Item | Value |
---|---|
geneid | 55366 |
ensemblid | ENSG00000205213.14 |
hgncid | 13299 |
symbol | LGR4 |
name | leucine rich repeat containing G protein-coupled receptor 4 |
refseq_nuc | NM_018490.5 |
refseq_prot | NP_060960.2 |
ensembl_nuc | ENST00000379214.9 |
ensembl_prot | ENSP00000368516.4 |
mane_status | MANE Select |
chr | chr11 |
start | 27365961 |
end | 27472790 |
strand | - |
ver | v1.2 |
region | chr11:27365961-27472790 |
region5000 | chr11:27360961-27477790 |
regionname0 | LGR4_chr11_27365961_27472790 |
regionname5000 | LGR4_chr11_27360961_27477790 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 951 | 223 | 57 | 35 | 99 | 12 | 18 | 78 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0002 | 0/0 | 951 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0003 | 0/0 | 951 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0004 | 0/0 | 951 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0005 | 0/0 | 951 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0006 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
a0007 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | MPGPL others(946): Show |
chr11 | 27360961 | 27477790 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2853 | 129 | 24 | 24 | 60 | 7 | 13 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0002 | 0/0 | 2853 | 81 | 23 | 11 | 38 | 4 | 5 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0004 | 0/0 | 2853 | 6 | 6 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0005 | 0/0 | 2853 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0010 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0013 | 0/0 | 2853 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0001c0014 | 0/1 | 2853 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0002c0003 | 0/0 | 2853 | 10 | 9 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0002c0011 | 0/0 | 2853 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0003c0006 | 0/0 | 2853 | 3 | 2 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0004c0007 | 0/0 | 2853 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0005c0009 | 0/0 | 2853 | 2 | 0 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0006c0008 | 0/0 | 2853 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 | ||
a0007c0012 | 0/0 | 2853 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | ATGCC others(2848): Show |
chr11 | 27360961 | 27477790 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5250 | 26 | 6 | 6 | 9 | 2 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0002 | 0/0 | 5250 | 29 | 0 | 7 | 20 | 1 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0003 | 0/0 | 5250 | 25 | 2 | 5 | 12 | 3 | 3 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0006 | 1/0 | 5250 | 2 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0007 | 0/0 | 5250 | 13 | 4 | 3 | 4 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0009 | 0/0 | 5250 | 8 | 5 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0010 | 0/0 | 5250 | 4 | 2 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0012 | 0/0 | 5250 | 6 | 0 | 0 | 6 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0015 | 0/0 | 5250 | 3 | 0 | 0 | 3 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0016 | 0/0 | 5250 | 3 | 0 | 3 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0019 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0021 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0024 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0027 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0028 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0029 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0030 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0032 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0034 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0001t0036 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0001 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0004 | 0/0 | 5250 | 22 | 2 | 4 | 13 | 2 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0005 | 0/0 | 5250 | 17 | 7 | 4 | 3 | 2 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0006 | 0/0 | 5250 | 9 | 7 | 0 | 2 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0008 | 0/0 | 5250 | 12 | 0 | 2 | 10 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0010 | 0/0 | 5250 | 2 | 1 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0011 | 0/0 | 5250 | 6 | 0 | 0 | 5 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0017 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0018 | 0/0 | 5250 | 2 | 2 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0020 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0022 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0023 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0025 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0026 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0033 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0002t0037 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0004t0013 | 0/0 | 5250 | 5 | 5 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0004t0035 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0005t0014 | 0/0 | 5250 | 4 | 4 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0010t0007 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0013t0005 | 0/0 | 5250 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0001c0014t0004 | 0/1 | 5250 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0002c0003t0004 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0002c0003t0005 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0002c0003t0006 | 0/0 | 5250 | 6 | 6 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0002c0003t0031 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0002c0011t0003 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0003c0006t0002 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0003c0006t0003 | 0/0 | 5250 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0003c0006t0007 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0004c0007t0001 | 0/0 | 5250 | 2 | 1 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0005c0009t0005 | 0/0 | 5250 | 2 | 0 | 0 | 0 | 0 | 2 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0006c0008t0001 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0006c0008t0009 | 0/0 | 5250 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
a0007c0012t0004 | 0/0 | 5250 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | AGAGC others(5245): Show |
chr11 | 27360961 | 27477790 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0006g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0010g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0015g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0016g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0021g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0024g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0028g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0029g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0030g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0032g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0034g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0001t0036g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0008g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0018g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0018g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0022g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0023g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0025g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0026g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0033g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0002t0037g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0004t0035g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0005t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0010t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0013t0005g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0001c0014t0004g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0003t0031g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0002c0011t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0003c0006t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0004c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0004c0007t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0005c0009t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0005c0009t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0006c0008t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0006c0008t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
a0007c0012t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0029 | g0104 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00099 | hp2 | a0001 | c0002 | t0004 | g0134 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00408 | hp2 | a0001 | c0002 | t0008 | g0192 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0072 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00544 | hp2 | a0001 | c0010 | t0007 | g0050 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0017 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00609 | hp2 | a0001 | c0001 | t0034 | g0204 | EAS | CHS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0061 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00735 | hp2 | a0001 | c0001 | t0016 | g0128 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0049 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0112 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0048 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0028 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01109 | hp1 | a0002 | c0003 | t0005 | g0044 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0024 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01243 | hp2 | a0003 | c0006 | t0003 | g0139 | AMR | PUR | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0070 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01257 | hp1 | a0004 | c0007 | t0001 | g0115 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01257 | hp2 | a0001 | c0002 | t0005 | g0025 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0060 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0071 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0002 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01517 | hp2 | a0001 | c0002 | t0005 | g0002 | EUR | IBS | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01891 | hp1 | a0001 | c0002 | t0005 | g0033 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01943 | hp1 | a0001 | c0002 | t0004 | g0132 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01943 | hp2 | a0001 | c0002 | t0008 | g0194 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01975 | hp2 | a0001 | c0002 | t0008 | g0191 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0021 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG01981 | hp2 | a0001 | c0001 | t0016 | g0111 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02004 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02027 | hp2 | a0001 | c0002 | t0004 | g0120 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02055 | hp1 | a0002 | c0003 | t0006 | g0197 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0047 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02071 | hp1 | a0001 | c0001 | t0009 | g0215 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02071 | hp2 | a0001 | c0002 | t0011 | g0075 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02074 | hp2 | a0001 | c0002 | t0004 | g0106 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02080 | hp1 | a0001 | c0002 | t0037 | g0241 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02080 | hp2 | a0001 | c0002 | t0008 | g0187 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02132 | hp1 | a0001 | c0002 | t0010 | g0046 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02135 | hp1 | a0001 | c0002 | t0006 | g0237 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02135 | hp2 | a0001 | c0001 | t0012 | g0081 | EAS | KHV | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0150 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02148 | hp2 | a0001 | c0001 | t0016 | g0125 | AMR | PEL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02165 | hp1 | a0007 | c0012 | t0004 | g0062 | EAS | CDX | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02165 | hp2 | a0001 | c0002 | t0004 | g0084 | EAS | CDX | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02451 | hp2 | a0002 | c0003 | t0031 | g0180 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02572 | hp1 | a0001 | c0004 | t0013 | g0045 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0232 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02615 | hp1 | a0002 | c0003 | t0006 | g0183 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02615 | hp2 | a0001 | c0005 | t0014 | g0149 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0173 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02622 | hp2 | a0001 | c0002 | t0018 | g0238 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02630 | hp1 | a0001 | c0002 | t0005 | g0008 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02630 | hp2 | a0001 | c0002 | t0018 | g0239 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02647 | hp1 | a0001 | c0005 | t0014 | g0148 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02683 | hp2 | a0005 | c0009 | t0005 | g0018 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02717 | hp1 | a0001 | c0002 | t0006 | g0199 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02717 | hp2 | a0003 | c0006 | t0002 | g0167 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02809 | hp1 | a0001 | c0002 | t0006 | g0186 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02809 | hp2 | a0003 | c0006 | t0007 | g0037 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02818 | hp1 | a0001 | c0001 | t0032 | g0174 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0218 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0011 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02896 | hp1 | a0001 | c0002 | t0017 | g0006 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02897 | hp1 | a0001 | c0002 | t0017 | g0007 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0182 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02970 | hp2 | a0001 | c0001 | t0030 | g0166 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02976 | hp1 | a0001 | c0004 | t0013 | g0041 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0176 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0023 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0009 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03139 | hp2 | a0002 | c0003 | t0006 | g0177 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03225 | hp1 | a0001 | c0002 | t0006 | g0185 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03225 | hp2 | a0006 | c0008 | t0009 | g0235 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03453 | hp1 | a0001 | c0005 | t0014 | g0154 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03453 | hp2 | a0001 | c0004 | t0013 | g0035 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0031 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03486 | hp2 | a0006 | c0008 | t0001 | g0145 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03492 | hp1 | a0001 | c0001 | t0019 | g0004 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03540 | hp1 | a0002 | c0003 | t0006 | g0200 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03540 | hp2 | a0001 | c0004 | t0013 | g0014 | AFR | GWD | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03579 | hp1 | a0001 | c0004 | t0013 | g0034 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03579 | hp2 | a0001 | c0002 | t0005 | g0012 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03654 | hp1 | a0001 | c0002 | t0023 | g0055 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0022 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03669 | hp2 | a0001 | c0002 | t0004 | g0076 | SAS | PJL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03834 | hp2 | a0001 | c0002 | t0022 | g0053 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04184 | hp1 | a0001 | c0001 | t0024 | g0124 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04184 | hp2 | a0001 | c0001 | t0010 | g0016 | SAS | BEB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0057 | SAS | STU | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG04228 | hp2 | a0005 | c0009 | t0005 | g0056 | SAS | STU | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18522 | hp1 | a0002 | c0011 | t0003 | g0155 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0178 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18612 | hp2 | a0001 | c0002 | t0008 | g0189 | EAS | CHB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18906 | hp1 | a0001 | c0001 | t0027 | g0137 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18906 | hp2 | a0002 | c0003 | t0004 | g0144 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18944 | hp1 | a0001 | c0001 | t0021 | g0027 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18944 | hp2 | a0001 | c0002 | t0008 | g0203 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18946 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18950 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18959 | hp1 | a0001 | c0002 | t0008 | g0169 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18960 | hp1 | a0001 | c0002 | t0033 | g0170 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18960 | hp2 | a0001 | c0001 | t0015 | g0029 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18964 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0065 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18967 | hp1 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18967 | hp2 | a0001 | c0002 | t0008 | g0195 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18975 | hp1 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0052 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18982 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18982 | hp2 | a0001 | c0002 | t0011 | g0143 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18984 | hp1 | a0001 | c0002 | t0006 | g0222 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0168 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18985 | hp2 | a0001 | c0002 | t0011 | g0078 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18990 | hp1 | a0001 | c0002 | t0011 | g0157 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18992 | hp2 | a0001 | c0002 | t0026 | g0119 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18993 | hp2 | a0001 | c0002 | t0008 | g0202 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18994 | hp1 | a0001 | c0002 | t0020 | g0005 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA18994 | hp2 | a0001 | c0001 | t0028 | g0092 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19004 | hp1 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0123 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0086 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0198 | AFR | LWK | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | LWK | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0083 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19057 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19058 | hp1 | a0001 | c0001 | t0012 | g0117 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19062 | hp1 | a0001 | c0002 | t0008 | g0227 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19068 | hp2 | a0001 | c0002 | t0011 | g0162 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19075 | hp1 | a0001 | c0002 | t0005 | g0043 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19076 | hp1 | a0001 | c0001 | t0015 | g0042 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19081 | hp1 | a0001 | c0002 | t0008 | g0193 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19082 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19082 | hp2 | a0001 | c0002 | t0008 | g0236 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19085 | hp2 | a0001 | c0001 | t0015 | g0019 | EAS | JPT | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0010 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0140 | AFR | YRI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0064 | EUR | TSI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20752 | hp2 | a0001 | c0013 | t0005 | g0026 | EUR | TSI | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20905 | hp1 | a0001 | c0002 | t0011 | g0088 | SAS | GIH | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0054 | SAS | GIH | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02109 | hp2 | a0002 | c0003 | t0006 | g0184 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02486 | hp1 | a0001 | c0002 | t0006 | g0196 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02486 | hp2 | a0001 | c0001 | t0036 | g0240 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02559 | hp1 | a0001 | c0002 | t0025 | g0090 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG02559 | hp2 | a0001 | c0005 | t0014 | g0153 | AFR | ACB | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03471 | hp1 | a0004 | c0007 | t0001 | g0096 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG03471 | hp2 | a0001 | c0004 | t0035 | g0175 | AFR | MSL | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG06807 | hp1 | a0001 | c0002 | t0005 | g0032 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20300 | hp1 | a0002 | c0003 | t0006 | g0206 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | USA | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
homoSapiens | chm13v2 | a0001 | c0014 | t0004 | g0069 | REF | REF | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0179 | REF | REF | LGR4_chr11_27360961_27477790 | LGR4 | chr11 | 27360961 | 27477790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27368475 | C | T | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2248G>A | p.Ala750Thr | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2736/5250 | 2248/2856 | 750/951 | chr11 | 27368475 | |||
chr11:27368597 | G | A | 2 | a0004 a0006 |
4 | HG01257.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.2126C>T | p.Thr709Met | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2614/5250 | 2126/2856 | 709/951 | chr11 | 27368597 | |||
chr11:27368673 | T | C | 1 | a0003 | 3 | HG01243.hp2 HG02717.hp2 HG02809.hp2 |
missense_variant | MODERATE | c.2050A>G | p.Arg684Gly | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2538/5250 | 2050/2856 | 684/951 | chr11 | 27368673 | |||
chr11:27372339 | G | A | 2 | a0002 a0006 |
13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
missense_variant | MODERATE | c.1439C>T | p.Ala480Val | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 16/18 | 1927/5250 | 1439/2856 | 480/951 | chr11 | 27372339 | |||
chr11:27377180 | C | A | 1 | a0005 | 2 | HG02683.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.1087G>T | p.Gly363Cys | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/18 | 1575/5250 | 1087/2856 | 363/951 | chr11 | 27377180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27368134 | C | T | 1 | a0001c0013 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.2589G>A | p.Ser863Ser | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 3077/5250 | 2589/2856 | 863/951 | chr11 | 27368134 | |||
chr11:27368620 | C | T | 1 | a0001c0010 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.2103G>A | p.Thr701Thr | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2591/5250 | 2103/2856 | 701/951 | chr11 | 27368620 | |||
chr11:27368929 | A | G | 1 | a0002c0003 | 10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
synonymous_variant | LOW | c.1794T>C | p.Asp598Asp | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2282/5250 | 1794/2856 | 598/951 | chr11 | 27368929 | |||
chr11:27368941 | T | C | 2 | a0001c0004 a0001c0005 |
10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
synonymous_variant | LOW | c.1782A>G | p.Leu594Leu | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 2270/5250 | 1782/2856 | 594/951 | chr11 | 27368941 | |||
chr11:27385297 | G | A | 5 | a0001c0002 a0001c0005 a0001c0013 others(2): Show |
89 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
synonymous_variant | LOW | c.573C>T | p.Ser191Ser | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/18 | 1061/5250 | 573/2856 | 191/951 | chr11 | 27385297 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27366085 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1782C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1782 | chr11 | 27366085 | ||||||
