0002t0002g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.202-580C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30455891 | |||||||
chr7:30456157 | G | C | 3 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 |
3 | HG01109.hp2 HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.201+564C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456157 | |||||||
chr7:30456296 | T | C | 5 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+425A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456296 | |||||||
chr7:30456338 | G | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+383C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456338 | |||||||
chr7:30456348 | C | T | 1 | a0002c0002t0027g0123 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.201+373G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456348 | |||||||
chr7:30456377 | C | T | 8 | a0003c0005t0002g0133 a0003c0005t0008g0064 a0003c0005t0008g0073 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.201+344G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456377 | |||||||
chr7:30456434 | C | G | 132 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(129): Show |
160 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.201+287G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456434 | |||||||
chr7:30456470 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.201+251T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456470 | |||||||
chr7:30456693 | G | GC | 132 | a0001c0001t0002g0139 a0001c0001t0012g0054 a0001c0001t0012g0055 others(129): Show |
160 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.201+27dupG | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 4/13 | chr7 | 30456693 | |||||||
chr7:30457092 | T | C | 157 | a0001c0001t0001g0077 a0001c0001t0002g0139 a0001c0001t0007g0033 others(154): Show |
185 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-121-50A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457092 | |||||||
chr7:30457136 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0201 |
2 | HG02040.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.-121-94C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457136 | |||||||
chr7:30457199 | C | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121-157G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457199 | |||||||
chr7:30457278 | A | C | 135 | a0001c0001t0002g0139 a0001c0001t0007g0033 a0001c0001t0007g0035 others(132): Show |
163 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.-121-236T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457278 | |||||||
chr7:30457302 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0006g0024 a0001c0001t0006g0047 |
4 | HG02559.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-260T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457302 | |||||||
chr7:30457322 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-121-280C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457322 | |||||||
chr7:30457557 | T | C | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-121-515A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457557 | |||||||
chr7:30457799 | C | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0251 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-757G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457799 | |||||||
chr7:30457893 | T | A | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-121-851A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457893 | |||||||
chr7:30457916 | T | C | 14 | a0002c0002t0002g0132 a0002c0002t0002g0146 a0002c0002t0003g0009 others(11): Show |
18 | HG01167.hp1 HG01169.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-121-874A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30457916 | |||||||
chr7:30458128 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-122+1024A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458128 | |||||||
chr7:30458226 | T | A | 145 | a0001c0001t0002g0139 a0001c0001t0009g0038 a0001c0001t0009g0039 others(142): Show |
173 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.-122+926A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458226 | |||||||
chr7:30458360 | C | CAG | 17 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(14): Show |
27 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-122+790_-122+791d others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458360 | |||||||
chr7:30458381 | G | GT | 4 | a0001c0001t0001g0192 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | NA18978.hp1 NA18978.hp2 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122+770dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458381 | |||||||
chr7:30458383 | T | A | 1 | a0002c0022t0002g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-122+769A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458383 | |||||||
chr7:30458421 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(16): Show |
19 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-122+731G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458421 | |||||||
chr7:30458740 | C | CT | 93 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0002g0139 others(90): Show |
115 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-122+411dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458740 | |||||||
chr7:30458740 | C | T | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-122+412G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458740 | |||||||
chr7:30458741 | T | C | 1 | a0002c0002t0002g0097 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-122+411A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458741 | |||||||
chr7:30458806 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-122+346C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458806 | |||||||
chr7:30458988 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-122+164G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30458988 | |||||||
chr7:30459113 | A | G | 1 | a0001c0003t0004g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-122+39T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 3/13 | chr7 | 30459113 | |||||||
chr7:30459495 | C | G | 21 | a0001c0001t0012g0054 a0001c0001t0012g0055 a0001c0001t0012g0056 others(18): Show |
22 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-210-255G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 2/13 | chr7 | 30459495 | |||||||
chr7:30459835 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(77): Show |
95 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-211+66T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 2/13 | chr7 | 30459835 | |||||||
