Item | Value |
---|---|
geneid | 221395 |
ensemblid | ENSG00000069122.19 |
hgncid | 19030 |
symbol | ADGRF5 |
name | adhesion G protein-coupled receptor F5 |
refseq_nuc | NM_001098518.2 |
refseq_prot | NP_001091988.1 |
ensembl_nuc | ENST00000283296.12 |
ensembl_prot | ENSP00000283296.7 |
mane_status | MANE Select |
chr | chr6 |
start | 46852522 |
end | 46921938 |
strand | - |
ver | v1.2 |
region | chr6:46852522-46921938 |
region5000 | chr6:46847522-46926938 |
regionname0 | ADGRF5_chr6_46852522_46921938 |
regionname5000 | ADGRF5_chr6_46847522_46926938 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1346 | 167 | 13 | 41 | 82 | 9 | 22 | 62 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0002 | 0/0 | 1346 | 134 | 27 | 15 | 74 | 4 | 14 | 55 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0003 | 1/0 | 1346 | 52 | 39 | 8 | 1 | 1 | 2 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0004 | 0/0 | 1346 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0005 | 0/0 | 1346 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0006 | 0/1 | 1346 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0007 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0008 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0009 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0010 | 0/0 | 1346 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0011 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0012 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0013 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0014 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0015 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0016 | 0/0 | 1346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0017 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0018 | 0/0 | 1346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0019 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
a0020 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | MKSPR others(1341): Show |
chr6 | 46847522 | 46926938 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4038 | 133 | 11 | 39 | 63 | 7 | 13 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0001c0004 | 0/0 | 4038 | 28 | 1 | 2 | 14 | 2 | 9 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0001c0012 | 0/0 | 4038 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0001c0013 | 0/0 | 4038 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0001c0019 | 0/0 | 4038 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0001c0028 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0002c0002 | 0/0 | 4038 | 114 | 19 | 13 | 64 | 4 | 14 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0002c0005 | 0/0 | 4038 | 10 | 2 | 1 | 7 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0002c0006 | 0/0 | 4038 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0002c0014 | 0/0 | 4038 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0002c0017 | 0/0 | 4038 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0003c0003 | 0/0 | 4038 | 44 | 36 | 5 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0003c0007 | 1/0 | 4038 | 6 | 1 | 3 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0003c0025 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0003c0034 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0004c0008 | 0/0 | 4038 | 5 | 5 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0004c0009 | 0/0 | 4038 | 3 | 2 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0004c0011 | 0/0 | 4038 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0004c0029 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0005c0010 | 0/0 | 4038 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0006c0015 | 0/1 | 4038 | 2 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0007c0020 | 0/0 | 4038 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0008c0022 | 0/0 | 4038 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0009c0030 | 0/0 | 4038 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0010c0035 | 0/0 | 4038 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0011c0031 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0012c0023 | 0/0 | 4038 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0013c0033 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0014c0032 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0015c0024 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0016c0026 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0017c0021 | 0/0 | 4038 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0018c0016 | 0/0 | 4038 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0019c0027 | 0/0 | 4038 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 | ||
a0020c0018 | 0/0 | 4038 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | ATGAA others(4033): Show |
chr6 | 46847522 | 46926938 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5761 | 128 | 10 | 39 | 60 | 7 | 12 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0001t0002 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0001t0012 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0001t0026 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0001t0029 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0001t0030 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0004t0001 | 0/0 | 5761 | 26 | 0 | 2 | 13 | 2 | 9 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0004t0015 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0004t0027 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0012t0001 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0013t0001 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0019t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0001c0028t0004 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0002 | 0/0 | 5761 | 105 | 15 | 13 | 60 | 4 | 13 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0010 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0013 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0017 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0019 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0020 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0021 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0022 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0002t0028 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0005t0002 | 0/0 | 5761 | 10 | 2 | 1 | 7 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0006t0002 | 0/0 | 5761 | 7 | 6 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0014t0002 | 0/0 | 5761 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0002c0017t0002 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0003 | 0/0 | 5760 | 30 | 23 | 4 | 1 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0004 | 0/0 | 5761 | 6 | 5 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0006 | 0/0 | 5760 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0009 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0011 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5806): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0014 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0003c0003t0016 | 0/0 | 5727 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5722): Show |
chr6 | 46847522 | 46926938 |
a0003c0007t0003 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0003c0007t0005 | 1/0 | 5761 | 5 | 1 | 2 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0003c0025t0003 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0003c0034t0006 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0004c0008t0004 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0004c0008t0007 | 0/0 | 5761 | 3 | 3 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0004c0008t0023 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0004c0009t0008 | 0/0 | 5760 | 2 | 1 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0004c0009t0025 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0004c0011t0004 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0004c0011t0018 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0004c0029t0024 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0005c0010t0001 | 0/0 | 5761 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0006c0015t0001 | 0/1 | 5761 | 2 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0007c0020t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0008c0022t0001 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0009c0030t0001 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0010c0035t0002 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0011c0031t0003 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0012c0023t0002 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0013c0033t0011 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5806): Show |
chr6 | 46847522 | 46926938 |
a0014c0032t0003 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5755): Show |
chr6 | 46847522 | 46926938 |
a0015c0024t0002 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0016c0026t0001 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0017c0021t0001 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0018c0016t0001 | 0/0 | 5761 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0019c0027t0002 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
a0020c0018t0001 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | GACTC others(5756): Show |
chr6 | 46847522 | 46926938 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0026g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0029g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0001t0030g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0004t0027g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0012t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0012t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0013t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0013t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0019t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0001c0028t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0019g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0020g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0022g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0002t0028g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0005t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0006t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0014t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0014t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0002c0017t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0003t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0005g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0007t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0025t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0003c0034t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0008t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0008t0007g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0008t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0008t0023g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0009t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0009t0008g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0009t0025g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0011t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0011t0018g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0004c0029t0024g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0005c0010t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0005c0010t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0006c0015t0001g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0006c0015t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0007c0020t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0008c0022t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0009c0030t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0010c0035t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0011c0031t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0012c0023t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0013c0033t0011g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0014c0032t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0015c0024t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0016c0026t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0017c0021t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0018c0016t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0019c0027t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
a0020c0018t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0362 | EUR | GBR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | GBR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0248 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00280 | hp2 | a0003 | c0007 | t0005 | g0130 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0352 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0359 | EUR | FIN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00544 | hp1 | a0007 | c0020 | t0001 | g0332 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00642 | hp1 | a0002 | c0006 | t0002 | g0198 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00673 | hp2 | a0002 | c0005 | t0002 | g0144 | EAS | CHS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00738 | hp2 | a0008 | c0022 | t0001 | g0300 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG00741 | hp2 | a0003 | c0003 | t0003 | g0193 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01071 | hp2 | a0003 | c0007 | t0005 | g0235 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0347 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0354 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01106 | hp2 | a0004 | c0009 | t0008 | g0023 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0131 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0123 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0252 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01192 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01243 | hp2 | a0003 | c0003 | t0004 | g0343 | AMR | PUR | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01255 | hp1 | a0003 | c0007 | t0003 | g0188 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0239 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01346 | hp1 | a0003 | c0003 | t0003 | g0205 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01346 | hp2 | a0003 | c0007 | t0005 | g0147 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0361 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0358 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0363 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0115 | EUR | IBS | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0245 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01884 | hp2 | a0003 | c0003 | t0004 | g0338 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01891 | hp1 | a0003 | c0003 | t0003 | g0179 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01891 | hp2 | a0002 | c0005 | t0002 | g0058 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0150 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01978 | hp1 | a0009 | c0030 | t0001 | g0101 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02004 | hp1 | a0002 | c0005 | t0002 | g0151 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02004 | hp2 | a0010 | c0035 | t0002 | g0186 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02015 | hp1 | a0002 | c0014 | t0002 | g0032 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02055 | hp1 | a0002 | c0006 | t0002 | g0060 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02055 | hp2 | a0003 | c0007 | t0005 | g0167 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02083 | hp1 | a0002 | c0005 | t0002 | g0321 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02129 | hp1 | a0002 | c0005 | t0002 | g0159 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0017 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02145 | hp2 | a0003 | c0003 | t0003 | g0336 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02257 | hp1 | a0004 | c0009 | t0008 | g0022 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02258 | hp1 | a0005 | c0010 | t0001 | g0178 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02258 | hp2 | a0002 | c0005 | t0002 | g0341 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02280 | hp1 | a0003 | c0003 | t0006 | g0018 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02280 | hp2 | a0004 | c0008 | t0007 | g0010 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0241 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0127 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02572 | hp1 | a0003 | c0003 | t0003 | g0129 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02572 | hp2 | a0003 | c0034 | t0006 | g0014 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02602 | hp1 | a0006 | c0015 | t0001 | g0234 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0364 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02615 | hp2 | a0003 | c0003 | t0003 | g0027 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02622 | hp1 | a0002 | c0006 | t0002 | g0062 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02622 | hp2 | a0003 | c0003 | t0006 | g0016 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02630 | hp1 | a0001 | c0004 | t0015 | g0025 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02630 | hp2 | a0002 | c0006 | t0002 | g0197 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02647 | hp1 | a0003 | c0003 | t0003 | g0172 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02647 | hp2 | a0002 | c0006 | t0002 | g0064 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02683 | hp2 | a0012 | c0023 | t0002 | g0285 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0204 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02717 | hp1 | a0003 | c0003 | t0004 | g0337 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02717 | hp2 | a0003 | c0003 | t0009 | g0021 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02723 | hp1 | a0003 | c0003 | t0009 | g0020 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02723 | hp2 | a0003 | c0003 | t0003 | g0065 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02809 | hp1 | a0013 | c0033 | t0011 | g0335 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02809 | hp2 | a0003 | c0003 | t0003 | g0195 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02818 | hp1 | a0014 | c0032 | t0003 | g0201 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02818 | hp2 | a0005 | c0010 | t0001 | g0194 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02886 | hp2 | a0004 | c0009 | t0025 | g0028 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02895 | hp1 | a0015 | c0024 | t0002 | g0190 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02896 | hp1 | a0004 | c0008 | t0023 | g0348 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02896 | hp2 | a0003 | c0003 | t0003 | g0346 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02897 | hp1 | a0003 | c0003 | t0003 | g0345 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02922 | hp2 | a0003 | c0003 | t0003 | g0133 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02965 | hp1 | a0003 | c0003 | t0003 | g0173 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02965 | hp2 | a0003 | c0003 | t0011 | g0330 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02970 | hp1 | a0003 | c0003 | t0003 | g0192 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02970 | hp2 | a0002 | c0006 | t0002 | g0061 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0339 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02976 | hp2 | a0016 | c0026 | t0001 | g0331 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03098 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03130 | hp1 | a0004 | c0008 | t0007 | g0010 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03130 | hp2 | a0002 | c0002 | t0010 | g0120 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03139 | hp1 | a0004 | c0008 | t0004 | g0349 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03139 | hp2 | a0004 | c0008 | t0007 | g0029 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03195 | hp1 | a0002 | c0006 | t0002 | g0059 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03225 | hp1 | a0004 | c0029 | t0024 | g0132 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03225 | hp2 | a0003 | c0003 | t0004 | g0242 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03239 | hp1 | a0017 | c0021 | t0001 | g0164 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03453 | hp1 | a0003 | c0003 | t0003 | g0171 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03453 | hp2 | a0003 | c0025 | t0003 | g0240 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03486 | hp1 | a0003 | c0003 | t0003 | g0004 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0128 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03491 | hp2 | a0018 | c0016 | t0001 | g0202 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03516 | hp1 | a0003 | c0003 | t0003 | g0189 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03516 | hp2 | a0003 | c0003 | t0003 | g0196 | AFR | ESN | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03540 | hp1 | a0003 | c0003 | t0014 | g0024 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03540 | hp2 | a0002 | c0002 | t0017 | g0063 | AFR | GWD | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03579 | hp2 | a0003 | c0003 | t0003 | g0340 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0162 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0050 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0174 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0175 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0312 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03834 | hp2 | a0003 | c0003 | t0003 | g0227 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03927 | hp2 | a0002 | c0002 | t0022 | g0031 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0040 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0356 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04115 | hp2 | a0001 | c0004 | t0001 | g0166 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04184 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0176 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0165 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04204 | hp1 | a0003 | c0003 | t0003 | g0238 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0316 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0163 | SAS | STU | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18522 | hp1 | a0002 | c0002 | t0010 | g0066 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18522 | hp2 | a0002 | c0002 | t0013 | g0019 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | CHB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18747 | hp2 | a0002 | c0017 | t0002 | g0148 | EAS | CHB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18939 | hp1 | a0001 | c0013 | t0001 | g0251 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18941 | hp2 | a0001 | c0004 | t0001 | g0154 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18943 | hp2 | a0002 | c0002 | t0019 | g0184 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18944 | hp1 | a0019 | c0027 | t0002 | g0140 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18946 | hp2 | a0003 | c0003 | t0003 | g0228 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18948 | hp1 | a0001 | c0012 | t0001 | g0276 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18948 | hp2 | a0002 | c0005 | t0002 | g0076 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18949 | hp2 | a0002 | c0002 | t0021 | g0089 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18951 | hp2 | a0001 | c0004 | t0001 | g0153 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0139 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18953 | hp1 | a0002 | c0002 | t0020 | g0055 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18954 | hp1 | a0001 | c0013 | t0001 | g0278 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18959 | hp1 | a0001 | c0001 | t0029 | g0288 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18959 | hp2 | a0002 | c0005 | t0002 | g0143 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18960 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18965 | hp1 | a0001 | c0001 | t0026 | g0119 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18979 | hp2 | a0001 | c0012 | t0001 | g0296 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18981 | hp2 | a0001 | c0004 | t0001 | g0155 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18984 | hp2 | a0002 | c0005 | t0002 | g0137 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18989 | hp1 | a0001 | c0004 | t0001 | g0146 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18993 | hp1 | a0002 | c0014 | t0002 | g0210 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18993 | hp2 | a0001 | c0001 | t0030 | g0368 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19007 | hp1 | a0001 | c0019 | t0001 | g0271 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19030 | hp2 | a0004 | c0011 | t0004 | g0036 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19043 | hp1 | a0003 | c0003 | t0016 | g0026 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19056 | hp1 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19060 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19062 | hp1 | a0001 | c0004 | t0001 | g0136 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19070 | hp1 | a0001 | c0004 | t0027 | g0145 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19078 | hp2 | a0020 | c0018 | t0001 | g0160 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0152 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19085 | hp2 | a0002 | c0002 | t0028 | g0279 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19086 | hp2 | a0001 | c0004 | t0001 | g0077 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19091 | hp2 | a0002 | c0005 | t0002 | g0156 | EAS | JPT | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0351 | AFR | YRI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ASW | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20129 | hp2 | a0003 | c0003 | t0003 | g0191 | AFR | ASW | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0069 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0083 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0070 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | TSI | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0161 | SAS | GIH | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | GIH | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02109 | hp2 | a0003 | c0003 | t0003 | g0121 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02486 | hp1 | a0004 | c0011 | t0018 | g0263 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02486 | hp2 | a0003 | c0003 | t0003 | g0200 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02559 | hp1 | a0003 | c0003 | t0006 | g0015 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG02559 | hp2 | a0011 | c0031 | t0003 | g0199 | AFR | ACB | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03471 | hp1 | a0003 | c0003 | t0004 | g0342 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | MSL | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20300 | hp1 | a0003 | c0003 | t0003 | g0170 | AFR | USA | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | USA | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA21309 | hp1 | a0001 | c0028 | t0004 | g0236 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | LWK | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
homoSapiens | chm13v2 | a0006 | c0015 | t0001 | g0213 | REF | REF | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
homoSapiens | grch38p0 | a0003 | c0007 | t0005 | g0149 | REF | REF | ADGRF5_chr6_46847522_46926938 | ADGRF5 | chr6 | 46847522 | 46926938 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46856740 | C | T | 1 | a0007 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3854G>A | p.Arg1285Lys | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/21 | 4104/5761 | 3854/4041 | 1285/1346 | chr6 | 46856740 | |||
chr6:46859336 | A | G | 10 | a0001 a0005 a0006 others(7): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
missense_variant | MODERATE | c.2567T>C | p.Met856Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2817/5761 | 2567/4041 | 856/1346 | chr6 | 46859336 | |||
chr6:46859358 | T | C | 1 | a0019 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.2545A>G | p.Thr849Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2795/5761 | 2545/4041 | 849/1346 | chr6 | 46859358 | |||