chr11:27366106 | G | C | 1 | a0001c0001t0029 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1761C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1761 | chr11 | 27366106 | ||||||
chr11:27366115 | C | A | 1 | a0001c0002t0033 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1752G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1752 | chr11 | 27366115 | ||||||
chr11:27366144 | T | C | 2 | a0001c0001t0021 a0001c0001t0028 |
2 | NA18944.hp1 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1723A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1723 | chr11 | 27366144 | ||||||
chr11:27366468 | A | T | 1 | a0002c0003t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1399T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1399 | chr11 | 27366468 | ||||||
chr11:27366633 | G | A | 1 | a0001c0001t0032 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 1234 | chr11 | 27366633 | ||||||
chr11:27366883 | C | T | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0034 |
10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*984G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 984 | chr11 | 27366883 | ||||||
chr11:27366901 | C | T | 1 | a0001c0002t0026 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*966G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 966 | chr11 | 27366901 | ||||||
chr11:27366907 | G | A | 1 | a0001c0001t0027 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 960 | chr11 | 27366907 | ||||||
chr11:27366957 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 910 | chr11 | 27366957 | ||||||
chr11:27366984 | T | C | 4 | a0001c0002t0008 a0001c0002t0011 a0001c0002t0022 others(1): Show |
20 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*883A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 883 | chr11 | 27366984 | ||||||
chr11:27367077 | C | T | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(11): Show |
61 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*790G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 790 | chr11 | 27367077 | ||||||
chr11:27367302 | C | G | 1 | a0001c0002t0025 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*565G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 565 | chr11 | 27367302 | ||||||
chr11:27367363 | T | C | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(11): Show |
61 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*504A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 504 | chr11 | 27367363 | ||||||
chr11:27367417 | T | C | 3 | a0001c0004t0013 a0001c0004t0035 a0001c0005t0014 |
10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*450A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 450 | chr11 | 27367417 | ||||||
chr11:27367436 | G | A | 1 | a0001c0002t0023 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 431 | chr11 | 27367436 | ||||||
chr11:27367839 | C | T | 1 | a0001c0001t0024 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 28 | chr11 | 27367839 | ||||||
chr11:27367856 | C | T | 1 | a0001c0001t0016 | 3 | HG00735.hp2 HG01981.hp2 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 18/18 | 11 | chr11 | 27367856 | ||||||
chr11:27472332 | C | G | 14 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0015 others(11): Show |
54 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-30G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 30 | chr11 | 27472332 | ||||||
chr11:27472335 | G | A | 1 | a0001c0001t0030 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 33 | chr11 | 27472335 | ||||||
chr11:27472423 | C | G | 1 | a0001c0002t0017 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 121 | chr11 | 27472423 | ||||||
chr11:27472549 | C | G | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(35): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-247G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472549 | |||||||
chr11:27472561 | C | A | 2 | a0001c0001t0036 a0001c0002t0018 |
3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-259G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472561 | |||||||
chr11:27472671 | C | G | 1 | a0001c0002t0020 | 1 | NA18994.hp1 | 5_prime_UTR_variant | MODIFIER | c.-369G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 369 | chr11 | 27472671 | ||||||
chr11:27472673 | G | A | 1 | a0001c0002t0037 | 1 | HG02080.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-371C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | chr11 | 27472673 | |||||||
chr11:27472712 | C | T | 1 | a0001c0001t0019 | 1 | HG03492.hp1 | 5_prime_UTR_variant | MODIFIER | c.-410G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/18 | 410 | chr11 | 27472712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:27369160 | C | G | 1 | a0001c0002t0006g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1580-17G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369160 | |||||||
chr11:27369240 | T | A | 2 | a0001c0001t0002g0207 a0001c0001t0024g0124 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1580-97A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369240 | |||||||
chr11:27369903 | T | C | 61 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(58): Show |
61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1580-760A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369903 | |||||||
chr11:27369978 | T | C | 10 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(7): Show |
10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1580-835A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27369978 | |||||||
chr11:27370094 | G | T | 1 | a0001c0002t0005g0001 | 2 | NA18946.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1580-951C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370094 | |||||||
chr11:27370160 | T | G | 236 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1580-1017A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370160 | |||||||
chr11:27370323 | G | A | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-1180C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370323 | |||||||
chr11:27370327 | T | A | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1580-1184A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370327 | |||||||
chr11:27370414 | C | G | 2 | a0001c0002t0004g0112 a0001c0002t0005g0025 |
2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1579+1201G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370414 | |||||||
chr11:27370642 | G | C | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+973C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370642 | |||||||
chr11:27370725 | C | G | 1 | a0003c0006t0003g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579+890G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370725 | |||||||
chr11:27370751 | T | C | 1 | a0007c0012t0004g0062 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1579+864A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370751 | |||||||
chr11:27370956 | T | C | 1 | a0001c0002t0005g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1579+659A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370956 | |||||||
chr11:27370958 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1579+657G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27370958 | |||||||
chr11:27371027 | T | C | 181 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0151 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1579+588A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371027 | |||||||
chr11:27371369 | C | T | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1579+246G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371369 | |||||||
chr11:27371370 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1579+245C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371370 | |||||||
chr11:27371486 | C | T | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1579+129G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 17/17 | chr11 | 27371486 | |||||||
chr11:27372266 | G | A | 105 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(102): Show |
108 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1495+17C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 16/17 | chr11 | 27372266 | |||||||
chr11:27372448 | T | C | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1380-50A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372448 | |||||||
chr11:27372528 | G | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0136 a0001c0001t0009g0215 |
3 | HG02071.hp1 NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1380-130C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372528 | |||||||
chr11:27372737 | C | T | 1 | a0002c0003t0006g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1380-339G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372737 | |||||||
chr11:27372868 | CT | C | 105 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(102): Show |
108 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1380-471delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372868 | |||||||
chr11:27372949 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1380-551A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27372949 | |||||||
chr11:27373105 | C | A | 84 | a0001c0002t0004g0060 a0001c0002t0004g0061 a0001c0002t0004g0065 others(81): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1379+446G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373105 | |||||||
chr11:27373154 | G | A | 84 | a0001c0002t0004g0060 a0001c0002t0004g0061 a0001c0002t0004g0065 others(81): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1379+397C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373154 | |||||||
chr11:27373160 | C | T | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1379+391G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373160 | |||||||
chr11:27373368 | T | C | 1 | a0001c0001t0003g0103 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1379+183A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 15/17 | chr11 | 27373368 | |||||||
chr11:27373694 | C | G | 2 | a0003c0006t0002g0167 a0003c0006t0007g0037 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1254-18G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373694 | |||||||
chr11:27373824 | G | A | 181 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0151 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1254-148C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373824 | |||||||
chr11:27373830 | G | A | 84 | a0001c0002t0004g0060 a0001c0002t0004g0061 a0001c0002t0004g0065 others(81): Show |
86 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1253+145C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373830 | |||||||
chr11:27373900 | C | T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1253+75G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373900 | |||||||
chr11:27373924 | T | C | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1253+51A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373924 | |||||||
chr11:27373940 | A | G | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1253+35T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 14/17 | chr11 | 27373940 | |||||||
chr11:27374328 | C | A | 108 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(105): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1182-282G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374328 | |||||||
chr11:27374338 | A | G | 1 | a0001c0001t0024g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1182-292T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374338 | |||||||
chr11:27374455 | C | T | 1 | a0001c0002t0004g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1182-409G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374455 | |||||||
chr11:27374604 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1182-558C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374604 | |||||||
chr11:27374710 | A | C | 1 | a0001c0002t0004g0066 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1182-664T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374710 | |||||||
chr11:27374756 | G | T | 236 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1182-710C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27374756 | |||||||
chr11:27375077 | T | A | 236 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1182-1031A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375077 | |||||||
chr11:27375116 | T | C | 1 | a0001c0001t0003g0089 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1182-1070A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375116 | |||||||
chr11:27375121 | C | CA | 13 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0003 others(10): Show |
14 | HG00140.hp2 HG00408.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1182-1076dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375121 | |||||||
chr11:27375194 | T | G | 2 | a0001c0002t0004g0074 a0001c0002t0004g0082 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1181+1105A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375194 | |||||||
chr11:27375263 | C | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181+1036G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375263 | |||||||
chr11:27375297 | C | CA | 125 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1181+1001dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375297 | |||||||
chr11:27375297 | C | CAA | 9 | a0001c0001t0001g0126 a0001c0001t0002g0188 a0001c0001t0002g0190 others(6): Show |
9 | HG01109.hp1 HG02027.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181+1000_1181+100 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375297 | |||||||
chr11:27375520 | A | G | 87 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(84): Show |
89 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1181+779T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375520 | |||||||
chr11:27375651 | C | T | 1 | a0001c0001t0029g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1181+648G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375651 | |||||||
chr11:27375768 | C | T | 2 | a0001c0002t0004g0140 a0001c0002t0005g0013 |
2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1181+531G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375768 | |||||||
chr11:27375843 | G | A | 8 | a0001c0001t0002g0229 a0001c0001t0003g0156 a0001c0001t0003g0158 others(5): Show |
8 | NA18951.hp1 NA18952.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+456C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375843 | |||||||
chr11:27375921 | TA | T | 83 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(80): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1181+377delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375921 | |||||||
chr11:27375977 | CT | C | 5 | a0001c0001t0003g0131 a0001c0001t0003g0141 a0001c0001t0007g0039 others(2): Show |
6 | HG02451.hp1 HG06807.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+321delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375977 | |||||||
chr11:27375980 | T | C | 13 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+319A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27375980 | |||||||
chr11:27376101 | C | T | 108 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(105): Show |
111 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1181+198G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376101 | |||||||
chr11:27376158 | T | TAG | 66 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0152 others(63): Show |
66 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1181+139_1181+140d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376158 | |||||||
chr11:27376177 | C | T | 13 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181+122G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376177 | |||||||
chr11:27376212 | G | A | 2 | a0003c0006t0002g0167 a0003c0006t0007g0037 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1181+87C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376212 | |||||||
chr11:27376238 | A | G | 1 | a0001c0002t0004g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1181+61T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376238 | |||||||
chr11:27376247 | T | C | 1 | a0001c0002t0005g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1181+52A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 13/17 | chr11 | 27376247 | |||||||
chr11:27376441 | G | T | 21 | a0001c0001t0003g0141 a0001c0001t0007g0039 a0001c0001t0007g0040 others(18): Show |
21 | HG00609.hp2 HG01257.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1110-71C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376441 | |||||||
chr11:27376468 | T | G | 12 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(9): Show |
12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110-98A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376468 | |||||||
chr11:27376518 | T | C | 3 | a0001c0001t0016g0111 a0001c0001t0016g0125 a0001c0001t0016g0128 |
3 | HG00735.hp2 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1110-148A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376518 | |||||||
chr11:27376641 | G | T | 1 | a0001c0001t0036g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110-271C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376641 | |||||||
chr11:27376721 | C | A | 23 | a0001c0001t0001g0098 a0001c0001t0003g0141 a0001c0001t0007g0039 others(20): Show |
23 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1110-351G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376721 | |||||||
chr11:27376724 | C | T | 31 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1110-354G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376724 | |||||||
chr11:27376768 | T | C | 3 | a0001c0001t0003g0141 a0001c0001t0007g0039 a0001c0001t0007g0040 |
3 | HG02451.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1109+390A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376768 | |||||||
chr11:27376953 | G | A | 2 | a0005c0009t0005g0018 a0005c0009t0005g0056 |
2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1109+205C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27376953 | |||||||
chr11:27377007 | C | T | 1 | a0001c0001t0009g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1109+151G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27377007 | |||||||
chr11:27377097 | G | A | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1109+61C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 12/17 | chr11 | 27377097 | |||||||
chr11:27377266 | A | C | 2 | a0003c0006t0002g0167 a0003c0006t0007g0037 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1044-43T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377266 | |||||||
chr11:27377298 | G | A | 96 | a0001c0001t0001g0098 a0001c0001t0001g0142 a0001c0001t0001g0146 others(93): Show |
96 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1044-75C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377298 | |||||||
chr11:27377524 | G | T | 235 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1044-301C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377524 | |||||||
chr11:27377559 | T | C | 10 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(7): Show |
10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1044-336A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377559 | |||||||
chr11:27377721 | A | C | 1 | a0001c0002t0020g0005 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1044-498T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377721 | |||||||
chr11:27377866 | A | G | 31 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1044-643T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27377866 | |||||||
chr11:27378019 | A | G | 62 | a0001c0001t0001g0142 a0001c0001t0002g0188 a0001c0001t0002g0190 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1043+678T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378019 | |||||||
chr11:27378498 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1043+199A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378498 | |||||||
chr11:27378545 | G | T | 1 | a0001c0002t0020g0005 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1043+152C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 11/17 | chr11 | 27378545 | |||||||
chr11:27379119 | G | A | 1 | a0001c0002t0005g0043 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.972-351C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379119 | |||||||
chr11:27379170 | C | T | 131 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.972-402G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379170 | |||||||
chr11:27379186 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.972-418A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379186 | |||||||
chr11:27379264 | A | G | 8 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.972-496T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379264 | |||||||
chr11:27379415 | C | T | 4 | a0001c0005t0014g0148 a0001c0005t0014g0149 a0001c0005t0014g0153 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-647G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379415 | |||||||
chr11:27379564 | C | T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+707G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379564 | |||||||
chr11:27379622 | T | C | 235 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.971+649A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379622 | |||||||
chr11:27379643 | A | G | 68 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0151 others(65): Show |
68 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.971+628T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379643 | |||||||
chr11:27379654 | G | A | 1 | a0001c0002t0005g0002 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.971+617C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379654 | |||||||
chr11:27379779 | A | C | 1 | a0001c0001t0010g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.971+492T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379779 | |||||||
chr11:27379842 | C | T | 31 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.971+429G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379842 | |||||||
chr11:27379902 | TAAA | T | 139 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.971+366_971+368del others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27379902 | |||||||
chr11:27380156 | G | A | 8 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(5): Show |
9 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+115C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27380156 | |||||||
chr11:27380196 | A | T | 139 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.971+75T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 10/17 | chr11 | 27380196 | |||||||
chr11:27380380 | T | G | 87 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(84): Show |
89 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.903-41A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 9/17 | chr11 | 27380380 | |||||||
chr11:27380393 | T | A | 139 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.903-54A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 9/17 | chr11 | 27380393 | |||||||
chr11:27380833 | G | C | 12 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(9): Show |
12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.830+62C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380833 | |||||||
chr11:27380842 | C | T | 2 | a0005c0009t0005g0018 a0005c0009t0005g0056 |
2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.830+53G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380842 | |||||||
chr11:27380866 | C | T | 1 | a0001c0004t0013g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.830+29G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 8/17 | chr11 | 27380866 | |||||||
chr11:27381035 | T | G | 22 | a0001c0001t0001g0098 a0001c0001t0007g0039 a0001c0001t0007g0040 others(19): Show |
22 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.759-69A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381035 | |||||||
chr11:27381180 | A | G | 8 | a0001c0001t0009g0173 a0001c0001t0009g0176 a0001c0001t0009g0182 others(5): Show |
8 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-214T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381180 | |||||||
chr11:27381363 | C | T | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.759-397G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381363 | |||||||
chr11:27381421 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.759-455T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381421 | |||||||