chr7:30459838 | G | A | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-211+63C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 2/13 | chr7 | 30459838 | |||||||
chr7:30460077 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-351-36C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460077 | |||||||
chr7:30460102 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0222 |
2 | NA18966.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-351-61T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460102 | |||||||
chr7:30460156 | A | G | 1 | a0002c0002t0002g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-351-115T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460156 | |||||||
chr7:30460211 | G | T | 5 | a0002c0013t0025g0068 a0003c0005t0010g0065 a0003c0007t0008g0067 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-351-170C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460211 | |||||||
chr7:30460305 | A | T | 1 | a0002c0002t0003g0138 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-351-264T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460305 | |||||||
chr7:30460345 | T | C | 33 | a0001c0003t0002g0084 a0002c0002t0002g0005 a0002c0002t0002g0010 others(30): Show |
43 | HG00408.hp2 HG01081.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.-351-304A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460345 | |||||||
chr7:30460703 | C | G | 1 | a0002c0002t0002g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-351-662G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30460703 | |||||||
chr7:30461008 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-967A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461008 | |||||||
chr7:30461074 | A | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-1033T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461074 | |||||||
chr7:30461159 | C | T | 5 | a0002c0002t0002g0081 a0002c0002t0002g0083 a0002c0002t0002g0097 others(2): Show |
5 | NA18949.hp1 NA18974.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-1118G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461159 | |||||||
chr7:30461164 | A | C | 12 | a0001c0003t0004g0171 a0001c0003t0004g0235 a0001c0003t0004g0236 others(9): Show |
12 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-351-1123T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461164 | |||||||
chr7:30461264 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-351-1223C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461264 | |||||||
chr7:30461416 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-351-1375C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461416 | |||||||
chr7:30461620 | G | C | 1 | a0002c0002t0002g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-351-1579C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461620 | |||||||
chr7:30461723 | AG | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-1683delC | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461723 | |||||||
chr7:30461802 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-1761T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461802 | |||||||
chr7:30461831 | C | T | 7 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-351-1790G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461831 | |||||||
chr7:30461986 | C | A | 1 | a0004c0006t0006g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-351-1945G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30461986 | |||||||
chr7:30462010 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-351-1969A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462010 | |||||||
chr7:30462063 | G | C | 144 | a0001c0001t0001g0077 a0001c0001t0002g0001 a0001c0001t0002g0014 others(141): Show |
181 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-351-2022C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462063 | |||||||
chr7:30462148 | A | C | 7 | a0002c0002t0002g0132 a0002c0002t0003g0009 a0002c0002t0003g0019 others(4): Show |
10 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-351-2107T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462148 | |||||||
chr7:30462201 | A | G | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-2160T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462201 | |||||||
chr7:30462333 | C | T | 7 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-351-2292G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462333 | |||||||
chr7:30462335 | C | T | 1 | a0002c0002t0002g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-351-2294G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462335 | |||||||
chr7:30462342 | T | C | 5 | a0002c0004t0005g0015 a0002c0004t0005g0086 a0002c0004t0005g0087 others(2): Show |
6 | HG01255.hp2 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-351-2301A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462342 | |||||||
chr7:30462394 | C | T | 3 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 |
3 | HG01109.hp2 HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-351-2353G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462394 | |||||||
chr7:30462426 | G | GT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0186 a0001c0001t0001g0187 others(55): Show |
68 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-351-2386dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462426 | |||||||
chr7:30462426 | G | GTT | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(43): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-2387_-351-238 others(6): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462426 | |||||||
chr7:30462426 | G | GTTT | 8 | a0001c0001t0001g0027 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
9 | HG01346.hp2 HG01361.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.-351-2388_-351-238 others(7): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462426 | |||||||
chr7:30462426 | GT | G | 7 | a0001c0001t0001g0167 a0001c0001t0001g0224 a0001c0001t0009g0038 others(4): Show |
7 | HG01516.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-351-2386delA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462426 | |||||||
chr7:30462431 | T | G | 3 | a0005c0008t0001g0078 a0005c0008t0001g0079 a0005c0008t0001g0080 |
3 | HG02976.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-351-2390A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462431 | |||||||
chr7:30462456 | T | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-2415A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462456 | |||||||
chr7:30462637 | G | T | 1 | a0001c0001t0009g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-351-2596C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462637 | |||||||
