Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3082 |
| ensemblid | ENSG00000019991.18 |
| hgncid | 4893 |
| symbol | HGF |
| name | hepatocyte growth factor |
| refseq_nuc | NM_000601.6 |
| refseq_prot | NP_000592.3 |
| ensembl_nuc | ENST00000222390.11 |
| ensembl_prot | ENSP00000222390.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 81699010 |
| end | 81770047 |
| strand | - |
| ver | v1.2 |
| region | chr7:81699010-81770047 |
| region5000 | chr7:81694010-81775047 |
| regionname0 | HGF_chr7_81699010_81770047 |
| regionname5000 | HGF_chr7_81694010_81775047 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 728 | 267 | 83 | 46 | 100 | 4 | 32 | 70 | HGF_chr7_81694010_81775047 | HGF | MWVTK others(723): Show |
chr7 | 81694010 | 81775047 |
| a0002 | 0/0 | 728 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | MWVTK others(723): Show |
chr7 | 81694010 | 81775047 |
| a0003 | 0/0 | 728 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | MWVTK others(723): Show |
chr7 | 81694010 | 81775047 |
| a0004 | 0/0 | 728 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | MWVTK others(723): Show |
chr7 | 81694010 | 81775047 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2184 | 225 | 54 | 43 | 93 | 4 | 29 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0002 | 0/0 | 2184 | 33 | 26 | 3 | 1 | 0 | 3 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0004 | 0/0 | 2184 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0005 | 0/0 | 2184 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0007 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0008 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0009 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0001c0011 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0002c0003 | 0/0 | 2184 | 3 | 0 | 2 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0003c0006 | 0/0 | 2184 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 | ||
| a0004c0010 | 0/0 | 2184 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | ATGTG others(2179): Show |
chr7 | 81694010 | 81775047 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5834 | 130 | 21 | 23 | 60 | 3 | 23 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0002 | 1/1 | 5834 | 40 | 3 | 9 | 20 | 1 | 5 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0003 | 0/0 | 5834 | 29 | 8 | 9 | 11 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0004 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0005 | 0/0 | 5832 | 8 | 8 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0006 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0007 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0008 | 0/0 | 5829 | 5 | 5 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5824): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0009 | 0/0 | 5832 | 3 | 3 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0010 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0011 | 0/0 | 5834 | 2 | 0 | 2 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0012 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0013 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0001t0014 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0001 | 0/0 | 5834 | 5 | 2 | 0 | 1 | 0 | 2 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0002 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0003 | 0/0 | 5834 | 5 | 4 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0004 | 0/0 | 5832 | 9 | 9 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0005 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0006 | 0/0 | 5834 | 3 | 1 | 1 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0007 | 0/0 | 5834 | 4 | 3 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0009 | 0/0 | 5832 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5827): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0010 | 0/0 | 5834 | 3 | 3 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0002t0015 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0004t0001 | 0/0 | 5834 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0005t0006 | 0/0 | 5834 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0007t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0008t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0009t0001 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0001c0011t0006 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0002c0003t0001 | 0/0 | 5834 | 3 | 0 | 2 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0003c0006t0001 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| a0004c0010t0003 | 0/0 | 5834 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | AGGCA others(5829): Show |
chr7 | 81694010 | 81775047 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0002g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0002t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0005t0006g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0007t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0009t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0001c0011t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0003c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| a0004c0010t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0100 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01069 | hp1 | a0001 | c0002 | t0006 | g0094 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0186 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0096 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0239 | AMR | PUR | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0062 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02027 | hp2 | a0001 | c0009 | t0001 | g0196 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02055 | hp1 | a0001 | c0002 | t0010 | g0124 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0178 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0247 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02165 | hp2 | a0001 | c0001 | t0013 | g0042 | EAS | CDX | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0250 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0118 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0251 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0245 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02280 | hp2 | a0001 | c0002 | t0007 | g0112 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0093 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0249 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0248 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02630 | hp2 | a0001 | c0002 | t0015 | g0113 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0114 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02809 | hp2 | a0001 | c0011 | t0006 | g0116 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0115 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0122 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0103 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03017 | hp2 | a0003 | c0006 | t0001 | g0172 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03041 | hp1 | a0001 | c0002 | t0010 | g0243 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0077 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0125 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03130 | hp2 | a0001 | c0005 | t0006 | g0007 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0111 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0123 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0253 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03942 | hp1 | a0001 | c0002 | t0006 | g0095 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0117 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18984 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19005 | hp1 | a0001 | c0007 | t0001 | g0084 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19058 | hp2 | a0001 | c0008 | t0001 | g0068 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19240 | hp1 | a0004 | c0010 | t0003 | g0179 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | YRI | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ASW | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0074 | SAS | GIH | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02486 | hp1 | a0001 | c0005 | t0006 | g0007 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0244 | AFR | ACB | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | USA | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0205 | REF | REF | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0194 | REF | REF | HGF_chr7_81694010_81775047 | HGF | chr7 | 81694010 | 81775047 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81705746 | C | T | 1 | a0003 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1765G>A | p.Val589Ile | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 16/18 | 1841/5834 | 1765/2187 | 589/728 | chr7 | 81705746 | |||
| chr7:81729735 | C | T | 1 | a0002 | 3 | HG01175.hp2 HG01361.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.910G>A | p.Glu304Lys | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/18 | 986/5834 | 910/2187 | 304/728 | chr7 | 81729735 | |||
| chr7:81752221 | T | C | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.524A>G | p.Asn175Ser | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/18 | 600/5834 | 524/2187 | 175/728 | chr7 | 81752221 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81705738 | A | G | 1 | a0001c0007 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1773T>C | p.Asp591Asp | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 16/18 | 1849/5834 | 1773/2187 | 591/728 | chr7 | 81705738 | |||
| chr7:81706382 | G | A | 1 | a0001c0004 | 3 | NA18946.hp1 NA18979.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.1662C>T | p.His554His | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/18 | 1738/5834 | 1662/2187 | 554/728 | chr7 | 81706382 | |||
| chr7:81743429 | G | A | 1 | a0001c0008 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.789C>T | p.Pro263Pro | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/18 | 865/5834 | 789/2187 | 263/728 | chr7 | 81743429 | |||