chr11:27381525 | T | A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00735.hp1 HG02004.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-559A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381525 | |||||||
chr11:27381589 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.758+599C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381589 | |||||||
chr11:27381649 | C | T | 86 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(83): Show |
88 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.758+539G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381649 | |||||||
chr11:27381706 | C | CA | 61 | a0001c0001t0001g0146 a0001c0001t0002g0188 a0001c0001t0002g0190 others(58): Show |
61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.758+481dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381706 | |||||||
chr11:27381706 | CA | C | 167 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.758+481delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381706 | |||||||
chr11:27381734 | C | T | 13 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.758+454G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381734 | |||||||
chr11:27381785 | C | T | 61 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(58): Show |
61 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.758+403G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27381785 | |||||||
chr11:27382053 | T | C | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.758+135A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 7/17 | chr11 | 27382053 | |||||||
chr11:27382279 | A | G | 1 | a0001c0002t0005g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.690-23T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382279 | |||||||
chr11:27382332 | A | G | 2 | a0001c0002t0011g0088 a0001c0002t0022g0053 |
2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.690-76T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382332 | |||||||
chr11:27382386 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.690-130G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382386 | |||||||
chr11:27382406 | G | A | 62 | a0001c0001t0001g0142 a0001c0001t0002g0188 a0001c0001t0002g0190 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.690-150C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382406 | |||||||
chr11:27382434 | AC | A | 31 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.690-179delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382434 | |||||||
chr11:27382442 | GA | G | 3 | a0001c0001t0003g0141 a0003c0006t0002g0167 a0003c0006t0007g0037 |
3 | HG02717.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.690-187delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382442 | |||||||
chr11:27382704 | C | T | 1 | a0001c0005t0014g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690-448G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382704 | |||||||
chr11:27382869 | T | C | 3 | a0001c0001t0015g0019 a0001c0001t0015g0029 a0001c0001t0015g0042 |
3 | NA18960.hp2 NA19076.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.690-613A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382869 | |||||||
chr11:27382897 | G | T | 22 | a0001c0001t0001g0098 a0001c0001t0007g0039 a0001c0001t0007g0040 others(19): Show |
22 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.690-641C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27382897 | |||||||
chr11:27383010 | T | C | 236 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.690-754A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383010 | |||||||
chr11:27383222 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.690-966G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383222 | |||||||
chr11:27383309 | T | C | 83 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(80): Show |
85 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.689+1027A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383309 | |||||||
chr11:27383317 | G | T | 236 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.689+1019C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383317 | |||||||
chr11:27383330 | G | C | 87 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(84): Show |
89 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.689+1006C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383330 | |||||||
chr11:27383382 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.689+954C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383382 | |||||||
chr11:27383477 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.689+859G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383477 | |||||||
chr11:27383668 | T | G | 1 | a0001c0001t0002g0212 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.689+668A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383668 | |||||||
chr11:27383730 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.689+606C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383730 | |||||||
chr11:27383740 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(4): Show |
8 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+596C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383740 | |||||||
chr11:27383933 | G | A | 10 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(7): Show |
10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.689+403C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27383933 | |||||||
chr11:27384147 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.689+189G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 6/17 | chr11 | 27384147 | |||||||
chr11:27384599 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.618-192C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384599 | |||||||
chr11:27384798 | C | G | 1 | a0001c0001t0009g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-391G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384798 | |||||||
chr11:27384866 | C | A | 1 | a0001c0001t0002g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.617+387G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384866 | |||||||
chr11:27384900 | C | T | 1 | a0001c0002t0006g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.617+353G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 5/17 | chr11 | 27384900 | |||||||
chr11:27385531 | C | G | 1 | a0001c0001t0007g0020 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.402-63G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385531 | |||||||
chr11:27385736 | T | C | 1 | a0001c0001t0002g0212 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.402-268A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385736 | |||||||
chr11:27385815 | C | CA | 97 | a0001c0002t0001g0138 a0001c0002t0004g0060 a0001c0002t0004g0061 others(94): Show |
99 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.402-348dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | |||||||
chr11:27385815 | C | CAA | 110 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.402-349_402-348dup others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | |||||||
chr11:27385815 | C | CAAA | 13 | a0001c0001t0003g0089 a0001c0001t0007g0039 a0001c0001t0007g0040 others(10): Show |
13 | HG00609.hp2 HG01070.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.402-350_402-348dup others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385815 | |||||||
chr11:27385919 | A | G | 24 | a0001c0001t0001g0098 a0001c0001t0007g0015 a0001c0001t0007g0038 others(21): Show |
24 | HG00609.hp2 HG01257.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.402-451T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385919 | |||||||
chr11:27385980 | A | G | 85 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0060 others(82): Show |
87 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.402-512T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27385980 | |||||||
chr11:27386742 | CTGG | C | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.402-1277_402-1275d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386742 | |||||||
chr11:27386870 | C | T | 143 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(140): Show |
145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.402-1402G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386870 | |||||||
chr11:27386922 | A | G | 1 | a0001c0010t0007g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.402-1454T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386922 | |||||||
chr11:27386938 | G | C | 7 | a0001c0001t0009g0173 a0001c0001t0009g0176 a0001c0001t0009g0182 others(4): Show |
7 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.402-1470C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386938 | |||||||
chr11:27386967 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0121 |
2 | HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.402-1499G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27386967 | |||||||
chr11:27387010 | C | G | 235 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.402-1542G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387010 | |||||||
chr11:27387042 | G | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.402-1574C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387042 | |||||||
chr11:27387139 | A | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.402-1671T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387139 | |||||||
chr11:27387317 | A | G | 12 | a0002c0003t0004g0144 a0002c0003t0005g0031 a0002c0003t0005g0044 others(9): Show |
12 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.402-1849T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387317 | |||||||
chr11:27387343 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.402-1875T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387343 | |||||||
chr11:27387417 | C | T | 229 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(226): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.402-1949G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387417 | |||||||
chr11:27387466 | T | TAAAGAAA others(341): Show |
1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.402-1999_402-1998i others(350): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387466 | |||||||
chr11:27387641 | A | T | 229 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(226): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.402-2173T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387641 | |||||||
chr11:27387945 | G | A | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.402-2477C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27387945 | |||||||
chr11:27388036 | A | C | 1 | a0001c0001t0003g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.402-2568T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388036 | |||||||
chr11:27388044 | T | C | 146 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0188 others(143): Show |
148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.402-2576A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388044 | |||||||
chr11:27388079 | C | T | 63 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(60): Show |
63 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.402-2611G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388079 | |||||||
chr11:27388082 | A | G | 3 | a0001c0002t0006g0196 a0001c0002t0018g0238 a0001c0002t0018g0239 |
3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.402-2614T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388082 | |||||||
chr11:27388177 | A | G | 1 | a0001c0001t0003g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.402-2709T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388177 | |||||||
chr11:27388349 | A | C | 235 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.401+2745T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388349 | |||||||
chr11:27388383 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.401+2711A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388383 | |||||||
chr11:27388452 | T | A | 1 | a0002c0003t0006g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.401+2642A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388452 | |||||||
chr11:27388824 | G | T | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401+2270C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27388824 | |||||||
chr11:27389143 | A | G | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401+1951T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389143 | |||||||
chr11:27389389 | C | T | 3 | a0001c0002t0006g0196 a0001c0002t0018g0238 a0001c0002t0018g0239 |
3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.401+1705G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389389 | |||||||
chr11:27389408 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+1686A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389408 | |||||||
chr11:27389456 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.401+1638G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389456 | |||||||
chr11:27389507 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+1587G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389507 | |||||||
chr11:27389751 | G | A | 192 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.401+1343C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389751 | |||||||
chr11:27389799 | T | C | 1 | a0001c0002t0005g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.401+1295A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27389799 | |||||||
chr11:27390174 | TTA | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+918_401+919del others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390174 | |||||||
chr11:27390237 | G | A | 6 | a0001c0001t0001g0142 a0001c0002t0006g0196 a0001c0002t0018g0238 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+857C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390237 | |||||||
chr11:27390415 | G | A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+679C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390415 | |||||||
chr11:27390475 | T | G | 6 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.401+619A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390475 | |||||||
chr11:27390735 | C | T | 2 | a0001c0001t0007g0015 a0001c0001t0007g0038 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.401+359G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390735 | |||||||
chr11:27390988 | C | T | 186 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.401+106G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27390988 | |||||||
chr11:27391019 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.401+75A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 4/17 | chr11 | 27391019 | |||||||
chr11:27391235 | C | CTTTT | 5 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.330-74_330-71dupAA others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | |||||||
chr11:27391235 | CTT | C | 193 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(190): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.330-72_330-71delAA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | |||||||
chr11:27391235 | CTTT | C | 34 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.330-73_330-71delAA others(1): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391235 | |||||||
chr11:27391307 | G | A | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330-142C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391307 | |||||||
chr11:27391585 | C | G | 2 | a0001c0001t0006g0233 a0001c0001t0030g0166 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.330-420G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391585 | |||||||
chr11:27391689 | GAAAT | G | 128 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(125): Show |
130 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.330-528_330-525del others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391689 | |||||||
chr11:27391761 | T | C | 228 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(225): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.330-596A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391761 | |||||||
chr11:27391940 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.329+507G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27391940 | |||||||
chr11:27392254 | GT | G | 8 | a0001c0001t0009g0173 a0001c0001t0009g0176 a0001c0001t0009g0182 others(5): Show |
8 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.329+192delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392254 | |||||||
chr11:27392308 | T | C | 235 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.329+139A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392308 | |||||||
chr11:27392378 | C | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+69G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 3/17 | chr11 | 27392378 | |||||||
chr11:27392524 | GAA | G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(4): Show |
8 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.258-8_258-7delTT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27392524 | |||||||
chr11:27392661 | C | A | 6 | a0001c0001t0001g0142 a0001c0002t0006g0196 a0001c0002t0018g0238 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-143G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27392661 | |||||||
chr11:27393361 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-843A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393361 | |||||||
chr11:27393437 | T | G | 4 | a0001c0001t0006g0233 a0001c0001t0027g0137 a0001c0001t0030g0166 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-919A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393437 | |||||||
chr11:27393503 | T | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-985A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393503 | |||||||
chr11:27393512 | CCT | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-996_258-995del others(2): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393512 | |||||||
chr11:27393856 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(48): Show |
51 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.258-1338A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393856 | |||||||
chr11:27393937 | AT | A | 29 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0095 others(26): Show |
29 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.258-1420delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393937 | |||||||
chr11:27393938 | T | TG | 10 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0152 others(7): Show |
11 | HG00140.hp2 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.258-1421_258-1420i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | |||||||
chr11:27393938 | T | TGG | 3 | a0001c0001t0001g0098 a0001c0001t0009g0178 a0004c0007t0001g0096 |
3 | HG01891.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.258-1421_258-1420i others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | |||||||
chr11:27393938 | T | TGGGGG | 4 | a0001c0001t0009g0176 a0001c0001t0009g0182 a0001c0001t0009g0220 others(1): Show |
4 | HG02145.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1421_258-1420i others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393938 | |||||||
chr11:27393939 | T | G | 71 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0098 others(68): Show |
72 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.258-1421A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | |||||||
chr11:27393939 | T | TG | 33 | a0001c0001t0002g0201 a0001c0001t0002g0207 a0001c0001t0002g0219 others(30): Show |
33 | HG00544.hp2 HG01169.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-1422dupC | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | |||||||
chr11:27393939 | T | TGG | 49 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0205 others(46): Show |
50 | HG00544.hp1 HG00609.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.258-1423_258-1422d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | |||||||
chr11:27393939 | T | TGGG | 24 | a0001c0001t0002g0208 a0001c0001t0002g0210 a0001c0001t0002g0213 others(21): Show |
24 | HG00408.hp1 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.258-1424_258-1422d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393939 | |||||||
chr11:27393943 | G | A | 1 | a0002c0003t0031g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.258-1425C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393943 | |||||||
chr11:27393943 | G | GC | 4 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(1): Show |
4 | HG02135.hp2 NA18989.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-1426_258-1425i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393943 | |||||||
chr11:27393944 | G | C | 6 | a0001c0001t0012g0117 a0001c0001t0012g0118 a0001c0001t0015g0019 others(3): Show |
6 | HG00609.hp2 NA18960.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-1426C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393944 | |||||||
chr11:27393944 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-1426C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393944 | |||||||
chr11:27393945 | G | C | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.258-1427C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393945 | |||||||
chr11:27393949 | G | C | 38 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(35): Show |
38 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.258-1431C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393949 | |||||||
chr11:27393950 | G | A | 4 | a0001c0001t0006g0233 a0001c0001t0027g0137 a0001c0001t0030g0166 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-1432C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393950 | |||||||
chr11:27393955 | C | G | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.258-1437G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27393955 | |||||||
chr11:27394063 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-1545G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394063 | |||||||
chr11:27394064 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.258-1546C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394064 | |||||||
chr11:27394088 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.258-1570A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394088 | |||||||
chr11:27394381 | C | T | 7 | a0001c0002t0004g0074 a0001c0002t0004g0082 a0001c0002t0004g0083 others(4): Show |
7 | HG02080.hp1 NA18964.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-1863G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394381 | |||||||
chr11:27394547 | C | T | 1 | a0003c0006t0003g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.258-2029G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394547 | |||||||
chr11:27394560 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.258-2042C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394560 | |||||||
chr11:27394592 | G | A | 19 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0209 others(16): Show |
19 | HG00733.hp1 HG01975.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.258-2074C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394592 | |||||||
chr11:27394725 | A | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0006g0233 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.258-2207T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27394725 | |||||||
chr11:27395062 | T | C | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-2544A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395062 | |||||||
chr11:27395134 | T | C | 1 | a0001c0001t0002g0188 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.258-2616A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395134 | |||||||
chr11:27395166 | C | T | 10 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(7): Show |
10 | HG00609.hp2 HG02135.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-2648G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395166 | |||||||
chr11:27395202 | G | C | 29 | a0001c0001t0001g0146 a0001c0001t0002g0003 a0001c0001t0002g0171 others(26): Show |
30 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.258-2684C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395202 | |||||||
chr11:27395300 | A | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0004t0013g0014 others(5): Show |
8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-2782T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395300 | |||||||
chr11:27395354 | T | TA | 10 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0006g0233 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.258-2837dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395354 | |||||||
chr11:27395354 | TA | T | 9 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0006g0196 others(6): Show |
9 | HG00642.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-2837delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395354 | |||||||