chr7:30462775 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-351-2734G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462775 | |||||||
chr7:30462812 | C | T | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-2771G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462812 | |||||||
chr7:30462948 | C | CA | 105 | a0001c0001t0001g0170 a0001c0001t0001g0282 a0001c0001t0002g0139 others(102): Show |
131 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.-351-2908dupT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462948 | |||||||
chr7:30462948 | CA | C | 43 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(40): Show |
58 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.-351-2908delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462948 | |||||||
chr7:30462999 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-351-2958T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30462999 | |||||||
chr7:30463163 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-3122T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463163 | |||||||
chr7:30463270 | A | G | 5 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-3229T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463270 | |||||||
chr7:30463314 | A | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-351-3273T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463314 | |||||||
chr7:30463398 | AAAAC | A | 97 | a0001c0001t0002g0139 a0001c0003t0002g0084 a0002c0002t0002g0003 others(94): Show |
123 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.-351-3361_-351-335 others(8): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463398 | |||||||
chr7:30463571 | C | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-3530G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463571 | |||||||
chr7:30463664 | T | C | 214 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(211): Show |
267 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-351-3623A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463664 | |||||||
chr7:30463706 | TA | T | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(136): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-351-3666delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463706 | |||||||
chr7:30463706 | TAA | T | 71 | a0001c0001t0002g0139 a0001c0003t0002g0084 a0002c0002t0002g0005 others(68): Show |
89 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-351-3667_-351-366 others(6): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463706 | |||||||
chr7:30463747 | A | T | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(168): Show |
212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-351-3706T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463747 | |||||||
chr7:30463792 | C | T | 5 | a0002c0013t0025g0068 a0003c0005t0010g0065 a0003c0007t0008g0067 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-351-3751G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463792 | |||||||
chr7:30463832 | A | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-3791T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463832 | |||||||
chr7:30463870 | A | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-3829T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463870 | |||||||
chr7:30463875 | C | A | 12 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
18 | HG02080.hp2 HG02273.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.-351-3834G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30463875 | |||||||
chr7:30464051 | T | C | 1 | a0002c0002t0011g0155 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-351-4010A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464051 | |||||||
chr7:30464176 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-4135C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464176 | |||||||
chr7:30464233 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-4192G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464233 | |||||||
chr7:30464296 | A | C | 1 | a0002c0002t0002g0121 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-351-4255T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464296 | |||||||
chr7:30464322 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-4281C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464322 | |||||||
chr7:30464335 | A | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-4294T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464335 | |||||||
chr7:30464341 | G | A | 1 | a0001c0001t0016g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-351-4300C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464341 | |||||||
chr7:30464544 | C | T | 96 | a0001c0001t0002g0139 a0002c0002t0002g0003 a0002c0002t0002g0005 others(93): Show |
122 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.-351-4503G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464544 | |||||||
chr7:30464590 | A | G | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-4549T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464590 | |||||||
chr7:30464657 | G | A | 76 | a0001c0001t0002g0139 a0002c0002t0002g0003 a0002c0002t0002g0005 others(73): Show |
97 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-351-4616C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464657 | |||||||
chr7:30464907 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-4866C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464907 | |||||||
chr7:30464948 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-351-4907A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30464948 | |||||||
chr7:30465084 | C | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-5043G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465084 | |||||||
chr7:30465086 | G | T | 1 | a0002c0002t0002g0150 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-351-5045C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465086 | |||||||
chr7:30465104 | CA | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(45): Show |
63 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-351-5064delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465104 | |||||||
chr7:30465105 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-351-5064T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465105 | |||||||
chr7:30465116 | G | A | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-5075C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465116 | |||||||
chr7:30465265 | G | C | 1 | a0001c0001t0028g0058 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-351-5224C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465265 | |||||||