chr6:46859466 | C | T | 1 | a0009 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2437G>A | p.Val813Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2687/5761 | 2437/4041 | 813/1346 | chr6 | 46859466 | |||
chr6:46859502 | C | T | 5 | a0002 a0010 a0012 others(2): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
missense_variant | MODERATE | c.2401G>A | p.Val801Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2651/5761 | 2401/4041 | 801/1346 | chr6 | 46859502 | |||
chr6:46863070 | C | T | 1 | a0020 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.2017G>A | p.Val673Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2267/5761 | 2017/4041 | 673/1346 | chr6 | 46863070 | |||
chr6:46866948 | G | A | 15 | a0001 a0002 a0004 others(12): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
missense_variant | MODERATE | c.1811C>T | p.Thr604Met | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 2061/5761 | 1811/4041 | 604/1346 | chr6 | 46866948 | |||
chr6:46867077 | A | G | 1 | a0017 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1682T>C | p.Ile561Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 1932/5761 | 1682/4041 | 561/1346 | chr6 | 46867077 | |||
chr6:46871962 | G | A | 2 | a0011 a0014 |
2 | HG02559.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.1292C>T | p.Ala431Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1542/5761 | 1292/4041 | 431/1346 | chr6 | 46871962 | |||
chr6:46871995 | A | C | 1 | a0015 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1259T>G | p.Ile420Arg | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1509/5761 | 1259/4041 | 420/1346 | chr6 | 46871995 | |||
chr6:46872008 | G | C | 1 | a0014 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1246C>G | p.Pro416Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/21 | 1496/5761 | 1246/4041 | 416/1346 | chr6 | 46872008 | |||
chr6:46878306 | T | A | 1 | a0006 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1136A>T | p.Lys379Met | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/21 | 1386/5761 | 1136/4041 | 379/1346 | chr6 | 46878306 | |||
chr6:46879836 | T | C | 1 | a0013 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1018A>G | p.Ile340Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/21 | 1268/5761 | 1018/4041 | 340/1346 | chr6 | 46879836 | |||
chr6:46881517 | A | G | 1 | a0012 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.752T>C | p.Val251Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/21 | 1002/5761 | 752/4041 | 251/1346 | chr6 | 46881517 | |||
chr6:46882092 | C | T | 1 | a0005 | 2 | HG02258.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.628G>A | p.Gly210Arg | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/21 | 878/5761 | 628/4041 | 210/1346 | chr6 | 46882092 | |||
chr6:46883597 | C | T | 1 | a0008 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.574G>A | p.Ala192Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 824/5761 | 574/4041 | 192/1346 | chr6 | 46883597 | |||
chr6:46888404 | G | A | 1 | a0010 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.259C>T | p.Leu87Phe | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/21 | 509/5761 | 259/4041 | 87/1346 | chr6 | 46888404 | |||
chr6:46900034 | C | T | 1 | a0018 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.152G>A | p.Arg51Gln | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/21 | 402/5761 | 152/4041 | 51/1346 | chr6 | 46900034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46858240 | A | G | 1 | a0001c0019 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.3663T>C | p.Ile1221Ile | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3913/5761 | 3663/4041 | 1221/1346 | chr6 | 46858240 | |||
chr6:46858285 | T | C | 2 | a0004c0011 a0004c0029 |
3 | HG02486.hp1 HG03225.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.3618A>G | p.Pro1206Pro | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3868/5761 | 3618/4041 | 1206/1346 | chr6 | 46858285 | |||
chr6:46858399 | G | A | 1 | a0002c0017 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.3504C>T | p.Asp1168Asp | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3754/5761 | 3504/4041 | 1168/1346 | chr6 | 46858399 | |||
chr6:46858690 | G | A | 1 | a0004c0029 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3213C>T | p.Val1071Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3463/5761 | 3213/4041 | 1071/1346 | chr6 | 46858690 | |||
chr6:46858771 | G | A | 28 | a0001c0001 a0001c0004 a0001c0012 others(25): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.3132C>T | p.Asn1044Asn | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3382/5761 | 3132/4041 | 1044/1346 | chr6 | 46858771 | |||
chr6:46858978 | T | A | 28 | a0001c0001 a0001c0004 a0001c0012 others(25): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.2925A>T | p.Val975Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3175/5761 | 2925/4041 | 975/1346 | chr6 | 46858978 | |||
chr6:46859056 | G | A | 1 | a0001c0028 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2847C>T | p.Gly949Gly | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3097/5761 | 2847/4041 | 949/1346 | chr6 | 46859056 | |||
chr6:46859107 | T | C | 28 | a0001c0001 a0001c0004 a0001c0012 others(25): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.2796A>G | p.Thr932Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 3046/5761 | 2796/4041 | 932/1346 | chr6 | 46859107 | |||
chr6:46859173 | G | A | 28 | a0001c0001 a0001c0004 a0001c0012 others(25): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.2730C>T | p.Ala910Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2980/5761 | 2730/4041 | 910/1346 | chr6 | 46859173 | |||
chr6:46859218 | C | T | 1 | a0003c0025 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.2685G>A | p.Ser895Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2935/5761 | 2685/4041 | 895/1346 | chr6 | 46859218 | |||
chr6:46859242 | A | G | 11 | a0002c0002 a0002c0005 a0002c0006 others(8): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
synonymous_variant | LOW | c.2661T>C | p.Tyr887Tyr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2911/5761 | 2661/4041 | 887/1346 | chr6 | 46859242 | |||
chr6:46859389 | C | T | 28 | a0001c0001 a0001c0004 a0001c0012 others(25): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
synonymous_variant | LOW | c.2514G>A | p.Ser838Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/21 | 2764/5761 | 2514/4041 | 838/1346 | chr6 | 46859389 | |||
chr6:46862900 | G | C | 1 | a0001c0013 | 2 | NA18939.hp1 NA18954.hp1 |
synonymous_variant | LOW | c.2187C>G | p.Leu729Leu | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2437/5761 | 2187/4041 | 729/1346 | chr6 | 46862900 | |||
chr6:46863050 | C | T | 1 | a0001c0012 | 2 | NA18948.hp1 NA18979.hp2 |
synonymous_variant | LOW | c.2037G>A | p.Pro679Pro | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/21 | 2287/5761 | 2037/4041 | 679/1346 | chr6 | 46863050 | |||
chr6:46865076 | G | A | 14 | a0001c0001 a0001c0004 a0001c0012 others(11): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
synonymous_variant | LOW | c.1956C>T | p.Val652Val | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/21 | 2206/5761 | 1956/4041 | 652/1346 | chr6 | 46865076 | |||
chr6:46866998 | G | A | 1 | a0002c0014 | 2 | HG02015.hp1 NA18993.hp1 |
synonymous_variant | LOW | c.1761C>T | p.His587His | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/21 | 2011/5761 | 1761/4041 | 587/1346 | chr6 | 46866998 | |||
chr6:46879885 | G | A | 1 | a0017c0021 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.969C>T | p.Thr323Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/21 | 1219/5761 | 969/4041 | 323/1346 | chr6 | 46879885 | |||
chr6:46883559 | C | T | 1 | a0002c0006 | 7 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.612G>A | p.Ala204Ala | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 862/5761 | 612/4041 | 204/1346 | chr6 | 46883559 | |||
chr6:46883598 | G | A | 1 | a0003c0034 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.573C>T | p.Ser191Ser | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/21 | 823/5761 | 573/4041 | 191/1346 | chr6 | 46883598 | |||
chr6:46888363 | G | A | 26 | a0001c0001 a0001c0012 a0001c0013 others(23): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
synonymous_variant | LOW | c.300C>T | p.Thr100Thr | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/21 | 550/5761 | 300/4041 | 100/1346 | chr6 | 46888363 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46852636 | CA | C | 12 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0011 others(9): Show |
44 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1355delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1355 | chr6 | 46852636 | ||||||
chr6:46852653 | G | A | 1 | a0002c0002t0021 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1339C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1339 | chr6 | 46852653 | ||||||
chr6:46852660 | A | G | 1 | a0002c0002t0020 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1332 | chr6 | 46852660 | ||||||
chr6:46852675 | A | AATCCTTG others(44): Show |
2 | a0003c0003t0011 a0013c0033t0011 |
2 | HG02809.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1316_*1317insCCCA others(47): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1316 | chr6 | 46852675 | ||||||
chr6:46852710 | G | C | 3 | a0003c0003t0011 a0003c0003t0014 a0013c0033t0011 |
3 | HG02809.hp1 HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1282C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1282 | chr6 | 46852710 | ||||||
chr6:46852745 | G | C | 1 | a0004c0029t0024 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1247 | chr6 | 46852745 | ||||||
chr6:46852749 | A | C | 1 | a0004c0029t0024 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1243T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1243 | chr6 | 46852749 | ||||||
chr6:46852772 | C | T | 2 | a0004c0008t0007 a0004c0008t0023 |
4 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1220G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1220 | chr6 | 46852772 | ||||||
chr6:46852887 | G | T | 12 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0011 others(9): Show |
45 | HG00741.hp2 HG01074.hp1 HG01255.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1105C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1105 | chr6 | 46852887 | ||||||
chr6:46852932 | A | G | 1 | a0004c0008t0023 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1060T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 1060 | chr6 | 46852932 | ||||||
chr6:46853162 | G | A | 28 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0029 others(25): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*830C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 830 | chr6 | 46853162 | ||||||
chr6:46853169 | T | C | 1 | a0002c0002t0022 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*823A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 823 | chr6 | 46853169 | ||||||
chr6:46853348 | C | G | 19 | a0001c0001t0002 a0001c0001t0026 a0002c0002t0002 others(16): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*644G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 644 | chr6 | 46853348 | ||||||
chr6:46853419 | A | C | 1 | a0002c0002t0019 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*573T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 573 | chr6 | 46853419 | ||||||
chr6:46853515 | T | C | 1 | a0001c0004t0027 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 477 | chr6 | 46853515 | ||||||
chr6:46853580 | T | C | 20 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0026 others(17): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*412A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 412 | chr6 | 46853580 | ||||||
chr6:46853696 | G | A | 1 | a0002c0002t0028 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 296 | chr6 | 46853696 | ||||||
chr6:46853798 | G | A | 1 | a0001c0001t0029 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*194C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 194 | chr6 | 46853798 | ||||||
chr6:46853900 | C | T | 1 | a0002c0002t0010 | 2 | HG03130.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 92 | chr6 | 46853900 | ||||||
chr6:46853970 | C | T | 2 | a0002c0002t0017 a0004c0011t0018 |
2 | HG02486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 21/21 | 22 | chr6 | 46853970 | ||||||
chr6:46921812 | G | A | 1 | a0001c0001t0030 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15050 | chr6 | 46921812 | ||||||
chr6:46921838 | GAGAACCA others(27): Show |
G | 1 | a0003c0003t0016 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-184_-151delGCCTGA others(28): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15077 | chr6 | 46921838 | ||||||
chr6:46921840 | G | T | 12 | a0001c0001t0001 a0001c0001t0026 a0001c0004t0001 others(9): Show |
77 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-152C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15078 | chr6 | 46921840 | ||||||
chr6:46921884 | C | T | 5 | a0001c0004t0015 a0002c0002t0013 a0003c0003t0009 others(2): Show |
7 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15122 | chr6 | 46921884 | ||||||
chr6:46921897 | C | G | 3 | a0001c0001t0012 a0003c0003t0006 a0003c0034t0006 |
5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-209G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/21 | 15135 | chr6 | 46921897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:46854283 | C | G | 9 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3962-212G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854283 | |||||||
chr6:46854455 | C | G | 334 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(331): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.3962-384G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854455 | |||||||
chr6:46854612 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3962-541T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854612 | |||||||
chr6:46854637 | G | A | 4 | a0004c0008t0004g0349 a0004c0008t0007g0010 a0004c0008t0007g0029 others(1): Show |
5 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3962-566C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854637 | |||||||
chr6:46854669 | A | G | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.3962-598T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854669 | |||||||
chr6:46854709 | C | T | 1 | a0002c0002t0002g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3962-638G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854709 | |||||||
chr6:46854779 | C | A | 1 | a0001c0004t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3962-708G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854779 | |||||||
chr6:46854791 | T | C | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3962-720A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854791 | |||||||
chr6:46854804 | C | T | 1 | a0001c0004t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3962-733G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854804 | |||||||
chr6:46854852 | A | C | 132 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(129): Show |
138 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.3962-781T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854852 | |||||||
chr6:46854900 | G | GA | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3962-830dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854900 | |||||||
chr6:46854917 | G | A | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3962-846C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46854917 | |||||||
chr6:46855014 | G | C | 1 | a0002c0002t0002g0141 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3962-943C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855014 | |||||||
chr6:46855032 | A | C | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3961+942T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855032 | |||||||
chr6:46855132 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0350 a0001c0001t0012g0017 others(6): Show |
10 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3961+842T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855132 | |||||||
chr6:46855191 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3961+783A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855191 | |||||||
chr6:46855232 | A | G | 1 | a0002c0002t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3961+742T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855232 | |||||||
chr6:46855297 | T | C | 1 | a0001c0004t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3961+677A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855297 | |||||||
chr6:46855632 | C | T | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.3961+342G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855632 | |||||||
chr6:46855763 | T | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0297 |
2 | HG02080.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3961+211A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855763 | |||||||
chr6:46855775 | G | T | 9 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3961+199C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855775 | |||||||
chr6:46855795 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3961+179G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855795 | |||||||
chr6:46855952 | G | A | 1 | a0009c0030t0001g0101 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3961+22C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855952 | |||||||
chr6:46855958 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3961+16C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 20/20 | chr6 | 46855958 | |||||||
chr6:46856068 | A | AG | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3877-11dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856068 | |||||||
chr6:46856089 | A | G | 5 | a0002c0002t0002g0007 a0002c0002t0002g0257 a0002c0002t0002g0259 others(2): Show |
6 | HG00423.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.3877-31T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856089 | |||||||
chr6:46856162 | G | A | 2 | a0002c0014t0002g0032 a0002c0014t0002g0210 |
2 | HG02015.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3877-104C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856162 | |||||||
chr6:46856428 | T | A | 136 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(133): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.3876+290A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856428 | |||||||
chr6:46856542 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.3876+176T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856542 | |||||||
chr6:46856711 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
splice_region_variant&intron_variant | LOW | c.3876+7T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 19/20 | chr6 | 46856711 | |||||||
chr6:46856823 | C | T | 4 | a0004c0008t0004g0349 a0004c0008t0007g0010 a0004c0008t0007g0029 others(1): Show |
5 | HG02280.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3816+44G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856823 | |||||||
chr6:46856838 | T | C | 1 | a0002c0005t0002g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3816+29A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856838 | |||||||
chr6:46856860 | C | T | 1 | a0002c0002t0002g0088 | 1 | NA19056.hp2 | splice_region_variant&intron_variant | LOW | c.3816+7G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 18/20 | chr6 | 46856860 | |||||||
chr6:46856913 | G | GA | 9 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.3775-6dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46856913 | |||||||
chr6:46857061 | C | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3775-153G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857061 | |||||||
chr6:46857331 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3775-423C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857331 | |||||||
chr6:46857349 | C | G | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3775-441G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857349 | |||||||
chr6:46857431 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3775-523T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857431 | |||||||
chr6:46857458 | C | T | 1 | a0002c0002t0002g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3775-550G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857458 | |||||||
chr6:46857509 | C | T | 2 | a0003c0003t0003g0192 a0003c0003t0003g0193 |
2 | HG00741.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3775-601G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857509 | |||||||
chr6:46857582 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3774+547C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857582 | |||||||
chr6:46857707 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(167): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.3774+422T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857707 | |||||||
chr6:46857735 | AAGGTCTC others(4): Show |
A | 1 | a0003c0003t0003g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3774+383_3774+393d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857735 | |||||||
chr6:46857748 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3774+381C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857748 | |||||||
chr6:46857760 | T | C | 1 | a0002c0002t0002g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3774+369A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857760 | |||||||
chr6:46857787 | C | CT | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3774+341dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857787 | |||||||
chr6:46857791 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3774+338G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857791 | |||||||
chr6:46857858 | G | A | 139 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(136): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.3774+271C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857858 | |||||||
chr6:46857873 | A | C | 4 | a0003c0003t0003g0227 a0003c0003t0003g0228 a0003c0025t0003g0240 others(1): Show |
4 | HG02572.hp2 HG03453.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3774+256T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857873 | |||||||
chr6:46857895 | G | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.3774+234C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46857895 | |||||||
chr6:46858084 | T | C | 1 | a0002c0006t0002g0062 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3774+45A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 17/20 | chr6 | 46858084 | |||||||
chr6:46859608 | T | C | 1 | a0003c0003t0003g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2380-85A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859608 | |||||||
chr6:46859728 | T | C | 1 | a0001c0001t0002g0364 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2380-205A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859728 | |||||||
chr6:46859773 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2380-250G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859773 | |||||||
chr6:46859817 | C | CTATTT | 4 | a0002c0002t0002g0011 a0002c0002t0002g0351 a0002c0002t0017g0063 others(1): Show |
5 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2380-299_2380-295d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | C | CTATTTTA others(3): Show |
205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.2380-304_2380-295d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | C | CTATTTTA others(8): Show |
31 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0001g0229 others(28): Show |
33 | HG00544.hp1 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.2380-309_2380-295d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | C | CTATTTTA others(11): Show |
1 | a0002c0002t0028g0279 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2380-312_2380-295d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | C | CTATTTTA others(13): Show |
62 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0007 others(59): Show |
65 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.2380-314_2380-295d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | C | CTATTTTA others(18): Show |
6 | a0002c0002t0002g0057 a0002c0002t0002g0092 a0002c0002t0002g0094 others(3): Show |
6 | HG00423.hp1 HG00558.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.2380-319_2380-295d others(27): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859817 | CTATTT | C | 9 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2380-299_2380-295d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859817 | |||||||
chr6:46859821 | T | TTTATTTT others(8): Show |
1 | a0002c0002t0002g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2380-299_2380-298i others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859821 | |||||||
chr6:46859825 | T | TTTTATTT others(3): Show |
3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2380-303_2380-302i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859825 | |||||||
chr6:46859876 | G | A | 139 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(136): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2380-353C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859876 | |||||||
chr6:46859919 | A | G | 1 | a0003c0003t0006g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2380-396T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859919 | |||||||
chr6:46859937 | G | T | 2 | a0002c0002t0002g0108 a0002c0002t0002g0109 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.2380-414C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859937 | |||||||
chr6:46859953 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2380-430T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859953 | |||||||
chr6:46859981 | C | T | 4 | a0003c0003t0003g0065 a0003c0003t0003g0128 a0003c0003t0003g0129 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-458G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46859981 | |||||||
chr6:46860232 | C | G | 1 | a0002c0017t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2379+483G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860232 | |||||||
chr6:46860371 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2379+344G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860371 | |||||||
chr6:46860422 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2379+293C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860422 | |||||||
chr6:46860437 | C | T | 1 | a0003c0003t0004g0242 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2379+278G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860437 | |||||||
chr6:46860599 | A | G | 1 | a0014c0032t0003g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2379+116T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860599 | |||||||
chr6:46860643 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2379+72C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 16/20 | chr6 | 46860643 | |||||||
chr6:46860933 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2200-39T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46860933 | |||||||
chr6:46861058 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2200-164G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861058 | |||||||
chr6:46861099 | A | G | 25 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0051 others(22): Show |
28 | HG00438.hp1 HG00741.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.2200-205T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861099 | |||||||
chr6:46861137 | T | C | 314 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(311): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2200-243A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861137 | |||||||
chr6:46861190 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0350 a0001c0001t0012g0017 others(2): Show |
6 | HG02145.hp1 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2200-296C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861190 | |||||||
chr6:46861305 | G | A | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2200-411C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861305 | |||||||
chr6:46861456 | T | C | 334 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(331): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.2200-562A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861456 | |||||||
chr6:46861484 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2200-590G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861484 | |||||||
chr6:46861509 | AC | A | 5 | a0002c0002t0002g0072 a0002c0002t0002g0073 a0002c0002t0002g0095 others(2): Show |