chr11:27395679 | T | C | 106 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(103): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.258-3161A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395679 | |||||||
chr11:27395746 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.258-3228G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395746 | |||||||
chr11:27395757 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-3239C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27395757 | |||||||
chr11:27396087 | C | A | 1 | a0001c0002t0025g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258-3569G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396087 | |||||||
chr11:27396088 | C | A | 1 | a0001c0002t0025g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.258-3570G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396088 | |||||||
chr11:27396149 | C | A | 73 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-3631G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396149 | |||||||
chr11:27396255 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258-3737G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396255 | |||||||
chr11:27396403 | C | T | 1 | a0002c0003t0005g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.258-3885G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396403 | |||||||
chr11:27396536 | A | AT | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0004t0013g0014 others(5): Show |
8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-4019dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396536 | |||||||
chr11:27396539 | T | A | 12 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0003g0091 others(9): Show |
12 | HG00735.hp1 HG01243.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.258-4021A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396539 | |||||||
chr11:27396563 | G | A | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258-4045C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396563 | |||||||
chr11:27396678 | G | T | 73 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258-4160C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27396678 | |||||||
chr11:27397033 | C | T | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0004t0013g0014 others(5): Show |
8 | HG02572.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-4515G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397033 | |||||||
chr11:27397053 | A | G | 2 | a0006c0008t0001g0145 a0006c0008t0009g0235 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-4535T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397053 | |||||||
chr11:27397083 | T | C | 3 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0086 |
3 | NA18989.hp1 NA19010.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.258-4565A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397083 | |||||||
chr11:27397254 | C | T | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-4736G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397254 | |||||||
chr11:27397332 | G | A | 1 | a0001c0001t0002g0229 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.258-4814C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397332 | |||||||
chr11:27397444 | C | A | 28 | a0001c0001t0001g0146 a0001c0001t0002g0003 a0001c0001t0002g0171 others(25): Show |
29 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-4926G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397444 | |||||||
chr11:27397510 | T | G | 1 | a0001c0002t0004g0065 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.258-4992A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397510 | |||||||
chr11:27397587 | T | C | 91 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.258-5069A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397587 | |||||||
chr11:27397640 | G | C | 1 | a0001c0001t0002g0207 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.258-5122C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397640 | |||||||
chr11:27397673 | G | A | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0010g0010 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.258-5155C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397673 | |||||||
chr11:27397769 | C | G | 1 | a0001c0001t0003g0160 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.258-5251G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27397769 | |||||||
chr11:27398205 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0009g0178 a0003c0006t0002g0167 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-5687C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398205 | |||||||
chr11:27398235 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.258-5717C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398235 | |||||||
chr11:27398308 | T | C | 1 | a0001c0002t0008g0236 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.258-5790A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398308 | |||||||
chr11:27398339 | A | G | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-5821T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398339 | |||||||
chr11:27398516 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-5998G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398516 | |||||||
chr11:27398598 | G | A | 18 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(15): Show |
19 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.258-6080C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398598 | |||||||
chr11:27398994 | C | T | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(2): Show |
5 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-6476G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27398994 | |||||||
chr11:27399034 | C | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-6516G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399034 | |||||||
chr11:27399059 | T | C | 143 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(140): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.258-6541A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399059 | |||||||
chr11:27399165 | C | A | 17 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0209 others(14): Show |
17 | HG01975.hp1 HG02148.hp1 NA18971.hp1 others(14): Show |
intron_variant | MODIFIER | c.258-6647G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399165 | |||||||
chr11:27399262 | G | A | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-6744C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399262 | |||||||
chr11:27399581 | G | A | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-7063C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399581 | |||||||
chr11:27399615 | G | T | 3 | a0001c0001t0003g0107 a0001c0001t0016g0111 a0001c0001t0016g0125 |
3 | HG00733.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.258-7097C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27399615 | |||||||
chr11:27400388 | G | A | 1 | a0001c0002t0004g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.258-7870C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400388 | |||||||
chr11:27400523 | G | A | 1 | a0001c0001t0029g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.258-8005C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400523 | |||||||
chr11:27400612 | C | T | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-8094G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400612 | |||||||
chr11:27400725 | G | A | 1 | a0001c0001t0006g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258-8207C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400725 | |||||||
chr11:27400799 | T | C | 1 | a0005c0009t0005g0018 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.258-8281A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400799 | |||||||
chr11:27400839 | G | A | 1 | a0001c0002t0005g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258-8321C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400839 | |||||||
chr11:27400906 | C | T | 6 | a0001c0001t0001g0098 a0001c0001t0007g0015 a0001c0001t0007g0038 others(3): Show |
6 | HG01891.hp2 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-8388G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400906 | |||||||
chr11:27400924 | T | C | 22 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(19): Show |
23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-8406A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400924 | |||||||
chr11:27400983 | C | A | 1 | a0001c0005t0014g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.258-8465G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27400983 | |||||||
chr11:27401043 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258-8525A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401043 | |||||||
chr11:27401083 | A | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.258-8565T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401083 | |||||||
chr11:27401098 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(18): Show |
22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-8580A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401098 | |||||||
chr11:27401106 | C | G | 21 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(18): Show |
22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-8588G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401106 | |||||||
chr11:27401118 | G | A | 1 | a0001c0002t0010g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.258-8600C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401118 | |||||||
chr11:27401159 | C | T | 112 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(109): Show |
115 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.258-8641G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401159 | |||||||
chr11:27401424 | C | T | 56 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0001g0142 others(53): Show |
58 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.258-8906G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401424 | |||||||
chr11:27401539 | C | T | 54 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0007g0017 others(51): Show |
56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-9021G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401539 | |||||||
chr11:27401615 | T | C | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.258-9097A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401615 | |||||||
chr11:27401627 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.258-9109A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401627 | |||||||
chr11:27401706 | A | C | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-9188T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401706 | |||||||
chr11:27401795 | C | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-9277G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27401795 | |||||||
chr11:27402076 | C | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.258-9558G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402076 | |||||||
chr11:27402132 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-9614C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402132 | |||||||
chr11:27402220 | C | A | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-9702G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402220 | |||||||
chr11:27402339 | C | T | 1 | a0001c0001t0034g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.258-9821G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402339 | |||||||
chr11:27402415 | TA | T | 105 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(102): Show |
108 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.258-9898delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402415 | |||||||
chr11:27402577 | C | T | 1 | a0001c0010t0007g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.258-10059G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402577 | |||||||
chr11:27402826 | G | A | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.257+9963C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402826 | |||||||
chr11:27402902 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.257+9887T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27402902 | |||||||
chr11:27403206 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.257+9583G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403206 | |||||||
chr11:27403320 | G | T | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(4): Show |
7 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+9469C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403320 | |||||||
chr11:27403731 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+9058G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403731 | |||||||
chr11:27403821 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0136 a0001c0002t0004g0135 |
3 | NA18978.hp1 NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.257+8968A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403821 | |||||||
chr11:27403878 | T | C | 1 | a0001c0002t0006g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.257+8911A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403878 | |||||||
chr11:27403949 | G | A | 7 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(4): Show |
7 | NA18971.hp1 NA18984.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+8840C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27403949 | |||||||
chr11:27404236 | C | T | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(10): Show |
13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+8553G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404236 | |||||||
chr11:27404293 | C | T | 1 | a0001c0004t0013g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.257+8496G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404293 | |||||||
chr11:27404485 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.257+8304A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404485 | |||||||
chr11:27404795 | TC | T | 113 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.257+7993delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404795 | |||||||
chr11:27404844 | G | A | 143 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(140): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.257+7945C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404844 | |||||||
chr11:27404967 | T | G | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+7822A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27404967 | |||||||
chr11:27405260 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.257+7529G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405260 | |||||||
chr11:27405474 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0136 others(1): Show |
4 | NA18971.hp2 NA18978.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+7315C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405474 | |||||||
chr11:27405648 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+7141T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405648 | |||||||
chr11:27405949 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+6840G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27405949 | |||||||
chr11:27406123 | C | G | 1 | a0001c0001t0003g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.257+6666G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406123 | |||||||
chr11:27406241 | C | G | 2 | a0002c0003t0005g0031 a0002c0003t0006g0177 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.257+6548G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406241 | |||||||
chr11:27406330 | C | T | 1 | a0001c0001t0007g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.257+6459G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406330 | |||||||
chr11:27406349 | C | T | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+6440G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406349 | |||||||
chr11:27406481 | G | A | 1 | a0001c0002t0004g0079 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.257+6308C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406481 | |||||||
chr11:27406717 | C | A | 31 | a0001c0001t0001g0087 a0001c0001t0007g0017 a0001c0002t0004g0060 others(28): Show |
33 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.257+6072G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406717 | |||||||
chr11:27406956 | C | T | 4 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+5833G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27406956 | |||||||
chr11:27407208 | G | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+5581C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407208 | |||||||
chr11:27407587 | A | C | 1 | a0002c0003t0005g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.257+5202T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407587 | |||||||
chr11:27407670 | TA | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+5118delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407670 | |||||||
chr11:27407979 | A | C | 1 | a0001c0001t0002g0217 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.257+4810T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27407979 | |||||||
chr11:27408273 | T | C | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+4516A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408273 | |||||||
chr11:27408392 | T | C | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.257+4397A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408392 | |||||||
chr11:27408439 | C | T | 55 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0007g0017 others(52): Show |
57 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.257+4350G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408439 | |||||||
chr11:27408867 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+3922G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27408867 | |||||||
chr11:27409057 | A | C | 1 | a0001c0001t0003g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.257+3732T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409057 | |||||||
chr11:27409197 | C | G | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.257+3592G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409197 | |||||||
chr11:27409573 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+3216G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409573 | |||||||
chr11:27409619 | T | C | 2 | a0001c0001t0007g0028 a0001c0001t0010g0047 |
2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.257+3170A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409619 | |||||||
chr11:27409732 | A | C | 4 | a0001c0001t0032g0174 a0002c0011t0003g0155 a0003c0006t0002g0167 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+3057T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409732 | |||||||
chr11:27409843 | C | T | 95 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0001g0113 others(92): Show |
98 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.257+2946G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27409843 | |||||||
chr11:27410130 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+2659G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410130 | |||||||
chr11:27410159 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.257+2630C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410159 | |||||||
chr11:27410204 | G | A | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+2585C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410204 | |||||||
chr11:27410212 | C | T | 1 | a0001c0005t0014g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.257+2577G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410212 | |||||||
chr11:27410249 | G | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 others(11): Show |
14 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.257+2540C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410249 | |||||||
chr11:27410706 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.257+2083T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410706 | |||||||
chr11:27410711 | T | G | 17 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0209 others(14): Show |
17 | HG01975.hp1 HG02148.hp1 NA18971.hp1 others(14): Show |
intron_variant | MODIFIER | c.257+2078A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410711 | |||||||
chr11:27410796 | T | C | 1 | a0004c0007t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.257+1993A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27410796 | |||||||
chr11:27411332 | T | C | 54 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0007g0017 others(51): Show |
56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.257+1457A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27411332 | |||||||
chr11:27411949 | T | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+840A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27411949 | |||||||
chr11:27412039 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+750G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412039 | |||||||
chr11:27412285 | A | G | 112 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(109): Show |
115 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.257+504T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412285 | |||||||
chr11:27412306 | C | G | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.257+483G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412306 | |||||||
chr11:27412473 | C | T | 1 | a0002c0003t0006g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.257+316G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 2/17 | chr11 | 27412473 | |||||||
chr11:27412870 | G | A | 1 | a0001c0002t0004g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.186-10C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27412870 | |||||||
chr11:27413359 | T | C | 18 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0209 others(15): Show |
18 | HG01975.hp1 HG02148.hp1 NA18950.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-499A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413359 | |||||||
chr11:27413544 | G | A | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-684C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413544 | |||||||
chr11:27413612 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-752C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413612 | |||||||
chr11:27413651 | G | A | 1 | a0001c0002t0005g0033 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.186-791C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413651 | |||||||
chr11:27413740 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-880A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413740 | |||||||
chr11:27413748 | G | A | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-888C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413748 | |||||||
chr11:27413750 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.186-890G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413750 | |||||||
chr11:27413945 | T | G | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-1085A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27413945 | |||||||
chr11:27414375 | T | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-1515A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414375 | |||||||
chr11:27414376 | T | A | 1 | a0001c0001t0012g0118 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.186-1516A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414376 | |||||||
chr11:27414396 | T | TA | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0006g0233 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-1537dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414396 | |||||||
chr11:27414396 | TA | T | 22 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(19): Show |
23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-1537delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414396 | |||||||
chr11:27414584 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.186-1724C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414584 | |||||||
chr11:27414586 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.186-1726C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414586 | |||||||
chr11:27414759 | CAGAAA | C | 54 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0007g0017 others(51): Show |
56 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.186-1904_186-1900d others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414759 | |||||||
chr11:27414766 | G | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-1906C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414766 | |||||||