chr7:30465371 | T | TAGAG | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-5331_-351-533 others(8): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465371 | |||||||
chr7:30465505 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-351-5464G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465505 | |||||||
chr7:30465556 | T | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-5515A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465556 | |||||||
chr7:30465657 | C | CT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-5617dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465657 | |||||||
chr7:30465949 | A | G | 1 | a0002c0004t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-351-5908T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465949 | |||||||
chr7:30465951 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-351-5910G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465951 | |||||||
chr7:30465988 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-5947G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30465988 | |||||||
chr7:30466216 | C | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-6175G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466216 | |||||||
chr7:30466304 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-6263T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466304 | |||||||
chr7:30466381 | T | C | 3 | a0002c0002t0002g0082 a0002c0002t0002g0112 a0002c0002t0002g0113 |
3 | HG02135.hp1 NA18991.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-351-6340A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466381 | |||||||
chr7:30466417 | C | T | 2 | a0001c0003t0014g0013 a0001c0003t0014g0032 |
3 | HG03209.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-351-6376G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466417 | |||||||
chr7:30466425 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-351-6384G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466425 | |||||||
chr7:30466465 | C | G | 16 | a0001c0003t0004g0171 a0001c0003t0004g0235 a0001c0003t0004g0236 others(13): Show |
17 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-351-6424G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466465 | |||||||
chr7:30466560 | C | T | 6 | a0002c0002t0002g0017 a0002c0002t0002g0116 a0002c0002t0002g0117 others(3): Show |
7 | HG01081.hp2 HG01123.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.-351-6519G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466560 | |||||||
chr7:30466617 | T | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-351-6576A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466617 | |||||||
chr7:30466829 | C | G | 3 | a0002c0002t0002g0018 a0002c0002t0002g0130 a0002c0002t0002g0157 |
4 | HG01069.hp2 HG01071.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-351-6788G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466829 | |||||||
chr7:30466848 | G | A | 8 | a0001c0001t0012g0054 a0001c0001t0012g0055 a0001c0001t0012g0056 others(5): Show |
8 | HG00735.hp1 HG01981.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-351-6807C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466848 | |||||||
chr7:30466941 | G | A | 1 | a0006c0009t0007g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-351-6900C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30466941 | |||||||
chr7:30467028 | C | T | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(168): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-351-6987G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467028 | |||||||
chr7:30467145 | G | C | 1 | a0001c0001t0028g0058 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-351-7104C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467145 | |||||||
chr7:30467344 | G | GT | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(72): Show |
99 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-351-7304dupA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467344 | |||||||
chr7:30467344 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-351-7303C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467344 | |||||||
chr7:30467370 | C | T | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-7329G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467370 | |||||||
chr7:30467423 | A | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG00438.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-351-7382T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467423 | |||||||
chr7:30467476 | A | T | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-7435T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467476 | |||||||
chr7:30467508 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-351-7467G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467508 | |||||||
chr7:30467523 | C | G | 6 | a0001c0001t0024g0074 a0004c0006t0001g0175 a0004c0006t0001g0176 others(3): Show |
6 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-351-7482G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467523 | |||||||
chr7:30467657 | G | A | 1 | a0002c0002t0002g0023 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-351-7616C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467657 | |||||||
chr7:30467764 | T | C | 194 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(191): Show |
246 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-351-7723A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467764 | |||||||
chr7:30467972 | G | C | 1 | a0002c0002t0002g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-351-7931C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467972 | |||||||
chr7:30467994 | A | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-351-7953T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30467994 | |||||||
chr7:30468097 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-351-8056A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468097 | |||||||
chr7:30468132 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0284 |
3 | HG00438.hp1 HG02135.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-351-8091A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468132 | |||||||
chr7:30468242 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-351-8201A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468242 | |||||||
chr7:30468572 | A | G | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-351-8531T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468572 | |||||||
chr7:30468675 | T | A | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0251 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-351-8634A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468675 | |||||||
chr7:30468733 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-351-8692T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468733 | |||||||