5 | HG00733.hp1 HG01109.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200-616delG | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861509 | |||||||
chr6:46861558 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2200-664G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861558 | |||||||
chr6:46861618 | C | T | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2200-724G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861618 | |||||||
chr6:46861627 | T | C | 1 | a0003c0003t0009g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2200-733A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861627 | |||||||
chr6:46861642 | C | T | 4 | a0003c0003t0003g0065 a0003c0003t0003g0128 a0003c0003t0003g0129 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200-748G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861642 | |||||||
chr6:46861711 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0047 others(66): Show |
71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.2200-817T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861711 | |||||||
chr6:46861791 | T | A | 2 | a0001c0004t0001g0126 a0001c0004t0001g0135 |
2 | NA18952.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2200-897A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861791 | |||||||
chr6:46861817 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
118 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.2200-923C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861817 | |||||||
chr6:46861891 | T | C | 2 | a0002c0002t0002g0123 a0002c0002t0002g0131 |
2 | HG01167.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2199+997A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46861891 | |||||||
chr6:46862012 | A | T | 2 | a0003c0003t0011g0330 a0013c0033t0011g0335 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2199+876T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862012 | |||||||
chr6:46862079 | T | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2199+809A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862079 | |||||||
chr6:46862115 | G | A | 4 | a0003c0003t0003g0065 a0003c0003t0003g0128 a0003c0003t0003g0129 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2199+773C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862115 | |||||||
chr6:46862199 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2199+689C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862199 | |||||||
chr6:46862253 | T | A | 1 | a0002c0002t0022g0031 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2199+635A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862253 | |||||||
chr6:46862323 | A | G | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2199+565T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862323 | |||||||
chr6:46862358 | T | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0287 |
2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2199+530A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862358 | |||||||
chr6:46862361 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2199+527G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862361 | |||||||
chr6:46862363 | G | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0357 a0001c0001t0001g0358 others(3): Show |
6 | HG00738.hp1 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2199+525C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862363 | |||||||
chr6:46862396 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2199+492C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862396 | |||||||
chr6:46862506 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2199+382A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862506 | |||||||
chr6:46862561 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2199+327A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862561 | |||||||
chr6:46862622 | G | A | 1 | a0004c0011t0018g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2199+266C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862622 | |||||||
chr6:46862637 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2199+251C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862637 | |||||||
chr6:46862703 | C | CT | 11 | a0001c0004t0001g0050 a0002c0002t0002g0072 a0003c0003t0003g0170 others(8): Show |
11 | HG00741.hp2 HG01071.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2199+184dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTT | 31 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0074 others(28): Show |
31 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2199+180_2199+184d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTT | 17 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0086 others(14): Show |
17 | HG01106.hp2 HG01934.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.2199+179_2199+184d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(2): Show |
16 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0046 others(13): Show |
16 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2199+176_2199+184d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(3): Show |
32 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0034 others(29): Show |
33 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.2199+175_2199+184d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(4): Show |
20 | a0002c0002t0002g0035 a0002c0002t0002g0053 a0002c0002t0002g0084 others(17): Show |
20 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.2199+174_2199+184d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(5): Show |
14 | a0002c0002t0002g0007 a0002c0002t0002g0040 a0002c0002t0002g0047 others(11): Show |
14 | HG01168.hp1 HG02055.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.2199+173_2199+184d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(6): Show |
22 | a0002c0002t0002g0007 a0002c0002t0002g0011 a0002c0002t0002g0057 others(19): Show |
23 | HG00408.hp2 HG00423.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2199+172_2199+184d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(7): Show |
17 | a0002c0002t0002g0002 a0002c0002t0002g0083 a0002c0002t0002g0090 others(14): Show |
18 | HG00673.hp2 HG01516.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.2199+171_2199+184d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(8): Show |
8 | a0002c0002t0002g0093 a0002c0002t0002g0220 a0002c0002t0002g0223 others(5): Show |
8 | HG00438.hp2 HG00597.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2199+170_2199+184d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(9): Show |
4 | a0002c0002t0002g0073 a0002c0002t0002g0252 a0002c0002t0002g0334 others(1): Show |
4 | HG00423.hp1 HG00733.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.2199+169_2199+184d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(11): Show |
1 | a0002c0002t0002g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2199+167_2199+184d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | C | CTTTTTTT others(12): Show |
1 | a0002c0002t0002g0254 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2199+166_2199+184d others(21): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | CT | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
46 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.2199+184delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | CTT | C | 84 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(81): Show |
85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.2199+183_2199+184d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862703 | CTTT | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0209 others(6): Show |
10 | HG01515.hp1 HG02630.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.2199+182_2199+184d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862703 | |||||||
chr6:46862711 | T | A | 2 | a0001c0013t0001g0251 a0001c0013t0001g0278 |
2 | NA18939.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2199+177A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862711 | |||||||
chr6:46862754 | T | C | 1 | a0002c0006t0002g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2199+134A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 15/20 | chr6 | 46862754 | |||||||
chr6:46863166 | C | T | 1 | a0001c0001t0001g0344 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1991-70G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863166 | |||||||
chr6:46863230 | A | T | 1 | a0003c0003t0003g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1991-134T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863230 | |||||||
chr6:46863231 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1991-135G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863231 | |||||||
chr6:46863323 | C | T | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1991-227G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863323 | |||||||
chr6:46863452 | G | T | 1 | a0001c0004t0001g0204 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1991-356C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863452 | |||||||
chr6:46863490 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1991-394C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863490 | |||||||
chr6:46863527 | C | T | 1 | a0003c0003t0003g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1991-431G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863527 | |||||||
chr6:46863540 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1991-444A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863540 | |||||||
chr6:46863633 | T | C | 1 | a0003c0003t0003g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1991-537A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863633 | |||||||
chr6:46863655 | T | C | 1 | a0004c0009t0025g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1991-559A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863655 | |||||||
chr6:46863710 | C | T | 2 | a0001c0001t0001g0357 a0001c0001t0001g0358 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1991-614G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863710 | |||||||
chr6:46863759 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1991-663A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863759 | |||||||
chr6:46863776 | A | G | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1991-680T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863776 | |||||||
chr6:46863783 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1991-687T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46863783 | |||||||
chr6:46864035 | T | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1991-939A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864035 | |||||||
chr6:46864082 | A | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+960T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864082 | |||||||
chr6:46864092 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+950C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864092 | |||||||
chr6:46864107 | T | C | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1990+935A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864107 | |||||||
chr6:46864135 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+907G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864135 | |||||||
chr6:46864218 | C | T | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+824G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864218 | |||||||
chr6:46864320 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+722C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864320 | |||||||
chr6:46864361 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+681A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864361 | |||||||
chr6:46864509 | C | G | 1 | a0004c0011t0018g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1990+533G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864509 | |||||||
chr6:46864526 | A | AT | 9 | a0001c0001t0001g0100 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1990+515dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | |||||||
chr6:46864526 | A | ATT | 12 | a0003c0003t0003g0004 a0003c0003t0003g0189 a0003c0003t0003g0191 others(9): Show |
13 | HG01106.hp2 HG01255.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1990+514_1990+515d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | |||||||
chr6:46864526 | AT | A | 26 | a0001c0001t0001g0226 a0001c0001t0001g0261 a0001c0001t0001g0293 others(23): Show |
26 | HG01074.hp1 HG01891.hp1 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.1990+515delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | |||||||
chr6:46864526 | ATT | A | 10 | a0002c0002t0002g0158 a0002c0002t0002g0231 a0002c0002t0002g0246 others(7): Show |
11 | HG02056.hp1 HG02071.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1990+514_1990+515d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | |||||||
chr6:46864526 | ATTT | A | 126 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(123): Show |
132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1990+513_1990+515d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864526 | |||||||
chr6:46864628 | G | A | 3 | a0004c0011t0004g0036 a0004c0011t0018g0263 a0004c0029t0024g0132 |
3 | HG02486.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1990+414C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864628 | |||||||
chr6:46864753 | T | C | 3 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 |
3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1990+289A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864753 | |||||||
chr6:46864799 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+243A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864799 | |||||||
chr6:46864816 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+226T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864816 | |||||||
chr6:46864820 | G | A | 1 | a0008c0022t0001g0300 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1990+222C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864820 | |||||||
chr6:46864825 | A | G | 2 | a0003c0003t0011g0330 a0013c0033t0011g0335 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1990+217T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864825 | |||||||
chr6:46864905 | A | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+137T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46864905 | |||||||
chr6:46865004 | T | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1990+38A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 14/20 | chr6 | 46865004 | |||||||
chr6:46865231 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0168 others(8): Show |
12 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1835-34T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865231 | |||||||
chr6:46865652 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1835-455G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865652 | |||||||
chr6:46865925 | C | T | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1835-728G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865925 | |||||||
chr6:46865935 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1835-738C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865935 | |||||||
chr6:46865958 | A | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1835-761T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865958 | |||||||
chr6:46865974 | A | G | 1 | a0001c0004t0001g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1835-777T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46865974 | |||||||
chr6:46866005 | AT | A | 350 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(347): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.1835-809delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866005 | |||||||
chr6:46866046 | G | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1835-849C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866046 | |||||||
chr6:46866107 | C | A | 136 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(133): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1834+818G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866107 | |||||||
chr6:46866165 | A | T | 1 | a0003c0003t0003g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1834+760T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866165 | |||||||
chr6:46866311 | A | G | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1834+614T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866311 | |||||||
chr6:46866316 | CTT | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1834+607_1834+608d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866316 | |||||||
chr6:46866346 | T | G | 1 | a0002c0002t0002g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1834+579A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866346 | |||||||
chr6:46866393 | G | A | 139 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(136): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1834+532C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866393 | |||||||
chr6:46866444 | G | A | 2 | a0004c0011t0018g0263 a0004c0029t0024g0132 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1834+481C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866444 | |||||||
chr6:46866564 | AT | A | 4 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1834+360delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866564 | |||||||
chr6:46866659 | A | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1834+266T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866659 | |||||||
chr6:46866662 | A | G | 1 | a0001c0001t0001g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1834+263T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866662 | |||||||
chr6:46866699 | T | C | 8 | a0003c0003t0003g0179 a0003c0003t0003g0227 a0003c0003t0003g0228 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1834+226A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866699 | |||||||
chr6:46866704 | A | T | 139 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(136): Show |
146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1834+221T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866704 | |||||||
chr6:46866730 | C | T | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1834+195G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866730 | |||||||
chr6:46866736 | T | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1834+189A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 13/20 | chr6 | 46866736 | |||||||
chr6:46867169 | TG | T | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1622-33delC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867169 | |||||||
chr6:46867467 | A | G | 9 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622-330T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867467 | |||||||
chr6:46867491 | G | C | 4 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-354C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867491 | |||||||
chr6:46867565 | C | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0233 others(8): Show |
13 | HG00609.hp1 NA18939.hp1 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-428G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867565 | |||||||
chr6:46867638 | G | C | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1622-501C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867638 | |||||||
chr6:46867760 | C | T | 4 | a0001c0004t0001g0077 a0001c0004t0001g0150 a0001c0004t0001g0161 others(1): Show |
4 | HG00544.hp1 HG01975.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-623G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867760 | |||||||
chr6:46867794 | TGC | T | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1622-659_1622-658d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867794 | |||||||
chr6:46867941 | T | A | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1622-804A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46867941 | |||||||
chr6:46868017 | T | C | 13 | a0003c0003t0003g0004 a0003c0003t0003g0121 a0003c0003t0003g0189 others(10): Show |
14 | HG00741.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1621+866A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868017 | |||||||
chr6:46868035 | C | A | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1621+848G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868035 | |||||||
chr6:46868669 | G | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1621+214C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868669 | |||||||
chr6:46868785 | T | C | 1 | a0003c0003t0003g0200 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1621+98A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868785 | |||||||
chr6:46868815 | A | G | 1 | a0002c0002t0002g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1621+68T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 12/20 | chr6 | 46868815 | |||||||
chr6:46869109 | C | G | 2 | a0002c0002t0002g0224 a0002c0002t0002g0225 |
2 | HG00408.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1412-17G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869109 | |||||||
chr6:46869140 | A | G | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1412-48T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869140 | |||||||
chr6:46869258 | T | C | 335 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(332): Show |
348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1412-166A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869258 | |||||||
chr6:46869270 | G | A | 4 | a0003c0003t0003g0065 a0003c0003t0003g0128 a0003c0003t0003g0129 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412-178C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869270 | |||||||
chr6:46869468 | C | T | 130 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(127): Show |
136 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1412-376G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869468 | |||||||
chr6:46869653 | C | T | 137 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0003 others(134): Show |
144 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1412-561G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869653 | |||||||
chr6:46869770 | C | T | 3 | a0004c0009t0008g0022 a0004c0009t0008g0023 a0004c0009t0025g0028 |
3 | HG01106.hp2 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1412-678G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869770 | |||||||
chr6:46869812 | G | A | 2 | a0002c0002t0002g0052 a0002c0002t0002g0054 |
2 | NA18951.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1412-720C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869812 | |||||||
chr6:46869832 | A | G | 1 | a0003c0003t0003g0200 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1412-740T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869832 | |||||||
chr6:46869967 | A | G | 6 | a0001c0001t0001g0045 a0001c0004t0001g0162 a0001c0004t0001g0163 others(3): Show |
6 | HG03239.hp1 HG03492.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-875T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46869967 | |||||||
chr6:46870263 | A | C | 312 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(309): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1412-1171T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870263 | |||||||
chr6:46870279 | A | G | 1 | a0002c0002t0002g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1412-1187T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870279 | |||||||
chr6:46870304 | C | T | 2 | a0004c0009t0008g0022 a0004c0009t0008g0023 |
2 | HG01106.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1412-1212G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870304 | |||||||
chr6:46870305 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1412-1213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870305 | |||||||
chr6:46870330 | A | T | 1 | a0001c0019t0001g0271 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1412-1238T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870330 | |||||||
chr6:46870379 | G | A | 1 | a0001c0012t0001g0296 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1412-1287C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870379 | |||||||
chr6:46870390 | C | G | 313 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(310): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.1412-1298G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870390 | |||||||
chr6:46870737 | GCTTAACA others(4): Show |
G | 1 | a0001c0001t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1411+1095_1411+110 others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870737 | |||||||
chr6:46870837 | G | A | 2 | a0003c0003t0011g0330 a0013c0033t0011g0335 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1411+1006C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870837 | |||||||
chr6:46870922 | T | TTG | 345 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(342): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1411+919_1411+920d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870922 | |||||||
chr6:46870957 | T | C | 1 | a0002c0002t0002g0246 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1411+886A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870957 | |||||||
chr6:46870961 | T | C | 1 | a0003c0025t0003g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1411+882A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870961 | |||||||
chr6:46870981 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0272 a0001c0004t0001g0154 |
3 | HG03831.hp1 NA18941.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1411+862T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46870981 | |||||||
chr6:46871026 | C | T | 1 | a0002c0017t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1411+817G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871026 | |||||||
chr6:46871072 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1411+771T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871072 | |||||||
chr6:46871183 | A | G | 147 | a0001c0001t0001g0012 a0001c0001t0001g0350 a0001c0001t0001g0353 others(144): Show |
155 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1411+660T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871183 | |||||||
chr6:46871211 | T | C | 13 | a0003c0003t0003g0004 a0003c0003t0003g0121 a0003c0003t0003g0189 others(10): Show |
14 | HG00741.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1411+632A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871211 | |||||||
chr6:46871325 | A | G | 1 | a0003c0003t0014g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1411+518T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871325 | |||||||
chr6:46871453 | A | G | 3 | a0001c0004t0001g0126 a0001c0004t0001g0127 a0001c0004t0001g0135 |
3 | HG02523.hp1 NA18952.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1411+390T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871453 | |||||||
chr6:46871524 | A | G | 9 | a0002c0002t0002g0245 a0002c0002t0013g0019 a0003c0003t0004g0343 others(6): Show |
10 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1411+319T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871524 | |||||||
chr6:46871571 | C | A | 5 | a0003c0003t0003g0200 a0003c0003t0003g0227 a0003c0003t0009g0020 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411+272G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871571 | |||||||
chr6:46871620 | T | G | 298 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(295): Show |
311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1411+223A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871620 | |||||||
chr6:46871698 | T | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0237 others(18): Show |
23 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1411+145A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871698 | |||||||
chr6:46871725 | A | T | 2 | a0002c0002t0013g0019 a0004c0008t0007g0029 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1411+118T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871725 | |||||||
chr6:46871738 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0310 a0008c0022t0001g0300 |
3 | HG00738.hp2 HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1411+105C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871738 | |||||||
chr6:46871807 | C | G | 1 | a0003c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1411+36G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 11/20 | chr6 | 46871807 | |||||||
chr6:46872021 | G | A | 1 | a0001c0001t0001g0005 | 2 | NA18956.hp1 NA18984.hp1 |
splice_region_variant&intron_variant | LOW | c.1241-8C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872021 | |||||||
chr6:46872085 | A | AT | 6 | a0002c0002t0002g0011 a0002c0002t0002g0241 a0002c0002t0002g0351 others(3): Show |