chr11:27414771 | G | A | 4 | a0001c0001t0009g0173 a0001c0001t0009g0176 a0001c0001t0009g0182 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-1911C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414771 | |||||||
chr11:27414809 | G | C | 84 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(81): Show |
85 | HG00140.hp2 HG00609.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.186-1949C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414809 | |||||||
chr11:27414810 | T | C | 7 | a0001c0001t0012g0073 a0001c0001t0012g0080 a0001c0001t0012g0081 others(4): Show |
7 | HG00609.hp2 HG02135.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-1950A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414810 | |||||||
chr11:27414887 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-2027G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414887 | |||||||
chr11:27414940 | G | A | 1 | a0001c0004t0013g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-2080C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27414940 | |||||||
chr11:27415342 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-2482G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415342 | |||||||
chr11:27415416 | C | T | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-2556G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415416 | |||||||
chr11:27415490 | G | T | 1 | a0001c0001t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.186-2630C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415490 | |||||||
chr11:27415499 | C | T | 1 | a0001c0002t0006g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2639G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415499 | |||||||
chr11:27415651 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.186-2791G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415651 | |||||||
chr11:27415809 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-2949C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27415809 | |||||||
chr11:27416056 | T | C | 1 | a0001c0001t0003g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.186-3196A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416056 | |||||||
chr11:27416154 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-3294T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416154 | |||||||
chr11:27416246 | G | A | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(10): Show |
13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-3386C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416246 | |||||||
chr11:27416254 | G | A | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-3394C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416254 | |||||||
chr11:27416281 | T | C | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-3421A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416281 | |||||||
chr11:27416361 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-3501T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416361 | |||||||
chr11:27416544 | T | A | 31 | a0001c0001t0001g0087 a0001c0001t0007g0017 a0001c0002t0004g0060 others(28): Show |
33 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-3684A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416544 | |||||||
chr11:27416950 | A | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-4090T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27416950 | |||||||
chr11:27417076 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-4216C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417076 | |||||||
chr11:27417205 | T | C | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-4345A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417205 | |||||||
chr11:27417504 | T | C | 1 | a0001c0002t0037g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.186-4644A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417504 | |||||||
chr11:27417972 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-5112G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27417972 | |||||||
chr11:27418091 | C | A | 2 | a0001c0001t0007g0054 a0001c0002t0022g0053 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.186-5231G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418091 | |||||||
chr11:27418091 | C | G | 1 | a0001c0002t0011g0078 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.186-5231G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418091 | |||||||
chr11:27418127 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-5267A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418127 | |||||||
chr11:27418138 | T | A | 1 | a0001c0002t0004g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186-5278A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418138 | |||||||
chr11:27418168 | T | G | 2 | a0001c0001t0001g0098 a0001c0001t0009g0178 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-5308A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418168 | |||||||
chr11:27418412 | G | A | 20 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0009g0215 others(17): Show |
20 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.186-5552C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418412 | |||||||
chr11:27418486 | G | C | 1 | a0001c0001t0007g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-5626C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418486 | |||||||
chr11:27418736 | T | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0110 |
3 | NA18951.hp2 NA18952.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.186-5876A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418736 | |||||||
chr11:27418825 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-5965A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418825 | |||||||
chr11:27418832 | CT | C | 48 | a0001c0001t0001g0098 a0001c0001t0001g0113 a0001c0001t0001g0114 others(45): Show |
49 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.186-5973delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418832 | |||||||
chr11:27418832 | CTT | C | 37 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0142 others(34): Show |
37 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.186-5974_186-5973d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418832 | |||||||
chr11:27418851 | G | T | 1 | a0001c0002t0006g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-5991C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418851 | |||||||
chr11:27418853 | G | A | 1 | a0001c0002t0006g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-5993C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27418853 | |||||||
chr11:27419025 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.186-6165T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419025 | |||||||
chr11:27419258 | T | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-6398A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419258 | |||||||
chr11:27419274 | C | A | 14 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 others(11): Show |
14 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-6414G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419274 | |||||||
chr11:27419393 | T | G | 1 | a0001c0001t0003g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-6533A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419393 | |||||||
chr11:27419580 | T | TTA | 143 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(140): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.186-6722_186-6721d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419580 | |||||||
chr11:27419721 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-6861A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419721 | |||||||
chr11:27419849 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-6989G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27419849 | |||||||
chr11:27420627 | C | T | 1 | a0005c0009t0005g0056 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.186-7767G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420627 | |||||||
chr11:27420785 | C | T | 24 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(21): Show |
25 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.186-7925G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420785 | |||||||
chr11:27420838 | A | C | 6 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(3): Show |
6 | NA18971.hp1 NA18984.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-7978T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27420838 | |||||||
chr11:27421257 | C | T | 4 | a0001c0001t0032g0174 a0002c0011t0003g0155 a0003c0006t0002g0167 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-8397G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421257 | |||||||
chr11:27421517 | G | T | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-8657C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421517 | |||||||
chr11:27421604 | T | C | 114 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(111): Show |
117 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.186-8744A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421604 | |||||||
chr11:27421629 | A | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.186-8769T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421629 | |||||||
chr11:27421665 | C | T | 1 | a0001c0002t0010g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186-8805G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421665 | |||||||
chr11:27421714 | C | A | 2 | a0001c0001t0007g0015 a0001c0001t0007g0038 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.186-8854G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421714 | |||||||
chr11:27421852 | T | C | 2 | a0001c0001t0001g0136 a0001c0002t0004g0135 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-8992A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421852 | |||||||
chr11:27421968 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9108A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421968 | |||||||
chr11:27421970 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9110T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421970 | |||||||
chr11:27421973 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.186-9113C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421973 | |||||||
chr11:27421994 | GT | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-9135delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27421994 | |||||||
chr11:27422159 | G | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-9299C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422159 | |||||||
chr11:27422283 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0009g0168 |
2 | HG02004.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.186-9423A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422283 | |||||||
chr11:27422471 | G | T | 1 | a0002c0003t0005g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.186-9611C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422471 | |||||||
chr11:27422608 | C | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-9748G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422608 | |||||||
chr11:27422628 | C | T | 60 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(57): Show |
61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-9768G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422628 | |||||||
chr11:27422889 | C | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-10029G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422889 | |||||||
chr11:27422970 | T | C | 53 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0007g0017 others(50): Show |
55 | HG00099.hp2 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.186-10110A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27422970 | |||||||
chr11:27423039 | A | G | 1 | a0001c0002t0004g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186-10179T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423039 | |||||||
chr11:27423071 | T | C | 1 | a0001c0001t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.186-10211A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423071 | |||||||
chr11:27423461 | CCTT | C | 5 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-10604_186-1060 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423461 | |||||||
chr11:27423583 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(18): Show |
22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-10723A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423583 | |||||||
chr11:27423621 | A | G | 60 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(57): Show |
61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-10761T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423621 | |||||||
chr11:27423966 | A | T | 1 | a0001c0001t0016g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.186-11106T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27423966 | |||||||
chr11:27424118 | A | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-11258T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424118 | |||||||
chr11:27424292 | T | C | 1 | a0004c0007t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.186-11432A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424292 | |||||||
chr11:27424298 | G | A | 1 | a0001c0001t0003g0160 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.186-11438C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424298 | |||||||
chr11:27424305 | C | T | 2 | a0001c0001t0007g0028 a0001c0001t0010g0047 |
2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.186-11445G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424305 | |||||||
chr11:27424507 | C | A | 60 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(57): Show |
61 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.186-11647G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424507 | |||||||
chr11:27424705 | A | G | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-11845T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424705 | |||||||
chr11:27424732 | T | G | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-11872A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424732 | |||||||
chr11:27424844 | T | C | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-11984A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424844 | |||||||
chr11:27424895 | G | A | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-12035C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27424895 | |||||||
chr11:27425079 | C | G | 1 | a0001c0010t0007g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.186-12219G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425079 | |||||||
chr11:27425124 | G | C | 6 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(3): Show |
6 | HG02027.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-12264C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425124 | |||||||
chr11:27425326 | G | GTT | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(10): Show |
13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-12468_186-1246 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425326 | |||||||
chr11:27425329 | T | A | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-12469A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425329 | |||||||
chr11:27425338 | G | GTT | 21 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(18): Show |
22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-12480_186-1247 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425338 | |||||||
chr11:27425803 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-12943G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425803 | |||||||
chr11:27425828 | T | A | 1 | a0001c0001t0030g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.186-12968A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425828 | |||||||
chr11:27425983 | G | T | 1 | a0001c0001t0009g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186-13123C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425983 | |||||||
chr11:27425999 | T | C | 3 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 |
3 | HG00642.hp2 HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.186-13139A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27425999 | |||||||
chr11:27426128 | T | C | 1 | a0001c0002t0004g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.186-13268A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426128 | |||||||
chr11:27426295 | T | C | 1 | a0001c0001t0007g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-13435A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426295 | |||||||
chr11:27426343 | T | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-13483A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426343 | |||||||
chr11:27426478 | C | T | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-13618G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426478 | |||||||
chr11:27426613 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-13753A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426613 | |||||||
chr11:27426736 | C | G | 1 | a0001c0002t0008g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.186-13876G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426736 | |||||||
chr11:27426788 | A | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-13928T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426788 | |||||||
chr11:27426862 | G | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(19): Show |
23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-14002C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27426862 | |||||||
chr11:27427097 | G | C | 1 | a0001c0002t0010g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.186-14237C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427097 | |||||||
chr11:27427104 | G | A | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-14244C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427104 | |||||||
chr11:27427258 | C | T | 1 | a0001c0001t0007g0017 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.186-14398G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427258 | |||||||
chr11:27427363 | G | A | 3 | a0001c0001t0007g0054 a0001c0001t0019g0004 a0001c0002t0022g0053 |
3 | HG03492.hp1 HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.186-14503C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427363 | |||||||
chr11:27427380 | G | A | 1 | a0002c0003t0031g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186-14520C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427380 | |||||||
chr11:27427450 | A | G | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14590T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427450 | |||||||
chr11:27427452 | C | A | 1 | a0001c0002t0025g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-14592G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427452 | |||||||
chr11:27427521 | C | A | 29 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0099 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.186-14661G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427521 | |||||||
chr11:27427664 | C | T | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14804G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427664 | |||||||
chr11:27427688 | A | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-14828T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427688 | |||||||
chr11:27427798 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-14938C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427798 | |||||||
chr11:27427805 | C | T | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14945G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427805 | |||||||
chr11:27427814 | G | A | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-14954C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427814 | |||||||
chr11:27427823 | A | G | 1 | a0001c0002t0004g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.186-14963T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427823 | |||||||
chr11:27427862 | G | A | 6 | a0001c0001t0001g0142 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-15002C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427862 | |||||||
chr11:27427922 | C | T | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-15062G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427922 | |||||||
chr11:27427998 | G | A | 1 | a0001c0001t0010g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186-15138C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27427998 | |||||||
chr11:27428139 | C | CT | 22 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(19): Show |
23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-15280dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428139 | |||||||
chr11:27428139 | CT | C | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-15280delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428139 | |||||||
chr11:27428223 | T | C | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-15363A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428223 | |||||||
chr11:27428287 | C | T | 44 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0113 others(41): Show |
45 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.186-15427G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428287 | |||||||
chr11:27428362 | T | C | 61 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(58): Show |
62 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.186-15502A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428362 | |||||||
chr11:27428432 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0009g0178 a0001c0002t0004g0061 |
3 | HG00639.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-15572G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428432 | |||||||
chr11:27428492 | G | A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-15632C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428492 | |||||||
chr11:27428500 | T | C | 22 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(19): Show |
23 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-15640A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428500 | |||||||
chr11:27428619 | T | C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(10): Show |
13 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-15759A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428619 | |||||||
chr11:27428636 | C | CTAGATAG others(2): Show |
4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-15777_186-1577 others(13): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428636 | |||||||
chr11:27428640 | A | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0004c0007t0001g0096 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-15780T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428640 | |||||||
chr11:27428749 | T | G | 1 | a0001c0002t0004g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.186-15889A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428749 | |||||||
chr11:27428763 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.186-15903G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428763 | |||||||
chr11:27428818 | G | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-15958C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428818 | |||||||
chr11:27428855 | C | T | 1 | a0001c0001t0006g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-15995G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428855 | |||||||
chr11:27428984 | A | G | 115 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(112): Show |
118 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.186-16124T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27428984 | |||||||
chr11:27429217 | G | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-16357C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429217 | |||||||
chr11:27429254 | G | A | 2 | a0006c0008t0001g0145 a0006c0008t0009g0235 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.186-16394C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429254 | |||||||
chr11:27429343 | G | A | 26 | a0001c0001t0001g0142 a0001c0001t0006g0233 a0001c0001t0012g0073 others(23): Show |
26 | HG00609.hp2 HG00642.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-16483C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429343 | |||||||
chr11:27429470 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-16610C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429470 | |||||||
chr11:27429482 | C | CA | 11 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0007g0015 others(8): Show |
11 | HG00735.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-16623dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429482 | |||||||
chr11:27429499 | A | C | 3 | a0001c0001t0032g0174 a0003c0006t0002g0167 a0003c0006t0007g0037 |