chr7:30468738 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0278 a0001c0001t0001g0279 |
5 | HG00408.hp1 HG00438.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.-351-8697A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468738 | |||||||
chr7:30468807 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-351-8766A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30468807 | |||||||
chr7:30469168 | T | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-351-9127A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469168 | |||||||
chr7:30469296 | C | G | 2 | a0002c0002t0002g0114 a0002c0002t0002g0115 |
2 | NA18947.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-351-9255G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469296 | |||||||
chr7:30469376 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-352+9230G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469376 | |||||||
chr7:30469377 | T | C | 1 | a0002c0002t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-352+9229A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469377 | |||||||
chr7:30469435 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-352+9171C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469435 | |||||||
chr7:30469815 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-352+8791T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30469815 | |||||||
chr7:30470029 | G | A | 12 | a0002c0013t0025g0068 a0003c0005t0008g0064 a0003c0005t0008g0073 others(9): Show |
12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-352+8577C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470029 | |||||||
chr7:30470205 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-352+8401G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470205 | |||||||
chr7:30470455 | G | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-352+8151C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470455 | |||||||
chr7:30470781 | G | T | 1 | a0003c0005t0010g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-352+7825C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470781 | |||||||
chr7:30470909 | G | T | 4 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-352+7697C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470909 | |||||||
chr7:30470918 | G | A | 102 | a0001c0001t0002g0139 a0002c0002t0002g0003 a0002c0002t0002g0005 others(99): Show |
129 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.-352+7688C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30470918 | |||||||
chr7:30471072 | G | GGGCTC | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7533_-352+753 others(9): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471072 | |||||||
chr7:30471076 | ATCGCT | A | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7525_-352+752 others(9): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471076 | |||||||
chr7:30471084 | C | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7522G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471084 | |||||||
chr7:30471087 | A | AACAG | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7518_-352+751 others(8): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471087 | |||||||
chr7:30471091 | GCT | G | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7513_-352+751 others(6): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471091 | |||||||
chr7:30471095 | A | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7511T>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471095 | |||||||
chr7:30471097 | C | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7509G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471097 | |||||||
chr7:30471098 | T | C | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7508A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471098 | |||||||
chr7:30471099 | G | C | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7507C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471099 | |||||||
chr7:30471102 | G | GCCACCTA others(172): Show |
5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+7503_-352+750 others(183): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471102 | |||||||
chr7:30471237 | A | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-352+7369T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471237 | |||||||
chr7:30471516 | C | T | 1 | a0003c0005t0008g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-352+7090G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471516 | |||||||
chr7:30471568 | CA | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(46): Show |
64 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-352+7037delT | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471568 | |||||||
chr7:30471586 | T | A | 1 | a0002c0004t0020g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-352+7020A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471586 | |||||||
chr7:30471594 | G | A | 1 | a0002c0002t0003g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-352+7012C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471594 | |||||||
chr7:30471638 | C | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-352+6968G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471638 | |||||||
chr7:30471665 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-352+6941C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471665 | |||||||
chr7:30471808 | G | A | 6 | a0002c0002t0002g0010 a0002c0002t0002g0020 a0002c0002t0002g0089 others(3): Show |
9 | NA18943.hp2 NA18946.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-352+6798C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471808 | |||||||
chr7:30471854 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-352+6752C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471854 | |||||||
chr7:30471935 | G | T | 12 | a0002c0013t0025g0068 a0003c0005t0008g0064 a0003c0005t0008g0073 others(9): Show |
12 | HG01891.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-352+6671C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30471935 | |||||||
chr7:30472021 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(41): Show |
59 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.-352+6585A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472021 | |||||||
chr7:30472178 | C | T | 213 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(210): Show |
266 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.-352+6428G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472178 | |||||||
chr7:30472210 | G | A | 1 | a0002c0002t0003g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-352+6396C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472210 | |||||||
