Item | Value |
---|---|
geneid | 266977 |
ensemblid | ENSG00000153292.16 |
hgncid | 18990 |
symbol | ADGRF1 |
name | adhesion G protein-coupled receptor F1 |
refseq_nuc | NM_153840.4 |
refseq_prot | NP_722582.2 |
ensembl_nuc | ENST00000371253.7 |
ensembl_prot | ENSP00000360299.2 |
mane_status | MANE Select |
chr | chr6 |
start | 46997708 |
end | 47042332 |
strand | - |
ver | v1.2 |
region | chr6:46997708-47042332 |
region5000 | chr6:46992708-47047332 |
regionname0 | ADGRF1_chr6_46997708_47042332 |
regionname5000 | ADGRF1_chr6_46992708_47047332 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 910 | 284 | 44 | 54 | 144 | 9 | 31 | 116 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0002 | 0/0 | 910 | 84 | 38 | 12 | 33 | 0 | 1 | 25 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0003 | 0/0 | 910 | 9 | 2 | 5 | 0 | 1 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0004 | 0/0 | 910 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0005 | 0/0 | 910 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0006 | 0/0 | 910 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0007 | 0/0 | 910 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0008 | 0/0 | 910 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0009 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0010 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0011 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0012 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(518): Show |
chr6 | 46992708 | 47047332 |
a0013 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0014 | 0/0 | 910 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
a0015 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | MKVGV others(905): Show |
chr6 | 46992708 | 47047332 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2730 | 256 | 29 | 44 | 142 | 9 | 31 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0003 | 0/1 | 2730 | 13 | 9 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0006 | 0/0 | 2730 | 6 | 3 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0007 | 0/0 | 2730 | 5 | 0 | 3 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0012 | 0/0 | 2730 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0016 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0001c0017 | 0/0 | 2730 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0002c0002 | 0/0 | 2730 | 76 | 31 | 11 | 33 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0002c0008 | 0/0 | 2730 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0002c0019 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0002c0024 | 0/0 | 2730 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0002c0025 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0003c0004 | 0/0 | 2730 | 9 | 2 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0004c0005 | 0/0 | 2730 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0005c0010 | 0/0 | 2730 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0006c0009 | 0/0 | 2730 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0007c0013 | 0/0 | 2730 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0008c0011 | 0/0 | 2730 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0009c0014 | 0/0 | 2730 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0010c0023 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0011c0020 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0012c0022 | 0/0 | 2730 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0013c0021 | 0/0 | 2730 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0014c0015 | 0/0 | 2730 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 | ||
a0015c0018 | 0/0 | 2730 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | ATGAA others(2725): Show |
chr6 | 46992708 | 47047332 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5432 | 137 | 6 | 26 | 86 | 4 | 14 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0002 | 0/0 | 5432 | 51 | 14 | 11 | 17 | 3 | 6 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0004 | 0/0 | 5432 | 26 | 2 | 3 | 14 | 2 | 5 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0005 | 0/0 | 5432 | 16 | 1 | 1 | 12 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0007 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0012 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0016 | 0/0 | 5432 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0017 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0018 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0024 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0027 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0028 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0029 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0030 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0031 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0033 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0035 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0036 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0039 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0040 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0042 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0001t0044 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0001 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0004 | 0/0 | 5432 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0017 | 0/1 | 5431 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0022 | 0/0 | 5431 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0023 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0037 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0003t0038 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0006t0001 | 0/0 | 5432 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0006t0004 | 0/0 | 5432 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0007t0015 | 0/0 | 5432 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0007t0025 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0012t0005 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0016t0004 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0001c0017t0026 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0003 | 0/0 | 5431 | 37 | 5 | 7 | 25 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0006 | 0/0 | 5431 | 12 | 6 | 1 | 4 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0008 | 0/0 | 5432 | 5 | 3 | 1 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0009 | 0/0 | 5432 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0010 | 0/0 | 5432 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0011 | 0/0 | 5432 | 4 | 3 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0013 | 0/0 | 5432 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0014 | 0/0 | 5431 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0020 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0002t0034 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0008t0003 | 0/0 | 5431 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0002c0008t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0002c0019t0008 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0024t0043 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0002c0025t0032 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0003c0004t0007 | 0/0 | 5432 | 9 | 2 | 5 | 0 | 1 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0004c0005t0002 | 0/0 | 5432 | 4 | 0 | 0 | 4 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0004c0005t0005 | 0/0 | 5432 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0005c0010t0019 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0005c0010t0041 | 0/0 | 5432 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0006c0009t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0006c0009t0021 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0007c0013t0003 | 0/0 | 5431 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0008c0011t0002 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0008c0011t0005 | 0/0 | 5432 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0009c0014t0002 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0010c0023t0001 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0011c0020t0003 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0012c0022t0006 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
a0013c0021t0002 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0014c0015t0001 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5427): Show |
chr6 | 46992708 | 47047332 |
a0015c0018t0006 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | AGTGA others(5426): Show |
chr6 | 46992708 | 47047332 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 1 | 7 | 7 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0016g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0018g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0024g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0028g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0029g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0030g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0031g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0033g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0035g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0036g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0039g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0040g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0042g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0001t0044g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0017g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0022g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0022g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0023g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0037g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0003t0038g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0006t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0015g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0015g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0025g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0007t0025g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0012t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0012t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0016t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0001c0017t0026g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0010g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0013g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0014g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0020g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0002t0034g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0008t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0019t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0024t0043g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0002c0025t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0003c0004t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0004c0005t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0010t0019g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0010t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0005c0010t0041g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0009t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0009t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0006c0009t0021g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0007c0013t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0008c0011t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0008c0011t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0009c0014t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0010c0023t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0011c0020t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0012c0022t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0013c0021t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0014c0015t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
a0015c0018t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0279 | EUR | GBR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00408 | hp2 | a0002 | c0002 | t0003 | g0077 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00558 | hp2 | a0002 | c0002 | t0014 | g0064 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00597 | hp2 | a0002 | c0002 | t0006 | g0239 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00621 | hp2 | a0002 | c0002 | t0003 | g0167 | EAS | CHS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00639 | hp2 | a0001 | c0006 | t0004 | g0265 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0277 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00642 | hp2 | a0001 | c0006 | t0004 | g0261 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG00741 | hp2 | a0002 | c0002 | t0013 | g0155 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01069 | hp2 | a0001 | c0001 | t0030 | g0113 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01074 | hp1 | a0001 | c0003 | t0022 | g0294 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01074 | hp2 | a0001 | c0001 | t0031 | g0187 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01106 | hp1 | a0002 | c0024 | t0043 | g0308 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01106 | hp2 | a0001 | c0017 | t0026 | g0204 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01109 | hp2 | a0003 | c0004 | t0007 | g0186 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01168 | hp1 | a0003 | c0004 | t0007 | g0026 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01169 | hp2 | a0003 | c0004 | t0007 | g0026 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01192 | hp1 | a0003 | c0004 | t0007 | g0198 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01192 | hp2 | a0001 | c0001 | t0044 | g0278 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01243 | hp1 | a0002 | c0002 | t0011 | g0131 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0143 | AMR | PUR | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01255 | hp1 | a0005 | c0010 | t0041 | g0296 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01255 | hp2 | a0003 | c0004 | t0007 | g0209 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0050 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0301 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01884 | hp1 | a0002 | c0002 | t0010 | g0080 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01884 | hp2 | a0002 | c0002 | t0006 | g0305 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01891 | hp2 | a0006 | c0009 | t0006 | g0314 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0102 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01928 | hp2 | a0001 | c0003 | t0022 | g0280 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01975 | hp2 | a0001 | c0007 | t0015 | g0019 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01981 | hp2 | a0001 | c0007 | t0015 | g0019 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02004 | hp1 | a0001 | c0007 | t0015 | g0101 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02004 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02056 | hp1 | a0001 | c0001 | t0028 | g0089 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0076 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02074 | hp1 | a0001 | c0001 | t0016 | g0240 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0061 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02132 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0109 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02145 | hp2 | a0002 | c0002 | t0009 | g0038 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02148 | hp1 | a0002 | c0002 | t0008 | g0116 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02155 | hp2 | a0002 | c0002 | t0003 | g0184 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02257 | hp1 | a0001 | c0012 | t0005 | g0137 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02257 | hp2 | a0002 | c0008 | t0006 | g0313 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02258 | hp1 | a0002 | c0002 | t0009 | g0040 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0122 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02273 | hp2 | a0002 | c0002 | t0006 | g0260 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02280 | hp1 | a0002 | c0008 | t0003 | g0033 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0068 | AMR | PEL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02451 | hp1 | a0006 | c0009 | t0021 | g0312 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02451 | hp2 | a0002 | c0002 | t0006 | g0283 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02572 | hp1 | a0005 | c0010 | t0019 | g0118 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02572 | hp2 | a0002 | c0002 | t0010 | g0011 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02615 | hp1 | a0002 | c0002 | t0009 | g0040 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02622 | hp1 | a0002 | c0002 | t0006 | g0307 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02622 | hp2 | a0002 | c0002 | t0006 | g0304 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02630 | hp1 | a0002 | c0008 | t0003 | g0207 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02630 | hp2 | a0001 | c0003 | t0023 | g0041 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02647 | hp1 | a0001 | c0003 | t0023 | g0041 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02647 | hp2 | a0001 | c0001 | t0027 | g0140 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02683 | hp1 | a0009 | c0014 | t0002 | g0228 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0281 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02717 | hp1 | a0002 | c0002 | t0011 | g0130 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02723 | hp1 | a0001 | c0016 | t0004 | g0285 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0291 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0276 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02818 | hp1 | a0006 | c0009 | t0021 | g0311 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02896 | hp2 | a0005 | c0010 | t0019 | g0124 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02922 | hp1 | a0010 | c0023 | t0001 | g0110 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02965 | hp1 | a0002 | c0002 | t0020 | g0309 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02970 | hp1 | a0002 | c0002 | t0009 | g0287 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02970 | hp2 | a0002 | c0002 | t0006 | g0303 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02976 | hp1 | a0002 | c0002 | t0009 | g0038 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03017 | hp2 | a0001 | c0001 | t0033 | g0234 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03130 | hp2 | a0011 | c0020 | t0003 | g0144 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03139 | hp1 | a0002 | c0002 | t0008 | g0043 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0297 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03195 | hp2 | a0001 | c0001 | t0018 | g0205 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0047 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03225 | hp2 | a0001 | c0003 | t0037 | g0298 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0302 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03453 | hp1 | a0002 | c0002 | t0003 | g0046 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03453 | hp2 | a0002 | c0019 | t0008 | g0148 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03486 | hp2 | a0002 | c0002 | t0034 | g0295 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03492 | hp2 | a0001 | c0001 | t0042 | g0259 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03516 | hp1 | a0002 | c0002 | t0010 | g0011 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03516 | hp2 | a0003 | c0004 | t0007 | g0154 | AFR | ESN | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03540 | hp1 | a0002 | c0002 | t0011 | g0132 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03540 | hp2 | a0002 | c0002 | t0013 | g0139 | AFR | GWD | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03579 | hp2 | a0002 | c0002 | t0013 | g0079 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03654 | hp2 | a0002 | c0002 | t0006 | g0250 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0300 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03704 | hp2 | a0003 | c0004 | t0007 | g0211 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03710 | hp2 | a0013 | c0021 | t0002 | g0267 | SAS | PJL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0288 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04115 | hp2 | a0001 | c0001 | t0035 | g0274 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04204 | hp1 | a0014 | c0015 | t0001 | g0212 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | STU | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18522 | hp1 | a0002 | c0008 | t0003 | g0206 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18612 | hp2 | a0001 | c0007 | t0025 | g0217 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18747 | hp2 | a0002 | c0002 | t0008 | g0066 | EAS | CHB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18906 | hp1 | a0003 | c0004 | t0007 | g0153 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18906 | hp2 | a0002 | c0002 | t0006 | g0306 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18941 | hp1 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18941 | hp2 | a0001 | c0001 | t0016 | g0213 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18944 | hp1 | a0001 | c0007 | t0025 | g0218 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18946 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18947 | hp2 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18949 | hp1 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18953 | hp2 | a0001 | c0001 | t0036 | g0269 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18954 | hp2 | a0002 | c0002 | t0006 | g0035 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18959 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18965 | hp1 | a0001 | c0001 | t0012 | g0119 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18967 | hp2 | a0007 | c0013 | t0003 | g0023 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18974 | hp2 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18980 | hp1 | a0001 | c0001 | t0012 | g0174 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18980 | hp2 | a0001 | c0001 | t0029 | g0083 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18986 | hp2 | a0015 | c0018 | t0006 | g0266 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18990 | hp2 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18991 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18991 | hp2 | a0001 | c0001 | t0016 | g0233 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18994 | hp1 | a0008 | c0011 | t0002 | g0254 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0069 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18995 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18997 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18998 | hp1 | a0007 | c0013 | t0003 | g0023 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18998 | hp2 | a0004 | c0005 | t0005 | g0191 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18999 | hp1 | a0004 | c0005 | t0002 | g0244 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19003 | hp2 | a0001 | c0001 | t0017 | g0168 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19004 | hp2 | a0004 | c0005 | t0005 | g0074 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19005 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19009 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0195 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19030 | hp1 | a0002 | c0002 | t0003 | g0121 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19030 | hp2 | a0001 | c0001 | t0039 | g0315 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19043 | hp1 | a0002 | c0002 | t0011 | g0048 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19043 | hp2 | a0002 | c0008 | t0003 | g0033 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19060 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19067 | hp1 | a0001 | c0001 | t0024 | g0252 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19067 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19074 | hp2 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19075 | hp2 | a0004 | c0005 | t0002 | g0014 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19076 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19076 | hp2 | a0002 | c0002 | t0006 | g0035 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19077 | hp1 | a0002 | c0002 | t0014 | g0016 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19078 | hp1 | a0008 | c0011 | t0005 | g0147 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19079 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19080 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19084 | hp2 | a0002 | c0002 | t0014 | g0016 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19086 | hp1 | a0002 | c0002 | t0006 | g0237 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19087 | hp2 | a0001 | c0001 | t0024 | g0255 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0133 | AFR | YRI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ASW | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0262 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20805 | hp1 | a0003 | c0004 | t0007 | g0210 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20905 | hp2 | a0001 | c0001 | t0040 | g0257 | SAS | GIH | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02109 | hp1 | a0002 | c0002 | t0020 | g0310 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0293 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02559 | hp1 | a0001 | c0003 | t0038 | g0292 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03471 | hp1 | a0012 | c0022 | t0006 | g0290 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG03471 | hp2 | a0002 | c0025 | t0032 | g0044 | AFR | MSL | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
HG06807 | hp2 | a0002 | c0002 | t0010 | g0011 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20300 | hp1 | a0002 | c0002 | t0008 | g0149 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA21309 | hp1 | a0002 | c0002 | t0008 | g0112 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
NA21309 | hp2 | a0001 | c0012 | t0005 | g0138 | AFR | LWK | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
homoSapiens | chm13v2 | a0001 | c0003 | t0017 | g0188 | REF | REF | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0176 | REF | REF | ADGRF1_chr6_46992708_47047332 | ADGRF1 | chr6 | 46992708 | 47047332 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47007284 | A | T | 1 | a0015 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.2501T>A | p.Ile834Asn | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/15 | 2686/5432 | 2501/2733 | 834/910 | chr6 | 47007284 | |||
chr6:47009003 | A | G | 1 | a0008 | 2 | NA18994.hp1 NA19078.hp1 |
missense_variant | MODERATE | c.2432T>C | p.Ile811Thr | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2617/5432 | 2432/2733 | 811/910 | chr6 | 47009003 | |||
chr6:47009028 | T | G | 1 | a0005 | 3 | HG01255.hp1 HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.2407A>C | p.Thr803Pro | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2592/5432 | 2407/2733 | 803/910 | chr6 | 47009028 | |||
chr6:47009076 | T | C | 5 | a0002 a0005 a0006 others(2): Show |
93 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(90): Show |
missense_variant | MODERATE | c.2359A>G | p.Ile787Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2544/5432 | 2359/2733 | 787/910 | chr6 | 47009076 | |||
chr6:47009273 | G | A | 1 | a0007 | 2 | NA18967.hp2 NA18998.hp1 |
missense_variant | MODERATE | c.2162C>T | p.Thr721Met | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2347/5432 | 2162/2733 | 721/910 | chr6 | 47009273 | |||
chr6:47009722 | T | C | 6 | a0002 a0005 a0006 others(3): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
missense_variant | MODERATE | c.1713A>G | p.Ile571Met | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1898/5432 | 1713/2733 | 571/910 | chr6 | 47009722 | |||
chr6:47009865 | T | A | 1 | a0012 | 1 | HG03471.hp1 | stop_gained | HIGH | c.1570A>T | p.Lys524* | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1755/5432 | 1570/2733 | 524/910 | chr6 | 47009865 | |||
chr6:47010047 | C | T | 1 | a0003 | 9 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
missense_variant | MODERATE | c.1388G>A | p.Arg463His | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1573/5432 | 1388/2733 | 463/910 | chr6 | 47010047 | |||
chr6:47010113 | A | T | 1 | a0004 | 6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
missense_variant | MODERATE | c.1322T>A | p.Leu441His | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1507/5432 | 1322/2733 | 441/910 | chr6 | 47010113 | |||
chr6:47010158 | C | T | 1 | a0006 | 3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1277G>A | p.Arg426Gln | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1462/5432 | 1277/2733 | 426/910 | chr6 | 47010158 | |||
chr6:47016637 | G | C | 1 | a0011 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.743C>G | p.Ser248Cys | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/15 | 928/5432 | 743/2733 | 248/910 | chr6 | 47016637 | |||
chr6:47020740 | G | A | 1 | a0013 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.602C>T | p.Thr201Ile | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/15 | 787/5432 | 602/2733 | 201/910 | chr6 | 47020740 | |||
chr6:47024207 | G | C | 1 | a0012 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.288C>G | p.Ser96Arg | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/15 | 473/5432 | 288/2733 | 96/910 | chr6 | 47024207 | |||
chr6:47026003 | C | T | 1 | a0014 | 1 | HG04204.hp1 | missense_variant&splice_region_variant | MODERATE | c.128G>A | p.Gly43Asp | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/15 | 313/5432 | 128/2733 | 43/910 | chr6 | 47026003 | |||
chr6:47027752 | C | T | 1 | a0009 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.79G>A | p.Gly27Ser | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/15 | 264/5432 | 79/2733 | 27/910 | chr6 | 47027752 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47008954 | A | G | 1 | a0001c0017 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.2481T>C | p.Asn827Asn | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2666/5432 | 2481/2733 | 827/910 | chr6 | 47008954 | |||
chr6:47008999 | C | T | 1 | a0001c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.2436G>A | p.Val812Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2621/5432 | 2436/2733 | 812/910 | chr6 | 47008999 | |||
chr6:47009188 | G | A | 1 | a0003c0004 | 9 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
synonymous_variant | LOW | c.2247C>T | p.Val749Val | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2432/5432 | 2247/2733 | 749/910 | chr6 | 47009188 | |||
chr6:47009541 | G | A | 3 | a0001c0003 a0002c0008 a0012c0022 |
18 | HG01069.hp1 HG01074.hp1 HG01928.hp2 others(15): Show |
synonymous_variant | LOW | c.1894C>T | p.Leu632Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2079/5432 | 1894/2733 | 632/910 | chr6 | 47009541 | |||
chr6:47009581 | T | C | 1 | a0001c0012 | 2 | HG02257.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.1854A>G | p.Gln618Gln | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 2039/5432 | 1854/2733 | 618/910 | chr6 | 47009581 | |||
chr6:47009739 | A | G | 1 | a0001c0006 | 6 | HG00639.hp2 HG00642.hp2 HG01243.hp2 others(3): Show |
synonymous_variant | LOW | c.1696T>C | p.Leu566Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/15 | 1881/5432 | 1696/2733 | 566/910 | chr6 | 47009739 | |||
chr6:47012160 | T | A | 1 | a0002c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.963A>T | p.Ala321Ala | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/15 | 1148/5432 | 963/2733 | 321/910 | chr6 | 47012160 | |||
chr6:47016648 | T | C | 1 | a0002c0025 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.732A>G | p.Leu244Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/15 | 917/5432 | 732/2733 | 244/910 | chr6 | 47016648 | |||
chr6:47025917 | A | G | 1 | a0001c0007 | 5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
synonymous_variant | LOW | c.214T>C | p.Leu72Leu | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/15 | 399/5432 | 214/2733 | 72/910 | chr6 | 47025917 | |||
chr6:47029014 | G | A | 3 | a0002c0024 a0002c0025 a0010c0023 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.48C>T | p.Asp16Asp | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | 233/5432 | 48/2733 | 16/910 | chr6 | 47029014 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46997812 | CA | C | 12 | a0001c0001t0017 a0001c0003t0022 a0002c0002t0003 others(9): Show |
66 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2409delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2409 | chr6 | 46997812 | ||||||
chr6:46997849 | C | T | 1 | a0002c0025t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2373G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2373 | chr6 | 46997849 | ||||||
chr6:46997882 | T | C | 1 | a0001c0001t0035 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2340A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2340 | chr6 | 46997882 | ||||||
chr6:46998102 | T | C | 1 | a0001c0001t0028 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2120A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2120 | chr6 | 46998102 | ||||||
chr6:46998110 | C | G | 1 | a0006c0009t0021 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2112G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2112 | chr6 | 46998110 | ||||||
chr6:46998121 | C | T | 12 | a0001c0001t0017 a0001c0003t0022 a0002c0002t0003 others(9): Show |
66 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2101G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2101 | chr6 | 46998121 | ||||||
chr6:46998156 | A | C | 2 | a0001c0007t0015 a0001c0007t0025 |
5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2066T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2066 | chr6 | 46998156 | ||||||
chr6:46998159 | A | G | 1 | a0001c0003t0023 | 2 | HG02630.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2063T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2063 | chr6 | 46998159 | ||||||
chr6:46998167 | T | C | 1 | a0002c0025t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2055A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2055 | chr6 | 46998167 | ||||||
chr6:46998198 | G | A | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(16): Show |
108 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2024C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 2024 | chr6 | 46998198 | ||||||
chr6:46998285 | C | T | 12 | a0001c0001t0017 a0001c0003t0022 a0002c0002t0003 others(9): Show |
66 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1937G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1937 | chr6 | 46998285 | ||||||
chr6:46998301 | G | A | 1 | a0001c0001t0029 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1921 | chr6 | 46998301 | ||||||
chr6:46998302 | T | C | 1 | a0001c0003t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1920A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1920 | chr6 | 46998302 | ||||||
chr6:46998390 | C | T | 1 | a0002c0002t0014 | 3 | HG00558.hp2 NA19077.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1832 | chr6 | 46998390 | ||||||
chr6:46998537 | G | T | 12 | a0001c0001t0017 a0001c0003t0022 a0002c0002t0003 others(9): Show |
66 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1685C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1685 | chr6 | 46998537 | ||||||
chr6:46998807 | G | C | 2 | a0001c0001t0027 a0002c0002t0010 |
5 | HG01884.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1415C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1415 | chr6 | 46998807 | ||||||
chr6:46998809 | G | A | 1 | a0001c0001t0039 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1413 | chr6 | 46998809 | ||||||
chr6:46998924 | G | A | 1 | a0001c0001t0030 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1298 | chr6 | 46998924 | ||||||
chr6:46998945 | A | G | 4 | a0002c0002t0009 a0002c0002t0013 a0005c0010t0019 others(1): Show |
11 | HG00741.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1277T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1277 | chr6 | 46998945 | ||||||
chr6:46998950 | T | C | 1 | a0001c0001t0040 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1272A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1272 | chr6 | 46998950 | ||||||
chr6:46998969 | C | T | 1 | a0002c0002t0020 | 2 | HG02109.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1253G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1253 | chr6 | 46998969 | ||||||
chr6:46999047 | G | A | 1 | a0001c0001t0035 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1175 | chr6 | 46999047 | ||||||