3 | HG02717.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.186-16639T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429499 | |||||||
chr11:27429514 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-16654C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429514 | |||||||
chr11:27429518 | G | A | 1 | a0001c0001t0009g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.186-16658C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429518 | |||||||
chr11:27429686 | A | G | 1 | a0001c0001t0003g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-16826T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27429686 | |||||||
chr11:27430015 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-17155C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430015 | |||||||
chr11:27430167 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
7 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-17307G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430167 | |||||||
chr11:27430212 | C | A | 62 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0098 others(59): Show |
63 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.186-17352G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430212 | |||||||
chr11:27430405 | GA | G | 5 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-17546delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430405 | |||||||
chr11:27430478 | A | G | 4 | a0001c0001t0002g0207 a0001c0001t0007g0054 a0001c0001t0019g0004 others(1): Show |
4 | HG02698.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-17618T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430478 | |||||||
chr11:27430879 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0005t0014g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-18019G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430879 | |||||||
chr11:27430913 | A | C | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-18053T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27430913 | |||||||
chr11:27431011 | G | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0171 a0001c0001t0002g0172 others(18): Show |
22 | HG00140.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-18151C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431011 | |||||||
chr11:27431159 | A | G | 6 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-18299T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431159 | |||||||
chr11:27431387 | C | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-18527G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431387 | |||||||
chr11:27431583 | C | T | 1 | a0001c0001t0007g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-18723G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431583 | |||||||
chr11:27431584 | G | A | 3 | a0001c0002t0006g0196 a0001c0002t0018g0238 a0001c0002t0018g0239 |
3 | HG02486.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.186-18724C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431584 | |||||||
chr11:27431587 | C | T | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-18727G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431587 | |||||||
chr11:27431772 | T | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0032g0174 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-18912A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431772 | |||||||
chr11:27431866 | T | C | 5 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(2): Show |
5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-19006A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27431866 | |||||||
chr11:27432032 | C | T | 3 | a0001c0001t0027g0137 a0001c0001t0030g0166 a0003c0006t0003g0139 |
3 | HG01243.hp2 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.186-19172G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432032 | |||||||
chr11:27432196 | A | G | 2 | a0001c0001t0002g0181 a0001c0001t0002g0234 |
2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.186-19336T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432196 | |||||||
chr11:27432205 | A | C | 19 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0012g0073 others(16): Show |
20 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.186-19345T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432205 | |||||||
chr11:27432374 | G | A | 2 | a0001c0005t0014g0148 a0001c0005t0014g0153 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.186-19514C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432374 | |||||||
chr11:27432545 | A | C | 5 | a0001c0004t0013g0014 a0001c0004t0013g0034 a0001c0004t0013g0035 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-19685T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432545 | |||||||
chr11:27432668 | C | G | 4 | a0001c0001t0009g0178 a0001c0002t0004g0061 a0001c0002t0004g0150 others(1): Show |
4 | HG00639.hp1 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-19808G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27432668 | |||||||
chr11:27433222 | T | C | 8 | a0001c0001t0006g0233 a0001c0001t0010g0036 a0001c0002t0004g0061 others(5): Show |
8 | HG00639.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-20362A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433222 | |||||||
chr11:27433312 | T | A | 1 | a0001c0002t0020g0005 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-20452A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433312 | |||||||
chr11:27433341 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.186-20481A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433341 | |||||||
chr11:27433387 | A | C | 1 | a0001c0001t0003g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.186-20527T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433387 | |||||||
chr11:27433397 | CT | C | 162 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(159): Show |
164 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.186-20538delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433397 | |||||||
chr11:27433615 | T | C | 6 | a0001c0001t0010g0036 a0001c0004t0013g0014 a0001c0004t0013g0034 others(3): Show |
6 | HG02572.hp1 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-20755A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433615 | |||||||
chr11:27433946 | A | G | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-21086T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433946 | |||||||
chr11:27433950 | T | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-21090A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27433950 | |||||||
chr11:27434029 | T | C | 221 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.186-21169A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434029 | |||||||
chr11:27434035 | C | T | 165 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(162): Show |
167 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.186-21175G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434035 | |||||||
chr11:27434321 | T | G | 1 | a0001c0002t0006g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-21461A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434321 | |||||||
chr11:27434512 | C | T | 165 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(162): Show |
167 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.186-21652G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434512 | |||||||
chr11:27434887 | T | C | 3 | a0001c0001t0009g0178 a0001c0002t0004g0061 a0001c0004t0035g0175 |
3 | HG00639.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.186-22027A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434887 | |||||||
chr11:27434941 | T | C | 165 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(162): Show |
167 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.186-22081A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27434941 | |||||||
chr11:27435129 | G | A | 9 | a0001c0001t0032g0174 a0001c0002t0005g0008 a0001c0002t0005g0009 others(6): Show |
9 | HG01891.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-22269C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435129 | |||||||
chr11:27435205 | C | T | 27 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(24): Show |
28 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-22345G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435205 | |||||||
chr11:27435287 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0003g0141 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.186-22427A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435287 | |||||||
chr11:27435348 | AAAC | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-22491_186-2248 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435348 | |||||||
chr11:27435415 | A | G | 2 | a0001c0001t0001g0142 a0003c0006t0002g0167 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.186-22555T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435415 | |||||||
chr11:27435488 | G | A | 32 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(29): Show |
33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22628C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435488 | |||||||
chr11:27435512 | A | G | 32 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(29): Show |
33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22652T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435512 | |||||||
chr11:27435548 | T | G | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.186-22688A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435548 | |||||||
chr11:27435581 | G | A | 6 | a0001c0002t0004g0134 a0001c0002t0005g0002 a0001c0002t0005g0024 others(3): Show |
7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-22721C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435581 | |||||||
chr11:27435646 | C | T | 32 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(29): Show |
33 | HG00642.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.186-22786G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435646 | |||||||
chr11:27435774 | A | C | 165 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(162): Show |
167 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.186-22914T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435774 | |||||||
chr11:27435933 | C | T | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-23073G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435933 | |||||||
chr11:27435965 | C | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-23105G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27435965 | |||||||
chr11:27436037 | GAGTTGCT others(8): Show |
G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(6): Show |
9 | HG02572.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-23192_186-2317 others(19): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436037 | |||||||
chr11:27436057 | G | A | 20 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0038 others(17): Show |
21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-23197C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436057 | |||||||
chr11:27436113 | G | A | 27 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(24): Show |
28 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.186-23253C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436113 | |||||||
chr11:27436204 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0003g0133 others(1): Show |
4 | HG01109.hp2 HG01243.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-23344G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436204 | |||||||
chr11:27436206 | T | G | 1 | a0001c0001t0007g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-23346A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436206 | |||||||
chr11:27436293 | G | A | 1 | a0001c0002t0005g0011 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.186-23433C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436293 | |||||||
chr11:27436302 | C | T | 28 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(25): Show |
29 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-23442G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436302 | |||||||
chr11:27436347 | G | GAGAA | 66 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(63): Show |
66 | HG00735.hp2 HG01070.hp2 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.186-23491_186-2348 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436347 | |||||||
chr11:27436347 | GAGAA | G | 28 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0007g0015 others(25): Show |
29 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-23491_186-2348 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436347 | |||||||
chr11:27436371 | AAGAG | A | 7 | a0001c0001t0001g0142 a0001c0001t0030g0166 a0001c0002t0017g0006 others(4): Show |
7 | HG02717.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-23515_186-2351 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436371 | |||||||
chr11:27436373 | G | GAA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0010g0036 others(5): Show |
8 | HG02572.hp1 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-23514_186-2351 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436373 | |||||||
chr11:27436602 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.186-23742A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436602 | |||||||
chr11:27436674 | T | C | 5 | a0001c0001t0007g0020 a0001c0001t0015g0019 a0001c0001t0015g0029 others(2): Show |
6 | NA18946.hp2 NA18960.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-23814A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436674 | |||||||
chr11:27436750 | A | G | 1 | a0001c0002t0005g0013 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.186-23890T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436750 | |||||||
chr11:27436863 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.186-24003A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27436863 | |||||||
chr11:27437297 | AT | A | 14 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 others(11): Show |
14 | HG00639.hp1 HG01099.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-24438delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437297 | |||||||
chr11:27437435 | C | T | 1 | a0001c0001t0007g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-24575G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437435 | |||||||
chr11:27437564 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.186-24704G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437564 | |||||||
chr11:27437660 | A | AGGTGTGT others(4): Show |
1 | a0001c0001t0012g0117 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.186-24801_186-2480 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGT | 15 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0207 others(12): Show |
15 | HG01099.hp1 HG01255.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-24802_186-2480 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGT | 17 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(14): Show |
17 | HG00639.hp1 HG02027.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-24804_186-2480 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGTGT | 47 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0093 others(44): Show |
47 | HG00735.hp2 HG01255.hp2 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.186-24806_186-2480 others(10): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGTGTG others(1): Show |
31 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0001g0114 others(28): Show |
32 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-24808_186-2480 others(12): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGTGTG others(3): Show |
40 | a0001c0001t0001g0142 a0001c0001t0002g0209 a0001c0001t0003g0085 others(37): Show |
41 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.186-24810_186-2480 others(14): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGTGTG others(5): Show |
8 | a0001c0001t0010g0057 a0001c0001t0012g0080 a0001c0001t0030g0166 others(5): Show |
8 | HG02132.hp1 HG02970.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-24812_186-2480 others(16): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0003g0089 a0001c0001t0032g0174 a0002c0003t0004g0144 |
3 | HG01070.hp2 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.186-24814_186-2480 others(18): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | AGT | A | 11 | a0001c0001t0006g0233 a0001c0001t0009g0182 a0001c0001t0009g0220 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-24802_186-2480 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | AGTGT | A | 4 | a0001c0001t0007g0040 a0001c0002t0004g0076 a0001c0005t0014g0148 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-24804_186-2480 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437660 | AGTGTGTG others(7): Show |
A | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-24814_186-2480 others(18): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437660 | |||||||
chr11:27437712 | A | T | 1 | a0001c0004t0013g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186-24852T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437712 | |||||||
chr11:27437771 | GCAGGAGG others(5): Show |
G | 82 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0093 others(79): Show |
82 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.186-24923_186-2491 others(16): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437771 | |||||||
chr11:27437805 | C | T | 16 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(13): Show |
16 | HG01981.hp1 HG02004.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.186-24945G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27437805 | |||||||
chr11:27438443 | T | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-25583A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438443 | |||||||
chr11:27438559 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-25699C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438559 | |||||||
chr11:27438604 | A | G | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.186-25744T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438604 | |||||||
chr11:27438610 | A | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-25750T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438610 | |||||||
chr11:27438655 | GCCT | G | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-25798_186-2579 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438655 | |||||||
chr11:27438665 | A | G | 3 | a0002c0003t0006g0183 a0002c0003t0006g0184 a0002c0003t0006g0197 |
3 | HG02055.hp1 HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.186-25805T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438665 | |||||||
chr11:27438988 | C | T | 1 | a0001c0001t0024g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.186-26128G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27438988 | |||||||
chr11:27439079 | A | G | 1 | a0004c0007t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.186-26219T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439079 | |||||||
chr11:27439092 | C | T | 2 | a0001c0001t0002g0228 a0001c0002t0008g0189 |
2 | NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.186-26232G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439092 | |||||||
chr11:27439164 | T | C | 185 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.186-26304A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439164 | |||||||
chr11:27439169 | C | A | 1 | a0006c0008t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186-26309G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439169 | |||||||
chr11:27439207 | T | G | 1 | a0001c0002t0004g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.186-26347A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439207 | |||||||
chr11:27439221 | T | C | 68 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0003g0085 others(65): Show |
70 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.186-26361A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439221 | |||||||
chr11:27439226 | C | G | 1 | a0001c0001t0010g0016 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.186-26366G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439226 | |||||||
chr11:27439492 | C | A | 1 | a0004c0007t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-26632G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439492 | |||||||
chr11:27439609 | G | T | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.186-26749C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439609 | |||||||
chr11:27439684 | T | C | 2 | a0001c0005t0014g0148 a0001c0005t0014g0153 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.186-26824A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439684 | |||||||
chr11:27439899 | CTCTT | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0105 others(7): Show |
10 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.186-27043_186-2704 others(8): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439899 | |||||||
chr11:27439901 | C | CT | 8 | a0001c0001t0002g0188 a0001c0001t0002g0205 a0001c0001t0002g0219 others(5): Show |
8 | HG01891.hp1 HG01975.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-27042dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | |||||||
chr11:27439901 | CT | C | 14 | a0001c0001t0002g0217 a0001c0001t0003g0068 a0001c0001t0003g0077 others(11): Show |
14 | HG01070.hp2 HG01256.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-27042delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | |||||||
chr11:27439901 | CTT | C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(10): Show |
13 | HG00642.hp2 HG01243.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.186-27043_186-2704 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | |||||||
chr11:27439901 | CTTT | C | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-27044_186-2704 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439901 | |||||||
chr11:27439928 | C | T | 2 | a0001c0001t0009g0182 a0001c0001t0009g0220 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.186-27068G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439928 | |||||||
chr11:27439982 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.186-27122A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27439982 | |||||||
chr11:27440023 | A | T | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-27163T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440023 | |||||||
chr11:27440066 | C | A | 1 | a0001c0002t0006g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-27206G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440066 | |||||||
chr11:27440232 | T | C | 72 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(69): Show |
72 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.186-27372A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440232 | |||||||
chr11:27440266 | G | A | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.186-27406C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440266 | |||||||
chr11:27440645 | TTG | T | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-27787_186-2778 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440645 | |||||||
chr11:27440683 | C | G | 163 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(160): Show |
165 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.186-27823G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440683 | |||||||
chr11:27440926 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(6): Show |
9 | HG02572.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-28066T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27440926 | |||||||
chr11:27441190 | C | G | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-28330G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441190 | |||||||
chr11:27441258 | T | C | 80 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0001g0151 others(77): Show |
82 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.186-28398A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441258 | |||||||
chr11:27441324 | C | CAGCCTCT others(46): Show |
1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-28517_186-2846 others(57): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441324 | |||||||
chr11:27441399 | T | C | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.186-28539A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441399 | |||||||
chr11:27441626 | C | T | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.186-28766G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441626 | |||||||
chr11:27441648 | AAG | A | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-28790_186-2878 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441648 | |||||||