| chr7:81745035 | A | G | 2 | a0001c0005 a0001c0011 |
3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.711T>C | p.His237His | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/18 | 787/5834 | 711/2187 | 237/728 | chr7 | 81745035 | |||
| chr7:81752157 | T | C | 1 | a0001c0009 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.588A>G | p.Val196Val | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/18 | 664/5834 | 588/2187 | 196/728 | chr7 | 81752157 | |||
| chr7:81758726 | T | C | 2 | a0001c0002 a0001c0011 |
34 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(31): Show |
synonymous_variant | LOW | c.333A>G | p.Glu111Glu | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/18 | 409/5834 | 333/2187 | 111/728 | chr7 | 81758726 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81699013 | T | C | 1 | a0001c0001t0011 | 2 | HG00639.hp1 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3568A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3568 | chr7 | 81699013 | ||||||
| chr7:81699165 | A | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(14): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*3416T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3416 | chr7 | 81699165 | ||||||
| chr7:81699477 | C | A | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3104G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 3104 | chr7 | 81699477 | ||||||
| chr7:81699720 | C | T | 1 | a0001c0001t0013 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2861G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2861 | chr7 | 81699720 | ||||||
| chr7:81699848 | A | G | 1 | a0001c0001t0012 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2733T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2733 | chr7 | 81699848 | ||||||
| chr7:81700351 | A | G | 2 | a0001c0001t0010 a0001c0002t0010 |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2230T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2230 | chr7 | 81700351 | ||||||
| chr7:81700549 | C | T | 2 | a0001c0001t0005 a0001c0002t0005 |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2032G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 2032 | chr7 | 81700549 | ||||||
| chr7:81700605 | G | A | 2 | a0001c0001t0010 a0001c0002t0010 |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1976C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1976 | chr7 | 81700605 | ||||||
| chr7:81700666 | TAGG | T | 1 | a0001c0001t0008 | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1912_*1914delCCT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1912 | chr7 | 81700666 | ||||||
| chr7:81700903 | C | A | 3 | a0001c0001t0007 a0001c0002t0007 a0001c0002t0015 |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1678 | chr7 | 81700903 | ||||||
| chr7:81700926 | G | A | 4 | a0001c0001t0006 a0001c0002t0006 a0001c0005t0006 others(1): Show |
8 | HG01069.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1655C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1655 | chr7 | 81700926 | ||||||
| chr7:81700959 | A | G | 2 | a0001c0001t0010 a0001c0002t0010 |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1622 | chr7 | 81700959 | ||||||
| chr7:81701064 | C | G | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(14): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1517G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1517 | chr7 | 81701064 | ||||||
| chr7:81701311 | C | T | 3 | a0001c0001t0003 a0001c0002t0003 a0004c0010t0003 |
35 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1270 | chr7 | 81701311 | ||||||
| chr7:81701547 | C | T | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 others(1): Show |
19 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 1034 | chr7 | 81701547 | ||||||
| chr7:81701601 | T | C | 1 | a0001c0001t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 980 | chr7 | 81701601 | ||||||
| chr7:81702053 | TAA | T | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(4): Show |
28 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*527delTT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 526 | chr7 | 81702053 | ||||||
| chr7:81702069 | G | A | 1 | a0001c0002t0015 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 512 | chr7 | 81702069 | ||||||
| chr7:81702114 | T | C | 1 | a0001c0001t0008 | 5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*467A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 18/18 | 467 | chr7 | 81702114 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:81702835 | G | T | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-78C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702835 | |||||||
| chr7:81702897 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0041 others(11): Show |
15 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.2011-140A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702897 | |||||||
| chr7:81702917 | T | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2011-160A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81702917 | |||||||
| chr7:81703239 | C | CT | 10 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0166 others(7): Show |
10 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2011-483dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703239 | |||||||
| chr7:81703452 | T | C | 1 | a0001c0002t0006g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2011-695A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703452 | |||||||
| chr7:81703677 | T | A | 219 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(216): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2011-920A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703677 | |||||||
| chr7:81703862 | C | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2011-1105G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81703862 | |||||||
| chr7:81704231 | G | A | 3 | a0001c0001t0003g0213 a0001c0001t0003g0228 a0001c0001t0003g0230 |
3 | HG01123.hp2 HG02280.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2010+1159C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704231 | |||||||
| chr7:81704303 | G | A | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010+1087C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704303 | |||||||
| chr7:81704607 | C | T | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2010+783G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704607 | |||||||
| chr7:81704962 | C | T | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2010+428G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81704962 | |||||||
| chr7:81705033 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2010+357C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705033 | |||||||
| chr7:81705208 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2010+182C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705208 | |||||||
| chr7:81705277 | T | C | 2 | a0001c0001t0002g0159 a0001c0001t0002g0188 |
2 | NA18955.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2010+113A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 17/17 | chr7 | 81705277 | |||||||
| chr7:81705870 | TA | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1758-118delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81705870 | |||||||
| chr7:81705870 | TAA | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0044 others(8): Show |
11 | HG00544.hp1 HG01070.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1758-119_1758-118d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81705870 | |||||||
| chr7:81706014 | G | T | 9 | a0001c0001t0005g0098 a0001c0001t0005g0135 a0001c0001t0005g0136 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-261C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706014 | |||||||
| chr7:81706141 | G | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0145 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1757+146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706141 | |||||||
| chr7:81706144 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(75): Show |
80 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1757+143G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 15/17 | chr7 | 81706144 | |||||||
| chr7:81706581 | C | G | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-154G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706581 | |||||||
| chr7:81706602 | A | C | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617-175T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706602 | |||||||
| chr7:81706645 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0151 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1617-218C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706645 | |||||||
| chr7:81706716 | T | G | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-289A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706716 | |||||||
| chr7:81706935 | A | C | 22 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(19): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1616+355T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706935 | |||||||
| chr7:81706949 | C | T | 219 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(216): Show |
230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1616+341G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706949 | |||||||
| chr7:81706974 | G | GA | 22 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(19): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1616+315dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81706974 | |||||||
| chr7:81707068 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1616+222C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707068 | |||||||
| chr7:81707123 | T | C | 28 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1616+167A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707123 | |||||||
| chr7:81707219 | C | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0056 others(6): Show |