chr6:46999079 | C | A | 1 | a0002c0002t0013 | 3 | HG00741.hp2 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1143G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1143 | chr6 | 46999079 | ||||||
chr6:46999156 | G | A | 1 | a0001c0001t0031 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1066 | chr6 | 46999156 | ||||||
chr6:46999175 | T | C | 1 | a0001c0001t0018 | 2 | HG03195.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1047A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 1047 | chr6 | 46999175 | ||||||
chr6:46999377 | G | A | 1 | a0006c0009t0021 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*845C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 845 | chr6 | 46999377 | ||||||
chr6:46999448 | C | T | 1 | a0001c0003t0037 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 774 | chr6 | 46999448 | ||||||
chr6:46999556 | C | G | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0018 others(12): Show |
91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*666G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 666 | chr6 | 46999556 | ||||||
chr6:46999601 | C | T | 15 | a0002c0002t0003 a0002c0002t0006 a0002c0002t0008 others(12): Show |
76 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*621G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 621 | chr6 | 46999601 | ||||||
chr6:46999640 | G | A | 20 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(17): Show |
105 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*582C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 582 | chr6 | 46999640 | ||||||
chr6:46999716 | C | T | 1 | a0001c0001t0036 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 506 | chr6 | 46999716 | ||||||
chr6:46999804 | C | G | 23 | a0001c0001t0027 a0001c0001t0035 a0002c0002t0003 others(20): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 418 | chr6 | 46999804 | ||||||
chr6:47000041 | C | T | 2 | a0002c0002t0009 a0002c0002t0013 |
8 | HG00741.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*181G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 181 | chr6 | 47000041 | ||||||
chr6:47000148 | A | C | 1 | a0001c0017t0026 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 74 | chr6 | 47000148 | ||||||
chr6:47000168 | C | T | 1 | a0001c0001t0033 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*54G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 15/15 | 54 | chr6 | 47000168 | ||||||
chr6:47029082 | G | A | 2 | a0002c0024t0043 a0002c0025t0032 |
2 | HG01106.hp1 HG03471.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | chr6 | 47029082 | |||||||
chr6:47029098 | T | C | 1 | a0001c0001t0044 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/15 | 37 | chr6 | 47029098 | ||||||
chr6:47042215 | G | C | 34 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0016 others(31): Show |
138 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(135): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/15 | chr6 | 47042215 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:47000370 | C | A | 2 | a0001c0001t0005g0071 a0001c0001t0005g0072 |
2 | NA18948.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2660-75G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000370 | |||||||
chr6:47000431 | C | T | 149 | a0001c0001t0001g0058 a0001c0001t0001g0189 a0001c0001t0002g0008 others(146): Show |
184 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.2660-136G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000431 | |||||||
chr6:47000701 | C | T | 1 | a0002c0002t0003g0078 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2660-406G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000701 | |||||||
chr6:47000901 | TC | T | 63 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(60): Show |
81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.2659+599delG | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47000901 | |||||||
chr6:47001301 | G | T | 88 | a0001c0001t0001g0058 a0001c0001t0001g0189 a0001c0001t0002g0008 others(85): Show |
106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2659+200C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 14/14 | chr6 | 47001301 | |||||||
chr6:47001723 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2593-156A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47001723 | |||||||
chr6:47001888 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2593-321T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47001888 | |||||||
chr6:47002090 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2593-523T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002090 | |||||||
chr6:47002096 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2593-529G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002096 | |||||||
chr6:47002309 | G | T | 4 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-742C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002309 | |||||||
chr6:47002383 | G | GA | 7 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2593-817dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002383 | |||||||
chr6:47002399 | A | C | 1 | a0001c0001t0001g0002 | 7 | NA18949.hp2 NA18961.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.2593-832T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002399 | |||||||
chr6:47002488 | A | C | 160 | a0001c0001t0001g0058 a0001c0001t0001g0189 a0001c0001t0002g0008 others(157): Show |
196 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.2593-921T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002488 | |||||||
chr6:47002582 | T | C | 4 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-1015A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002582 | |||||||
chr6:47002635 | A | G | 1 | a0009c0014t0002g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2593-1068T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002635 | |||||||
chr6:47002747 | A | T | 68 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(65): Show |
86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.2593-1180T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002747 | |||||||
chr6:47002790 | G | A | 12 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(9): Show |
22 | HG01358.hp1 HG01928.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.2593-1223C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002790 | |||||||
chr6:47002837 | T | C | 1 | a0001c0001t0031g0187 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2593-1270A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002837 | |||||||
chr6:47002858 | G | C | 1 | a0002c0002t0014g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2593-1291C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002858 | |||||||
chr6:47002949 | C | T | 4 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-1382G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002949 | |||||||
chr6:47002998 | A | G | 2 | a0001c0001t0004g0214 a0001c0001t0004g0236 |
2 | HG02155.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2593-1431T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47002998 | |||||||
chr6:47003011 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2593-1444C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003011 | |||||||
chr6:47003695 | A | G | 1 | a0003c0004t0007g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2592+2122T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003695 | |||||||
chr6:47003724 | C | T | 1 | a0001c0003t0004g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2592+2093G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003724 | |||||||
chr6:47003828 | G | A | 1 | a0001c0003t0037g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2592+1989C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003828 | |||||||
chr6:47003875 | A | G | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2592+1942T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47003875 | |||||||
chr6:47004168 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0177 a0001c0001t0004g0238 |
3 | HG00544.hp1 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2592+1649G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004168 | |||||||
chr6:47004169 | G | A | 1 | a0013c0021t0002g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2592+1648C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004169 | |||||||
chr6:47004409 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2592+1408A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004409 | |||||||
chr6:47004434 | A | T | 56 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(53): Show |
72 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.2592+1383T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004434 | |||||||
chr6:47004483 | T | C | 72 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(69): Show |
90 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2592+1334A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004483 | |||||||
chr6:47004507 | T | C | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2592+1310A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004507 | |||||||
chr6:47004707 | C | T | 1 | a0001c0017t0026g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2592+1110G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004707 | |||||||
chr6:47004731 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18951.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2592+1086G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004731 | |||||||
chr6:47004917 | G | A | 1 | a0001c0007t0025g0218 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2592+900C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004917 | |||||||
chr6:47004930 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2592+887C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004930 | |||||||
chr6:47004964 | C | T | 160 | a0001c0001t0001g0058 a0001c0001t0001g0189 a0001c0001t0002g0008 others(157): Show |
196 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.2592+853G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004964 | |||||||
chr6:47004966 | T | G | 1 | a0001c0001t0004g0262 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2592+851A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47004966 | |||||||
chr6:47005060 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0094 |
5 | NA18955.hp2 NA18986.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2592+757A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005060 | |||||||
chr6:47005165 | T | C | 1 | a0002c0002t0006g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2592+652A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005165 | |||||||
chr6:47005217 | C | T | 4 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+600G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005217 | |||||||
chr6:47005317 | C | A | 7 | a0001c0001t0002g0251 a0001c0001t0002g0253 a0001c0001t0002g0270 others(4): Show |
7 | HG00609.hp1 HG02056.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2592+500G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005317 | |||||||
chr6:47005344 | A | G | 1 | a0001c0003t0001g0208 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2592+473T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005344 | |||||||
chr6:47005507 | T | C | 1 | a0003c0004t0007g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2592+310A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005507 | |||||||
chr6:47005569 | A | T | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2592+248T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005569 | |||||||
chr6:47005727 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2592+90G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 13/14 | chr6 | 47005727 | |||||||
chr6:47005935 | C | G | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2533-59G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005935 | |||||||
chr6:47005946 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2533-70C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005946 | |||||||
chr6:47005972 | A | G | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2533-96T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47005972 | |||||||
chr6:47006177 | A | G | 3 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2533-301T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006177 | |||||||
chr6:47006415 | A | T | 1 | a0002c0002t0006g0304 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2533-539T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006415 | |||||||
chr6:47006461 | AATTTT | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
201 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.2533-590_2533-586d others(7): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006461 | |||||||
chr6:47006552 | T | C | 2 | a0001c0003t0022g0280 a0001c0003t0022g0294 |
2 | HG01074.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.2533-676A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006552 | |||||||
chr6:47006690 | C | T | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2532+563G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006690 | |||||||
chr6:47006820 | C | T | 1 | a0004c0005t0005g0191 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2532+433G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006820 | |||||||
chr6:47006833 | T | C | 4 | a0004c0005t0002g0014 a0004c0005t0002g0244 a0004c0005t0005g0074 others(1): Show |
6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.2532+420A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47006833 | |||||||
chr6:47007034 | TTTACA | T | 3 | a0002c0002t0013g0079 a0002c0002t0013g0139 a0002c0002t0013g0155 |
3 | HG00741.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2532+214_2532+218d others(7): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007034 | |||||||
chr6:47007040 | T | G | 1 | a0001c0001t0039g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2532+213A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007040 | |||||||
chr6:47007076 | G | T | 66 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(63): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2532+177C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 12/14 | chr6 | 47007076 | |||||||
chr6:47007383 | A | G | 4 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-89T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007383 | |||||||
chr6:47007422 | G | T | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-128C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007422 | |||||||
chr6:47007423 | T | A | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-129A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007423 | |||||||
chr6:47007424 | A | AGAGACT | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-131_2491-130i others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007424 | |||||||
chr6:47007429 | C | CCTTAAGA others(2): Show |
3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2491-136_2491-135i others(11): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007429 | |||||||
chr6:47007530 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2491-236G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007530 | |||||||
chr6:47007659 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
103 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.2491-365G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007659 | |||||||
chr6:47007761 | T | C | 1 | a0001c0007t0025g0217 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2491-467A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007761 | |||||||
chr6:47007957 | A | G | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2491-663T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007957 | |||||||
chr6:47007978 | A | G | 4 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-684T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47007978 | |||||||
chr6:47008162 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2490+783G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008162 | |||||||
chr6:47008429 | G | A | 2 | a0002c0002t0020g0309 a0002c0002t0020g0310 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2490+516C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008429 | |||||||
chr6:47008658 | A | G | 7 | a0002c0002t0008g0043 a0002c0002t0008g0149 a0002c0002t0011g0048 others(4): Show |
7 | HG01243.hp1 HG02717.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490+287T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008658 | |||||||
chr6:47008672 | T | C | 3 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2490+273A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008672 | |||||||
chr6:47008833 | G | A | 2 | a0001c0001t0018g0133 a0001c0001t0018g0205 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2490+112C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008833 | |||||||
chr6:47008900 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0004g0227 |
2 | NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2490+45A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 11/14 | chr6 | 47008900 | |||||||
chr6:47010639 | C | T | 27 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(24): Show |
30 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1117-321G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010639 | |||||||
chr6:47010973 | G | GCAGAGTG others(1): Show |
5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-656_1117-655i others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010973 | |||||||
chr6:47010976 | C | G | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-658G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010976 | |||||||
chr6:47010977 | C | G | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-659G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010977 | |||||||
chr6:47010983 | A | G | 1 | a0001c0016t0004g0285 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1117-665T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47010983 | |||||||
chr6:47011132 | A | T | 65 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(62): Show |
83 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1117-814T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011132 | |||||||
chr6:47011149 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1117-831A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011149 | |||||||
chr6:47011432 | T | A | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1116+575A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011432 | |||||||
chr6:47011667 | T | C | 67 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(64): Show |