chr7:30472329 | G | T | 26 | a0002c0002t0002g0003 a0002c0002t0002g0016 a0002c0002t0002g0081 others(23): Show |
34 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.-352+6277C>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472329 | |||||||
chr7:30472333 | C | A | 101 | a0001c0001t0002g0139 a0001c0003t0002g0084 a0002c0002t0002g0003 others(98): Show |
128 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-352+6273G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472333 | |||||||
chr7:30472390 | G | C | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-352+6216C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472390 | |||||||
chr7:30472414 | G | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(43): Show |
61 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-352+6192C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472414 | |||||||
chr7:30472471 | T | C | 1 | a0001c0001t0009g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-352+6135A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472471 | |||||||
chr7:30472566 | C | A | 2 | a0001c0001t0007g0035 a0001c0001t0007g0036 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-352+6040G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472566 | |||||||
chr7:30472603 | T | C | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
56 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-352+6003A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472603 | |||||||
chr7:30472878 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-352+5728G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30472878 | |||||||
chr7:30473079 | A | G | 186 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(183): Show |
238 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-352+5527T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473079 | |||||||
chr7:30473081 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-352+5525C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473081 | |||||||
chr7:30473122 | G | A | 210 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(207): Show |
262 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.-352+5484C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473122 | |||||||
chr7:30473155 | A | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(188): Show |
243 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-352+5451T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473155 | |||||||
chr7:30473436 | G | A | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-352+5170C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473436 | |||||||
chr7:30473519 | A | G | 1 | a0001c0001t0022g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-352+5087T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473519 | |||||||
chr7:30473543 | G | A | 178 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(175): Show |
230 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.-352+5063C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473543 | |||||||
chr7:30473593 | G | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(23): Show |
36 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-352+5013C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473593 | |||||||
chr7:30473645 | C | T | 5 | a0004c0006t0001g0175 a0004c0006t0001g0176 a0004c0006t0006g0173 others(2): Show |
5 | HG01978.hp1 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+4961G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473645 | |||||||
chr7:30473667 | T | G | 1 | a0004c0006t0006g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-352+4939A>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30473667 | |||||||
chr7:30474104 | GTAGAGTT others(22): Show |
G | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-352+4473_-352+450 others(33): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474104 | |||||||
chr7:30474301 | C | G | 1 | a0002c0002t0003g0093 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-352+4305G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474301 | |||||||
chr7:30474447 | T | A | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-352+4159A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474447 | |||||||
chr7:30474539 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): Show |
8 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-352+4067T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474539 | |||||||
chr7:30474652 | C | T | 1 | a0001c0003t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-352+3954G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474652 | |||||||
chr7:30474676 | C | T | 1 | a0002c0004t0005g0049 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-352+3930G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474676 | |||||||
chr7:30474719 | T | A | 1 | a0006c0009t0007g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-352+3887A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474719 | |||||||
chr7:30474738 | T | C | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(38): Show |
56 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-352+3868A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474738 | |||||||
chr7:30474825 | A | G | 25 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(22): Show |
36 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-352+3781T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30474825 | |||||||
chr7:30475087 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18993.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-352+3519T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475087 | |||||||
chr7:30475208 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-352+3398A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475208 | |||||||
chr7:30475237 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): Show |
8 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-352+3369T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475237 | |||||||
chr7:30475269 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-352+3337A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475269 | |||||||
chr7:30475287 | G | C | 123 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(120): Show |
160 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.-352+3319C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475287 | |||||||
chr7:30475288 | A | C | 1 | a0002c0002t0002g0156 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-352+3318T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475288 | |||||||