9 | HG01074.hp1 HG01952.hp1 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.1616+71G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707219 | |||||||
| chr7:81707268 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0204 |
2 | HG00544.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1616+22T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 14/17 | chr7 | 81707268 | |||||||
| chr7:81707464 | C | T | 1 | a0001c0001t0008g0077 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1542-100G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707464 | |||||||
| chr7:81707490 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1542-126G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707490 | |||||||
| chr7:81707578 | A | C | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1542-214T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707578 | |||||||
| chr7:81707816 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1542-452A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707816 | |||||||
| chr7:81707879 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-515A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707879 | |||||||
| chr7:81707906 | G | T | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-542C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707906 | |||||||
| chr7:81707945 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0207 a0003c0006t0001g0172 |
3 | HG03017.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1542-581T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81707945 | |||||||
| chr7:81708123 | GT | G | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-760delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708123 | |||||||
| chr7:81708130 | A | G | 22 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(19): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1542-766T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708130 | |||||||
| chr7:81708258 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1542-894A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708258 | |||||||
| chr7:81708264 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-900C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708264 | |||||||
| chr7:81708297 | A | G | 1 | a0003c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1542-933T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708297 | |||||||
| chr7:81708310 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1542-946T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708310 | |||||||
| chr7:81708524 | C | CT | 15 | a0001c0001t0001g0106 a0001c0001t0001g0207 a0001c0001t0002g0092 others(12): Show |
15 | HG00639.hp1 HG01099.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1542-1161dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708524 | C | CTT | 26 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG01346.hp1 HG02109.hp2 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.1542-1162_1542-116 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708524 | C | CTTT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(97): Show |
108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1542-1163_1542-116 others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708524 | C | CTTTT | 51 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0029 others(48): Show |
52 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.1542-1164_1542-116 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708524 | C | CTTTTTTT | 7 | a0001c0001t0001g0048 a0001c0001t0008g0028 a0001c0001t0008g0077 others(4): Show |
7 | HG02055.hp1 HG02145.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1542-1167_1542-116 others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708524 | CTTTTTTT | C | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-1167_1542-116 others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708524 | |||||||
| chr7:81708660 | C | G | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1542-1296G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708660 | |||||||
| chr7:81708682 | A | G | 2 | a0001c0002t0007g0239 a0001c0002t0015g0113 |
2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1542-1318T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708682 | |||||||
| chr7:81708875 | C | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0021 others(29): Show |
33 | HG00280.hp2 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.1541+1272G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708875 | |||||||
| chr7:81708956 | A | G | 22 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(19): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1541+1191T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708956 | |||||||
| chr7:81708980 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1541+1167T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81708980 | |||||||
| chr7:81709104 | A | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1541+1043T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709104 | |||||||
| chr7:81709334 | A | G | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+813T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709334 | |||||||
| chr7:81709539 | A | C | 1 | a0001c0002t0003g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1541+608T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709539 | |||||||
| chr7:81709666 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1541+481T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709666 | |||||||
| chr7:81709677 | G | C | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+470C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709677 | |||||||
| chr7:81709689 | A | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1541+458T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709689 | |||||||
| chr7:81709718 | A | C | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1541+429T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709718 | |||||||
| chr7:81709891 | C | T | 9 | a0001c0001t0003g0139 a0001c0001t0003g0214 a0001c0001t0003g0229 others(6): Show |
9 | HG01243.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+256G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709891 | |||||||
| chr7:81709926 | A | G | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1541+221T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709926 | |||||||
| chr7:81709988 | A | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(184): Show |
197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1541+159T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81709988 | |||||||
| chr7:81710031 | A | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0075 |
2 | HG01934.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1541+116T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 13/17 | chr7 | 81710031 | |||||||
| chr7:81710590 | A | G | 22 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(19): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1445-347T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710590 | |||||||
| chr7:81710782 | CATAAT | C | 19 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(16): Show |
19 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1445-544_1445-540d others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710782 | |||||||
| chr7:81710918 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(238): Show |
258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1444+563G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81710918 | |||||||
| chr7:81711191 | G | A | 2 | a0001c0002t0003g0247 a0004c0010t0003g0179 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1444+290C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711191 | |||||||
| chr7:81711199 | C | T | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+282G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711199 | |||||||
| chr7:81711233 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1444+248C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711233 | |||||||
| chr7:81711456 | C | T | 2 | a0001c0001t0002g0091 a0001c0001t0002g0092 |
2 | NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1444+25G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 12/17 | chr7 | 81711456 | |||||||
| chr7:81711678 | C | T | 1 | a0001c0001t0003g0220 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1406-159G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711678 | |||||||
| chr7:81711733 | T | G | 1 | a0001c0001t0002g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1406-214A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711733 | |||||||
| chr7:81711739 | G | A | 1 | a0001c0002t0006g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1406-220C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711739 | |||||||
| chr7:81711746 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1406-227G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711746 | |||||||
| chr7:81711782 | C | A | 1 | a0001c0001t0003g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1406-263G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711782 | |||||||
| chr7:81711788 | C | G | 1 | a0001c0001t0002g0159 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1406-269G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711788 | |||||||
| chr7:81711848 | G | T | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1406-329C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711848 | |||||||
| chr7:81711870 | C | G | 1 | a0001c0011t0006g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1406-351G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711870 | |||||||
| chr7:81711871 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1406-352A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81711871 | |||||||
| chr7:81712210 | C | T | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1406-691G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712210 | |||||||