85 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1116+340A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 10/14 | chr6 | 47011667 | |||||||
chr6:47012203 | C | T | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.928-8G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012203 | |||||||
chr6:47012204 | G | A | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.928-9C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012204 | |||||||
chr6:47012379 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
294 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.928-184C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012379 | |||||||
chr6:47012416 | C | G | 1 | a0011c0020t0003g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.928-221G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012416 | |||||||
chr6:47012611 | G | A | 1 | a0006c0009t0021g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-416C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012611 | |||||||
chr6:47012622 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
201 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.928-427C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012622 | |||||||
chr6:47012688 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.928-493C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012688 | |||||||
chr6:47012721 | G | A | 2 | a0001c0001t0018g0133 a0001c0001t0018g0205 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.928-526C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012721 | |||||||
chr6:47012753 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0012g0028 |
5 | NA18964.hp1 NA18974.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.928-558C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012753 | |||||||
chr6:47012798 | C | T | 1 | a0002c0002t0003g0194 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.928-603G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012798 | |||||||
chr6:47012911 | C | T | 1 | a0001c0001t0044g0278 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.928-716G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47012911 | |||||||
chr6:47013013 | C | T | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.928-818G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013013 | |||||||
chr6:47013067 | C | T | 1 | a0001c0006t0001g0143 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.928-872G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013067 | |||||||
chr6:47013124 | C | A | 4 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-929G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013124 | |||||||
chr6:47013190 | C | T | 2 | a0002c0002t0011g0131 a0002c0002t0011g0132 |
2 | HG01243.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.928-995G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013190 | |||||||
chr6:47013202 | C | T | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1007G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013202 | |||||||
chr6:47013218 | G | A | 1 | a0002c0002t0034g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.928-1023C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013218 | |||||||
chr6:47013253 | G | T | 3 | a0006c0009t0006g0314 a0006c0009t0021g0311 a0006c0009t0021g0312 |
3 | HG01891.hp2 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.928-1058C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013253 | |||||||
chr6:47013353 | C | A | 1 | a0001c0001t0002g0248 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.928-1158G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013353 | |||||||
chr6:47013719 | A | G | 1 | a0002c0002t0008g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.927+962T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013719 | |||||||
chr6:47013759 | G | C | 1 | a0001c0001t0004g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.927+922C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013759 | |||||||
chr6:47013878 | T | TTC | 13 | a0001c0001t0001g0111 a0001c0001t0002g0219 a0001c0001t0002g0229 others(10): Show |
14 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+801_927+802dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013878 | |||||||
chr6:47013878 | TTC | T | 71 | a0001c0001t0005g0182 a0002c0002t0003g0003 a0002c0002t0003g0006 others(68): Show |
88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.927+801_927+802del others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013878 | |||||||
chr6:47013939 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0173 |
8 | NA18949.hp2 NA18961.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+742G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013939 | |||||||
chr6:47013947 | A | G | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+734T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47013947 | |||||||
chr6:47014056 | T | C | 23 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(20): Show |
26 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.927+625A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014056 | |||||||
chr6:47014114 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.927+567G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014114 | |||||||
chr6:47014218 | A | C | 2 | a0001c0001t0002g0279 a0001c0001t0005g0183 |
2 | HG00099.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.927+463T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014218 | |||||||
chr6:47014259 | C | T | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+422G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014259 | |||||||
chr6:47014539 | G | A | 5 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+142C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014539 | |||||||
chr6:47014607 | T | C | 1 | a0002c0002t0008g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.927+74A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014607 | |||||||
chr6:47014611 | C | T | 6 | a0002c0002t0008g0043 a0002c0002t0008g0112 a0002c0002t0008g0149 others(3): Show |
8 | HG01884.hp1 HG02572.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+70G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 9/14 | chr6 | 47014611 | |||||||
chr6:47014866 | A | G | 6 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(3): Show |
6 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-22T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014866 | |||||||
chr6:47014892 | G | T | 5 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0006c0009t0006g0314 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-48C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014892 | |||||||
chr6:47014924 | A | C | 5 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0006c0009t0006g0314 others(2): Show |
5 | HG01891.hp2 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-80T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014924 | |||||||
chr6:47014987 | T | C | 1 | a0001c0001t0005g0202 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.764-143A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47014987 | |||||||
chr6:47015045 | C | T | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.764-201G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015045 | |||||||
chr6:47015073 | T | G | 79 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0085 others(76): Show |
95 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.764-229A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015073 | |||||||
chr6:47015218 | A | G | 28 | a0002c0002t0003g0003 a0002c0002t0003g0006 a0002c0002t0003g0017 others(25): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.764-374T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015218 | |||||||
chr6:47015236 | G | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0196 others(3): Show |
6 | HG01070.hp1 HG01261.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-392C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015236 | |||||||
chr6:47015415 | A | AT | 68 | a0001c0001t0001g0051 a0001c0001t0001g0091 a0001c0001t0001g0117 others(65): Show |
84 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.764-572dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015415 | |||||||
chr6:47015415 | AT | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0092 others(3): Show |
6 | NA18947.hp1 NA18963.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-572delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015415 | |||||||
chr6:47015420 | T | TA | 3 | a0002c0002t0009g0038 a0002c0002t0009g0040 a0002c0002t0009g0287 |
5 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-577_764-576ins others(1): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015420 | |||||||
chr6:47015519 | A | T | 165 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0117 others(162): Show |
203 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.764-675T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015519 | |||||||
chr6:47015573 | G | A | 3 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 |
3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.764-729C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015573 | |||||||
chr6:47015574 | C | CTATT | 5 | a0001c0001t0002g0251 a0001c0001t0031g0187 a0002c0002t0006g0250 others(2): Show |
5 | HG01074.hp2 HG03471.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-734_764-731dup others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | |||||||
chr6:47015574 | C | CTATTTAT others(5): Show |
48 | a0001c0001t0001g0051 a0001c0001t0001g0117 a0001c0001t0004g0238 others(45): Show |
58 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.764-742_764-731dup others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | |||||||
chr6:47015574 | C | CTATTTAT others(9): Show |
16 | a0002c0002t0003g0003 a0002c0002t0003g0020 a0002c0002t0003g0065 others(13): Show |
23 | HG00741.hp2 HG01255.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.764-746_764-731dup others(16): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | |||||||
chr6:47015574 | C | CTATTTAT others(13): Show |
2 | a0002c0002t0003g0017 a0002c0002t0003g0063 |
3 | NA18947.hp2 NA18959.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.764-750_764-731dup others(20): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | |||||||
chr6:47015574 | CTATT | C | 6 | a0002c0002t0011g0048 a0002c0002t0011g0130 a0002c0002t0011g0131 others(3): Show |
6 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-734_764-731del others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015574 | |||||||
chr6:47015610 | C | A | 2 | a0002c0002t0034g0295 a0002c0025t0032g0044 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.764-766G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015610 | |||||||
chr6:47015661 | C | T | 4 | a0004c0005t0002g0014 a0004c0005t0002g0244 a0004c0005t0005g0074 others(1): Show |
6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-817G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015661 | |||||||
chr6:47015671 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.764-827A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015671 | |||||||
chr6:47015691 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.764-847C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015691 | |||||||
chr6:47015702 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.764-858G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015702 | |||||||
chr6:47015732 | T | C | 1 | a0002c0002t0034g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763+885A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015732 | |||||||
chr6:47015734 | T | C | 16 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(13): Show |
17 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.763+883A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015734 | |||||||
chr6:47015746 | C | T | 15 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0002t0003g0045 others(12): Show |
17 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.763+871G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015746 | |||||||
chr6:47015754 | AT | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
307 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.763+862delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015754 | |||||||
chr6:47015786 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.763+831G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015786 | |||||||
chr6:47015806 | C | T | 10 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(7): Show |
11 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.763+811G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015806 | |||||||
chr6:47015939 | C | T | 15 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(12): Show |
16 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.763+678G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015939 | |||||||
chr6:47015974 | G | T | 2 | a0001c0001t0002g0215 a0001c0001t0002g0216 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.763+643C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015974 | |||||||
chr6:47015991 | G | A | 1 | a0001c0001t0004g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.763+626C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47015991 | |||||||
chr6:47016018 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.763+599C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016018 | |||||||
chr6:47016027 | T | C | 167 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0114 others(164): Show |
205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.763+590A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016027 | |||||||
chr6:47016197 | A | G | 2 | a0001c0012t0005g0137 a0001c0012t0005g0138 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.763+420T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016197 | |||||||
chr6:47016214 | T | TTG | 14 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0002t0003g0046 others(11): Show |
16 | HG01255.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.763+401_763+402dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016214 | |||||||
chr6:47016272 | C | A | 1 | a0001c0001t0005g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.763+345G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016272 | |||||||
chr6:47016352 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.763+265G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016352 | |||||||
chr6:47016363 | G | A | 2 | a0001c0003t0001g0027 a0005c0010t0019g0118 |
3 | HG02572.hp1 HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.763+254C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016363 | |||||||
chr6:47016487 | G | A | 3 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.763+130C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016487 | |||||||
chr6:47016529 | C | T | 2 | a0002c0002t0020g0309 a0002c0002t0020g0310 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.763+88G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016529 | |||||||
chr6:47016539 | C | T | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.763+78G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 8/14 | chr6 | 47016539 | |||||||
chr6:47016827 | C | G | 5 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(2): Show |
5 | HG01106.hp1 HG01243.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-59G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016827 | |||||||
chr6:47016828 | G | A | 1 | a0001c0001t0031g0187 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.612-60C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016828 | |||||||
chr6:47016852 | T | C | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.612-84A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016852 | |||||||
chr6:47016937 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.612-169T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016937 | |||||||
chr6:47016949 | G | GAT | 3 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.612-183_612-182dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016949 | |||||||
chr6:47016971 | C | T | 9 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0004g0297 others(6): Show |
10 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.612-203G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47016971 | |||||||
chr6:47017084 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-316T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017084 | |||||||
chr6:47017150 | C | T | 4 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.612-382G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017150 | |||||||
chr6:47017151 | G | C | 1 | a0001c0001t0002g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-383C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017151 | |||||||
chr6:47017157 | A | T | 1 | a0001c0001t0002g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.612-389T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017157 | |||||||
chr6:47017194 | T | C | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.612-426A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017194 | |||||||
chr6:47017320 | G | A | 18 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0196 others(15): Show |
19 | HG01070.hp1 HG01261.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.612-552C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017320 | |||||||
chr6:47017353 | C | T | 1 | a0001c0001t0004g0302 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.612-585G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017353 | |||||||
chr6:47017490 | A | G | 1 | a0006c0009t0006g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.612-722T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017490 | |||||||
chr6:47017685 | G | A | 1 | a0001c0001t0005g0182 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.612-917C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017685 | |||||||
chr6:47017690 | T | A | 10 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(7): Show |
12 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.612-922A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017690 | |||||||
chr6:47017692 | C | CA | 17 | a0001c0001t0001g0093 a0001c0001t0001g0178 a0001c0001t0002g0036 others(14): Show |
18 | HG00099.hp1 HG01175.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.612-925dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017692 | |||||||
chr6:47017692 | CA | C | 58 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(55): Show |