7 | HG02451.hp1 HG02615.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1241-73dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872085 | |||||||
chr6:46872337 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
118 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1241-324A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872337 | |||||||
chr6:46872369 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1241-356C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872369 | |||||||
chr6:46872646 | G | A | 1 | a0002c0002t0002g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-633C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872646 | |||||||
chr6:46872681 | A | G | 1 | a0002c0002t0002g0087 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1241-668T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872681 | |||||||
chr6:46872709 | A | C | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1241-696T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872709 | |||||||
chr6:46872799 | C | T | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241-786G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872799 | |||||||
chr6:46872875 | C | T | 1 | a0002c0017t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1241-862G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872875 | |||||||
chr6:46872876 | G | A | 1 | a0003c0003t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1241-863C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872876 | |||||||
chr6:46872967 | G | C | 6 | a0001c0001t0001g0350 a0001c0001t0012g0017 a0002c0002t0002g0177 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-954C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46872967 | |||||||
chr6:46873024 | C | T | 15 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0207 others(12): Show |
15 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1241-1011G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873024 | |||||||
chr6:46873101 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0258 others(13): Show |
18 | HG02071.hp2 NA18939.hp1 NA18941.hp1 others(15): Show |
intron_variant | MODIFIER | c.1241-1088A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873101 | |||||||
chr6:46873102 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1241-1089T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873102 | |||||||
chr6:46873119 | C | A | 1 | a0002c0002t0002g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1241-1106G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873119 | |||||||
chr6:46873138 | C | T | 1 | a0003c0003t0003g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1241-1125G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873138 | |||||||
chr6:46873146 | G | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
115 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1241-1133C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873146 | |||||||
chr6:46873296 | G | A | 1 | a0004c0011t0004g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-1283C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873296 | |||||||
chr6:46873569 | T | C | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1241-1556A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873569 | |||||||
chr6:46873630 | C | G | 63 | a0001c0001t0001g0080 a0001c0001t0001g0104 a0001c0001t0001g0111 others(60): Show |
64 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1241-1617G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873630 | |||||||
chr6:46873813 | T | A | 3 | a0002c0002t0002g0011 a0002c0002t0002g0351 a0002c0002t0017g0063 |
4 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-1800A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873813 | |||||||
chr6:46873853 | A | G | 3 | a0001c0001t0001g0350 a0001c0001t0012g0017 a0016c0026t0001g0331 |
3 | HG02145.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1241-1840T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873853 | |||||||
chr6:46873864 | C | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(221): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1241-1851G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873864 | |||||||
chr6:46873980 | C | A | 1 | a0003c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241-1967G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46873980 | |||||||
chr6:46874001 | T | C | 7 | a0002c0006t0002g0059 a0002c0006t0002g0060 a0002c0006t0002g0061 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-1988A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874001 | |||||||
chr6:46874069 | C | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(221): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1241-2056G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874069 | |||||||
chr6:46874132 | T | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | NA18950.hp2 NA18973.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1241-2119A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874132 | |||||||
chr6:46874170 | C | T | 1 | a0003c0003t0003g0228 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1241-2157G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874170 | |||||||
chr6:46874400 | C | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1241-2387G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874400 | |||||||
chr6:46874472 | G | T | 9 | a0003c0003t0003g0004 a0003c0003t0003g0189 a0003c0003t0003g0191 others(6): Show |
10 | HG00741.hp2 HG01255.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-2459C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874472 | |||||||
chr6:46874664 | C | A | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-2651G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874664 | |||||||
chr6:46874714 | T | G | 2 | a0001c0001t0001g0357 a0001c0001t0001g0358 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1241-2701A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874714 | |||||||
chr6:46874732 | G | A | 1 | a0002c0014t0002g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1241-2719C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874732 | |||||||
chr6:46874746 | T | G | 1 | a0001c0001t0026g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1241-2733A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874746 | |||||||
chr6:46874899 | G | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1241-2886C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874899 | |||||||
chr6:46874952 | G | T | 15 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0207 others(12): Show |
15 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1241-2939C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46874952 | |||||||
chr6:46875008 | G | A | 1 | a0003c0003t0003g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1241-2995C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875008 | |||||||
chr6:46875144 | C | T | 1 | a0005c0010t0001g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1240+3058G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875144 | |||||||
chr6:46875154 | T | A | 16 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0207 others(13): Show |
16 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+3048A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875154 | |||||||
chr6:46875197 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1240+3005C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875197 | |||||||
chr6:46875442 | C | T | 1 | a0001c0004t0015g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1240+2760G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875442 | |||||||
chr6:46875981 | C | T | 6 | a0001c0001t0001g0261 a0001c0001t0001g0325 a0001c0001t0001g0326 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+2221G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46875981 | |||||||
chr6:46876015 | G | A | 309 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(306): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1240+2187C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876015 | |||||||
chr6:46876056 | T | A | 1 | a0001c0004t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240+2146A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876056 | |||||||
chr6:46876139 | A | G | 1 | a0002c0002t0002g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1240+2063T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876139 | |||||||
chr6:46876227 | G | T | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+1975C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876227 | |||||||
chr6:46876359 | G | T | 3 | a0002c0002t0002g0248 a0002c0002t0002g0249 a0003c0003t0003g0227 |
3 | HG00280.hp1 HG01070.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240+1843C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876359 | |||||||
chr6:46876585 | G | C | 1 | a0002c0002t0002g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1240+1617C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876585 | |||||||
chr6:46876605 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0344 |
2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1240+1597A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876605 | |||||||
chr6:46876613 | T | C | 1 | a0003c0003t0003g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1240+1589A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876613 | |||||||
chr6:46876689 | G | T | 1 | a0003c0007t0005g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1240+1513C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876689 | |||||||
chr6:46876720 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0344 |
2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1240+1482G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876720 | |||||||
chr6:46876729 | A | G | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1240+1473T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876729 | |||||||
chr6:46876777 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1240+1425C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876777 | |||||||
chr6:46876832 | C | T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240+1370G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876832 | |||||||
chr6:46876841 | A | T | 44 | a0001c0001t0001g0080 a0001c0001t0001g0104 a0001c0001t0001g0111 others(41): Show |
45 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240+1361T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876841 | |||||||
chr6:46876899 | CT | C | 220 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1240+1302delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876899 | |||||||
chr6:46876939 | A | G | 3 | a0001c0001t0001g0350 a0001c0001t0012g0017 a0016c0026t0001g0331 |
3 | HG02145.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1240+1263T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46876939 | |||||||
chr6:46877046 | T | C | 2 | a0003c0003t0009g0020 a0003c0003t0009g0021 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1240+1156A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877046 | |||||||
chr6:46877056 | A | C | 1 | a0002c0002t0002g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240+1146T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877056 | |||||||
chr6:46877094 | A | G | 105 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(102): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1240+1108T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877094 | |||||||
chr6:46877100 | C | A | 1 | a0002c0002t0002g0088 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1240+1102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877100 | |||||||
chr6:46877225 | C | CTCTT | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0292 others(1): Show |
4 | HG00544.hp2 HG01175.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+973_1240+976d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | C | CTCTTTCT others(1): Show |
5 | a0001c0001t0001g0033 a0001c0001t0001g0363 a0002c0002t0002g0034 others(2): Show |
5 | HG01516.hp1 HG03195.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+969_1240+976d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | C | CTCTTTCT others(5): Show |
2 | a0002c0002t0022g0031 a0018c0016t0001g0202 |
2 | HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1240+965_1240+976d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | CTCTT | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0086 a0001c0001t0001g0102 others(10): Show |
13 | HG00597.hp1 HG00621.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240+973_1240+976d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | CTCTTTCT others(1): Show |
C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0168 others(7): Show |
11 | HG00099.hp1 HG00408.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1240+969_1240+976d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | CTCTTTCT others(5): Show |
C | 6 | a0001c0001t0001g0005 a0002c0002t0002g0254 a0002c0002t0002g0255 others(3): Show |
7 | HG01106.hp2 HG02257.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+965_1240+976d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877225 | CTCTTTCT others(9): Show |
C | 2 | a0001c0004t0001g0077 a0007c0020t0001g0332 |
2 | HG00544.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1240+961_1240+976d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877225 | |||||||
chr6:46877236 | T | C | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1240+966A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877236 | |||||||
chr6:46877275 | CTTTCTTT others(7): Show |
C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0211 a0001c0001t0001g0212 others(2): Show |
5 | HG01358.hp2 HG01952.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+913_1240+926d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877275 | |||||||
chr6:46877277 | TTCTTTCT others(9): Show |
T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0303 a0002c0002t0002g0252 others(1): Show |
4 | HG01175.hp1 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+909_1240+924d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877277 | |||||||
chr6:46877279 | CTTTCTT | C | 3 | a0003c0003t0003g0227 a0003c0003t0003g0340 a0003c0003t0014g0024 |
3 | HG03540.hp1 HG03579.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240+917_1240+922d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877279 | |||||||
chr6:46877281 | T | C | 1 | a0003c0025t0003g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240+921A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | |||||||
chr6:46877281 | TTCTTTCT others(3): Show |
T | 1 | a0003c0003t0003g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1240+911_1240+920d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | |||||||
chr6:46877281 | TTCTTTCT others(5): Show |
T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0229 others(12): Show |
15 | HG00639.hp2 HG01361.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240+909_1240+920d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877281 | |||||||
chr6:46877283 | CTT | C | 3 | a0001c0001t0001g0366 a0002c0002t0002g0052 a0002c0002t0019g0184 |
3 | NA18943.hp2 NA18989.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1240+917_1240+918d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877283 | |||||||
chr6:46877283 | CTTTCTT | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0359 a0002c0002t0017g0063 others(2): Show |
5 | HG00323.hp2 HG01975.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+913_1240+918d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877283 | |||||||
chr6:46877285 | T | C | 16 | a0001c0001t0001g0221 a0001c0001t0001g0282 a0001c0001t0001g0333 others(13): Show |
16 | HG00408.hp2 HG00597.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+917A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | |||||||
chr6:46877285 | TTCTTTC | T | 5 | a0001c0001t0001g0013 a0001c0004t0001g0138 a0001c0028t0004g0236 others(2): Show |
6 | HG01261.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+911_1240+916d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | |||||||
chr6:46877285 | TTCTTTCT others(1): Show |
T | 17 | a0001c0001t0001g0209 a0001c0001t0001g0268 a0001c0001t0001g0289 others(14): Show |
18 | HG00099.hp2 HG01168.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+909_1240+916d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877285 | |||||||
chr6:46877287 | CTT | C | 13 | a0001c0001t0001g0203 a0001c0001t0001g0262 a0001c0001t0002g0364 others(10): Show |
13 | HG00423.hp1 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+913_1240+914d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877287 | |||||||
chr6:46877289 | T | C | 48 | a0001c0001t0001g0113 a0001c0001t0001g0221 a0001c0001t0001g0233 others(45): Show |
48 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1240+913A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | |||||||
chr6:46877289 | T | TTCTTTCT others(7): Show |
1 | a0005c0010t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+912_1240+913i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | |||||||
chr6:46877289 | TTC | T | 7 | a0001c0001t0001g0048 a0003c0003t0003g0200 a0004c0008t0007g0010 others(4): Show |
8 | HG02280.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+911_1240+912d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | |||||||
chr6:46877289 | TTCTCTCT others(3): Show |
T | 1 | a0003c0003t0003g0172 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1240+903_1240+912d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877289 | |||||||
chr6:46877291 | C | CTT | 6 | a0001c0004t0001g0154 a0003c0003t0003g0238 a0003c0003t0004g0343 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+910_1240+911i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877291 | |||||||
chr6:46877293 | C | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0030 others(97): Show |
103 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1240+909G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877293 | |||||||
chr6:46877295 | C | CCTTCCTT others(7): Show |
1 | a0003c0025t0003g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1240+906_1240+907i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877295 | |||||||
chr6:46877295 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0333 a0003c0003t0004g0343 |
3 | HG00733.hp2 HG01243.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1240+907G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877295 | |||||||
chr6:46877297 | C | T | 29 | a0001c0001t0001g0099 a0001c0001t0001g0217 a0001c0001t0001g0307 others(26): Show |
29 | HG01071.hp2 HG01168.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1240+905G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877297 | |||||||
chr6:46877298 | T | C | 3 | a0001c0001t0001g0333 a0002c0006t0002g0061 a0003c0025t0003g0240 |
3 | HG00733.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1240+904A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877298 | |||||||
chr6:46877299 | C | CCT | 4 | a0001c0001t0001g0282 a0002c0002t0002g0182 a0002c0002t0002g0224 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+902_1240+903i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | |||||||
chr6:46877299 | C | CCTTCCT | 6 | a0001c0001t0001g0221 a0002c0002t0002g0177 a0002c0002t0002g0312 others(3): Show |
6 | HG00597.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+902_1240+903i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | |||||||
chr6:46877299 | C | CCTTCCTT others(7): Show |
1 | a0001c0001t0012g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1240+902_1240+903i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | |||||||
chr6:46877299 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0286 a0001c0001t0001g0323 others(6): Show |
9 | HG00642.hp2 HG00673.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+903G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877299 | |||||||
chr6:46877301 | C | T | 4 | a0001c0001t0001g0350 a0001c0004t0001g0162 a0002c0002t0002g0117 others(1): Show |
4 | HG02698.hp2 HG03209.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+901G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877301 | |||||||
chr6:46877302 | T | C | 25 | a0001c0001t0001g0113 a0001c0001t0001g0221 a0001c0001t0001g0282 others(22): Show |
25 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1240+900A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877302 | |||||||
chr6:46877303 | C | CCT | 7 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0001g0367 others(4): Show |
7 | HG00609.hp1 HG00741.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877303 | C | CCTTCCT | 4 | a0002c0002t0002g0180 a0002c0002t0002g0183 a0002c0002t0002g0247 others(1): Show |
4 | HG01943.hp1 HG02809.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877303 | C | CCTTCCTT others(3): Show |
6 | a0001c0001t0001g0353 a0002c0002t0002g0040 a0002c0002t0002g0046 others(3): Show |
6 | HG01074.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+898_1240+899i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877303 | C | CCTTCCTT others(15): Show |
1 | a0001c0001t0001g0350 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1240+898_1240+899i others(24): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877303 | C | CTTTCCTT others(19): Show |
1 | a0002c0002t0002g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+898_1240+899i others(28): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877303 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
91 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1240+899G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877303 | |||||||
chr6:46877305 | C | T | 1 | a0001c0004t0001g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+897G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877305 | |||||||
chr6:46877305 | CTT | C | 6 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0004t0001g0136 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+895_1240+896d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877305 | |||||||
chr6:46877306 | T | C | 132 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(129): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1240+896A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCC | 3 | a0001c0001t0001g0355 a0002c0002t0002g0001 a0003c0003t0003g0192 |
3 | HG01123.hp1 HG02970.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCCTTCC | 7 | a0002c0002t0002g0082 a0002c0002t0002g0181 a0002c0002t0002g0219 others(4): Show |
7 | HG01070.hp2 HG01099.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCCTTCCT others(3): Show |
13 | a0001c0001t0001g0226 a0001c0001t0001g0357 a0001c0001t0001g0363 others(10): Show |
14 | HG00438.hp1 HG00738.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCCTTCCT others(7): Show |
7 | a0002c0002t0002g0035 a0002c0002t0002g0187 a0002c0002t0002g0223 others(4): Show |
7 | HG00323.hp1 HG00642.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+895_1240+896i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCTCTCCT others(3): Show |
2 | a0001c0001t0001g0358 a0002c0002t0002g0054 |
2 | HG01515.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCTCTCCT others(7): Show |
2 | a0001c0001t0001g0012 a0002c0002t0002g0053 |
3 | HG01070.hp1 HG01071.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | T | TCTCTTTC others(5): Show |
2 | a0001c0001t0001g0318 a0002c0002t0002g0320 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1240+895_1240+896i others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877306 | TTTCCTTC others(9): Show |
T | 2 | a0002c0002t0002g0117 a0002c0002t0002g0356 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+880_1240+895d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877306 | |||||||
chr6:46877307 | T | C | 44 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0103 others(41): Show |
44 | HG01071.hp2 HG01168.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.1240+895A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877307 | |||||||
chr6:46877309 | CCT | C | 6 | a0001c0001t0001g0207 a0001c0001t0001g0214 a0001c0001t0001g0217 others(3): Show |
6 | HG01496.hp1 HG02602.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+891_1240+892d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877309 | |||||||
chr6:46877310 | C | T | 39 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0103 others(36): Show |
39 | HG01071.hp2 HG01168.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1240+892G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877310 | |||||||
chr6:46877311 | T | C | 8 | a0001c0001t0001g0099 a0001c0001t0026g0119 a0001c0004t0001g0135 others(5): Show |
8 | HG01071.hp2 HG01243.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+891A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877311 | |||||||
chr6:46877314 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0001g0217 a0001c0001t0026g0119 others(7): Show |
10 | HG01071.hp2 HG02647.hp1 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+888G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877314 | |||||||
chr6:46877315 | T | C | 3 | a0001c0001t0001g0217 a0001c0004t0001g0162 a0002c0014t0002g0210 |
3 | HG03654.hp2 NA18990.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1240+887A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877315 | |||||||
chr6:46877318 | C | T | 1 | a0001c0004t0001g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+884G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877318 | |||||||
chr6:46877319 | T | C | 1 | a0001c0004t0001g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+883A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877319 | |||||||
chr6:46877322 | C | T | 2 | a0001c0004t0001g0162 a0003c0003t0003g0172 |
2 | HG02647.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1240+880G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCT | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0157 others(4): Show |
7 | HG01106.hp2 HG01192.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+876_1240+879d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(1): Show |
C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0114 a0001c0001t0026g0119 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+872_1240+879d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(5): Show |
C | 11 | a0001c0001t0001g0116 a0001c0004t0001g0150 a0001c0004t0001g0165 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+868_1240+879d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(9): Show |
C | 19 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0102 others(16): Show |
19 | HG00639.hp1 HG00673.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1240+864_1240+879d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(13): Show |
C | 18 | a0001c0004t0001g0174 a0002c0002t0002g0083 a0002c0002t0002g0091 others(15): Show |
18 | HG01168.hp1 HG01346.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+860_1240+879d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(17): Show |
C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0104 others(26): Show |
31 | HG00558.hp2 HG00621.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.1240+856_1240+879d others(26): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(21): Show |
C | 30 | a0001c0001t0001g0048 a0001c0028t0004g0236 a0002c0002t0002g0057 others(27): Show |
31 | HG00733.hp1 HG01167.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1240+852_1240+879d others(30): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877322 | CTTCTTTC others(25): Show |
C | 2 | a0002c0002t0002g0244 a0003c0003t0003g0027 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+848_1240+879d others(34): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877322 | |||||||
chr6:46877323 | T | C | 3 | a0002c0002t0002g0117 a0002c0002t0002g0356 a0003c0003t0003g0172 |
3 | HG02647.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+879A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877323 | |||||||
chr6:46877326 | T | C | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1240+876A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877326 | |||||||
chr6:46877327 | T | C | 3 | a0002c0002t0002g0117 a0002c0002t0002g0356 a0003c0003t0003g0172 |
3 | HG02647.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1240+875A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877327 | |||||||
chr6:46877330 | T | C | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(169): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.1240+872A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877330 | |||||||
chr6:46877334 | T | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(130): Show |
140 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1240+868A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877334 | |||||||