chr11:27441836 | G | A | 8 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0011 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-28976C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441836 | |||||||
chr11:27441900 | G | A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0126 others(3): Show |
6 | HG00733.hp1 HG01981.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-29040C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441900 | |||||||
chr11:27441931 | T | G | 1 | a0006c0008t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.186-29071A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27441931 | |||||||
chr11:27442017 | A | G | 82 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(79): Show |
82 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.186-29157T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442017 | |||||||
chr11:27442045 | A | G | 3 | a0001c0001t0003g0068 a0001c0001t0003g0071 a0001c0002t0004g0070 |
3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.186-29185T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442045 | |||||||
chr11:27442180 | G | C | 1 | a0006c0008t0009g0235 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-29320C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442180 | |||||||
chr11:27442285 | A | G | 69 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(66): Show |
69 | HG00735.hp2 HG01070.hp2 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.186-29425T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442285 | |||||||
chr11:27442588 | C | T | 2 | a0001c0001t0002g0228 a0001c0002t0008g0189 |
2 | NA18612.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.185+29530G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442588 | |||||||
chr11:27442714 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0030g0166 a0001c0002t0017g0006 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+29404G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442714 | |||||||
chr11:27442781 | A | C | 185 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.185+29337T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27442781 | |||||||
chr11:27443082 | C | T | 26 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(23): Show |
27 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+29036G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443082 | |||||||
chr11:27443186 | CA | C | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+28931delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443186 | |||||||
chr11:27443325 | C | T | 6 | a0001c0002t0004g0134 a0001c0002t0005g0002 a0001c0002t0005g0024 others(3): Show |
7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+28793G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443325 | |||||||
chr11:27443358 | G | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+28760C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443358 | |||||||
chr11:27443367 | C | G | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+28751G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443367 | |||||||
chr11:27443518 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0003g0141 a0003c0006t0002g0167 |
3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+28600T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443518 | |||||||
chr11:27443589 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.185+28529C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27443589 | |||||||
chr11:27444044 | T | C | 63 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(60): Show |
63 | HG00735.hp2 HG01070.hp2 HG01255.hp2 others(60): Show |
intron_variant | MODIFIER | c.185+28074A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444044 | |||||||
chr11:27444094 | G | GA | 82 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(79): Show |
82 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.185+28023dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444094 | |||||||
chr11:27444478 | G | T | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185+27640C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444478 | |||||||
chr11:27444826 | G | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+27292C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444826 | |||||||
chr11:27444853 | C | A | 3 | a0001c0001t0009g0173 a0001c0001t0009g0182 a0001c0001t0009g0220 |
3 | HG02145.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.185+27265G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444853 | |||||||
chr11:27444891 | A | G | 20 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0038 others(17): Show |
21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+27227T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27444891 | |||||||
chr11:27445007 | A | T | 2 | a0002c0003t0005g0044 a0002c0003t0006g0206 |
2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.185+27111T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445007 | |||||||
chr11:27445040 | AGGCAGAA others(4): Show |
A | 3 | a0001c0001t0001g0146 a0001c0001t0003g0141 a0003c0006t0002g0167 |
3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+27067_185+2707 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445040 | |||||||
chr11:27445210 | G | A | 1 | a0001c0001t0007g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.185+26908C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445210 | |||||||
chr11:27445233 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0003g0141 a0003c0006t0002g0167 |
3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+26885G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445233 | |||||||
chr11:27445256 | G | A | 1 | a0001c0001t0010g0016 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+26862C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445256 | |||||||
chr11:27445272 | C | A | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+26846G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445272 | |||||||
chr11:27445283 | G | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+26835C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445283 | |||||||
chr11:27445374 | G | A | 10 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(7): Show |
10 | NA18951.hp1 NA18952.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+26744C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445374 | |||||||
chr11:27445453 | G | A | 1 | a0001c0002t0011g0143 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.185+26665C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445453 | |||||||
chr11:27445562 | A | C | 163 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(160): Show |
165 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+26556T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445562 | |||||||
chr11:27445564 | C | A | 8 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0011 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+26554G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445564 | |||||||
chr11:27445706 | G | A | 1 | a0001c0005t0014g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.185+26412C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445706 | |||||||
chr11:27445814 | T | G | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+26304A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445814 | |||||||
chr11:27445883 | T | TA | 71 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(68): Show |
71 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.185+26234dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27445883 | |||||||
chr11:27446154 | T | A | 70 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(67): Show |
70 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.185+25964A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446154 | |||||||
chr11:27446170 | AT | A | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+25947delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446170 | |||||||
chr11:27446371 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185+25747C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446371 | |||||||
chr11:27446436 | T | G | 1 | a0001c0001t0010g0016 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+25682A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446436 | |||||||
chr11:27446681 | C | T | 1 | a0002c0003t0005g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.185+25437G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446681 | |||||||
chr11:27446736 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185+25382C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446736 | |||||||
chr11:27446886 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0061 others(2): Show |
5 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+25232C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446886 | |||||||
chr11:27446917 | G | C | 70 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(67): Show |
70 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.185+25201C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27446917 | |||||||
chr11:27447048 | G | C | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+25070C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447048 | |||||||
chr11:27447053 | G | A | 66 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0003g0085 others(63): Show |
68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.185+25065C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447053 | |||||||
chr11:27447081 | T | C | 1 | a0001c0001t0006g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+25037A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447081 | |||||||
chr11:27447098 | C | T | 6 | a0001c0001t0001g0142 a0001c0001t0030g0166 a0001c0002t0017g0006 others(3): Show |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+25020G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447098 | |||||||
chr11:27447196 | A | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0006g0233 others(8): Show |
11 | HG01169.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.185+24922T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447196 | |||||||
chr11:27447389 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.185+24729A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447389 | |||||||
chr11:27447426 | T | G | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+24692A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447426 | |||||||
chr11:27447602 | T | A | 3 | a0001c0001t0001g0146 a0001c0001t0003g0141 a0003c0006t0002g0167 |
3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+24516A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447602 | |||||||
chr11:27447631 | A | G | 1 | a0001c0002t0011g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.185+24487T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27447631 | |||||||
chr11:27448295 | C | CT | 70 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(67): Show |
70 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.185+23822dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448295 | |||||||
chr11:27448355 | T | C | 1 | a0001c0002t0005g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.185+23763A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448355 | |||||||
chr11:27448417 | T | C | 92 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(89): Show |
94 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.185+23701A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448417 | |||||||
chr11:27448519 | C | G | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+23599G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448519 | |||||||
chr11:27448570 | G | A | 1 | a0004c0007t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.185+23548C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448570 | |||||||
chr11:27448571 | C | T | 1 | a0001c0004t0013g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.185+23547G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448571 | |||||||
chr11:27448683 | T | G | 1 | a0006c0008t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+23435A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448683 | |||||||
chr11:27448878 | A | G | 45 | a0001c0001t0001g0087 a0001c0001t0003g0085 a0001c0001t0003g0131 others(42): Show |
46 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.185+23240T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448878 | |||||||
chr11:27448970 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.185+23148G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27448970 | |||||||
chr11:27449195 | G | A | 1 | a0001c0001t0003g0161 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.185+22923C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449195 | |||||||
chr11:27449273 | AAT | A | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+22843_185+2284 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449273 | |||||||
chr11:27449301 | A | G | 65 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(62): Show |
66 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.185+22817T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449301 | |||||||
chr11:27449356 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0003g0141 a0003c0006t0002g0167 |
3 | HG02717.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+22762C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449356 | |||||||
chr11:27449373 | C | A | 162 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(159): Show |
164 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.185+22745G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449373 | |||||||
chr11:27449404 | G | A | 4 | a0001c0002t0001g0138 a0001c0002t0001g0147 a0001c0002t0004g0140 others(1): Show |
4 | HG00642.hp2 HG01243.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+22714C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449404 | |||||||
chr11:27449412 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.185+22706C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449412 | |||||||
chr11:27449808 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0003g0141 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.185+22310T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449808 | |||||||
chr11:27449883 | A | C | 13 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0027g0137 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+22235T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27449883 | |||||||
chr11:27450049 | A | G | 46 | a0001c0001t0001g0087 a0001c0001t0001g0142 a0001c0001t0003g0085 others(43): Show |
47 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+22069T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450049 | |||||||
chr11:27450173 | A | C | 25 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 others(22): Show |
25 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+21945T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450173 | |||||||
chr11:27450275 | T | C | 13 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0027g0137 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+21843A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450275 | |||||||
chr11:27450345 | T | A | 1 | a0001c0002t0004g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185+21773A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450345 | |||||||
chr11:27450545 | T | C | 1 | a0001c0002t0011g0078 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.185+21573A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450545 | |||||||
chr11:27450582 | A | C | 20 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0038 others(17): Show |
21 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+21536T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450582 | |||||||
chr11:27450582 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.185+21536T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450582 | |||||||
chr11:27450686 | G | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+21432C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450686 | |||||||
chr11:27450749 | T | C | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+21369A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27450749 | |||||||
chr11:27451083 | C | T | 1 | a0006c0008t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+21035G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451083 | |||||||
chr11:27451115 | A | C | 1 | a0001c0001t0003g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+21003T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451115 | |||||||
chr11:27451158 | A | G | 6 | a0001c0002t0004g0134 a0001c0002t0005g0002 a0001c0002t0005g0024 others(3): Show |
7 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+20960T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451158 | |||||||
chr11:27451230 | T | C | 70 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(67): Show |
70 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.185+20888A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451230 | |||||||
chr11:27451233 | A | T | 1 | a0001c0002t0004g0065 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.185+20885T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451233 | |||||||
chr11:27451425 | G | A | 6 | a0001c0001t0006g0233 a0001c0002t0001g0138 a0001c0002t0001g0147 others(3): Show |
6 | HG00639.hp1 HG00642.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+20693C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451425 | |||||||
chr11:27451521 | G | A | 26 | a0001c0001t0001g0142 a0001c0001t0007g0015 a0001c0001t0007g0020 others(23): Show |
27 | HG01891.hp1 HG02451.hp1 HG02630.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+20597C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451521 | |||||||
chr11:27451550 | T | C | 3 | a0001c0001t0036g0240 a0001c0002t0018g0238 a0001c0002t0018g0239 |
3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.185+20568A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451550 | |||||||
chr11:27451911 | A | G | 1 | a0001c0002t0004g0070 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.185+20207T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27451911 | |||||||
chr11:27452042 | A | T | 1 | a0001c0002t0008g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.185+20076T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452042 | |||||||
chr11:27452342 | C | T | 1 | a0002c0003t0006g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.185+19776G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452342 | |||||||
chr11:27452422 | C | A | 4 | a0002c0003t0006g0183 a0002c0003t0006g0184 a0002c0003t0006g0197 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+19696G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452422 | |||||||
chr11:27452434 | G | A | 85 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(82): Show |
85 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.185+19684C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452434 | |||||||
chr11:27452581 | AT | A | 82 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(79): Show |
82 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.185+19536delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452581 | |||||||
chr11:27452623 | G | GT | 31 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0113 others(28): Show |
31 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.185+19494dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | |||||||
chr11:27452623 | GT | G | 6 | a0001c0001t0002g0209 a0001c0001t0007g0030 a0001c0001t0007g0038 others(3): Show |
6 | HG00639.hp1 HG01975.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+19494delA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | |||||||
chr11:27452623 | GTTT | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+19492_185+1949 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452623 | |||||||
chr11:27452650 | CA | C | 55 | a0001c0001t0003g0131 a0001c0001t0007g0015 a0001c0001t0007g0017 others(52): Show |
57 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.185+19467delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452650 | |||||||
chr11:27452759 | G | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0151 others(7): Show |
10 | HG00639.hp1 HG00735.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+19359C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452759 | |||||||
chr11:27452784 | C | T | 1 | a0001c0002t0004g0079 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.185+19334G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452784 | |||||||
chr11:27452790 | A | AT | 5 | a0001c0001t0002g0219 a0001c0001t0010g0016 a0001c0002t0004g0072 others(2): Show |
5 | HG00544.hp1 HG02135.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+19327dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452790 | |||||||
chr11:27452823 | C | T | 5 | a0001c0001t0001g0142 a0001c0002t0001g0138 a0001c0002t0001g0147 others(2): Show |
5 | HG00642.hp2 HG01243.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+19295G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27452823 | |||||||
chr11:27453248 | T | C | 55 | a0001c0001t0003g0131 a0001c0001t0007g0015 a0001c0001t0007g0017 others(52): Show |
57 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.185+18870A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453248 | |||||||
chr11:27453345 | G | A | 1 | a0001c0001t0010g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.185+18773C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453345 | |||||||
chr11:27453358 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.185+18760G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453358 | |||||||
chr11:27453362 | C | G | 1 | a0001c0001t0032g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.185+18756G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453362 | |||||||
chr11:27453443 | T | TA | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0151 others(6): Show |
9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+18674dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27453443 | |||||||
chr11:27454161 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0151 others(6): Show |
9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+17957G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454161 | |||||||
chr11:27454514 | C | G | 1 | a0007c0012t0004g0062 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.185+17604G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454514 | |||||||
chr11:27454552 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0151 others(6): Show |
9 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+17566C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454552 | |||||||
chr11:27454761 | C | CA | 16 | a0001c0001t0001g0110 a0001c0001t0002g0172 a0001c0001t0010g0057 others(13): Show |
16 | HG01433.hp1 HG01981.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+17356dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454761 | |||||||
chr11:27454761 | CA | C | 60 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(57): Show |
60 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.185+17356delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454761 | |||||||
chr11:27454963 | A | C | 1 | a0001c0001t0003g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+17155T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27454963 | |||||||
chr11:27455079 | A | C | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+17039T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455079 | |||||||
chr11:27455252 | C | T | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+16866G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455252 | |||||||
chr11:27455269 | G | A | 11 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0001t0002g0209 others(8): Show |
11 | HG00609.hp2 HG01975.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+16849C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455269 | |||||||
chr11:27455350 | T | G | 1 | a0001c0002t0004g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.185+16768A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455350 | |||||||
chr11:27455389 | A | C | 65 | a0001c0001t0001g0142 a0001c0001t0003g0131 a0001c0001t0003g0141 others(62): Show |
67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+16729T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455389 | |||||||
chr11:27455727 | C | T | 2 | a0001c0001t0003g0133 a0001c0002t0004g0132 |
2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.185+16391G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455727 | |||||||