77 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.612-925delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017692 | |||||||
chr6:47017791 | C | T | 166 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0114 others(163): Show |
204 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.612-1023G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017791 | |||||||
chr6:47017852 | G | A | 7 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.612-1084C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017852 | |||||||
chr6:47017947 | A | T | 1 | a0001c0006t0001g0143 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.612-1179T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47017947 | |||||||
chr6:47018219 | C | T | 81 | a0001c0001t0001g0058 a0001c0001t0001g0151 a0001c0001t0001g0152 others(78): Show |
99 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.612-1451G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018219 | |||||||
chr6:47018453 | C | G | 1 | a0009c0014t0002g0228 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.612-1685G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018453 | |||||||
chr6:47018511 | C | A | 9 | a0001c0003t0004g0291 a0001c0003t0004g0293 a0001c0003t0004g0297 others(6): Show |
10 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.612-1743G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018511 | |||||||
chr6:47018643 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.612-1875C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018643 | |||||||
chr6:47018674 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.612-1906C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018674 | |||||||
chr6:47018681 | G | C | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.612-1913C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018681 | |||||||
chr6:47018705 | A | C | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.612-1937T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018705 | |||||||
chr6:47018710 | A | G | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.612-1942T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018710 | |||||||
chr6:47018766 | T | A | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+1965A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018766 | |||||||
chr6:47018770 | A | G | 90 | a0001c0001t0001g0058 a0001c0001t0001g0151 a0001c0001t0001g0152 others(87): Show |
109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.611+1961T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018770 | |||||||
chr6:47018834 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02135.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.611+1897G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018834 | |||||||
chr6:47018880 | G | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0169 a0001c0001t0001g0172 others(2): Show |
5 | HG01943.hp1 NA18960.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+1851C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018880 | |||||||
chr6:47018970 | A | G | 90 | a0001c0001t0001g0058 a0001c0001t0001g0151 a0001c0001t0001g0152 others(87): Show |
109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.611+1761T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47018970 | |||||||
chr6:47019028 | C | T | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.611+1703G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019028 | |||||||
chr6:47019045 | G | A | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1686C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019045 | |||||||
chr6:47019101 | A | C | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1630T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019101 | |||||||
chr6:47019180 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(264): Show |
330 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(327): Show |
intron_variant | MODIFIER | c.611+1551C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019180 | |||||||
chr6:47019384 | G | A | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+1347C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019384 | |||||||
chr6:47019468 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.611+1263C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019468 | |||||||
chr6:47019499 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.611+1232G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019499 | |||||||
chr6:47019561 | G | A | 1 | a0002c0002t0006g0239 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.611+1170C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019561 | |||||||
chr6:47019576 | C | G | 1 | a0001c0001t0004g0241 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.611+1155G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019576 | |||||||
chr6:47019595 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.611+1136C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019595 | |||||||
chr6:47019617 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0219 a0001c0001t0002g0220 |
5 | HG01081.hp1 HG01346.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+1114C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019617 | |||||||
chr6:47019631 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.611+1100G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019631 | |||||||
chr6:47019633 | G | A | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+1098C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019633 | |||||||
chr6:47019648 | C | T | 51 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(48): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.611+1083G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019648 | |||||||
chr6:47019663 | G | A | 2 | a0002c0002t0020g0309 a0002c0002t0020g0310 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.611+1068C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019663 | |||||||
chr6:47019683 | C | CAA | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+1046_611+1047d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019683 | |||||||
chr6:47019683 | CA | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
370 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.611+1047delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019683 | |||||||
chr6:47019802 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.611+929T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019802 | |||||||
chr6:47019897 | A | G | 8 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0196 others(5): Show |
8 | HG01070.hp1 HG01261.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+834T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47019897 | |||||||
chr6:47020025 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0189 |
2 | NA18970.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.611+706C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020025 | |||||||
chr6:47020027 | A | G | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+704T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020027 | |||||||
chr6:47020054 | C | T | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.611+677G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020054 | |||||||
chr6:47020089 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0273 |
3 | NA18984.hp2 NA19060.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.611+642A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020089 | |||||||
chr6:47020174 | C | T | 9 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.611+557G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020174 | |||||||
chr6:47020248 | C | T | 1 | a0001c0001t0039g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.611+483G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020248 | |||||||
chr6:47020258 | C | T | 2 | a0001c0007t0025g0217 a0002c0002t0003g0050 |
2 | HG01358.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.611+473G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020258 | |||||||
chr6:47020292 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0057 others(2): Show |
5 | HG00408.hp1 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.611+439T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020292 | |||||||
chr6:47020307 | A | G | 1 | a0001c0001t0033g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.611+424T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020307 | |||||||
chr6:47020324 | C | T | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+407G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020324 | |||||||
chr6:47020329 | C | G | 40 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(37): Show |
55 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.611+402G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020329 | |||||||
chr6:47020362 | G | A | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+369C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020362 | |||||||
chr6:47020370 | T | C | 167 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0114 others(164): Show |
205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.611+361A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020370 | |||||||
chr6:47020390 | G | A | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611+341C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020390 | |||||||
chr6:47020482 | C | T | 1 | a0001c0003t0037g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.611+249G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020482 | |||||||
chr6:47020502 | C | CA | 61 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(58): Show |
80 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.611+228dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | |||||||
chr6:47020502 | C | CAA | 8 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.611+227_611+228dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | |||||||
chr6:47020502 | C | CAAA | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.611+226_611+228dup others(3): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020502 | |||||||
chr6:47020609 | C | T | 3 | a0001c0001t0016g0213 a0001c0001t0016g0233 a0001c0001t0016g0240 |
3 | HG02074.hp1 NA18941.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.611+122G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020609 | |||||||
chr6:47020612 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.611+119T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 7/14 | chr6 | 47020612 | |||||||
chr6:47020809 | A | G | 2 | a0001c0001t0018g0133 a0001c0001t0018g0205 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.553-20T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020809 | |||||||
chr6:47020860 | T | C | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.553-71A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020860 | |||||||
chr6:47020912 | C | T | 167 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0114 others(164): Show |
205 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.553-123G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47020912 | |||||||
chr6:47021052 | G | A | 2 | a0002c0002t0020g0309 a0002c0002t0020g0310 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.553-263C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021052 | |||||||
chr6:47021085 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.553-296C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021085 | |||||||
chr6:47021362 | A | AT | 11 | a0001c0001t0001g0162 a0001c0003t0001g0208 a0003c0004t0007g0026 others(8): Show |
12 | HG01069.hp1 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-574dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021362 | |||||||
chr6:47021362 | A | ATTTTTTT others(524): Show |
1 | a0001c0003t0004g0291 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.553-574_553-573ins others(531): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021362 | |||||||
chr6:47021400 | A | G | 77 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(74): Show |
96 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.552+558T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021400 | |||||||
chr6:47021657 | G | A | 3 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.552+301C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021657 | |||||||
chr6:47021793 | G | A | 37 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(34): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.552+165C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021793 | |||||||
chr6:47021838 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.552+120C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021838 | |||||||
chr6:47021858 | G | A | 37 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(34): Show |
50 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.552+100C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021858 | |||||||
chr6:47021925 | C | T | 1 | a0001c0001t0028g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.552+33G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021925 | |||||||
chr6:47021943 | G | A | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.552+15C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 6/14 | chr6 | 47021943 | |||||||
chr6:47022092 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.452-34A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022092 | |||||||
chr6:47022112 | C | T | 63 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.452-54G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022112 | |||||||
chr6:47022153 | A | G | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.452-95T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022153 | |||||||
chr6:47022804 | C | CT | 78 | a0001c0001t0001g0126 a0001c0001t0001g0151 a0001c0001t0001g0152 others(75): Show |
91 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.452-747dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | |||||||
chr6:47022804 | C | CTT | 12 | a0001c0003t0001g0208 a0002c0008t0006g0313 a0003c0004t0007g0026 others(9): Show |
12 | HG01069.hp1 HG01109.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-748_452-747dup others(2): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | |||||||
chr6:47022804 | C | T | 1 | a0002c0008t0003g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.452-746G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | |||||||
chr6:47022804 | CT | C | 19 | a0001c0001t0001g0165 a0002c0002t0003g0045 a0002c0002t0003g0046 others(16): Show |
23 | HG00621.hp2 HG00741.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.452-747delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022804 | |||||||
chr6:47022809 | T | C | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452-751A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022809 | |||||||
chr6:47022837 | C | T | 1 | a0005c0010t0041g0296 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.452-779G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022837 | |||||||
chr6:47022888 | C | G | 4 | a0002c0008t0006g0313 a0006c0009t0006g0314 a0006c0009t0021g0311 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-830G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022888 | |||||||
chr6:47022957 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.452-899G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022957 | |||||||
chr6:47022973 | A | G | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-915T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47022973 | |||||||
chr6:47023010 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.452-952G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023010 | |||||||
chr6:47023062 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.451+982C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023062 | |||||||
chr6:47023124 | T | C | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.451+920A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023124 | |||||||
chr6:47023218 | C | A | 2 | a0005c0010t0019g0124 a0005c0010t0041g0296 |
2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.451+826G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023218 | |||||||
chr6:47023288 | G | A | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.451+756C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023288 | |||||||
chr6:47023312 | T | C | 1 | a0001c0001t0005g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.451+732A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023312 | |||||||
chr6:47023460 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0088 |
7 | NA18942.hp2 NA18946.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+584C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023460 | |||||||
chr6:47023686 | T | A | 1 | a0001c0003t0022g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.451+358A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023686 | |||||||
chr6:47023703 | C | T | 168 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0114 others(165): Show |
206 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.451+341G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023703 | |||||||
chr6:47023780 | A | G | 1 | a0001c0001t0004g0236 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.451+264T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023780 | |||||||
chr6:47023782 | C | A | 1 | a0001c0001t0031g0187 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.451+262G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023782 | |||||||
chr6:47023978 | G | A | 1 | a0002c0002t0006g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.451+66C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47023978 | |||||||
chr6:47024035 | G | C | 2 | a0001c0001t0007g0025 a0001c0001t0027g0140 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.451+9C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 5/14 | chr6 | 47024035 | |||||||
chr6:47024223 | C | G | 1 | a0001c0003t0004g0297 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.278-6G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024223 | |||||||
chr6:47024288 | AT | A | 9 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.278-72delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024288 | |||||||
chr6:47024322 | T | C | 63 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
81 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.278-105A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024322 | |||||||
chr6:47024429 | G | A | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.278-212C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024429 | |||||||