| chr7:81712221 | A | C | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1406-702T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712221 | |||||||
| chr7:81712339 | C | A | 21 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(18): Show |
21 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1406-820G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712339 | |||||||
| chr7:81712465 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1406-946G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712465 | |||||||
| chr7:81712492 | A | G | 1 | a0001c0001t0013g0042 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1406-973T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712492 | |||||||
| chr7:81712546 | A | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(180): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-1027T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712546 | |||||||
| chr7:81712722 | C | T | 19 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(16): Show |
19 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-1203G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712722 | |||||||
| chr7:81712744 | C | T | 1 | a0001c0001t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1406-1225G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712744 | |||||||
| chr7:81712873 | G | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1406-1354C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81712873 | |||||||
| chr7:81713011 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1406-1492C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713011 | |||||||
| chr7:81713023 | C | A | 2 | a0001c0001t0001g0058 a0001c0008t0001g0068 |
2 | NA18982.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1406-1504G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713023 | |||||||
| chr7:81713298 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1406-1779C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713298 | |||||||
| chr7:81713537 | C | CA | 208 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(205): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1406-2019dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713537 | |||||||
| chr7:81713631 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1406-2112G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713631 | |||||||
| chr7:81713692 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1406-2173C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713692 | |||||||
| chr7:81713777 | T | C | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(180): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-2258A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713777 | |||||||
| chr7:81713858 | T | A | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1406-2339A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713858 | |||||||
| chr7:81713890 | T | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(180): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1406-2371A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713890 | |||||||
| chr7:81713989 | C | CGT | 23 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0090 others(20): Show |
26 | HG00609.hp2 HG00733.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1406-2472_1406-247 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | C | CGTGT | 3 | a0001c0001t0001g0164 a0001c0001t0002g0010 a0001c0001t0002g0177 |
3 | HG02015.hp2 HG02559.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1406-2474_1406-247 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | CGT | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1406-2472_1406-247 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | CGTGT | C | 9 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0224 others(6): Show |
9 | HG02145.hp2 HG02615.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-2474_1406-247 others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | CGTGTGT | C | 4 | a0001c0001t0001g0009 a0001c0002t0001g0110 a0002c0003t0001g0015 others(1): Show |
5 | HG00280.hp2 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1406-2476_1406-247 others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0009g0102 a0001c0001t0009g0103 a0001c0001t0010g0178 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-2478_1406-247 others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713989 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0132 |
3 | HG00280.hp1 HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1406-2482_1406-247 others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713989 | |||||||
| chr7:81713991 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0082 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1406-2472A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713991 | |||||||
| chr7:81713992 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1406-2473C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81713992 | |||||||
| chr7:81714148 | G | A | 3 | a0001c0001t0002g0130 a0001c0001t0002g0147 a0001c0001t0002g0183 |
3 | HG00642.hp2 HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1406-2629C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714148 | |||||||
| chr7:81714199 | C | T | 7 | a0001c0001t0001g0048 a0001c0001t0006g0012 a0001c0002t0006g0093 others(4): Show |
9 | HG01069.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1406-2680G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714199 | |||||||
| chr7:81714251 | T | C | 1 | a0001c0002t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1406-2732A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714251 | |||||||
| chr7:81714346 | T | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1406-2827A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714346 | |||||||
| chr7:81714703 | TA | T | 8 | a0001c0001t0001g0158 a0001c0001t0002g0089 a0001c0001t0002g0197 others(5): Show |
8 | HG00558.hp1 HG00733.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1405+2528delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81714703 | |||||||
| chr7:81715327 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+1905T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715327 | |||||||
| chr7:81715359 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1405+1873A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715359 | |||||||
| chr7:81715362 | A | G | 1 | a0001c0002t0001g0252 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1405+1870T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715362 | |||||||
| chr7:81715446 | A | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0204 |
2 | HG00544.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1405+1786T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715446 | |||||||
| chr7:81715607 | C | T | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1625G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715607 | |||||||
| chr7:81715754 | C | A | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1478G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715754 | |||||||
| chr7:81715755 | A | T | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1405+1477T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715755 | |||||||
| chr7:81715908 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1405+1324C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81715908 | |||||||
| chr7:81716072 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1405+1160G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716072 | |||||||
| chr7:81716073 | G | A | 2 | a0001c0005t0006g0007 a0001c0011t0006g0116 |
3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+1159C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716073 | |||||||
| chr7:81716091 | G | A | 2 | a0001c0005t0006g0007 a0001c0011t0006g0116 |
3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+1141C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716091 | |||||||
| chr7:81716145 | A | T | 1 | a0001c0001t0002g0127 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1405+1087T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716145 | |||||||
| chr7:81716189 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1405+1043T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716189 | |||||||
| chr7:81716269 | C | T | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1405+963G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716269 | |||||||
| chr7:81716287 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0082 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1405+945C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716287 | |||||||
| chr7:81716591 | A | G | 2 | a0001c0005t0006g0007 a0001c0011t0006g0116 |
3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1405+641T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716591 | |||||||
| chr7:81716617 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+615G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716617 | |||||||
| chr7:81716750 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1405+482C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716750 | |||||||
| chr7:81716769 | T | C | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+463A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716769 | |||||||
| chr7:81716976 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1405+256T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81716976 | |||||||
| chr7:81717104 | G | A | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405+128C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 11/17 | chr7 | 81717104 | |||||||
| chr7:81717369 | T | C | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(188): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
splice_region_variant&intron_variant | LOW | c.1272-4A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717369 | |||||||
| chr7:81717382 | C | A | 1 | a0001c0002t0006g0094 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1272-17G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717382 | |||||||