chr6:46877338 | T | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0030 others(86): Show |
92 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1240+864A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877338 | |||||||
chr6:46877342 | T | C | 19 | a0001c0001t0001g0044 a0001c0001t0001g0103 a0001c0001t0001g0169 others(16): Show |
19 | HG00099.hp2 HG01081.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240+860A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877342 | |||||||
chr6:46877346 | T | C | 22 | a0001c0001t0001g0044 a0001c0001t0001g0284 a0002c0002t0002g0083 others(19): Show |
22 | HG01168.hp1 HG01192.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1240+856A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877346 | |||||||
chr6:46877350 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0080 a0001c0001t0001g0104 others(40): Show |
45 | HG00558.hp2 HG00621.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1240+852A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877350 | |||||||
chr6:46877351 | T | C | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1240+851A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877351 | |||||||
chr6:46877354 | T | C | 17 | a0001c0001t0001g0048 a0001c0028t0004g0236 a0002c0002t0002g0090 others(14): Show |
18 | HG01261.hp1 HG01884.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+848A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877354 | |||||||
chr6:46877357 | CTTTCTTT others(14): Show |
C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0211 others(5): Show |
8 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+824_1240+844d others(23): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877357 | |||||||
chr6:46877358 | T | C | 2 | a0003c0003t0003g0027 a0004c0011t0004g0036 |
2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1240+844A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877358 | |||||||
chr6:46877361 | CTTTCTTT others(10): Show |
C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02129.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1240+824_1240+840d others(19): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877361 | |||||||
chr6:46877362 | T | C | 1 | a0001c0004t0001g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+840A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877362 | |||||||
chr6:46877365 | CTTTCTTT others(6): Show |
C | 7 | a0001c0001t0001g0207 a0001c0001t0001g0214 a0001c0001t0001g0287 others(4): Show |
7 | HG01496.hp1 HG02109.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+824_1240+836d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877365 | |||||||
chr6:46877369 | CTTTCTTT others(2): Show |
C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0293 a0002c0014t0002g0210 |
3 | NA18990.hp2 NA18993.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1240+824_1240+832d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877369 | |||||||
chr6:46877373 | CTTTCT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0049 others(27): Show |
31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1240+824_1240+828d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877373 | |||||||
chr6:46877377 | CT | C | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(133): Show |
143 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1240+824delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877377 | |||||||
chr6:46877378 | T | TTTC | 26 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0169 others(23): Show |
27 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.1240+821_1240+823d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877378 | |||||||
chr6:46877378 | T | TTTCTTTC | 5 | a0001c0001t0001g0044 a0001c0001t0001g0284 a0001c0001t0001g0314 others(2): Show |
5 | HG01192.hp2 HG01258.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+817_1240+823d others(9): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877378 | |||||||
chr6:46877384 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+818A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877384 | |||||||
chr6:46877385 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+817G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877385 | |||||||
chr6:46877487 | G | C | 1 | a0003c0003t0003g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240+715C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877487 | |||||||
chr6:46877536 | A | G | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1240+666T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877536 | |||||||
chr6:46877545 | C | T | 2 | a0002c0002t0002g0141 a0002c0002t0002g0142 |
2 | NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1240+657G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877545 | |||||||
chr6:46877710 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1240+492C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877710 | |||||||
chr6:46877736 | T | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(107): Show |
115 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1240+466A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877736 | |||||||
chr6:46877753 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+449A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877753 | |||||||
chr6:46877759 | G | C | 1 | a0003c0003t0003g0347 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1240+443C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877759 | |||||||
chr6:46877860 | G | T | 2 | a0002c0002t0002g0248 a0002c0002t0002g0249 |
2 | HG00280.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1240+342C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46877860 | |||||||
chr6:46878042 | G | A | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+160C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46878042 | |||||||
chr6:46878052 | A | T | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1240+150T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 10/20 | chr6 | 46878052 | |||||||
chr6:46878489 | A | T | 3 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 |
3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-84T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878489 | |||||||
chr6:46878540 | G | A | 308 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1037-135C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878540 | |||||||
chr6:46878554 | C | G | 2 | a0001c0001t0001g0350 a0001c0001t0012g0017 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1037-149G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878554 | |||||||
chr6:46878657 | A | G | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1037-252T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878657 | |||||||
chr6:46878811 | A | G | 2 | a0001c0001t0001g0350 a0001c0001t0012g0017 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1037-406T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878811 | |||||||
chr6:46878967 | G | A | 1 | a0002c0005t0002g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1037-562C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46878967 | |||||||
chr6:46879034 | C | T | 3 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 |
3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1037-629G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879034 | |||||||
chr6:46879088 | A | G | 220 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1037-683T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879088 | |||||||
chr6:46879306 | G | GA | 7 | a0003c0003t0003g0200 a0003c0003t0006g0015 a0003c0003t0006g0016 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+511_1036+512i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879306 | |||||||
chr6:46879307 | T | C | 7 | a0003c0003t0003g0200 a0003c0003t0006g0015 a0003c0003t0006g0016 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+511A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879307 | |||||||
chr6:46879308 | G | A | 3 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 |
3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036+510C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879308 | |||||||
chr6:46879311 | C | A | 1 | a0001c0001t0001g0333 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1036+507G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879311 | |||||||
chr6:46879329 | C | T | 87 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0041 others(84): Show |
90 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1036+489G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879329 | |||||||
chr6:46879348 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1036+470C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879348 | |||||||
chr6:46879418 | G | A | 6 | a0001c0001t0001g0261 a0001c0001t0001g0325 a0001c0001t0001g0326 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1036+400C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879418 | |||||||
chr6:46879547 | G | C | 275 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1036+271C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879547 | |||||||
chr6:46879564 | C | G | 1 | a0002c0002t0002g0057 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1036+254G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879564 | |||||||
chr6:46879747 | A | G | 2 | a0002c0002t0002g0245 a0015c0024t0002g0190 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1036+71T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879747 | |||||||
chr6:46879764 | T | G | 82 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(79): Show |
87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1036+54A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 9/20 | chr6 | 46879764 | |||||||
chr6:46880289 | C | T | 1 | a0002c0002t0002g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.815-250G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880289 | |||||||
chr6:46880358 | T | TA | 290 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(287): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.815-320dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880358 | |||||||
chr6:46880522 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0207 others(4): Show |
7 | HG01358.hp2 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.815-483G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880522 | |||||||
chr6:46880561 | T | TAAGAGTG others(3): Show |
1 | a0001c0001t0001g0319 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.815-532_815-523dup others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880561 | |||||||
chr6:46880625 | T | G | 2 | a0001c0001t0001g0350 a0001c0001t0012g0017 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.815-586A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880625 | |||||||
chr6:46880708 | T | C | 3 | a0002c0002t0002g0011 a0002c0002t0002g0351 a0002c0002t0017g0063 |
4 | HG02615.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.815-669A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880708 | |||||||
chr6:46880740 | A | T | 1 | a0002c0002t0002g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.815-701T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880740 | |||||||
chr6:46880787 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.814+668A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880787 | |||||||
chr6:46880894 | C | T | 1 | a0003c0003t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.814+561G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880894 | |||||||
chr6:46880924 | C | G | 1 | a0002c0002t0013g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.814+531G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880924 | |||||||
chr6:46880940 | A | T | 2 | a0003c0003t0003g0027 a0003c0034t0006g0014 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.814+515T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46880940 | |||||||
chr6:46881014 | C | T | 8 | a0002c0002t0002g0245 a0002c0002t0002g0248 a0002c0002t0002g0249 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.814+441G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881014 | |||||||
chr6:46881104 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.814+351T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881104 | |||||||
chr6:46881320 | G | T | 18 | a0001c0001t0001g0203 a0001c0001t0001g0237 a0001c0001t0001g0350 others(15): Show |
19 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.814+135C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881320 | |||||||
chr6:46881336 | A | C | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.814+119T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881336 | |||||||
chr6:46881338 | C | A | 7 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.814+117G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 8/20 | chr6 | 46881338 | |||||||
chr6:46881630 | T | C | 3 | a0002c0002t0013g0019 a0003c0003t0004g0343 a0004c0008t0007g0029 |
3 | HG01243.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.672-33A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/20 | chr6 | 46881630 | |||||||
chr6:46881883 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0028t0004g0236 others(8): Show |
13 | HG01261.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.671+166A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 7/20 | chr6 | 46881883 | |||||||
chr6:46882432 | T | G | 315 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(312): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.613-325A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882432 | |||||||
chr6:46882456 | G | A | 1 | a0003c0003t0003g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.613-349C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882456 | |||||||
chr6:46882533 | C | T | 1 | a0006c0015t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.613-426G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882533 | |||||||
chr6:46882536 | T | C | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-429A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882536 | |||||||
chr6:46882543 | C | T | 2 | a0002c0002t0002g0122 a0002c0002t0002g0244 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.613-436G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882543 | |||||||
chr6:46882686 | C | T | 3 | a0002c0005t0002g0076 a0002c0005t0002g0143 a0002c0005t0002g0321 |
3 | HG02083.hp1 NA18948.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.613-579G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882686 | |||||||
chr6:46882969 | T | C | 1 | a0003c0003t0003g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.612+590A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46882969 | |||||||
chr6:46883047 | A | T | 2 | a0005c0010t0001g0178 a0005c0010t0001g0194 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.612+512T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883047 | |||||||
chr6:46883166 | G | A | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.612+393C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883166 | |||||||
chr6:46883179 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.612+380G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883179 | |||||||
chr6:46883185 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.612+374G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883185 | |||||||
chr6:46883219 | A | G | 6 | a0002c0002t0002g0177 a0003c0003t0003g0065 a0003c0003t0003g0128 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+340T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883219 | |||||||
chr6:46883229 | T | C | 1 | a0002c0002t0002g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.612+330A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883229 | |||||||
chr6:46883293 | C | T | 1 | a0002c0002t0021g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612+266G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883293 | |||||||
chr6:46883434 | T | C | 7 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.612+125A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883434 | |||||||
chr6:46883526 | G | A | 1 | a0002c0002t0002g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.612+33C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 6/20 | chr6 | 46883526 | |||||||
chr6:46883774 | C | G | 7 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.506-109G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883774 | |||||||
chr6:46883776 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.506-111G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883776 | |||||||
chr6:46883788 | C | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0028t0004g0236 others(8): Show |
13 | HG01261.hp1 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.506-123G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883788 | |||||||
chr6:46883799 | C | T | 1 | a0004c0011t0004g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-134G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883799 | |||||||
chr6:46883856 | C | T | 5 | a0002c0002t0002g0245 a0002c0002t0013g0019 a0003c0003t0004g0343 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.506-191G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883856 | |||||||
chr6:46883934 | G | T | 1 | a0002c0002t0002g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.505+161C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883934 | |||||||
chr6:46883993 | C | A | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0212 others(2): Show |
5 | HG01358.hp2 HG01952.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 5/20 | chr6 | 46883993 | |||||||
chr6:46884415 | T | A | 1 | a0002c0006t0002g0064 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.329-144A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884415 | |||||||
chr6:46884436 | T | G | 1 | a0003c0007t0003g0188 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.329-165A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884436 | |||||||
chr6:46884456 | C | T | 315 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(312): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.329-185G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884456 | |||||||
chr6:46884685 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.329-414C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884685 | |||||||
chr6:46884801 | G | C | 8 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
8 | HG02071.hp1 HG02135.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-530C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884801 | |||||||
chr6:46884810 | C | T | 2 | a0003c0003t0003g0196 a0003c0003t0003g0336 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.329-539G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46884810 | |||||||
chr6:46885194 | CA | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00621.hp1 HG01346.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.329-924delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | |||||||
chr6:46885194 | CAA | C | 78 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0080 others(75): Show |
80 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.329-925_329-924del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | |||||||
chr6:46885194 | CAAA | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(223): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.329-926_329-924del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885194 | |||||||
chr6:46885240 | G | T | 1 | a0002c0002t0010g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.329-969C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885240 | |||||||
chr6:46885328 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.329-1057G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885328 | |||||||
chr6:46885373 | C | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.329-1102G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885373 | |||||||
chr6:46885495 | G | C | 1 | a0002c0002t0002g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.329-1224C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885495 | |||||||
chr6:46885511 | G | A | 16 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(13): Show |
16 | HG01074.hp1 HG01106.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.329-1240C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885511 | |||||||
chr6:46885513 | T | C | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-1242A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885513 | |||||||
chr6:46885535 | G | T | 1 | a0006c0015t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.329-1264C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885535 | |||||||
chr6:46885683 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.329-1412T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885683 | |||||||
chr6:46885760 | T | C | 1 | a0007c0020t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.329-1489A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885760 | |||||||
chr6:46885849 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.329-1578T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885849 | |||||||
chr6:46885925 | C | A | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.329-1654G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46885925 | |||||||
chr6:46886128 | A | T | 5 | a0001c0001t0001g0268 a0001c0001t0001g0292 a0001c0001t0001g0298 others(2): Show |
5 | HG00544.hp2 HG00609.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-1857T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886128 | |||||||
chr6:46886144 | T | C | 4 | a0002c0002t0002g0083 a0002c0002t0002g0115 a0002c0002t0002g0117 others(1): Show |
4 | HG01516.hp2 HG02698.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-1873A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886144 | |||||||
chr6:46886307 | T | A | 3 | a0001c0004t0015g0025 a0004c0009t0008g0022 a0004c0009t0008g0023 |
3 | HG01106.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.328+2028A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886307 | |||||||
chr6:46886426 | T | C | 13 | a0001c0001t0001g0203 a0001c0001t0001g0237 a0001c0001t0001g0355 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.328+1909A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886426 | |||||||
chr6:46886624 | T | A | 8 | a0003c0003t0003g0004 a0003c0003t0003g0189 a0003c0003t0003g0191 others(5): Show |
9 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+1711A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886624 | |||||||
chr6:46886666 | G | A | 67 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(64): Show |
71 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.328+1669C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886666 | |||||||
chr6:46886670 | G | A | 8 | a0002c0002t0017g0063 a0002c0006t0002g0059 a0002c0006t0002g0060 others(5): Show |
8 | HG00642.hp1 HG02055.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+1665C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886670 | |||||||
chr6:46886893 | A | T | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.328+1442T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46886893 | |||||||
chr6:46887003 | C | T | 315 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(312): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.328+1332G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887003 | |||||||
chr6:46887024 | G | C | 1 | a0002c0002t0002g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328+1311C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887024 | |||||||
chr6:46887224 | A | G | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.328+1111T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887224 | |||||||
chr6:46887358 | G | A | 1 | a0003c0003t0003g0228 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.328+977C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887358 | |||||||
chr6:46887393 | A | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.328+942T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887393 | |||||||
chr6:46887545 | T | G | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+790A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887545 | |||||||
chr6:46887605 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.328+730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887605 | |||||||
chr6:46887798 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.328+537T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887798 | |||||||
chr6:46887903 | T | G | 7 | a0003c0003t0003g0200 a0003c0003t0006g0015 a0003c0003t0006g0016 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+432A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887903 | |||||||
chr6:46887997 | C | CAGGGAAG others(24): Show |
70 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.328+307_328+337dup others(31): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46887997 | |||||||
chr6:46888095 | C | T | 1 | a0004c0011t0004g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.328+240G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888095 | |||||||
chr6:46888119 | C | T | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.328+216G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888119 | |||||||
chr6:46888219 | C | T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.328+116G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 4/20 | chr6 | 46888219 | |||||||
chr6:46888526 | G | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-21C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888526 | |||||||
chr6:46888547 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.158-42C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888547 | |||||||
chr6:46888728 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.158-223C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888728 | |||||||
chr6:46888755 | G | T | 1 | a0001c0004t0001g0077 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.158-250C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888755 | |||||||
chr6:46888844 | T | G | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.158-339A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888844 | |||||||
chr6:46888847 | G | A | 2 | a0002c0002t0002g0108 a0002c0002t0002g0109 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.158-342C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888847 | |||||||
chr6:46888942 | C | G | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-437G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46888942 | |||||||
chr6:46889186 | C | CAT | 10 | a0001c0004t0015g0025 a0002c0002t0002g0241 a0002c0002t0010g0066 others(7): Show |
10 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-683_158-682dup others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | |||||||
chr6:46889186 | CAT | C | 196 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(193): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.158-683_158-682del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | |||||||
chr6:46889186 | CATAT | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0028t0004g0236 others(40): Show |
46 | HG00280.hp1 HG00741.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.158-685_158-682del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889186 | |||||||
chr6:46889209 | T | C | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-704A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889209 | |||||||
chr6:46889213 | T | G | 3 | a0002c0002t0002g0118 a0003c0003t0009g0020 a0003c0003t0009g0021 |
3 | HG02056.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.158-708A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889213 | |||||||
chr6:46889279 | TATATAGT others(29): Show |
T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-810_158-775del others(36): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889279 | |||||||
chr6:46889299 | GTATA | G | 4 | a0002c0002t0002g0083 a0002c0002t0002g0115 a0002c0002t0002g0117 others(1): Show |
4 | HG01516.hp2 HG02698.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-798_158-795del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889299 | |||||||
chr6:46889368 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.158-863T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889368 | |||||||
chr6:46889450 | T | C | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0085 others(10): Show |
13 | HG00639.hp1 HG01496.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-945A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889450 | |||||||
chr6:46889499 | T | G | 100 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(97): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.158-994A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889499 | |||||||