chr6:47024458 | G | A | 3 | a0001c0003t0001g0208 a0003c0004t0007g0153 a0003c0004t0007g0154 |
3 | HG01069.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.278-241C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024458 | |||||||
chr6:47024467 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0053 |
6 | NA18942.hp2 NA18946.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-250T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024467 | |||||||
chr6:47024594 | G | A | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-377C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024594 | |||||||
chr6:47024603 | C | T | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.278-386G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024603 | |||||||
chr6:47024806 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.278-589C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024806 | |||||||
chr6:47024843 | G | A | 3 | a0002c0008t0003g0033 a0002c0008t0003g0206 a0002c0008t0003g0207 |
4 | HG02280.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-626C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024843 | |||||||
chr6:47024850 | A | G | 51 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(48): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.278-633T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024850 | |||||||
chr6:47024873 | A | G | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.278-656T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024873 | |||||||
chr6:47024942 | T | C | 1 | a0003c0004t0007g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.278-725A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024942 | |||||||
chr6:47024958 | G | A | 3 | a0001c0001t0004g0276 a0001c0001t0004g0277 a0001c0001t0044g0278 |
3 | HG00642.hp1 HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.278-741C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47024958 | |||||||
chr6:47025171 | A | G | 51 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(48): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.277+683T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025171 | |||||||
chr6:47025245 | C | A | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.277+609G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025245 | |||||||
chr6:47025304 | A | C | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+550T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025304 | |||||||
chr6:47025539 | T | G | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.277+315A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025539 | |||||||
chr6:47025553 | C | T | 4 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0005c0010t0019g0124 others(1): Show |
4 | HG01255.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+301G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025553 | |||||||
chr6:47025554 | G | A | 1 | a0011c0020t0003g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.277+300C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025554 | |||||||
chr6:47025570 | G | A | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.277+284C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025570 | |||||||
chr6:47025746 | A | T | 6 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(3): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+108T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025746 | |||||||
chr6:47025809 | C | T | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+45G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025809 | |||||||
chr6:47025826 | T | C | 2 | a0002c0024t0043g0308 a0010c0023t0001g0110 |
2 | HG01106.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.277+28A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 4/14 | chr6 | 47025826 | |||||||
chr6:47026011 | GAGAA | G | 51 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(48): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.128-12_128-9delTTC others(1): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026011 | |||||||
chr6:47026102 | A | G | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-99T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026102 | |||||||
chr6:47026207 | C | T | 4 | a0002c0008t0006g0313 a0006c0009t0006g0314 a0006c0009t0021g0311 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-204G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026207 | |||||||
chr6:47026240 | C | T | 1 | a0001c0003t0037g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-237G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026240 | |||||||
chr6:47026472 | T | C | 1 | a0001c0003t0004g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.128-469A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026472 | |||||||
chr6:47026581 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.128-578G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026581 | |||||||
chr6:47026585 | T | C | 1 | a0001c0001t0002g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-582A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026585 | |||||||
chr6:47026709 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.128-706C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026709 | |||||||
chr6:47026725 | G | A | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.128-722C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026725 | |||||||
chr6:47026801 | C | T | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-798G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026801 | |||||||
chr6:47026826 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.128-823A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026826 | |||||||
chr6:47026907 | A | C | 1 | a0002c0002t0006g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.127+797T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026907 | |||||||
chr6:47026938 | A | T | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+766T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47026938 | |||||||
chr6:47027028 | A | T | 51 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(48): Show |
68 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.127+676T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027028 | |||||||
chr6:47027066 | G | A | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127+638C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027066 | |||||||
chr6:47027074 | T | C | 1 | a0001c0001t0002g0226 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.127+630A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027074 | |||||||
chr6:47027083 | G | A | 2 | a0002c0002t0008g0149 a0002c0019t0008g0148 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127+621C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027083 | |||||||
chr6:47027172 | A | T | 1 | a0002c0002t0008g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127+532T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027172 | |||||||
chr6:47027195 | G | T | 6 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(3): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.127+509C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027195 | |||||||
chr6:47027222 | C | G | 3 | a0002c0024t0043g0308 a0002c0025t0032g0044 a0010c0023t0001g0110 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+482G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027222 | |||||||
chr6:47027310 | C | T | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+394G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027310 | |||||||
chr6:47027311 | G | A | 41 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(38): Show |
56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.127+393C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027311 | |||||||
chr6:47027406 | C | T | 1 | a0012c0022t0006g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.127+298G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027406 | |||||||
chr6:47027507 | G | A | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127+197C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027507 | |||||||
chr6:47027695 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.127+9C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 3/14 | chr6 | 47027695 | |||||||
chr6:47027765 | T | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0196 others(3): Show |
6 | HG01070.hp1 HG01261.hp1 HG02683.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.70-4A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027765 | |||||||
chr6:47027772 | G | GA | 91 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0151 others(88): Show |
110 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.70-12dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027772 | |||||||
chr6:47027836 | A | C | 2 | a0001c0001t0007g0025 a0001c0001t0027g0140 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.70-75T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027836 | |||||||
chr6:47027888 | G | A | 4 | a0004c0005t0002g0014 a0004c0005t0002g0244 a0004c0005t0005g0074 others(1): Show |
6 | NA18941.hp1 NA18995.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-127C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027888 | |||||||
chr6:47027935 | A | G | 3 | a0002c0024t0043g0308 a0002c0025t0032g0044 a0010c0023t0001g0110 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.70-174T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47027935 | |||||||
chr6:47028066 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70-305C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028066 | |||||||
chr6:47028069 | A | T | 1 | a0001c0001t0002g0248 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.70-308T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028069 | |||||||
chr6:47028097 | C | T | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-336G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028097 | |||||||
chr6:47028161 | A | G | 2 | a0001c0001t0012g0119 a0001c0001t0012g0174 |
2 | NA18965.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.70-400T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028161 | |||||||
chr6:47028182 | T | C | 3 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 |
3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.70-421A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028182 | |||||||
chr6:47028265 | T | C | 34 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(31): Show |
47 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.70-504A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028265 | |||||||
chr6:47028280 | C | T | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-519G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028280 | |||||||
chr6:47028332 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.70-571A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028332 | |||||||
chr6:47028481 | C | T | 1 | a0002c0019t0008g0148 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+512G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028481 | |||||||
chr6:47028482 | C | G | 189 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0108 others(186): Show |
228 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(225): Show |
intron_variant | MODIFIER | c.69+511G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028482 | |||||||
chr6:47028515 | C | T | 1 | a0002c0008t0003g0033 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.69+478G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028515 | |||||||
chr6:47028540 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18964.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.69+453C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028540 | |||||||
chr6:47028553 | T | C | 2 | a0001c0001t0004g0271 a0001c0001t0004g0272 |
2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.69+440A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028553 | |||||||
chr6:47028671 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.69+322G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028671 | |||||||
chr6:47028702 | C | A | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+291G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028702 | |||||||
chr6:47028742 | C | A | 10 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(7): Show |
12 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+251G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028742 | |||||||
chr6:47028880 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.69+113T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028880 | |||||||
chr6:47028958 | G | T | 3 | a0002c0024t0043g0308 a0002c0025t0032g0044 a0010c0023t0001g0110 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.69+35C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 2/14 | chr6 | 47028958 | |||||||
chr6:47029298 | A | G | 2 | a0002c0002t0020g0309 a0002c0002t0020g0310 |
2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-43-194T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029298 | |||||||
chr6:47029358 | G | GT | 12 | a0001c0001t0001g0085 a0001c0001t0018g0133 a0001c0001t0018g0205 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-255dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029358 | |||||||
chr6:47029370 | T | A | 3 | a0002c0024t0043g0308 a0002c0025t0032g0044 a0010c0023t0001g0110 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-266A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029370 | |||||||
chr6:47029374 | C | T | 92 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0126 others(89): Show |
111 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.-43-270G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029374 | |||||||
chr6:47029415 | G | A | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-311C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029415 | |||||||
chr6:47029651 | C | G | 5 | a0002c0002t0008g0043 a0002c0002t0008g0149 a0002c0002t0010g0011 others(2): Show |
7 | HG01884.hp1 HG02572.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-547G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029651 | |||||||
chr6:47029794 | T | C | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-690A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47029794 | |||||||
chr6:47030050 | A | G | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-946T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030050 | |||||||
chr6:47030063 | T | C | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-959A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030063 | |||||||
chr6:47030171 | C | T | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-1067G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030171 | |||||||
chr6:47030174 | G | A | 1 | a0001c0001t0012g0174 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-43-1070C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030174 | |||||||
chr6:47030179 | G | A | 90 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0151 others(87): Show |
109 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-43-1075C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030179 | |||||||
chr6:47030341 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-43-1237G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030341 | |||||||
chr6:47030511 | G | A | 2 | a0002c0008t0006g0313 a0006c0009t0021g0312 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-43-1407C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030511 | |||||||
chr6:47030538 | A | T | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-1434T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030538 | |||||||
chr6:47030576 | A | ATG | 74 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(71): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-43-1474_-43-1473d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | A | ATGTG | 33 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0081 others(30): Show |
35 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43-1476_-43-1473d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | A | ATGTGTG | 35 | a0001c0001t0001g0151 a0001c0001t0001g0181 a0001c0001t0001g0189 others(32): Show |
42 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-43-1478_-43-1473d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | A | ATGTGTGT others(1): Show |
25 | a0001c0001t0002g0008 a0001c0001t0002g0036 a0001c0001t0002g0037 others(22): Show |
31 | HG00609.hp1 HG01168.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.-43-1480_-43-1473d others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | A | ATGTGTGT others(3): Show |
12 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0002g0009 others(9): Show |
17 | HG03239.hp2 HG03486.hp1 HG04115.hp2 others(14): Show |
intron_variant | MODIFIER | c.-43-1482_-43-1473d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | ATG | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-43-1474_-43-1473d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | ATGTGTG | A | 5 | a0001c0001t0004g0042 a0001c0003t0004g0297 a0002c0002t0003g0122 others(2): Show |
7 | HG02145.hp2 HG02258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-1478_-43-1473d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030576 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0005g0183 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-43-1482_-43-1473d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030576 | |||||||
chr6:47030618 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-43-1514C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030618 | |||||||
chr6:47030619 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-43-1515A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030619 | |||||||
chr6:47030732 | T | C | 6 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(3): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-1628A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030732 | |||||||
chr6:47030734 | G | T | 1 | a0001c0001t0002g0245 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-43-1630C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030734 | |||||||
chr6:47030745 | A | G | 1 | a0002c0002t0003g0062 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-43-1641T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030745 | |||||||
chr6:47030769 | C | CT | 34 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(31): Show |
47 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-43-1666dupA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030769 | |||||||
chr6:47030771 | C | T | 77 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(74): Show |