| chr7:81717485 | T | C | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-120A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717485 | |||||||
| chr7:81717609 | G | A | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(214): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1272-244C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717609 | |||||||
| chr7:81717647 | A | G | 1 | a0003c0006t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1272-282T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81717647 | |||||||
| chr7:81718076 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1272-711G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718076 | |||||||
| chr7:81718232 | T | G | 212 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(209): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1272-867A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718232 | |||||||
| chr7:81718325 | A | G | 1 | a0001c0001t0006g0012 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1272-960T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718325 | |||||||
| chr7:81718353 | T | A | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-988A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718353 | |||||||
| chr7:81718392 | GA | G | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1028delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718392 | |||||||
| chr7:81718430 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1272-1065G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718430 | |||||||
| chr7:81718437 | TG | T | 6 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1272-1073delC | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718437 | |||||||
| chr7:81718441 | G | A | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1272-1076C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718441 | |||||||
| chr7:81718581 | C | T | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1272-1216G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718581 | |||||||
| chr7:81718705 | C | T | 9 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(6): Show |
9 | HG02055.hp1 HG02145.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-1340G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718705 | |||||||
| chr7:81718935 | T | G | 1 | a0001c0001t0008g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1272-1570A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81718935 | |||||||
| chr7:81719267 | C | T | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1271+1478G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719267 | |||||||
| chr7:81719339 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1271+1406G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719339 | |||||||
| chr7:81719531 | G | T | 1 | a0001c0009t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1271+1214C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719531 | |||||||
| chr7:81719801 | T | C | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1271+944A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81719801 | |||||||
| chr7:81720096 | T | C | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1271+649A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720096 | |||||||
| chr7:81720102 | G | T | 1 | a0001c0007t0001g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1271+643C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720102 | |||||||
| chr7:81720203 | A | T | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1271+542T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720203 | |||||||
| chr7:81720356 | C | A | 30 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(27): Show |
30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1271+389G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720356 | |||||||
| chr7:81720374 | C | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0168 a0001c0001t0001g0206 |
3 | NA19005.hp2 NA19068.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1271+371G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720374 | |||||||
| chr7:81720536 | A | G | 7 | a0001c0001t0007g0097 a0001c0002t0003g0123 a0001c0002t0007g0112 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1271+209T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 10/17 | chr7 | 81720536 | |||||||
| chr7:81720892 | A | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-45T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720892 | |||||||
| chr7:81720907 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-60C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720907 | |||||||
| chr7:81720973 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1169-126G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81720973 | |||||||
| chr7:81721048 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1169-201T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721048 | |||||||
| chr7:81721056 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1169-209A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721056 | |||||||
| chr7:81721080 | CTT | C | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1169-235_1169-234d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721080 | |||||||
| chr7:81721129 | C | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(248): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1169-282G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721129 | |||||||
| chr7:81721150 | A | G | 5 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169-303T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721150 | |||||||
| chr7:81721164 | G | A | 18 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0010 others(15): Show |
24 | HG00609.hp2 HG01123.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1169-317C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721164 | |||||||
| chr7:81721179 | G | A | 7 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(4): Show |
8 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-332C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721179 | |||||||
| chr7:81721188 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0152 |
2 | HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1169-341G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721188 | |||||||
| chr7:81721221 | T | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1169-374A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721221 | |||||||
| chr7:81721257 | G | GA | 39 | a0001c0001t0004g0134 a0001c0001t0005g0098 a0001c0001t0005g0135 others(36): Show |
40 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.1169-411dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721257 | |||||||
| chr7:81721451 | T | G | 7 | a0001c0001t0007g0097 a0001c0002t0003g0123 a0001c0002t0007g0112 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-604A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721451 | |||||||
| chr7:81721502 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1169-655G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721502 | |||||||
| chr7:81721714 | T | C | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1169-867A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721714 | |||||||
| chr7:81721809 | C | T | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1169-962G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721809 | |||||||
| chr7:81721845 | T | C | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1169-998A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81721845 | |||||||
| chr7:81722010 | A | AT | 7 | a0001c0001t0007g0097 a0001c0002t0003g0123 a0001c0002t0007g0112 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1169-1164dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722010 | |||||||
| chr7:81722456 | C | T | 7 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(4): Show |
8 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-1609G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722456 | |||||||
| chr7:81722616 | C | G | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1169-1769G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722616 | |||||||
| chr7:81722800 | C | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-1953G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722800 | |||||||
| chr7:81722813 | C | CA | 169 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(166): Show |
177 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1169-1967dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722813 | |||||||
| chr7:81722813 | C | CAA | 16 | a0001c0001t0001g0031 a0001c0001t0001g0065 a0001c0001t0001g0066 others(13): Show |
16 | HG01071.hp1 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1169-1968_1169-196 others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722813 | |||||||
| chr7:81722845 | G | GTATATAT others(3): Show |
1 | a0001c0002t0010g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1169-2008_1169-199 others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(5): Show |
1 | a0001c0002t0010g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1169-2010_1169-199 others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(9): Show |
1 | a0001c0002t0009g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1169-2014_1169-199 others(20): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(11): Show |
3 | a0001c0001t0004g0134 a0001c0001t0009g0133 a0001c0002t0004g0017 |
3 | HG01884.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(13): Show |
8 | a0001c0001t0005g0098 a0001c0001t0005g0135 a0001c0001t0005g0136 others(5): Show |
8 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(24): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(15): Show |
1 | a0001c0001t0005g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1169-1999_1169-199 others(26): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(17): Show |
5 | a0001c0001t0005g0142 a0001c0002t0004g0248 a0001c0002t0004g0249 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1169-1999_1169-199 others(28): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722845 | G | GTATATAT others(23): Show |