chr6:46889501 | G | T | 6 | a0002c0002t0002g0248 a0002c0002t0002g0249 a0003c0003t0003g0227 others(3): Show |
7 | HG00280.hp1 HG01070.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-996C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889501 | |||||||
chr6:46889552 | A | ATG | 38 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(35): Show |
39 | HG00438.hp1 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.158-1049_158-1048d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | |||||||
chr6:46889552 | A | G | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-1047T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | |||||||
chr6:46889552 | ATG | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0305 a0001c0001t0001g0344 others(1): Show |
4 | NA18945.hp1 NA18952.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1049_158-1048d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889552 | |||||||
chr6:46889566 | GTGTA | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(99): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.158-1065_158-1062d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889566 | |||||||
chr6:46889568 | G | A | 2 | a0001c0004t0001g0154 a0003c0034t0006g0014 |
2 | HG02572.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.158-1063C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889568 | G | GTA | 4 | a0001c0004t0001g0150 a0002c0002t0002g0241 a0002c0005t0002g0151 others(1): Show |
4 | HG01975.hp1 HG02004.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1065_158-1064d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889568 | G | GTGTA | 70 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0080 others(67): Show |
71 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889568 | G | GTGTATA | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0361 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889568 | G | GTGTATAT others(1): Show |
4 | a0002c0002t0002g0177 a0003c0003t0003g0065 a0003c0003t0003g0128 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1064_158-1063i others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889568 | GTATA | G | 7 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(4): Show |
7 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.158-1067_158-1064d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889568 | |||||||
chr6:46889570 | A | G | 89 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0048 others(86): Show |
96 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.158-1065T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889570 | |||||||
chr6:46889572 | A | G | 4 | a0001c0001t0001g0013 a0003c0003t0003g0121 a0003c0003t0003g0196 others(1): Show |
5 | HG02109.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1067T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889572 | |||||||
chr6:46889621 | G | A | 1 | a0002c0014t0002g0032 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.158-1116C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889621 | |||||||
chr6:46889677 | T | C | 16 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0207 others(13): Show |
16 | HG00423.hp1 HG01243.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.158-1172A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889677 | |||||||
chr6:46889767 | AT | A | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1263delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889767 | |||||||
chr6:46889780 | G | GTA | 3 | a0001c0001t0001g0359 a0002c0005t0002g0137 a0003c0003t0016g0026 |
3 | HG00323.hp2 NA18984.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.158-1277_158-1276d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889780 | |||||||
chr6:46889780 | GTA | G | 187 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(184): Show |
196 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.158-1277_158-1276d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889780 | |||||||
chr6:46889782 | A | G | 2 | a0002c0002t0002g0220 a0003c0003t0014g0024 |
2 | HG01109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.158-1277T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889782 | |||||||
chr6:46889784 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.158-1279T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889784 | |||||||
chr6:46889799 | T | C | 4 | a0003c0003t0006g0015 a0003c0003t0006g0016 a0003c0003t0006g0018 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-1294A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889799 | |||||||
chr6:46889940 | T | C | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1435A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889940 | |||||||
chr6:46889992 | T | C | 2 | a0003c0003t0003g0192 a0003c0003t0003g0193 |
2 | HG00741.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.158-1487A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46889992 | |||||||
chr6:46890054 | A | G | 1 | a0002c0005t0002g0156 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.158-1549T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890054 | |||||||
chr6:46890090 | T | C | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-1585A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890090 | |||||||
chr6:46890132 | G | A | 28 | a0001c0001t0001g0221 a0001c0001t0001g0226 a0001c0001t0001g0233 others(25): Show |
31 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.158-1627C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890132 | |||||||
chr6:46890205 | G | C | 73 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(70): Show |
74 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.158-1700C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890205 | |||||||
chr6:46890262 | T | G | 1 | a0002c0002t0002g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.158-1757A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890262 | |||||||
chr6:46890332 | A | T | 1 | a0002c0002t0002g0158 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.158-1827T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890332 | |||||||
chr6:46890344 | T | C | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.158-1839A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890344 | |||||||
chr6:46890489 | G | A | 5 | a0001c0001t0001g0297 a0001c0001t0001g0306 a0001c0001t0001g0324 others(2): Show |
5 | HG00621.hp2 NA18947.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-1984C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890489 | |||||||
chr6:46890843 | A | G | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.158-2338T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890843 | |||||||
chr6:46890856 | T | C | 1 | a0002c0002t0002g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.158-2351A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890856 | |||||||
chr6:46890962 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.158-2457A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890962 | |||||||
chr6:46890972 | G | A | 1 | a0003c0003t0003g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.158-2467C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46890972 | |||||||
chr6:46891250 | C | A | 6 | a0002c0002t0002g0177 a0003c0003t0003g0065 a0003c0003t0003g0128 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-2745G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891250 | |||||||
chr6:46891256 | C | T | 70 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-2751G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891256 | |||||||
chr6:46891306 | T | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2801A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891306 | |||||||
chr6:46891401 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.158-2896G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891401 | |||||||
chr6:46891409 | C | A | 10 | a0001c0001t0001g0272 a0002c0002t0002g0107 a0002c0002t0002g0250 others(7): Show |
10 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-2904G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891409 | |||||||
chr6:46891611 | C | T | 320 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.158-3106G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891611 | |||||||
chr6:46891655 | C | T | 1 | a0002c0002t0002g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158-3150G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891655 | |||||||
chr6:46891721 | G | A | 70 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-3216C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891721 | |||||||
chr6:46891804 | G | A | 1 | a0002c0002t0002g0071 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.158-3299C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46891804 | |||||||
chr6:46892054 | C | T | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.158-3549G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892054 | |||||||
chr6:46892147 | TACACAAA others(5): Show |
T | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-3654_158-3643d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892147 | |||||||
chr6:46892155 | TACAC | T | 4 | a0001c0004t0001g0070 a0003c0007t0003g0188 a0003c0007t0005g0130 others(1): Show |
4 | HG00280.hp2 HG01255.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-3654_158-3651d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACAC | T | 22 | a0001c0001t0001g0169 a0001c0001t0001g0237 a0001c0004t0001g0050 others(19): Show |
22 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.158-3656_158-3651d others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(1): Show |
T | 37 | a0001c0001t0001g0275 a0001c0001t0001g0355 a0001c0004t0001g0069 others(34): Show |
37 | HG00544.hp1 HG01071.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.158-3658_158-3651d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(3): Show |
T | 66 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0114 others(63): Show |
67 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.158-3660_158-3651d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(5): Show |
T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
130 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.158-3662_158-3651d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(7): Show |
T | 76 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0048 others(73): Show |
82 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.158-3664_158-3651d others(16): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(9): Show |
T | 21 | a0001c0001t0001g0113 a0001c0001t0001g0222 a0001c0001t0001g0258 others(18): Show |
21 | HG00280.hp1 HG01070.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.158-3666_158-3651d others(18): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(11): Show |
T | 9 | a0002c0002t0002g0046 a0002c0002t0002g0134 a0002c0002t0002g0208 others(6): Show |
9 | HG01106.hp1 HG01175.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-3668_158-3651d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892155 | TACACACA others(13): Show |
T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | NA18950.hp2 NA18973.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-3670_158-3651d others(22): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892155 | |||||||
chr6:46892167 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.158-3662G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892167 | |||||||
chr6:46892177 | C | T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-3672G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892177 | |||||||
chr6:46892235 | C | T | 73 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(70): Show |
74 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.158-3730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892235 | |||||||
chr6:46892417 | G | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.158-3912C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892417 | |||||||
chr6:46892438 | A | G | 1 | a0004c0008t0023g0348 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.158-3933T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892438 | |||||||
chr6:46892480 | G | A | 2 | a0003c0003t0009g0020 a0003c0003t0009g0021 |
2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.158-3975C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892480 | |||||||
chr6:46892504 | C | T | 3 | a0002c0002t0002g0248 a0002c0002t0002g0249 a0003c0003t0003g0227 |
3 | HG00280.hp1 HG01070.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.158-3999G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892504 | |||||||
chr6:46892575 | C | T | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-4070G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892575 | |||||||
chr6:46892671 | A | T | 70 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 others(67): Show |
71 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-4166T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892671 | |||||||
chr6:46892706 | C | A | 2 | a0002c0002t0002g0047 a0002c0002t0002g0243 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.158-4201G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892706 | |||||||
chr6:46892783 | A | G | 87 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0079 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.158-4278T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892783 | |||||||
chr6:46892790 | T | C | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.158-4285A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892790 | |||||||
chr6:46892901 | C | T | 1 | a0003c0003t0003g0200 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.158-4396G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46892901 | |||||||
chr6:46893053 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158-4548G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893053 | |||||||
chr6:46893055 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.158-4550C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893055 | |||||||
chr6:46893058 | A | AT | 36 | a0001c0001t0001g0048 a0001c0001t0001g0211 a0001c0001t0001g0212 others(33): Show |
37 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.158-4554dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | A | ATT | 6 | a0001c0004t0001g0166 a0002c0006t0002g0060 a0003c0003t0003g0192 others(3): Show |
6 | HG00741.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4555_158-4554d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | A | ATTT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0037 others(5): Show |
9 | HG02155.hp2 HG03579.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-4556_158-4554d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | A | ATTTT | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(61): Show |
68 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.158-4557_158-4554d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | A | ATTTTT | 29 | a0001c0001t0001g0113 a0001c0001t0001g0168 a0001c0001t0001g0169 others(26): Show |
29 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.158-4558_158-4554d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | AT | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0075 others(56): Show |
64 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.158-4554delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | ATT | A | 61 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0074 others(58): Show |
62 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.158-4555_158-4554d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | ATTT | A | 12 | a0001c0004t0015g0025 a0002c0002t0002g0123 a0002c0002t0002g0131 others(9): Show |
12 | HG01106.hp2 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-4556_158-4554d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | ATTTTTTT others(4): Show |
A | 1 | a0007c0020t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.158-4564_158-4554d others(13): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893058 | ATTTTTTT others(6): Show |
A | 5 | a0003c0003t0003g0170 a0003c0003t0003g0171 a0003c0003t0003g0172 others(2): Show |
5 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-4566_158-4554d others(15): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893058 | |||||||
chr6:46893105 | C | T | 3 | a0001c0004t0001g0154 a0001c0004t0027g0145 a0002c0005t0002g0144 |
3 | HG00673.hp2 NA18941.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.158-4600G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893105 | |||||||
chr6:46893165 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.158-4660G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893165 | |||||||
chr6:46893191 | T | G | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.158-4686A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893191 | |||||||
chr6:46893276 | C | T | 6 | a0001c0001t0001g0261 a0001c0001t0001g0325 a0001c0001t0001g0326 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4771G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893276 | |||||||
chr6:46893324 | T | A | 6 | a0002c0002t0002g0177 a0003c0003t0003g0065 a0003c0003t0003g0128 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-4819A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893324 | |||||||
chr6:46893409 | T | G | 1 | a0002c0002t0002g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.158-4904A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893409 | |||||||
chr6:46893433 | G | A | 1 | a0002c0002t0002g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.158-4928C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893433 | |||||||
chr6:46893450 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.158-4945A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893450 | |||||||
chr6:46893615 | C | G | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-5110G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893615 | |||||||
chr6:46893617 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.158-5112C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893617 | |||||||
chr6:46893727 | A | G | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-5222T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893727 | |||||||
chr6:46893999 | G | A | 1 | a0004c0011t0004g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.158-5494C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46893999 | |||||||
chr6:46894053 | C | G | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-5548G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894053 | |||||||
chr6:46894107 | C | T | 4 | a0003c0003t0003g0170 a0003c0003t0003g0171 a0003c0003t0003g0172 others(1): Show |
4 | HG02647.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-5602G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894107 | |||||||
chr6:46894167 | T | A | 3 | a0003c0003t0003g0200 a0011c0031t0003g0199 a0014c0032t0003g0201 |
3 | HG02486.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.158-5662A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894167 | |||||||
chr6:46894303 | C | T | 2 | a0002c0002t0002g0108 a0002c0002t0002g0109 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.157+5726G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894303 | |||||||
chr6:46894950 | G | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+5079C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894950 | |||||||
chr6:46894953 | C | T | 4 | a0002c0002t0002g0177 a0003c0003t0003g0065 a0003c0003t0003g0128 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+5076G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894953 | |||||||
chr6:46894963 | G | A | 4 | a0002c0002t0002g0141 a0002c0002t0002g0142 a0002c0002t0002g0320 others(1): Show |
4 | NA18944.hp1 NA18966.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+5066C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894963 | |||||||
chr6:46894979 | C | T | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+5050G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894979 | |||||||
chr6:46894984 | C | A | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+5045G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46894984 | |||||||
chr6:46895131 | C | T | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+4898G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895131 | |||||||
chr6:46895191 | G | A | 2 | a0003c0007t0003g0188 a0007c0020t0001g0332 |
2 | HG00544.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.157+4838C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895191 | |||||||
chr6:46895223 | G | T | 15 | a0002c0002t0002g0245 a0002c0002t0013g0019 a0003c0003t0003g0004 others(12): Show |
16 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.157+4806C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895223 | |||||||
chr6:46895346 | G | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+4683C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895346 | |||||||
chr6:46895394 | G | A | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.157+4635C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895394 | |||||||
chr6:46895410 | T | A | 7 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(4): Show |
7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+4619A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895410 | |||||||
chr6:46895418 | G | C | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+4611C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895418 | |||||||
chr6:46895519 | C | T | 4 | a0001c0004t0001g0136 a0001c0004t0001g0138 a0001c0004t0001g0139 others(1): Show |
4 | NA18952.hp1 NA18984.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+4510G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895519 | |||||||
chr6:46895523 | C | A | 21 | a0002c0002t0002g0177 a0002c0002t0002g0245 a0002c0002t0013g0019 others(18): Show |
22 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.157+4506G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895523 | |||||||
chr6:46895542 | G | A | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+4487C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895542 | |||||||
chr6:46895688 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.157+4341C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895688 | |||||||
chr6:46895697 | T | C | 1 | a0002c0002t0002g0308 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.157+4332A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895697 | |||||||
chr6:46895782 | G | A | 8 | a0003c0003t0003g0004 a0003c0003t0003g0189 a0003c0003t0003g0191 others(5): Show |
9 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+4247C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895782 | |||||||
chr6:46895815 | T | C | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157+4214A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895815 | |||||||
chr6:46895880 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157+4149C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46895880 | |||||||
chr6:46896099 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157+3930C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896099 | |||||||
chr6:46896132 | C | A | 2 | a0002c0002t0002g0011 a0002c0002t0002g0351 |
3 | HG02615.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+3897G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896132 | |||||||
chr6:46896136 | G | T | 2 | a0001c0001t0001g0221 a0002c0002t0002g0051 |
2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.157+3893C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896136 | |||||||
chr6:46896211 | C | T | 1 | a0003c0003t0003g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+3818G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896211 | |||||||
chr6:46896231 | T | C | 1 | a0003c0003t0016g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+3798A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896231 | |||||||
chr6:46896299 | C | T | 12 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0081 others(9): Show |
15 | HG00741.hp1 HG01099.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+3730G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896299 | |||||||
chr6:46896517 | C | T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+3512G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896517 | |||||||
chr6:46896539 | T | C | 1 | a0003c0003t0003g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157+3490A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896539 | |||||||
chr6:46896549 | T | C | 1 | a0011c0031t0003g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.157+3480A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896549 | |||||||
chr6:46896660 | A | ATG | 144 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0048 others(141): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.157+3367_157+3368d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896660 | |||||||
chr6:46896714 | CAT | C | 4 | a0002c0002t0002g0047 a0002c0002t0002g0243 a0003c0003t0016g0026 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+3313_157+3314d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896714 | |||||||
chr6:46896977 | T | C | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+3052A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46896977 | |||||||
chr6:46897011 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.157+3018C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897011 | |||||||
chr6:46897079 | T | TAC | 5 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0003t0016g0026 others(2): Show |
5 | HG02451.hp1 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+2948_157+2949d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897079 | |||||||
chr6:46897137 | C | CAT | 23 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0079 others(20): Show |
24 | HG00423.hp1 HG00741.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.157+2890_157+2891d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | |||||||
chr6:46897137 | C | CATAT | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2888_157+2891d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | |||||||
chr6:46897137 | CAT | C | 3 | a0001c0004t0001g0135 a0001c0019t0001g0271 a0002c0005t0002g0159 |
3 | HG02129.hp1 NA18952.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.157+2890_157+2891d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897137 | |||||||
chr6:46897145 | T | C | 3 | a0001c0001t0001g0267 a0001c0004t0001g0291 a0004c0011t0004g0036 |
3 | NA18960.hp2 NA19007.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+2884A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TAC | 80 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0041 others(77): Show |
82 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.157+2882_157+2883d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TACACACA others(1): Show |
4 | a0003c0003t0006g0015 a0003c0003t0006g0016 a0003c0003t0006g0018 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+2876_157+2883d others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TATAC | 59 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0222 others(56): Show |
63 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TATACAC | 16 | a0001c0001t0001g0048 a0002c0002t0002g0248 a0003c0003t0003g0004 others(13): Show |
17 | HG00280.hp1 HG01261.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(8): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TATACACA others(1): Show |
11 | a0002c0002t0002g0249 a0003c0003t0003g0200 a0003c0003t0004g0242 others(8): Show |
12 | HG01070.hp2 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+2883_157+2884i others(10): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | T | TATACACA others(3): Show |
2 | a0003c0003t0004g0339 a0003c0003t0009g0021 |
2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.157+2883_157+2884i others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | TAC | T | 4 | a0001c0001t0001g0265 a0002c0002t0002g0011 a0002c0002t0002g0351 others(1): Show |
5 | HG01071.hp2 HG01261.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+2882_157+2883d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897145 | TACACACA others(5): Show |
T | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2872_157+2883d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897145 | |||||||
chr6:46897147 | C | T | 5 | a0001c0001t0001g0350 a0001c0001t0012g0017 a0003c0003t0003g0227 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+2882G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897147 | |||||||
chr6:46897149 | C | T | 3 | a0002c0002t0002g0011 a0002c0002t0002g0351 a0003c0003t0016g0026 |
4 | HG02615.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+2880G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897149 | |||||||