96 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-43-1667G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030771 | |||||||
chr6:47030864 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0097 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-43-1760C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030864 | |||||||
chr6:47030947 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-43-1843C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030947 | |||||||
chr6:47030953 | G | A | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-1849C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47030953 | |||||||
chr6:47031255 | G | A | 6 | a0002c0002t0011g0130 a0002c0002t0011g0131 a0002c0002t0011g0132 others(3): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-2151C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031255 | |||||||
chr6:47031257 | GTCTCTCT others(6): Show |
G | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2166_-43-2154d others(15): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031257 | |||||||
chr6:47031257 | GTCTCTCT others(54): Show |
G | 1 | a0001c0001t0002g0216 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-43-2214_-43-2154d others(63): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031257 | |||||||
chr6:47031270 | T | TTC | 8 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0001g0128 others(5): Show |
8 | HG01175.hp2 HG03710.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2168_-43-2167d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031270 | |||||||
chr6:47031270 | TTCTC | T | 13 | a0001c0001t0002g0036 a0001c0001t0002g0264 a0001c0001t0005g0159 others(10): Show |
13 | HG01255.hp1 HG01891.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-2170_-43-2167d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031270 | |||||||
chr6:47031288 | CTCTCTGT others(56): Show |
C | 1 | a0001c0001t0002g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-43-2247_-43-2185d others(65): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031288 | |||||||
chr6:47031331 | TTCTCTCT others(25): Show |
T | 3 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 |
3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-43-2259_-43-2228d others(34): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031331 | |||||||
chr6:47031332 | T | C | 2 | a0001c0001t0001g0189 a0002c0002t0003g0061 |
2 | HG02129.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-43-2228A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031332 | |||||||
chr6:47031333 | C | T | 2 | a0001c0001t0001g0189 a0002c0002t0003g0061 |
2 | HG02129.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-43-2229G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031333 | |||||||
chr6:47031335 | CTCTCTCT others(9): Show |
C | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2247_-43-2232d others(18): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031335 | |||||||
chr6:47031347 | C | G | 1 | a0002c0024t0043g0308 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-43-2243G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031347 | |||||||
chr6:47031349 | CTG | C | 5 | a0002c0002t0003g0061 a0002c0008t0003g0033 a0002c0008t0003g0206 others(2): Show |
6 | HG01106.hp1 HG02129.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-2247_-43-2246d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031349 | |||||||
chr6:47031351 | G | C | 4 | a0001c0001t0001g0189 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-2247C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTC | 32 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(29): Show |
33 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-43-2249_-43-2248d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTCTC | 11 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(8): Show |
12 | HG00438.hp1 HG00642.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-2251_-43-2248d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTCTCTC | 3 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0004g0262 |
4 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-2253_-43-2248d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTCTCTCT others(3): Show |
2 | a0001c0012t0005g0137 a0001c0012t0005g0138 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-43-2257_-43-2248d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTCTCTCT others(5): Show |
1 | a0001c0003t0004g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-43-2259_-43-2248d others(14): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | G | GTCTCTCT others(7): Show |
1 | a0001c0003t0023g0041 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-43-2261_-43-2248d others(16): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTC | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0030 others(72): Show |
94 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-43-2249_-43-2248d others(4): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTCTC | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0160 others(35): Show |
57 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-43-2251_-43-2248d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTCTCTC | G | 10 | a0001c0001t0005g0123 a0001c0001t0007g0025 a0001c0001t0018g0133 others(7): Show |
11 | HG01255.hp1 HG01884.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-2253_-43-2248d others(8): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTCTCTCT others(1): Show |
G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
9 | HG00639.hp1 HG02135.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-2255_-43-2248d others(10): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTCTCTCT others(3): Show |
G | 2 | a0001c0001t0004g0042 a0002c0002t0003g0102 |
3 | HG01928.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2257_-43-2248d others(12): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031351 | GTCTCTCT others(5): Show |
G | 1 | a0006c0009t0006g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-2259_-43-2248d others(14): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031351 | |||||||
chr6:47031353 | C | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0189 a0001c0001t0002g0215 others(3): Show |
6 | HG01167.hp2 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-2249G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031353 | |||||||
chr6:47031355 | C | G | 4 | a0002c0002t0003g0061 a0002c0008t0003g0033 a0002c0008t0003g0206 others(1): Show |
5 | HG02129.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-2251G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031355 | |||||||
chr6:47031363 | C | G | 1 | a0010c0023t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-2259G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031363 | |||||||
chr6:47031386 | T | C | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-2282A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031386 | |||||||
chr6:47031416 | C | T | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2312G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031416 | |||||||
chr6:47031459 | A | G | 79 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0151 others(76): Show |
96 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-43-2355T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031459 | |||||||
chr6:47031508 | T | G | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-2404A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031508 | |||||||
chr6:47031524 | C | T | 1 | a0004c0005t0002g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-43-2420G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031524 | |||||||
chr6:47031572 | G | C | 3 | a0002c0024t0043g0308 a0002c0025t0032g0044 a0010c0023t0001g0110 |
3 | HG01106.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-2468C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031572 | |||||||
chr6:47031695 | G | C | 1 | a0002c0002t0003g0102 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-43-2591C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031695 | |||||||
chr6:47031744 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
5 | HG03491.hp2 HG03492.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-2640C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031744 | |||||||
chr6:47031809 | C | T | 61 | a0001c0001t0001g0051 a0001c0001t0001g0070 a0001c0001t0001g0114 others(58): Show |
78 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-43-2705G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031809 | |||||||
chr6:47031935 | T | C | 2 | a0001c0001t0004g0243 a0002c0002t0003g0158 |
2 | HG02132.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-43-2831A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031935 | |||||||
chr6:47031968 | C | G | 1 | a0003c0004t0007g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-43-2864G>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47031968 | |||||||
chr6:47032088 | G | A | 8 | a0002c0002t0003g0121 a0002c0002t0003g0122 a0002c0002t0006g0303 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2984C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032088 | |||||||
chr6:47032139 | G | T | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-43-3035C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032139 | |||||||
chr6:47032158 | C | T | 1 | a0012c0022t0006g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-43-3054G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032158 | |||||||
chr6:47032159 | G | A | 2 | a0001c0012t0005g0137 a0001c0012t0005g0138 |
2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-43-3055C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032159 | |||||||
chr6:47032270 | G | A | 3 | a0002c0002t0009g0038 a0002c0002t0009g0040 a0002c0002t0009g0287 |
5 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-3166C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032270 | |||||||
chr6:47032274 | C | A | 76 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0151 others(73): Show |
92 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-43-3170G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032274 | |||||||
chr6:47032325 | G | A | 8 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0008t0006g0313 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-3221C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032325 | |||||||
chr6:47032389 | A | T | 2 | a0002c0024t0043g0308 a0002c0025t0032g0044 |
2 | HG01106.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-3285T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032389 | |||||||
chr6:47032389 | AT | A | 3 | a0002c0008t0003g0033 a0002c0008t0003g0206 a0002c0008t0003g0207 |
4 | HG02280.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3286delA | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032389 | |||||||
chr6:47032479 | T | C | 5 | a0001c0001t0001g0060 a0001c0001t0004g0214 a0001c0001t0004g0236 others(2): Show |
5 | HG00438.hp2 HG02155.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-3375A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032479 | |||||||
chr6:47032769 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-43-3665T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032769 | |||||||
chr6:47032785 | T | C | 142 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0070 others(139): Show |
175 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(172): Show |
intron_variant | MODIFIER | c.-43-3681A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032785 | |||||||
chr6:47032793 | G | C | 4 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3689C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032793 | |||||||
chr6:47032925 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(97): Show |
131 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.-43-3821G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032925 | |||||||
chr6:47032929 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-43-3825T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032929 | |||||||
chr6:47032954 | G | C | 7 | a0001c0001t0018g0133 a0001c0001t0018g0205 a0002c0002t0011g0130 others(4): Show |
7 | HG00741.hp2 HG01243.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-3850C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032954 | |||||||
chr6:47032987 | C | T | 1 | a0001c0001t0002g0231 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-43-3883G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032987 | |||||||
chr6:47032988 | G | A | 2 | a0001c0003t0004g0297 a0001c0003t0023g0041 |
3 | HG02630.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-43-3884C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47032988 | |||||||
chr6:47033056 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-43-3952A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033056 | |||||||
chr6:47033066 | C | T | 1 | a0006c0009t0006g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-3962G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033066 | |||||||
chr6:47033165 | T | A | 6 | a0002c0002t0006g0303 a0002c0002t0006g0304 a0002c0002t0006g0305 others(3): Show |
6 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-4061A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033165 | |||||||
chr6:47033175 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43-4071C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033175 | |||||||
chr6:47033229 | C | T | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
7 | HG02148.hp2 NA18939.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-4125G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033229 | |||||||
chr6:47033292 | A | G | 6 | a0001c0001t0007g0025 a0001c0001t0018g0205 a0001c0001t0027g0140 others(3): Show |
8 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-4188T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033292 | |||||||
chr6:47033306 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18951.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-43-4202C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033306 | |||||||
chr6:47033382 | C | T | 3 | a0001c0006t0001g0022 a0001c0006t0001g0109 a0010c0023t0001g0110 |
4 | HG02145.hp1 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4278G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033382 | |||||||
chr6:47033416 | C | T | 5 | a0002c0002t0006g0303 a0002c0002t0006g0304 a0002c0002t0006g0305 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-4312G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033416 | |||||||
chr6:47033463 | T | C | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-43-4359A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033463 | |||||||
chr6:47033499 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-43-4395G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033499 | |||||||
chr6:47033602 | G | A | 1 | a0002c0002t0013g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-43-4498C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033602 | |||||||
chr6:47033711 | C | T | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4607G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033711 | |||||||
chr6:47033721 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-43-4617G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033721 | |||||||
chr6:47033773 | G | C | 13 | a0001c0001t0039g0315 a0002c0002t0006g0303 a0002c0002t0006g0304 others(10): Show |
13 | HG01106.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-4669C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033773 | |||||||
chr6:47033775 | G | C | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4671C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033775 | |||||||
chr6:47033846 | C | A | 5 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-4742G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033846 | |||||||
chr6:47033876 | T | C | 82 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0036 others(79): Show |
93 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-43-4772A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033876 | |||||||
chr6:47033903 | T | A | 82 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0036 others(79): Show |
93 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-43-4799A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47033903 | |||||||
chr6:47034227 | T | C | 1 | a0015c0018t0006g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-43-5123A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034227 | |||||||
chr6:47034281 | T | C | 3 | a0003c0004t0007g0209 a0003c0004t0007g0210 a0003c0004t0007g0211 |
3 | HG01255.hp2 HG03704.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-43-5177A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034281 | |||||||
chr6:47034326 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | NA18965.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-43-5222C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034326 | |||||||
chr6:47034364 | T | C | 2 | a0002c0002t0003g0003 a0002c0002t0003g0106 |
7 | NA18960.hp1 NA18997.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-5260A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034364 | |||||||
chr6:47034407 | C | T | 1 | a0002c0002t0003g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-43-5303G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034407 | |||||||
chr6:47034425 | T | C | 1 | a0002c0002t0009g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-43-5321A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034425 | |||||||
chr6:47034594 | A | G | 4 | a0001c0003t0001g0027 a0001c0012t0005g0137 a0001c0012t0005g0138 others(1): Show |
5 | HG02257.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-5490T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034594 | |||||||
chr6:47034734 | G | C | 1 | a0006c0009t0006g0314 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-5630C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034734 | |||||||
chr6:47034963 | C | A | 1 | a0001c0001t0039g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-5859G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47034963 | |||||||
chr6:47035116 | C | T | 1 | a0001c0017t0026g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-43-6012G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035116 | |||||||
chr6:47035125 | A | G | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-6021T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035125 | |||||||
chr6:47035173 | G | C | 8 | a0001c0001t0018g0205 a0001c0003t0001g0208 a0002c0008t0003g0033 others(5): Show |