1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1169-1999_1169-199 others(34): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722845 | |||||||
| chr7:81722854 | T | TATATATA others(29): Show |
2 | a0001c0001t0007g0097 a0001c0002t0015g0113 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(40): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | |||||||
| chr7:81722854 | T | TATATATA others(31): Show |
2 | a0001c0002t0007g0112 a0001c0002t0007g0114 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(42): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | |||||||
| chr7:81722854 | T | TATATATA others(33): Show |
2 | a0001c0002t0003g0123 a0001c0002t0007g0122 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1169-2008_1169-200 others(44): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | |||||||
| chr7:81722854 | T | TATATATA others(35): Show |
1 | a0001c0002t0007g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1169-2008_1169-200 others(46): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722854 | |||||||
| chr7:81722928 | C | T | 1 | a0001c0002t0004g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1169-2081G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722928 | |||||||
| chr7:81722929 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0191 |
3 | HG00280.hp2 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1169-2082C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81722929 | |||||||
| chr7:81723253 | G | T | 26 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(23): Show |
26 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1169-2406C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723253 | |||||||
| chr7:81723255 | A | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-2408T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723255 | |||||||
| chr7:81723270 | G | A | 210 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1169-2423C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723270 | |||||||
| chr7:81723308 | T | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1169-2461A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723308 | |||||||
| chr7:81723401 | T | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(176): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1168+2489A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723401 | |||||||
| chr7:81723722 | T | C | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168+2168A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723722 | |||||||
| chr7:81723744 | G | A | 26 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(23): Show |
26 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1168+2146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723744 | |||||||
| chr7:81723801 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0076 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1168+2089A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723801 | |||||||
| chr7:81723841 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1168+2049A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723841 | |||||||
| chr7:81723910 | G | A | 180 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(177): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1168+1980C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723910 | |||||||
| chr7:81723913 | G | T | 1 | a0001c0002t0004g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1168+1977C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723913 | |||||||
| chr7:81723978 | T | C | 2 | a0001c0002t0004g0005 a0001c0002t0004g0111 |
3 | HG02451.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1168+1912A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81723978 | |||||||
| chr7:81724245 | G | T | 7 | a0001c0001t0007g0097 a0001c0002t0003g0123 a0001c0002t0007g0112 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1645C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724245 | |||||||
| chr7:81724349 | G | T | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1168+1541C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724349 | |||||||
| chr7:81724696 | G | A | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1168+1194C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724696 | |||||||
| chr7:81724940 | A | G | 6 | a0001c0001t0004g0134 a0001c0002t0004g0017 a0001c0002t0004g0248 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+950T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81724940 | |||||||
| chr7:81725026 | A | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG02015.hp1 HG02074.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+864T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725026 | |||||||
| chr7:81725300 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1168+590A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725300 | |||||||
| chr7:81725552 | G | A | 4 | a0001c0001t0010g0178 a0001c0002t0010g0124 a0001c0002t0010g0125 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168+338C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725552 | |||||||
| chr7:81725750 | G | A | 210 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
220 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1168+140C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 9/17 | chr7 | 81725750 | |||||||
| chr7:81726080 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1041-63T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726080 | |||||||
| chr7:81726133 | T | A | 47 | a0001c0001t0001g0048 a0001c0001t0001g0143 a0001c0001t0001g0148 others(44): Show |
50 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1041-116A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726133 | |||||||
| chr7:81726158 | A | T | 1 | a0001c0001t0001g0149 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1041-141T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726158 | |||||||
| chr7:81726186 | T | A | 36 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0001t0005g0098 others(33): Show |
37 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1041-169A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726186 | |||||||
| chr7:81726336 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041-319T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726336 | |||||||
| chr7:81726356 | T | C | 15 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(12): Show |
17 | HG00609.hp1 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1041-339A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726356 | |||||||
| chr7:81726454 | T | A | 2 | a0001c0001t0001g0207 a0003c0006t0001g0172 |
2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1041-437A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726454 | |||||||
| chr7:81726701 | C | T | 220 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(217): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1041-684G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81726701 | |||||||
| chr7:81727039 | T | G | 2 | a0001c0001t0001g0061 a0001c0001t0002g0177 |
2 | HG02559.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1041-1022A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727039 | |||||||
| chr7:81727048 | TG | T | 8 | a0001c0001t0001g0157 a0001c0001t0008g0028 a0001c0001t0008g0077 others(5): Show |
9 | HG02486.hp1 HG02809.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041-1032delC | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727048 | |||||||
| chr7:81727049 | G | GT | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(183): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1041-1033dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727049 | |||||||
| chr7:81727073 | T | C | 2 | a0002c0003t0001g0015 a0002c0003t0001g0062 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1041-1056A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727073 | |||||||
| chr7:81727085 | A | C | 2 | a0002c0003t0001g0015 a0002c0003t0001g0062 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1041-1068T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727085 | |||||||
| chr7:81727187 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(176): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1041-1170G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727187 | |||||||
| chr7:81727197 | C | T | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1041-1180G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727197 | |||||||
| chr7:81727210 | GT | G | 217 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(214): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1041-1194delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727210 | |||||||
| chr7:81727271 | C | T | 2 | a0001c0002t0007g0239 a0001c0002t0015g0113 |
2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1041-1254G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727271 | |||||||
| chr7:81727339 | G | T | 2 | a0001c0002t0002g0246 a0001c0002t0006g0094 |
2 | HG01069.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1041-1322C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727339 | |||||||
| chr7:81727396 | G | T | 1 | a0001c0001t0002g0010 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1041-1379C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727396 | |||||||
| chr7:81727411 | C | A | 9 | a0001c0001t0002g0177 a0001c0001t0004g0134 a0001c0002t0002g0246 others(6): Show |
9 | HG01069.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041-1394G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727411 | |||||||
| chr7:81727553 | T | A | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-1536A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727553 | |||||||
| chr7:81727562 | C | G | 6 | a0001c0001t0004g0134 a0001c0002t0004g0017 a0001c0002t0004g0248 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-1545G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727562 | |||||||