chr11:27455756 | T | C | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+16362A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455756 | |||||||
chr11:27455769 | C | T | 1 | a0001c0002t0005g0001 | 2 | NA18946.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.185+16349G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455769 | |||||||
chr11:27455887 | G | C | 1 | a0001c0002t0006g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.185+16231C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27455887 | |||||||
chr11:27456303 | C | T | 1 | a0002c0003t0006g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185+15815G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456303 | |||||||
chr11:27456317 | A | AAC | 144 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(141): Show |
146 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.185+15799_185+1580 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456317 | |||||||
chr11:27456326 | T | C | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+15792A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27456326 | |||||||
chr11:27457030 | T | C | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+15088A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457030 | |||||||
chr11:27457044 | AG | A | 8 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0011 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+15073delC | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457044 | |||||||
chr11:27457223 | G | T | 1 | a0001c0002t0005g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.185+14895C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457223 | |||||||
chr11:27457409 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.185+14709C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457409 | |||||||
chr11:27457491 | C | A | 2 | a0001c0004t0013g0014 a0001c0004t0013g0045 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.185+14627G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457491 | |||||||
chr11:27457534 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+14584G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27457534 | |||||||
chr11:27458100 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 |
3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+14018C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458100 | |||||||
chr11:27458365 | T | C | 2 | a0001c0002t0008g0195 a0001c0002t0033g0170 |
2 | NA18960.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.185+13753A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458365 | |||||||
chr11:27458378 | A | G | 1 | a0002c0003t0006g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.185+13740T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458378 | |||||||
chr11:27458457 | T | C | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13661A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458457 | |||||||
chr11:27458518 | T | G | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13600A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458518 | |||||||
chr11:27458586 | T | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13532A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458586 | |||||||
chr11:27458601 | C | T | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+13517G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458601 | |||||||
chr11:27458669 | G | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13449C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27458669 | |||||||
chr11:27459076 | T | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+13042A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459076 | |||||||
chr11:27459147 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 |
3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+12971C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459147 | |||||||
chr11:27459280 | T | C | 65 | a0001c0001t0001g0142 a0001c0001t0003g0131 a0001c0001t0003g0141 others(62): Show |
67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+12838A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459280 | |||||||
chr11:27459315 | G | C | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0019g0004 others(5): Show |
8 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+12803C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459315 | |||||||
chr11:27459522 | G | T | 1 | a0001c0001t0010g0016 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.185+12596C>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459522 | |||||||
chr11:27459711 | A | G | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+12407T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459711 | |||||||
chr11:27459874 | T | C | 1 | a0001c0001t0003g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.185+12244A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27459874 | |||||||
chr11:27460052 | T | C | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+12066A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460052 | |||||||
chr11:27460211 | G | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.185+11907C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460211 | |||||||
chr11:27460356 | TAA | T | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+11760_185+1176 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460356 | |||||||
chr11:27460454 | C | T | 8 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0011 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+11664G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460454 | |||||||
chr11:27460805 | T | C | 163 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+11313A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27460805 | |||||||
chr11:27461048 | C | T | 2 | a0001c0001t0009g0176 a0001c0002t0006g0196 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.185+11070G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461048 | |||||||
chr11:27461084 | T | C | 1 | a0001c0004t0035g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.185+11034A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461084 | |||||||
chr11:27461354 | A | T | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+10764T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461354 | |||||||
chr11:27461366 | A | T | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+10752T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461366 | |||||||
chr11:27461632 | A | AT | 54 | a0001c0001t0003g0131 a0001c0001t0007g0015 a0001c0001t0007g0017 others(51): Show |
56 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.185+10485dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461632 | |||||||
chr11:27461715 | T | C | 163 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+10403A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461715 | |||||||
chr11:27461836 | A | AT | 95 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.185+10281dupA | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | |||||||
chr11:27461836 | A | ATT | 53 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0077 others(50): Show |
55 | HG00099.hp2 HG00544.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.185+10280_185+1028 others(6): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | |||||||
chr11:27461836 | A | ATTT | 15 | a0001c0001t0007g0017 a0001c0001t0007g0020 a0001c0001t0007g0021 others(12): Show |
15 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.185+10279_185+1028 others(7): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | |||||||
chr11:27461836 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+10271_185+1028 others(15): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461836 | |||||||
chr11:27461870 | G | C | 1 | a0001c0001t0002g0217 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.185+10248C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461870 | |||||||
chr11:27461923 | G | A | 21 | a0001c0001t0007g0015 a0001c0001t0007g0038 a0001c0001t0007g0039 others(18): Show |
21 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+10195C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27461923 | |||||||
chr11:27462084 | C | T | 1 | a0001c0002t0008g0169 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.185+10034G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462084 | |||||||
chr11:27462085 | G | A | 1 | a0001c0002t0006g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.185+10033C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462085 | |||||||
chr11:27462231 | G | A | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+9887C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462231 | |||||||
chr11:27462287 | G | A | 23 | a0001c0001t0002g0188 a0001c0001t0002g0190 a0001c0001t0002g0201 others(20): Show |
23 | HG00408.hp2 HG01943.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.185+9831C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27462287 | |||||||
chr11:27463067 | C | CA | 87 | a0001c0001t0001g0059 a0001c0001t0001g0087 a0001c0001t0001g0093 others(84): Show |
87 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.185+9050dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | |||||||
chr11:27463067 | C | CAA | 46 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0130 others(43): Show |
46 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.185+9049_185+9050d others(4): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | |||||||
chr11:27463067 | C | CAAA | 8 | a0001c0001t0001g0127 a0001c0001t0001g0142 a0001c0001t0002g0217 others(5): Show |
8 | HG00140.hp1 HG02071.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+9048_185+9050d others(5): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | |||||||
chr11:27463067 | CA | C | 45 | a0001c0001t0007g0015 a0001c0001t0007g0017 a0001c0001t0007g0020 others(42): Show |
47 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.185+9050delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | |||||||
chr11:27463067 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.185+9040_185+9050d others(13): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463067 | |||||||
chr11:27463135 | C | G | 1 | a0001c0002t0001g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.185+8983G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463135 | |||||||
chr11:27463160 | G | A | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+8958C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463160 | |||||||
chr11:27463188 | G | A | 65 | a0001c0001t0001g0142 a0001c0001t0003g0131 a0001c0001t0003g0141 others(62): Show |
67 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.185+8930C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463188 | |||||||
chr11:27463307 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 |
3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8811T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463307 | |||||||
chr11:27463470 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8648T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463470 | |||||||
chr11:27463809 | A | C | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+8309T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463809 | |||||||
chr11:27463824 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+8294A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27463824 | |||||||
chr11:27464205 | G | C | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+7913C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464205 | |||||||
chr11:27464425 | C | T | 1 | a0001c0001t0009g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.185+7693G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464425 | |||||||
chr11:27464468 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185+7650C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464468 | |||||||
chr11:27464589 | C | A | 2 | a0001c0001t0003g0163 a0001c0001t0003g0164 |
2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.185+7529G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464589 | |||||||
chr11:27464807 | T | C | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+7311A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464807 | |||||||
chr11:27464839 | G | A | 1 | a0001c0002t0006g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+7279C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27464839 | |||||||
chr11:27465268 | A | G | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+6850T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465268 | |||||||
chr11:27465274 | T | C | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+6844A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465274 | |||||||
chr11:27465395 | C | T | 3 | a0001c0001t0003g0068 a0001c0001t0003g0071 a0001c0002t0004g0070 |
3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.185+6723G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465395 | |||||||
chr11:27465670 | G | A | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+6448C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465670 | |||||||
chr11:27465914 | C | T | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+6204G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27465914 | |||||||
chr11:27466220 | A | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+5898T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466220 | |||||||
chr11:27466445 | C | T | 85 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(82): Show |
85 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.185+5673G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466445 | |||||||
chr11:27466564 | T | G | 1 | a0002c0003t0004g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185+5554A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466564 | |||||||
chr11:27466695 | G | A | 1 | a0003c0006t0002g0167 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185+5423C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466695 | |||||||
chr11:27466940 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.185+5178G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27466940 | |||||||
chr11:27467034 | C | T | 1 | a0001c0001t0027g0137 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185+5084G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467034 | |||||||
chr11:27467064 | G | A | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+5054C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467064 | |||||||
chr11:27467291 | G | C | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+4827C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467291 | |||||||
chr11:27467296 | G | A | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+4822C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467296 | |||||||
chr11:27467334 | G | A | 1 | a0001c0002t0006g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+4784C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467334 | |||||||
chr11:27467456 | C | T | 162 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0087 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.185+4662G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467456 | |||||||
chr11:27467480 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.185+4638A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467480 | |||||||
chr11:27467551 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.185+4567G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467551 | |||||||
chr11:27467566 | C | CA | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0226 others(6): Show |
9 | HG02055.hp2 HG02132.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.185+4551dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0004g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.185+4551_185+4552i others(21): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | C | CAAAAAAA others(14): Show |
1 | a0001c0005t0014g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.185+4551_185+4552i others(23): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.185+4551_185+4552i others(25): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | C | CAAAAAAA others(17): Show |
2 | a0001c0005t0014g0148 a0001c0005t0014g0153 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.185+4551_185+4552i others(26): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | C | CAAAAAAA others(18): Show |
1 | a0001c0005t0014g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+4551_185+4552i others(27): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467566 | CA | C | 5 | a0001c0001t0007g0015 a0001c0001t0019g0004 a0001c0002t0008g0169 others(2): Show |
5 | HG02622.hp2 HG02895.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+4551delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467566 | |||||||
chr11:27467581 | A | AC | 84 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.185+4536_185+4537i others(3): Show |
LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467581 | |||||||
chr11:27467789 | G | C | 2 | a0001c0002t0017g0006 a0001c0002t0017g0007 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185+4329C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467789 | |||||||
chr11:27467851 | G | A | 1 | a0006c0008t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+4267C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27467851 | |||||||
chr11:27468095 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0146 |
3 | HG02970.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+4023A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468095 | |||||||
chr11:27468112 | GA | G | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+4005delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468112 | |||||||
chr11:27468155 | A | G | 1 | a0001c0002t0004g0066 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.185+3963T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468155 | |||||||
chr11:27468253 | G | C | 3 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0229 |
3 | NA18974.hp1 NA19004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.185+3865C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468253 | |||||||
chr11:27468311 | T | A | 7 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(4): Show |
7 | NA18971.hp1 NA18974.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+3807A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468311 | |||||||
chr11:27468401 | C | T | 1 | a0001c0002t0004g0065 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.185+3717G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468401 | |||||||
chr11:27468422 | G | A | 1 | a0001c0005t0014g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.185+3696C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468422 | |||||||
chr11:27468528 | T | C | 1 | a0001c0002t0005g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.185+3590A>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468528 | |||||||
chr11:27468585 | A | G | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0002t0004g0060 |
3 | HG01515.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.185+3533T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468585 | |||||||
chr11:27468701 | GA | G | 84 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.185+3416delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468701 | |||||||
chr11:27468715 | A | G | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0002t0004g0060 |
3 | HG01515.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.185+3403T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27468715 | |||||||
chr11:27469040 | G | A | 6 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0011 others(3): Show |
6 | HG02630.hp1 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+3078C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469040 | |||||||
chr11:27469115 | A | T | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+3003T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469115 | |||||||
chr11:27469242 | C | T | 3 | a0001c0001t0036g0240 a0001c0002t0018g0238 a0001c0002t0018g0239 |
3 | HG02486.hp2 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.185+2876G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469242 | |||||||
chr11:27469319 | T | G | 3 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0165 |
3 | NA19006.hp2 NA19070.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.185+2799A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469319 | |||||||
chr11:27469432 | C | T | 1 | a0007c0012t0004g0062 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.185+2686G>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469432 | |||||||
chr11:27469529 | T | A | 1 | a0001c0002t0008g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+2589A>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469529 | |||||||
chr11:27469559 | C | A | 1 | a0001c0001t0019g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.185+2559G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469559 | |||||||
chr11:27469769 | G | A | 1 | a0001c0001t0036g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.185+2349C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27469769 | |||||||
chr11:27470074 | A | G | 1 | a0001c0004t0013g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.185+2044T>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470074 | |||||||
chr11:27470713 | G | GA | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0228 others(5): Show |
8 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1404dupT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470713 | |||||||
chr11:27470713 | GA | G | 87 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.185+1404delT | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470713 | |||||||
chr11:27470867 | G | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA18946.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.185+1251C>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27470867 | |||||||
chr11:27471058 | T | G | 1 | a0002c0011t0003g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.185+1060A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471058 | |||||||
chr11:27471112 | A | T | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+1006T>A | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471112 | |||||||
chr11:27471418 | T | G | 1 | a0001c0001t0003g0165 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.185+700A>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471418 | |||||||
chr11:27471554 | C | G | 1 | a0001c0001t0006g0233 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+564G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471554 | |||||||
chr11:27471787 | C | G | 1 | a0001c0002t0004g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+331G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471787 | |||||||
chr11:27471856 | G | A | 1 | a0001c0002t0006g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+262C>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471856 | |||||||
chr11:27471981 | A | C | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0002t0004g0150 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+137T>G | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27471981 | |||||||
chr11:27472020 | C | A | 3 | a0001c0001t0003g0133 a0001c0002t0004g0132 a0001c0002t0004g0134 |
3 | HG00099.hp2 HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.185+98G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472020 | |||||||
chr11:27472074 | C | A | 2 | a0001c0001t0001g0136 a0001c0002t0004g0135 |
2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.185+44G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472074 | |||||||
chr11:27472083 | T | TC | 22 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0234 others(19): Show |
22 | HG00544.hp2 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.185+34dupG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472083 | |||||||
chr11:27472083 | TC | T | 92 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0095 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.185+34delG | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472083 | |||||||
chr11:27472090 | C | A | 10 | a0001c0001t0003g0156 a0001c0001t0003g0158 a0001c0001t0003g0159 others(7): Show |
10 | NA18951.hp1 NA18952.hp2 NA18990.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+28G>T | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472090 | |||||||
chr11:27472090 | C | G | 1 | a0001c0002t0004g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.185+28G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472090 | |||||||
chr11:27472091 | C | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+27G>C | LGR4 | ENSG00000205213.14 | transcript | ENST00000379214.9 | protein_coding | 1/17 | chr11 | 27472091 |