9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-6069C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035173 | |||||||
chr6:47035187 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01516.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-43-6083C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035187 | |||||||
chr6:47035269 | A | C | 1 | a0001c0001t0004g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-43-6165T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035269 | |||||||
chr6:47035407 | T | TA | 4 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-6304dupT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035407 | |||||||
chr6:47035454 | TA | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
5 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6351delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035454 | |||||||
chr6:47035510 | T | A | 1 | a0013c0021t0002g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-6406A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035510 | |||||||
chr6:47035604 | C | T | 8 | a0001c0001t0002g0279 a0001c0001t0004g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-6500G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035604 | |||||||
chr6:47035704 | A | G | 2 | a0001c0001t0002g0231 a0001c0001t0002g0268 |
2 | NA18967.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-44+6487T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035704 | |||||||
chr6:47035732 | C | T | 1 | a0001c0001t0007g0025 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-44+6459G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035732 | |||||||
chr6:47035740 | G | A | 108 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-44+6451C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035740 | |||||||
chr6:47035920 | G | C | 1 | a0002c0002t0006g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-44+6271C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035920 | |||||||
chr6:47035921 | G | T | 1 | a0002c0002t0006g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-44+6270C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035921 | |||||||
chr6:47035956 | C | A | 8 | a0001c0001t0002g0279 a0001c0001t0004g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+6235G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47035956 | |||||||
chr6:47036046 | C | A | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6145G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036046 | |||||||
chr6:47036060 | A | G | 1 | a0001c0001t0035g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+6131T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036060 | |||||||
chr6:47036162 | G | A | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+6029C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036162 | |||||||
chr6:47036266 | A | T | 24 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0039 others(21): Show |
33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+5925T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036266 | |||||||
chr6:47036269 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-44+5922T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036269 | |||||||
chr6:47036290 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0004g0288 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-44+5901A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036290 | |||||||
chr6:47036355 | A | G | 10 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0224 others(7): Show |
10 | HG00735.hp2 HG01346.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+5836T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036355 | |||||||
chr6:47036380 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0012g0028 |
4 | HG02148.hp2 NA18969.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5811G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036380 | |||||||
chr6:47036459 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-44+5732C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036459 | |||||||
chr6:47036515 | C | A | 1 | a0001c0017t0026g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-44+5676G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036515 | |||||||
chr6:47036547 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
11 | HG02132.hp1 NA18939.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+5644T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036547 | |||||||
chr6:47036549 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(71): Show |
112 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-44+5642T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036549 | |||||||
chr6:47036742 | A | G | 3 | a0002c0002t0013g0155 a0003c0004t0007g0153 a0003c0004t0007g0154 |
3 | HG00741.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+5449T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47036742 | |||||||
chr6:47037156 | T | C | 1 | a0001c0001t0002g0268 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-44+5035A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037156 | |||||||
chr6:47037169 | T | C | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+5022A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037169 | |||||||
chr6:47037215 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-44+4976C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037215 | |||||||
chr6:47037247 | G | A | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+4944C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037247 | |||||||
chr6:47037398 | G | C | 1 | a0001c0001t0036g0269 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-44+4793C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037398 | |||||||
chr6:47037405 | A | T | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+4786T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037405 | |||||||
chr6:47037414 | A | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(238): Show |
306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.-44+4777T>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037414 | |||||||
chr6:47037490 | A | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0215 a0001c0001t0002g0216 others(4): Show |
9 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4701T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037490 | |||||||
chr6:47037616 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0004g0042 |
3 | HG02717.hp2 HG02886.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-44+4575G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037616 | |||||||
chr6:47037762 | C | A | 8 | a0001c0001t0018g0205 a0001c0003t0001g0208 a0002c0008t0003g0033 others(5): Show |
9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4429G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47037762 | |||||||
chr6:47038009 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-44+4182G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038009 | |||||||
chr6:47038063 | G | C | 8 | a0001c0001t0018g0205 a0001c0003t0001g0208 a0002c0008t0003g0033 others(5): Show |
9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+4128C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038063 | |||||||
chr6:47038101 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-44+4090A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038101 | |||||||
chr6:47038216 | A | G | 108 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0013 others(105): Show |
128 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-44+3975T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038216 | |||||||
chr6:47038289 | C | A | 24 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0039 others(21): Show |
33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+3902G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038289 | |||||||
chr6:47038289 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-44+3902G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038289 | |||||||
chr6:47038542 | G | C | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG01175.hp2 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+3649C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038542 | |||||||
chr6:47038604 | C | T | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3587G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038604 | |||||||
chr6:47038627 | T | A | 8 | a0001c0001t0002g0279 a0001c0001t0004g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+3564A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038627 | |||||||
chr6:47038645 | A | G | 24 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0039 others(21): Show |
33 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44+3546T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038645 | |||||||
chr6:47038677 | A | G | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3514T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038677 | |||||||
chr6:47038740 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-44+3451G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038740 | |||||||
chr6:47038817 | C | T | 3 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 |
3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44+3374G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038817 | |||||||
chr6:47038818 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-44+3373C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038818 | |||||||
chr6:47038906 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(246): Show |
315 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.-44+3285T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038906 | |||||||
chr6:47038920 | G | A | 2 | a0001c0001t0004g0271 a0001c0001t0004g0272 |
2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-44+3271C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47038920 | |||||||
chr6:47039081 | TC | T | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+3109delG | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039081 | |||||||
chr6:47039171 | A | G | 3 | a0001c0001t0005g0150 a0002c0002t0008g0149 a0002c0019t0008g0148 |
3 | HG02965.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-44+3020T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039171 | |||||||
chr6:47039189 | G | T | 17 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(14): Show |
20 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+3002C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039189 | |||||||
chr6:47039217 | G | T | 11 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0282 others(8): Show |
17 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+2974C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039217 | |||||||
chr6:47039290 | T | C | 1 | a0001c0001t0002g0273 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-44+2901A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039290 | |||||||
chr6:47039411 | T | A | 8 | a0001c0001t0018g0205 a0001c0003t0001g0208 a0002c0008t0003g0033 others(5): Show |
9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+2780A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039411 | |||||||
chr6:47039504 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(69): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-44+2687C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039504 | |||||||
chr6:47039527 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(143): Show |
192 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.-44+2664A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039527 | |||||||
chr6:47039646 | C | T | 1 | a0001c0003t0022g0280 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-44+2545G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039646 | |||||||
chr6:47039651 | T | C | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2540A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039651 | |||||||
chr6:47039753 | G | A | 1 | a0002c0002t0011g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+2438C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039753 | |||||||
chr6:47039872 | G | A | 8 | a0001c0001t0002g0279 a0001c0001t0004g0275 a0001c0001t0004g0276 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+2319C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039872 | |||||||
chr6:47039886 | T | G | 4 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(1): Show |
4 | HG01243.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2305A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039886 | |||||||
chr6:47039965 | A | AAAAT | 5 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2222_-44+2225d others(6): Show |
ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039965 | |||||||
chr6:47039984 | A | G | 1 | a0008c0011t0005g0147 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44+2207T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47039984 | |||||||
chr6:47040012 | G | T | 104 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0013 others(101): Show |
124 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-44+2179C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040012 | |||||||
chr6:47040015 | T | C | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+2176A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040015 | |||||||
chr6:47040066 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(95): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-44+2125C>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040066 | |||||||
chr6:47040103 | A | G | 1 | a0001c0001t0004g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-44+2088T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040103 | |||||||
chr6:47040116 | C | A | 104 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0013 others(101): Show |
124 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.-44+2075G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040116 | |||||||
chr6:47040190 | C | T | 5 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+2001G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040190 | |||||||
chr6:47040336 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-44+1855C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040336 | |||||||
chr6:47040365 | G | A | 8 | a0001c0001t0018g0205 a0001c0003t0001g0208 a0002c0008t0003g0033 others(5): Show |
9 | HG01069.hp1 HG01255.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+1826C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040365 | |||||||
chr6:47040380 | G | A | 25 | a0001c0001t0002g0009 a0001c0001t0002g0015 a0001c0001t0002g0039 others(22): Show |
34 | HG01074.hp1 HG01255.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.-44+1811C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040380 | |||||||
chr6:47040385 | T | A | 8 | a0001c0001t0039g0315 a0002c0002t0020g0309 a0002c0002t0020g0310 others(5): Show |
8 | HG01106.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+1806A>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040385 | |||||||
chr6:47040488 | TA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
175 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.-44+1702delT | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040488 | |||||||
chr6:47040493 | A | T | 106 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0013 others(103): Show |
126 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.-44+1698T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040493 | |||||||
chr6:47040573 | G | T | 4 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 others(1): Show |
4 | HG02055.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1618C>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040573 | |||||||
chr6:47040621 | C | T | 1 | a0001c0001t0016g0213 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-44+1570G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040621 | |||||||
chr6:47040683 | T | C | 1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-44+1508A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040683 | |||||||
chr6:47040912 | T | G | 2 | a0001c0001t0004g0300 a0001c0001t0004g0301 |
2 | HG01515.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-44+1279A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47040912 | |||||||
chr6:47041033 | G | A | 3 | a0001c0001t0018g0133 a0002c0002t0011g0131 a0002c0002t0011g0132 |
3 | HG01243.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+1158C>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041033 | |||||||
chr6:47041056 | T | C | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG01175.hp2 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1135A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041056 | |||||||
chr6:47041152 | C | T | 5 | a0002c0002t0006g0303 a0002c0002t0006g0304 a0002c0002t0006g0305 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+1039G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041152 | |||||||
chr6:47041175 | T | C | 1 | a0001c0001t0004g0302 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-44+1016A>G | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041175 | |||||||
chr6:47041257 | A | G | 5 | a0001c0001t0018g0133 a0002c0002t0011g0130 a0002c0002t0011g0131 others(2): Show |
5 | HG01243.hp1 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+934T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041257 | |||||||
chr6:47041456 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(99): Show |
143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-44+735G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041456 | |||||||
chr6:47041861 | C | T | 3 | a0002c0002t0003g0045 a0002c0002t0003g0046 a0002c0002t0003g0047 |
3 | HG02055.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44+330G>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47041861 | |||||||
chr6:47042042 | C | A | 1 | a0014c0015t0001g0212 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-44+149G>T | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042042 | |||||||
chr6:47042075 | T | G | 14 | a0001c0001t0004g0042 a0001c0001t0039g0315 a0002c0002t0006g0303 others(11): Show |
15 | HG01106.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-44+116A>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042075 | |||||||
chr6:47042090 | A | T | 1 | a0002c0025t0032g0044 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-44+101T>A | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042090 | |||||||
chr6:47042112 | A | G | 1 | a0002c0002t0008g0043 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44+79T>C | ADGRF1 | ENSG00000153292.16 | transcript | ENST00000371253.7 | protein_coding | 1/14 | chr6 | 47042112 |