| chr7:81727576 | A | AT | 16 | a0001c0001t0004g0134 a0001c0001t0010g0178 a0001c0002t0002g0246 others(13): Show |
16 | HG01069.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1041-1560dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727576 | |||||||
| chr7:81727581 | T | TA | 199 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
209 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1041-1565dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727581 | |||||||
| chr7:81727591 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1041-1574G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727591 | |||||||
| chr7:81727739 | T | C | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(198): Show |
211 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.1041-1722A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727739 | |||||||
| chr7:81727825 | A | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1040+1780T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727825 | |||||||
| chr7:81727994 | C | G | 9 | a0001c0001t0007g0097 a0001c0001t0009g0133 a0001c0001t0014g0131 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+1611G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81727994 | |||||||
| chr7:81728033 | T | G | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1040+1572A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728033 | |||||||
| chr7:81728541 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1040+1064G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728541 | |||||||
| chr7:81728710 | C | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+895G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728710 | |||||||
| chr7:81728744 | C | T | 32 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(29): Show |
34 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1040+861G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728744 | |||||||
| chr7:81728759 | G | A | 182 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(179): Show |
190 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.1040+846C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728759 | |||||||
| chr7:81728873 | G | A | 9 | a0001c0001t0005g0098 a0001c0001t0005g0135 a0001c0001t0005g0136 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1040+732C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728873 | |||||||
| chr7:81728910 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00438.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1040+695G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728910 | |||||||
| chr7:81728992 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1040+613A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81728992 | |||||||
| chr7:81729021 | GATACTCA others(267): Show |
G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(188): Show |
199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1040+310_1040+583d others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729021 | |||||||
| chr7:81729062 | A | G | 6 | a0001c0001t0010g0178 a0001c0002t0003g0123 a0001c0002t0007g0122 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+543T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729062 | |||||||
| chr7:81729396 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1040+209C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 8/17 | chr7 | 81729396 | |||||||
| chr7:81729800 | CA | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-22delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81729800 | |||||||
| chr7:81729873 | AT | A | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-95delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81729873 | |||||||
| chr7:81730187 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-408C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730187 | |||||||
| chr7:81730519 | T | A | 9 | a0001c0001t0005g0098 a0001c0001t0005g0135 a0001c0001t0005g0136 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-740A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730519 | |||||||
| chr7:81730563 | T | G | 3 | a0001c0001t0009g0133 a0001c0002t0004g0244 a0001c0002t0009g0245 |
3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.866-784A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730563 | |||||||
| chr7:81730634 | TA | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-856delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730634 | |||||||
| chr7:81730658 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0066 others(3): Show |
6 | HG01934.hp1 HG01978.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-879T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730658 | |||||||
| chr7:81730689 | C | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-910G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81730689 | |||||||
| chr7:81731058 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.866-1279A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731058 | |||||||
| chr7:81731115 | G | A | 9 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-1336C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731115 | |||||||
| chr7:81731463 | A | G | 9 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-1684T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731463 | |||||||
| chr7:81731473 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.866-1694C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731473 | |||||||
| chr7:81731912 | C | T | 5 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-2133G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731912 | |||||||
| chr7:81731947 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866-2168G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81731947 | |||||||
| chr7:81732067 | C | A | 1 | a0001c0001t0008g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.866-2288G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732067 | |||||||
| chr7:81732200 | C | A | 2 | a0001c0001t0005g0098 a0001c0001t0005g0145 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.866-2421G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732200 | |||||||
| chr7:81732258 | C | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
6 | HG00733.hp2 NA18982.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-2479G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732258 | |||||||
| chr7:81732311 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.866-2532G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732311 | |||||||
| chr7:81732451 | G | A | 15 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-2672C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732451 | |||||||
| chr7:81732535 | A | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0183 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.866-2756T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732535 | |||||||
| chr7:81732564 | G | A | 5 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(2): Show |
5 | HG02965.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-2785C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732564 | |||||||
| chr7:81732653 | G | A | 15 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-2874C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732653 | |||||||
| chr7:81732874 | C | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(188): Show |
199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.866-3095G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81732874 | |||||||
| chr7:81733068 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-3289G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733068 | |||||||
| chr7:81733090 | T | G | 1 | a0001c0002t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.866-3311A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733090 | |||||||
| chr7:81733173 | A | C | 1 | a0001c0001t0002g0089 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.866-3394T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733173 | |||||||
| chr7:81733190 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-3411G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733190 | |||||||
| chr7:81733242 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.866-3463C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733242 | |||||||
| chr7:81733271 | A | G | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(195): Show |
206 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.866-3492T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733271 | |||||||
| chr7:81733271 | A | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0203 |
2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.866-3492T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733271 | |||||||
| chr7:81733438 | C | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0020 others(36): Show |
40 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.866-3659G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733438 | |||||||
| chr7:81733455 | T | C | 15 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(12): Show |
17 | HG00609.hp1 HG00733.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.866-3676A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733455 | |||||||
| chr7:81733763 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.866-3984T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733763 | |||||||
| chr7:81733822 | T | C | 3 | a0001c0001t0003g0218 a0001c0001t0003g0222 a0001c0001t0003g0236 |
3 | HG01257.hp2 HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.866-4043A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81733822 | |||||||
| chr7:81734018 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(188): Show |
199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.866-4239C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734018 | |||||||
| chr7:81734054 | T | C | 1 | a0001c0001t0006g0012 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.866-4275A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734054 | |||||||