chr6:46897159 | C | T | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2870G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897159 | |||||||
chr6:46897161 | C | T | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2868G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897161 | |||||||
chr6:46897179 | T | C | 1 | a0002c0002t0002g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.157+2850A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897179 | |||||||
chr6:46897198 | T | A | 3 | a0002c0005t0002g0058 a0002c0005t0002g0341 a0004c0009t0025g0028 |
3 | HG01891.hp2 HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.157+2831A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897198 | |||||||
chr6:46897257 | A | G | 4 | a0003c0003t0006g0015 a0003c0003t0006g0016 a0003c0003t0006g0018 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+2772T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897257 | |||||||
chr6:46897523 | T | C | 321 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(318): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.157+2506A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897523 | |||||||
chr6:46897570 | G | A | 2 | a0002c0002t0002g0254 a0002c0002t0002g0255 |
2 | NA18981.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.157+2459C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897570 | |||||||
chr6:46897596 | A | G | 1 | a0016c0026t0001g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.157+2433T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897596 | |||||||
chr6:46897606 | G | A | 2 | a0002c0002t0002g0241 a0003c0025t0003g0240 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.157+2423C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897606 | |||||||
chr6:46897638 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.157+2391C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897638 | |||||||
chr6:46897659 | C | A | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2370G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897659 | |||||||
chr6:46897660 | C | A | 6 | a0001c0004t0015g0025 a0002c0005t0002g0058 a0002c0005t0002g0341 others(3): Show |
6 | HG01106.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+2369G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897660 | |||||||
chr6:46897716 | G | T | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+2313C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897716 | |||||||
chr6:46897823 | C | T | 1 | a0001c0028t0004g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.157+2206G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46897823 | |||||||
chr6:46898021 | T | A | 323 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(320): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.157+2008A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898021 | |||||||
chr6:46898106 | T | G | 5 | a0002c0002t0002g0245 a0002c0002t0013g0019 a0003c0003t0004g0343 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1923A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898106 | |||||||
chr6:46898224 | C | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.157+1805G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898224 | |||||||
chr6:46898718 | T | G | 1 | a0003c0003t0014g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.157+1311A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898718 | |||||||
chr6:46898723 | T | G | 1 | a0001c0004t0001g0204 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.157+1306A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898723 | |||||||
chr6:46898898 | G | A | 1 | a0003c0003t0003g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.157+1131C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898898 | |||||||
chr6:46898914 | C | T | 1 | a0002c0002t0002g0290 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.157+1115G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898914 | |||||||
chr6:46898935 | C | T | 2 | a0002c0005t0002g0058 a0002c0005t0002g0341 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.157+1094G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898935 | |||||||
chr6:46898936 | G | A | 3 | a0002c0002t0002g0241 a0003c0003t0014g0024 a0003c0025t0003g0240 |
3 | HG02451.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.157+1093C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46898936 | |||||||
chr6:46899062 | G | T | 1 | a0002c0005t0002g0143 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157+967C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899062 | |||||||
chr6:46899088 | A | G | 7 | a0003c0003t0003g0200 a0003c0003t0006g0015 a0003c0003t0006g0016 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+941T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899088 | |||||||
chr6:46899145 | C | T | 1 | a0003c0003t0003g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+884G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899145 | |||||||
chr6:46899179 | G | A | 3 | a0002c0002t0013g0019 a0003c0003t0004g0343 a0004c0008t0007g0029 |
3 | HG01243.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.157+850C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899179 | |||||||
chr6:46899240 | CAGA | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG02155.hp2 NA18994.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.157+786_157+788del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899240 | |||||||
chr6:46899309 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.157+720G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899309 | |||||||
chr6:46899344 | G | A | 19 | a0001c0001t0001g0013 a0001c0028t0004g0236 a0003c0003t0003g0196 others(16): Show |
21 | HG01074.hp1 HG01261.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.157+685C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899344 | |||||||
chr6:46899404 | C | T | 1 | a0002c0002t0002g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.157+625G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899404 | |||||||
chr6:46899480 | C | T | 3 | a0001c0001t0001g0359 a0001c0001t0001g0361 a0001c0001t0001g0362 |
3 | HG00099.hp1 HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.157+549G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899480 | |||||||
chr6:46899532 | G | A | 7 | a0003c0003t0003g0004 a0003c0003t0003g0189 a0003c0003t0003g0191 others(4): Show |
8 | HG00741.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+497C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899532 | |||||||
chr6:46899656 | GT | G | 6 | a0001c0004t0015g0025 a0002c0002t0002g0057 a0003c0003t0014g0024 others(3): Show |
6 | HG01106.hp2 HG01255.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+372delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899656 | |||||||
chr6:46899665 | T | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(93): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.157+364A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899665 | |||||||
chr6:46899666 | TTG | T | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(93): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.157+361_157+362del others(2): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899666 | |||||||
chr6:46899746 | G | A | 1 | a0002c0002t0020g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.157+283C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899746 | |||||||
chr6:46899863 | G | T | 1 | a0001c0001t0001g0350 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157+166C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899863 | |||||||
chr6:46899975 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.157+54T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899975 | |||||||
chr6:46899977 | A | G | 1 | a0001c0013t0001g0251 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.157+52T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899977 | |||||||
chr6:46899980 | C | T | 320 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(317): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.157+49G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 3/20 | chr6 | 46899980 | |||||||
chr6:46900109 | T | G | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-26A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900109 | |||||||
chr6:46900161 | TA | T | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(221): Show |
232 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.103-79delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900161 | |||||||
chr6:46900309 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): Show |
100 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.103-226C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900309 | |||||||
chr6:46900376 | C | T | 160 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(157): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.103-293G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900376 | |||||||
chr6:46900462 | G | A | 2 | a0001c0001t0001g0313 a0001c0001t0001g0314 |
2 | HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.103-379C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900462 | |||||||
chr6:46900521 | A | AG | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-439dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46900521 | |||||||
chr6:46901004 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-921G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901004 | |||||||
chr6:46901026 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.103-943A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901026 | |||||||
chr6:46901073 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.103-990C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901073 | |||||||
chr6:46901180 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.103-1097G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901180 | |||||||
chr6:46901330 | C | T | 1 | a0001c0001t0029g0288 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.103-1247G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901330 | |||||||
chr6:46901414 | C | T | 4 | a0003c0003t0003g0347 a0004c0008t0004g0349 a0004c0008t0007g0010 others(1): Show |
5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1331G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901414 | |||||||
chr6:46901429 | C | G | 8 | a0001c0001t0001g0262 a0001c0001t0001g0283 a0001c0001t0001g0284 others(5): Show |
8 | HG00642.hp2 HG01192.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-1346G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901429 | |||||||
chr6:46901727 | G | A | 4 | a0003c0003t0003g0347 a0004c0008t0004g0349 a0004c0008t0007g0010 others(1): Show |
5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1644C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901727 | |||||||
chr6:46901890 | C | T | 4 | a0001c0001t0012g0017 a0003c0003t0006g0015 a0003c0003t0006g0016 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1807G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901890 | |||||||
chr6:46901907 | T | C | 2 | a0002c0002t0002g0122 a0003c0003t0004g0343 |
2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.103-1824A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901907 | |||||||
chr6:46901930 | G | A | 2 | a0001c0001t0012g0017 a0003c0003t0006g0016 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.103-1847C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46901930 | |||||||
chr6:46902081 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.103-1998G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902081 | |||||||
chr6:46902121 | G | A | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-2038C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902121 | |||||||
chr6:46902158 | T | G | 319 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(316): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.103-2075A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902158 | |||||||
chr6:46902297 | A | G | 1 | a0002c0002t0002g0176 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.103-2214T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902297 | |||||||
chr6:46902421 | G | A | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-2338C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902421 | |||||||
chr6:46902591 | C | T | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.103-2508G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902591 | |||||||
chr6:46902746 | A | T | 1 | a0003c0003t0003g0340 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103-2663T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902746 | |||||||
chr6:46902842 | G | A | 1 | a0002c0006t0002g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.103-2759C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902842 | |||||||
chr6:46902861 | T | C | 60 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(57): Show |
61 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.103-2778A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902861 | |||||||
chr6:46902864 | C | G | 4 | a0003c0003t0003g0347 a0004c0008t0004g0349 a0004c0008t0007g0010 others(1): Show |
5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-2781G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902864 | |||||||
chr6:46902904 | C | G | 324 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(321): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.103-2821G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46902904 | |||||||
chr6:46903036 | T | A | 3 | a0002c0002t0002g0122 a0003c0003t0003g0121 a0003c0003t0004g0343 |
3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.103-2953A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903036 | |||||||
chr6:46903087 | C | T | 2 | a0002c0002t0002g0035 a0004c0011t0004g0036 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.103-3004G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903087 | |||||||
chr6:46903147 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.103-3064C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903147 | |||||||
chr6:46903214 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-3131C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903214 | |||||||
chr6:46903245 | C | T | 1 | a0011c0031t0003g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.103-3162G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903245 | |||||||
chr6:46903367 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0315 |
2 | HG01109.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.103-3284C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903367 | |||||||
chr6:46903394 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+3267C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903394 | |||||||
chr6:46903448 | C | T | 155 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(152): Show |
160 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.102+3213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903448 | |||||||
chr6:46903497 | G | A | 1 | a0002c0002t0002g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.102+3164C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903497 | |||||||
chr6:46903527 | T | A | 4 | a0001c0001t0001g0261 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG03041.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+3134A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903527 | |||||||
chr6:46903541 | G | C | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+3120C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903541 | |||||||
chr6:46903589 | G | A | 1 | a0002c0002t0002g0316 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.102+3072C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903589 | |||||||
chr6:46903608 | T | C | 7 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0189 others(4): Show |
8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+3053A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903608 | |||||||
chr6:46903626 | GCCCTGCC others(8): Show |
G | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.102+3020_102+3034d others(17): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903626 | |||||||
chr6:46903669 | T | C | 2 | a0001c0004t0001g0135 a0002c0005t0002g0159 |
2 | HG02129.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.102+2992A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903669 | |||||||
chr6:46903714 | C | A | 3 | a0002c0002t0002g0122 a0003c0003t0003g0121 a0003c0003t0004g0343 |
3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.102+2947G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903714 | |||||||
chr6:46903906 | C | T | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2755G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903906 | |||||||
chr6:46903972 | T | C | 1 | a0020c0018t0001g0160 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.102+2689A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46903972 | |||||||
chr6:46904017 | C | G | 22 | a0002c0002t0002g0177 a0002c0002t0002g0245 a0002c0006t0002g0197 others(19): Show |
23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+2644G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904017 | |||||||
chr6:46904178 | T | C | 319 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(316): Show |
332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.102+2483A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904178 | |||||||
chr6:46904205 | T | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+2456A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904205 | |||||||
chr6:46904248 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.102+2413A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904248 | |||||||
chr6:46904257 | A | T | 1 | a0002c0014t0002g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.102+2404T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904257 | |||||||
chr6:46904305 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.102+2356C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904305 | |||||||
chr6:46904377 | G | T | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102+2284C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904377 | |||||||
chr6:46904624 | G | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(15): Show |
18 | HG02015.hp1 HG02155.hp2 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+2037C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904624 | |||||||
chr6:46904691 | T | A | 1 | a0001c0001t0001g0365 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.102+1970A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904691 | |||||||
chr6:46904728 | C | G | 1 | a0002c0002t0002g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.102+1933G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904728 | |||||||
chr6:46904884 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.102+1777T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904884 | |||||||
chr6:46904902 | G | T | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+1759C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904902 | |||||||
chr6:46904916 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+1745T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46904916 | |||||||
chr6:46905088 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.102+1573A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905088 | |||||||
chr6:46905223 | A | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(13): Show |
16 | HG02015.hp1 HG02155.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+1438T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905223 | |||||||
chr6:46905257 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+1404T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905257 | |||||||
chr6:46905409 | G | A | 1 | a0001c0004t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.102+1252C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905409 | |||||||
chr6:46905647 | T | C | 1 | a0003c0034t0006g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.102+1014A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905647 | |||||||
chr6:46905658 | G | A | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.102+1003C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905658 | |||||||
chr6:46905733 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.102+928G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905733 | |||||||
chr6:46905743 | CAAT | C | 22 | a0002c0002t0002g0177 a0002c0002t0002g0245 a0002c0006t0002g0197 others(19): Show |
23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+915_102+917del others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905743 | |||||||
chr6:46905791 | G | A | 4 | a0003c0003t0003g0179 a0003c0003t0003g0195 a0003c0003t0003g0196 others(1): Show |
4 | HG01891.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+870C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905791 | |||||||
chr6:46905812 | G | T | 22 | a0002c0002t0002g0177 a0002c0002t0002g0245 a0002c0006t0002g0197 others(19): Show |
23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+849C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905812 | |||||||
chr6:46905880 | G | A | 4 | a0002c0002t0002g0177 a0003c0003t0003g0128 a0003c0003t0003g0129 others(1): Show |
4 | HG02145.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+781C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905880 | |||||||
chr6:46905931 | T | C | 37 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(34): Show |
37 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.102+730A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46905931 | |||||||
chr6:46906000 | A | G | 4 | a0002c0002t0002g0122 a0003c0003t0003g0121 a0003c0003t0004g0343 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+661T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906000 | |||||||
chr6:46906371 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.102+290C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906371 | |||||||
chr6:46906544 | A | G | 2 | a0002c0005t0002g0058 a0002c0006t0002g0059 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.102+117T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906544 | |||||||
chr6:46906588 | T | G | 5 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0363 others(2): Show |
5 | HG00738.hp1 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+73A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 2/20 | chr6 | 46906588 | |||||||
chr6:46907030 | G | T | 2 | a0002c0002t0002g0035 a0004c0011t0004g0036 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-24-244C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907030 | |||||||
chr6:46907399 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-24-613A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907399 | |||||||
chr6:46907413 | C | A | 7 | a0001c0001t0012g0017 a0003c0003t0003g0200 a0003c0003t0006g0015 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-627G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907413 | |||||||
chr6:46907434 | G | T | 155 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(152): Show |
160 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-24-648C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907434 | |||||||
chr6:46907480 | C | A | 2 | a0002c0002t0002g0231 a0002c0002t0002g0232 |
2 | HG02071.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-24-694G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907480 | |||||||
chr6:46907521 | T | A | 1 | a0003c0003t0003g0228 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-24-735A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907521 | |||||||
chr6:46907582 | T | C | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-796A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907582 | |||||||
chr6:46907614 | A | T | 1 | a0002c0002t0002g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-24-828T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907614 | |||||||
chr6:46907824 | T | C | 3 | a0002c0002t0002g0047 a0002c0002t0002g0243 a0002c0002t0010g0066 |
3 | HG02109.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-24-1038A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46907824 | |||||||
chr6:46908010 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG01167.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-24-1224C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908010 | |||||||
chr6:46908048 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-24-1262C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908048 | |||||||
chr6:46908183 | G | T | 95 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(92): Show |
99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-24-1397C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908183 | |||||||
chr6:46908348 | G | A | 1 | a0001c0012t0001g0276 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-24-1562C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908348 | |||||||
chr6:46908354 | T | C | 1 | a0002c0002t0010g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-1568A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908354 | |||||||
chr6:46908362 | G | C | 2 | a0001c0001t0001g0319 a0002c0002t0002g0320 |
2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-24-1576C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908362 | |||||||
chr6:46908469 | T | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-1683A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908469 | |||||||
chr6:46908506 | C | T | 95 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(92): Show |
99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-24-1720G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908506 | |||||||
chr6:46908637 | G | C | 3 | a0001c0001t0001g0203 a0003c0003t0003g0238 a0003c0003t0003g0239 |
3 | HG01261.hp1 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-24-1851C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908637 | |||||||
chr6:46908708 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-24-1922T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46908708 | |||||||
chr6:46909032 | T | G | 9 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0189 others(6): Show |
10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24-2246A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909032 | |||||||
chr6:46909138 | A | G | 1 | a0002c0002t0002g0072 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-24-2352T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909138 | |||||||
chr6:46909274 | T | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24-2488A>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909274 | |||||||
chr6:46909514 | C | G | 4 | a0001c0004t0001g0136 a0001c0004t0001g0138 a0001c0004t0001g0139 others(1): Show |
4 | NA18952.hp1 NA18984.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-2728G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909514 | |||||||
chr6:46909609 | C | A | 11 | a0002c0002t0013g0019 a0002c0002t0017g0063 a0002c0005t0002g0058 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-2823G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909609 | |||||||
chr6:46909687 | G | A | 1 | a0003c0003t0003g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24-2901C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909687 | |||||||
chr6:46909835 | G | GT | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-3050dupA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46909835 | |||||||
chr6:46910007 | C | CAATAA | 63 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(60): Show |
64 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.-24-3226_-24-3222d others(7): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | |||||||
chr6:46910007 | C | CAATAAAA others(3): Show |
8 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0002c0002t0002g0107 others(5): Show |
8 | HG00621.hp1 HG01243.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24-3231_-24-3222d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | |||||||
chr6:46910007 | CAATAAAA others(3): Show |
C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(97): Show |
105 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-24-3231_-24-3222d others(12): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910007 | |||||||
chr6:46910056 | G | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0282 |
2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-24-3270C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910056 | |||||||
chr6:46910115 | G | A | 39 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(36): Show |
39 | HG01106.hp1 HG01891.hp2 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.-24-3329C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910115 | |||||||