chr7:30475367 | T | C | 1 | a0001c0001t0024g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-352+3239A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475367 | |||||||
chr7:30475375 | T | C | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(185): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.-352+3231A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475375 | |||||||
chr7:30475594 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): Show |
8 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-352+3012C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30475594 | |||||||
chr7:30476015 | C | T | 1 | a0002c0002t0002g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-352+2591G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476015 | |||||||
chr7:30476196 | A | G | 14 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(11): Show |
24 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.-352+2410T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476196 | |||||||
chr7:30476272 | A | G | 1 | a0002c0004t0002g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-352+2334T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476272 | |||||||
chr7:30476280 | T | A | 1 | a0002c0002t0002g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-352+2326A>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476280 | |||||||
chr7:30476293 | C | A | 2 | a0003c0011t0008g0076 a0003c0011t0010g0075 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-352+2313G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476293 | |||||||
chr7:30476331 | A | C | 4 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(1): Show |
4 | HG01109.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-352+2275T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476331 | |||||||
chr7:30476350 | A | G | 8 | a0001c0001t0001g0077 a0001c0001t0007g0033 a0001c0001t0007g0035 others(5): Show |
8 | HG01106.hp2 HG01109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-352+2256T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476350 | |||||||
chr7:30476370 | T | C | 7 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-352+2236A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476370 | |||||||
chr7:30476582 | A | C | 1 | a0001c0018t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-352+2024T>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476582 | |||||||
chr7:30476643 | T | C | 4 | a0002c0002t0002g0154 a0002c0002t0011g0021 a0002c0002t0011g0153 others(1): Show |
5 | NA18944.hp2 NA18949.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-352+1963A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476643 | |||||||
chr7:30476899 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-352+1707C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476899 | |||||||
chr7:30476975 | C | T | 2 | a0001c0003t0014g0013 a0001c0003t0014g0032 |
3 | HG03209.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-352+1631G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30476975 | |||||||
chr7:30477106 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-352+1500T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477106 | |||||||
chr7:30477198 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | NA18962.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-352+1408A>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477198 | |||||||
chr7:30477295 | A | G | 1 | a0002c0002t0002g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-352+1311T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477295 | |||||||
chr7:30477461 | C | T | 1 | a0006c0009t0007g0012 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-352+1145G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477461 | |||||||
chr7:30477567 | C | G | 9 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0053 others(6): Show |
19 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-352+1039G>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477567 | |||||||
chr7:30477681 | AT | A | 90 | a0001c0001t0001g0092 a0001c0001t0001g0283 a0001c0001t0001g0284 others(87): Show |
116 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-352+924delA | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477681 | |||||||
chr7:30477681 | ATT | A | 20 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0043 others(17): Show |
22 | HG00609.hp2 HG01069.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-352+923_-352+924d others(4): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477681 | |||||||
chr7:30477681 | ATTTT | A | 17 | a0001c0001t0001g0077 a0001c0001t0024g0074 a0002c0013t0025g0068 others(14): Show |
17 | HG01106.hp2 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-352+921_-352+924d others(6): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477681 | |||||||
chr7:30477838 | G | C | 1 | a0001c0001t0018g0287 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-352+768C>G | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477838 | |||||||
chr7:30477846 | G | A | 14 | a0001c0001t0007g0033 a0001c0001t0007g0035 a0001c0001t0007g0036 others(11): Show |
16 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-352+760C>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477846 | |||||||
chr7:30477874 | CTAGCT | C | 118 | a0001c0001t0001g0077 a0001c0001t0001g0092 a0001c0001t0002g0139 others(115): Show |
145 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.-352+727_-352+731d others(7): Show |
NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30477874 | |||||||
chr7:30478034 | C | A | 4 | a0001c0001t0001g0077 a0005c0008t0001g0078 a0005c0008t0001g0079 others(1): Show |
4 | HG01106.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-352+572G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30478034 | |||||||
chr7:30478151 | C | A | 101 | a0001c0001t0001g0092 a0001c0001t0002g0139 a0001c0003t0002g0084 others(98): Show |
128 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-352+455G>T | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30478151 | |||||||
chr7:30478517 | A | G | 150 | a0001c0001t0001g0059 a0001c0001t0001g0077 a0001c0001t0001g0092 others(147): Show |
189 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-352+89T>C | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30478517 | |||||||
chr7:30478534 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-352+72G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30478534 | |||||||
chr7:30478593 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0017t0001g0046 |
3 | HG02698.hp2 HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-352+13G>A | NOD1 | ENSG00000106100.11 | transcript | ENST00000222823.9 | protein_coding | 1/13 | chr7 | 30478593 |