chr6:46910169 | G | A | 2 | a0001c0001t0001g0275 a0002c0005t0002g0321 |
2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-24-3383C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910169 | |||||||
chr6:46910212 | C | G | 1 | a0001c0004t0001g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-24-3426G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910212 | |||||||
chr6:46910278 | G | T | 1 | a0001c0001t0001g0350 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-24-3492C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910278 | |||||||
chr6:46910474 | G | A | 4 | a0003c0003t0003g0347 a0004c0008t0004g0349 a0004c0008t0007g0010 others(1): Show |
5 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3688C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910474 | |||||||
chr6:46910552 | A | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-3766T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910552 | |||||||
chr6:46910592 | C | T | 2 | a0003c0003t0003g0128 a0003c0003t0003g0336 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-24-3806G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910592 | |||||||
chr6:46910608 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-24-3822G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910608 | |||||||
chr6:46910610 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-24-3824C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910610 | |||||||
chr6:46910656 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-24-3870C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910656 | |||||||
chr6:46910693 | TCAAC | T | 11 | a0002c0002t0013g0019 a0002c0002t0017g0063 a0002c0005t0002g0058 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-3911_-24-3908d others(6): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910693 | |||||||
chr6:46910709 | A | C | 64 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(61): Show |
65 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-24-3923T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910709 | |||||||
chr6:46910713 | A | C | 7 | a0001c0004t0001g0068 a0001c0004t0001g0069 a0001c0004t0001g0070 others(4): Show |
7 | HG01192.hp1 HG02615.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-3927T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910713 | |||||||
chr6:46910766 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-24-3980C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910766 | |||||||
chr6:46910870 | G | T | 7 | a0001c0001t0012g0017 a0003c0003t0003g0200 a0003c0003t0006g0015 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24-4084C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910870 | |||||||
chr6:46910933 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-24-4147A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46910933 | |||||||
chr6:46911027 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-24-4241G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911027 | |||||||
chr6:46911155 | C | A | 1 | a0006c0015t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-24-4369G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911155 | |||||||
chr6:46911263 | T | C | 320 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(317): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-24-4477A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911263 | |||||||
chr6:46911449 | A | T | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-4663T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911449 | |||||||
chr6:46911555 | C | T | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-4769G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911555 | |||||||
chr6:46911699 | C | T | 22 | a0002c0002t0002g0177 a0002c0002t0002g0245 a0002c0006t0002g0197 others(19): Show |
23 | HG00642.hp1 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-24-4913G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911699 | |||||||
chr6:46911910 | A | G | 1 | a0001c0004t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24-5124T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911910 | |||||||
chr6:46911929 | C | T | 1 | a0004c0008t0007g0010 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-24-5143G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46911929 | |||||||
chr6:46912221 | A | G | 4 | a0003c0003t0004g0242 a0003c0003t0004g0337 a0003c0003t0004g0338 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-5435T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912221 | |||||||
chr6:46912400 | G | T | 50 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 others(47): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-24-5614C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912400 | |||||||
chr6:46912556 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-24-5770A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912556 | |||||||
chr6:46912559 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-5773C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912559 | |||||||
chr6:46912672 | G | T | 1 | a0002c0002t0013g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24-5886C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912672 | |||||||
chr6:46912814 | C | A | 1 | a0001c0001t0001g0333 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24-6028G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912814 | |||||||
chr6:46912959 | T | C | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-6173A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46912959 | |||||||
chr6:46913144 | G | C | 3 | a0003c0003t0011g0330 a0013c0033t0011g0335 a0016c0026t0001g0331 |
3 | HG02809.hp1 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-24-6358C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913144 | |||||||
chr6:46913187 | C | T | 1 | a0004c0029t0024g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24-6401G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913187 | |||||||
chr6:46913205 | A | G | 1 | a0001c0004t0001g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24-6419T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913205 | |||||||
chr6:46913223 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-6437G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913223 | |||||||
chr6:46913262 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0267 others(8): Show |
13 | NA18939.hp1 NA18943.hp1 NA18954.hp1 others(10): Show |
intron_variant | MODIFIER | c.-24-6476G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913262 | |||||||
chr6:46913271 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-24-6485C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913271 | |||||||
chr6:46913392 | G | A | 61 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(58): Show |
62 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-24-6606C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913392 | |||||||
chr6:46913409 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0353 a0002c0002t0002g0354 |
4 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-6623C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913409 | |||||||
chr6:46913499 | CA | C | 256 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-24-6714delT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913499 | |||||||
chr6:46913528 | G | C | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-24-6742C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913528 | |||||||
chr6:46913650 | A | C | 2 | a0002c0002t0002g0241 a0003c0025t0003g0240 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-6864T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913650 | |||||||
chr6:46913787 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-24-7001C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913787 | |||||||
chr6:46913856 | A | T | 314 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(311): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-24-7070T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46913856 | |||||||
chr6:46914103 | A | C | 1 | a0001c0012t0001g0276 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-24-7317T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914103 | |||||||
chr6:46914283 | G | A | 1 | a0016c0026t0001g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25+7430C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914283 | |||||||
chr6:46914323 | G | A | 2 | a0002c0002t0002g0122 a0003c0003t0004g0343 |
2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-25+7390C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914323 | |||||||
chr6:46914428 | C | T | 66 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(63): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-25+7285G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914428 | |||||||
chr6:46914429 | A | T | 1 | a0003c0003t0003g0195 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25+7284T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914429 | |||||||
chr6:46914432 | T | C | 1 | a0003c0003t0006g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-25+7281A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914432 | |||||||
chr6:46914656 | G | T | 7 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0189 others(4): Show |
8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+7057C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914656 | |||||||
chr6:46914857 | G | T | 1 | a0002c0002t0002g0131 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-25+6856C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914857 | |||||||
chr6:46914869 | T | G | 95 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(92): Show |
99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-25+6844A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914869 | |||||||
chr6:46914878 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-25+6835G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914878 | |||||||
chr6:46914879 | G | A | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+6834C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914879 | |||||||
chr6:46914908 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-25+6805A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46914908 | |||||||
chr6:46915134 | A | C | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+6579T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915134 | |||||||
chr6:46915135 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-25+6578G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915135 | |||||||
chr6:46915151 | C | T | 3 | a0002c0002t0002g0122 a0003c0003t0003g0121 a0003c0003t0004g0343 |
3 | HG01243.hp2 HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-25+6562G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915151 | |||||||
chr6:46915167 | A | G | 95 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(92): Show |
99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-25+6546T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915167 | |||||||
chr6:46915288 | T | TTAA | 12 | a0001c0001t0001g0116 a0001c0004t0001g0126 a0001c0004t0001g0127 others(9): Show |
12 | HG01496.hp2 HG01516.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25+6422_-25+6424d others(5): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | |||||||
chr6:46915288 | T | TTAATAAT others(2): Show |
19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(16): Show |
22 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.-25+6416_-25+6424d others(11): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | |||||||
chr6:46915288 | T | TTAATAAT others(5): Show |
3 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0003c0003t0003g0189 |
3 | HG02451.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-25+6413_-25+6424d others(14): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | |||||||
chr6:46915288 | T | TTAATAAT others(11): Show |
7 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0191 others(4): Show |
8 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+6407_-25+6424d others(20): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | |||||||
chr6:46915288 | T | TTAATAAT others(14): Show |
1 | a0003c0003t0003g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-25+6404_-25+6424d others(23): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915288 | |||||||
chr6:46915320 | C | G | 9 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0189 others(6): Show |
10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25+6393G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915320 | |||||||
chr6:46915448 | G | C | 1 | a0002c0002t0002g0056 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-25+6265C>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915448 | |||||||
chr6:46915529 | C | T | 1 | a0005c0010t0001g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-25+6184G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915529 | |||||||
chr6:46915552 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-25+6161C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915552 | |||||||
chr6:46915736 | C | G | 1 | a0003c0007t0005g0235 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-25+5977G>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915736 | |||||||
chr6:46915757 | C | T | 9 | a0001c0001t0001g0272 a0001c0019t0001g0271 a0002c0002t0002g0252 others(6): Show |
9 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+5956G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915757 | |||||||
chr6:46915823 | A | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | NA18943.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-25+5890T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915823 | |||||||
chr6:46915980 | G | A | 8 | a0001c0004t0015g0025 a0002c0002t0002g0122 a0003c0003t0003g0121 others(5): Show |
8 | HG01106.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+5733C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46915980 | |||||||
chr6:46916003 | A | C | 1 | a0001c0004t0001g0204 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-25+5710T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916003 | |||||||
chr6:46916042 | C | T | 50 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 others(47): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-25+5671G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916042 | |||||||
chr6:46916097 | A | G | 50 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 others(47): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-25+5616T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916097 | |||||||
chr6:46916259 | G | A | 1 | a0014c0032t0003g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25+5454C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916259 | |||||||
chr6:46916473 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25+5240C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916473 | |||||||
chr6:46916551 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-25+5162A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916551 | |||||||
chr6:46916556 | C | A | 1 | a0001c0004t0015g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-25+5157G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916556 | |||||||
chr6:46916782 | A | T | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+4931T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916782 | |||||||
chr6:46916944 | G | A | 317 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-25+4769C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916944 | |||||||
chr6:46916945 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
90 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-25+4768G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46916945 | |||||||
chr6:46917458 | C | T | 1 | a0003c0007t0005g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-25+4255G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917458 | |||||||
chr6:46917562 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(113): Show |
122 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-25+4151A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917562 | |||||||
chr6:46917597 | G | A | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+4116C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917597 | |||||||
chr6:46917622 | G | A | 1 | a0003c0007t0005g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-25+4091C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46917622 | |||||||
chr6:46918075 | T | G | 1 | a0002c0002t0002g0118 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-25+3638A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918075 | |||||||
chr6:46918106 | G | A | 1 | a0001c0001t0026g0119 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-25+3607C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918106 | |||||||
chr6:46918107 | G | A | 58 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0209 others(55): Show |
61 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-25+3606C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918107 | |||||||
chr6:46918206 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-25+3507A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918206 | |||||||
chr6:46918220 | A | T | 2 | a0001c0001t0001g0357 a0001c0001t0001g0358 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-25+3493T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918220 | |||||||
chr6:46918278 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-25+3435T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918278 | |||||||
chr6:46918420 | T | G | 317 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(314): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-25+3293A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918420 | |||||||
chr6:46918427 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-25+3286G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918427 | |||||||
chr6:46918435 | C | T | 13 | a0002c0002t0002g0177 a0002c0006t0002g0197 a0002c0006t0002g0198 others(10): Show |
13 | HG00642.hp1 HG01255.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+3278G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918435 | |||||||
chr6:46918568 | G | A | 2 | a0001c0004t0001g0174 a0001c0004t0001g0175 |
2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-25+3145C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918568 | |||||||
chr6:46918677 | T | C | 1 | a0007c0020t0001g0332 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-25+3036A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918677 | |||||||
chr6:46918768 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-25+2945C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918768 | |||||||
chr6:46918780 | C | T | 1 | a0002c0002t0002g0180 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-25+2933G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918780 | |||||||
chr6:46918825 | C | T | 2 | a0002c0002t0002g0241 a0003c0025t0003g0240 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-25+2888G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918825 | |||||||
chr6:46918941 | A | G | 1 | a0002c0002t0002g0057 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-25+2772T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918941 | |||||||
chr6:46918953 | A | G | 9 | a0002c0002t0002g0245 a0003c0003t0003g0004 a0003c0003t0003g0189 others(6): Show |
10 | HG00741.hp2 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25+2760T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46918953 | |||||||
chr6:46919000 | T | C | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2713A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919000 | |||||||
chr6:46919037 | G | GTT | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(88): Show |
96 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-25+2674_-25+2675d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919037 | |||||||
chr6:46919067 | G | T | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+2646C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919067 | |||||||
chr6:46919132 | A | G | 1 | a0003c0007t0003g0188 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-25+2581T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919132 | |||||||
chr6:46919215 | T | G | 137 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(134): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-25+2498A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919215 | |||||||
chr6:46919449 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-25+2264T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919449 | |||||||
chr6:46919529 | T | C | 1 | a0001c0001t0001g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-25+2184A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919529 | |||||||
chr6:46919645 | G | T | 2 | a0001c0004t0001g0126 a0001c0004t0001g0127 |
2 | HG02523.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-25+2068C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919645 | |||||||
chr6:46919656 | T | C | 1 | a0002c0002t0002g0177 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25+2057A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919656 | |||||||
chr6:46919674 | C | A | 6 | a0001c0004t0015g0025 a0003c0003t0009g0020 a0003c0003t0009g0021 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+2039G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919674 | |||||||
chr6:46919816 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(90): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-25+1897A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919816 | |||||||
chr6:46919902 | T | G | 1 | a0018c0016t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-25+1811A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919902 | |||||||
chr6:46919965 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-25+1748T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919965 | |||||||
chr6:46919966 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-25+1747C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46919966 | |||||||
chr6:46920177 | C | A | 1 | a0002c0002t0010g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1536G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920177 | |||||||
chr6:46920357 | A | G | 1 | a0003c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-25+1356T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920357 | |||||||
chr6:46920407 | A | T | 6 | a0001c0001t0012g0017 a0003c0003t0003g0027 a0003c0003t0006g0015 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1306T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920407 | |||||||
chr6:46920415 | A | G | 5 | a0001c0001t0012g0017 a0003c0003t0006g0015 a0003c0003t0006g0016 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1298T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920415 | |||||||
chr6:46920500 | C | T | 1 | a0003c0003t0003g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-25+1213G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920500 | |||||||
chr6:46920523 | AT | A | 10 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0180 others(7): Show |
13 | HG01943.hp1 HG02004.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+1189delA | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920523 | |||||||
chr6:46920525 | T | TG | 6 | a0002c0002t0002g0122 a0002c0002t0002g0246 a0002c0002t0002g0247 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1187_-25+1188i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920525 | |||||||
chr6:46920526 | T | G | 122 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(119): Show |
123 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-25+1187A>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | |||||||
chr6:46920526 | T | TG | 56 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0265 others(53): Show |
60 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-25+1186dupC | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | |||||||
chr6:46920526 | T | TGG | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(93): Show |
101 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-25+1185_-25+1186d others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920526 | |||||||
chr6:46920533 | G | GT | 74 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(71): Show |
75 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-25+1179_-25+1180i others(3): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920533 | |||||||
chr6:46920591 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-25+1122C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920591 | |||||||
chr6:46920770 | G | A | 2 | a0001c0001t0001g0124 a0002c0002t0002g0123 |
2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-25+943C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920770 | |||||||
chr6:46920841 | C | T | 6 | a0001c0001t0012g0017 a0003c0003t0003g0027 a0003c0003t0006g0015 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+872G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920841 | |||||||
chr6:46920974 | C | T | 1 | a0005c0010t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25+739G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46920974 | |||||||
chr6:46921033 | A | T | 51 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0030 others(48): Show |
54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.-25+680T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921033 | |||||||
chr6:46921062 | G | T | 1 | a0001c0013t0001g0251 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-25+651C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921062 | |||||||
chr6:46921141 | T | C | 309 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(306): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.-25+572A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921141 | |||||||
chr6:46921173 | G | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(90): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-25+540C>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921173 | |||||||
chr6:46921262 | GCTCC | G | 6 | a0001c0001t0012g0017 a0003c0003t0003g0027 a0003c0003t0006g0015 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+447_-25+450del others(4): Show |
ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921262 | |||||||
chr6:46921277 | T | C | 1 | a0001c0001t0001g0344 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-25+436A>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921277 | |||||||
chr6:46921418 | A | G | 1 | a0002c0002t0002g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-25+295T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921418 | |||||||
chr6:46921426 | G | GA | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(175): Show |
184 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-25+286dupT | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921426 | |||||||
chr6:46921482 | A | T | 76 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0078 others(73): Show |
77 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-25+231T>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921482 | |||||||
chr6:46921485 | C | T | 5 | a0001c0001t0012g0017 a0003c0003t0006g0015 a0003c0003t0006g0016 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+228G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921485 | |||||||
chr6:46921486 | G | A | 6 | a0003c0003t0003g0345 a0003c0003t0003g0346 a0003c0003t0003g0347 others(3): Show |
7 | HG01074.hp1 HG02280.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+227C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921486 | |||||||
chr6:46921547 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0350 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-25+166C>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921547 | |||||||
chr6:46921577 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0037 others(20): Show |
23 | HG02015.hp1 HG02109.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25+136T>C | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921577 | |||||||
chr6:46921584 | C | A | 11 | a0001c0001t0001g0357 a0001c0001t0001g0358 a0001c0001t0001g0359 others(8): Show |
11 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+129G>T | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921584 | |||||||
chr6:46921680 | A | C | 6 | a0001c0001t0012g0017 a0003c0003t0003g0027 a0003c0003t0006g0015 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+33T>G | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921680 | |||||||
chr6:46921691 | C | T | 6 | a0001c0001t0012g0017 a0003c0003t0003g0027 a0003c0003t0006g0015 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+22G>A | ADGRF5 | ENSG00000069122.19 | transcript | ENST00000283296.12 | protein_coding | 1/20 | chr6 | 46921691 |