| chr7:81734250 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.866-4471T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734250 | |||||||
| chr7:81734447 | C | T | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.866-4668G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734447 | |||||||
| chr7:81734552 | A | G | 3 | a0001c0001t0009g0133 a0001c0002t0004g0244 a0001c0002t0009g0245 |
3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.866-4773T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734552 | |||||||
| chr7:81734581 | T | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-4802A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734581 | |||||||
| chr7:81734625 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.866-4846G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734625 | |||||||
| chr7:81734791 | A | G | 1 | a0001c0002t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.866-5012T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734791 | |||||||
| chr7:81734813 | G | A | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.866-5034C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734813 | |||||||
| chr7:81734871 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-5092G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734871 | |||||||
| chr7:81734948 | C | G | 1 | a0001c0001t0002g0010 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.866-5169G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81734948 | |||||||
| chr7:81735119 | C | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-5340G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735119 | |||||||
| chr7:81735298 | A | G | 15 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-5519T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735298 | |||||||
| chr7:81735378 | G | T | 35 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(32): Show |
38 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.866-5599C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735378 | |||||||
| chr7:81735489 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866-5710T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735489 | |||||||
| chr7:81735874 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.866-6095T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81735874 | |||||||
| chr7:81736098 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.866-6319T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736098 | |||||||
| chr7:81736107 | C | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.866-6328G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736107 | |||||||
| chr7:81736260 | C | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0002t0001g0240 |
3 | HG00639.hp2 HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.866-6481G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736260 | |||||||
| chr7:81736326 | C | T | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.866-6547G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736326 | |||||||
| chr7:81736473 | A | G | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.866-6694T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736473 | |||||||
| chr7:81736512 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(90): Show |
98 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.866-6733T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736512 | |||||||
| chr7:81736549 | T | C | 5 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-6770A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736549 | |||||||
| chr7:81736718 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.865+6635C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736718 | |||||||
| chr7:81736894 | G | GGGGTGTG others(3): Show |
1 | a0001c0002t0007g0114 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.865+6458_865+6459i others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGGGTGTG others(5): Show |
3 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0015g0113 |
3 | HG02280.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.865+6458_865+6459i others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGT | 8 | a0001c0001t0002g0181 a0001c0001t0002g0193 a0001c0001t0010g0178 others(5): Show |
8 | HG01433.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.865+6457_865+6458d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGT | 4 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+6455_865+6458d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGT | 11 | a0001c0001t0003g0232 a0001c0001t0005g0145 a0001c0001t0008g0202 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.865+6453_865+6458d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(1): Show |
38 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0036 others(35): Show |
39 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.865+6451_865+6458d others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(3): Show |
67 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(64): Show |
70 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.865+6449_865+6458d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(5): Show |
59 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0020 others(56): Show |
62 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.865+6447_865+6458d others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(7): Show |
13 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.865+6445_865+6458d others(16): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(9): Show |
6 | a0001c0001t0001g0204 a0001c0001t0005g0135 a0001c0001t0005g0136 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+6443_865+6458d others(18): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GGTGTGTG others(13): Show |
2 | a0001c0001t0001g0132 a0001c0001t0005g0142 |
2 | HG02735.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.865+6439_865+6458d others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GTGTGTGT others(4): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0059 |
2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.865+6458_865+6459i others(13): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GTGTGTGT others(6): Show |
1 | a0001c0002t0003g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+6458_865+6459i others(15): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81736894 | G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0224 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.865+6458_865+6459i others(17): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81736894 | |||||||
| chr7:81737765 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.865+5588C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81737765 | |||||||
| chr7:81737864 | G | A | 15 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.865+5489C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81737864 | |||||||
| chr7:81738080 | T | A | 194 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(191): Show |
202 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.865+5273A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738080 | |||||||
| chr7:81738336 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+5017T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738336 | |||||||
| chr7:81738403 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.865+4950G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738403 | |||||||
| chr7:81738765 | A | G | 14 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+4588T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738765 | |||||||
| chr7:81738909 | AC | A | 8 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0166 others(5): Show |
8 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+4443delG | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738909 | |||||||
| chr7:81738962 | T | C | 1 | a0001c0002t0005g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.865+4391A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81738962 | |||||||
| chr7:81739111 | T | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(197): Show |
208 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.865+4242A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739111 | |||||||
| chr7:81739119 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+4234T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739119 | |||||||
| chr7:81739138 | A | G | 12 | a0001c0001t0004g0134 a0001c0001t0010g0178 a0001c0002t0003g0123 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+4215T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739138 | |||||||
| chr7:81739271 | A | C | 2 | a0001c0001t0004g0134 a0001c0002t0004g0017 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.865+4082T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739271 | |||||||
| chr7:81739361 | T | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+3992A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739361 | |||||||
| chr7:81739432 | G | GGACA | 7 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.865+3917_865+3920d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739432 | |||||||
| chr7:81739569 | AC | A | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.865+3783delG | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739569 | |||||||
| chr7:81739636 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+3717T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739636 | |||||||
| chr7:81739673 | T | C | 1 | a0001c0001t0013g0042 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.865+3680A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81739673 | |||||||
| chr7:81740103 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(45): Show |
49 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.865+3250T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740103 | |||||||
| chr7:81740141 | T | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+3212A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740141 | |||||||
| chr7:81740236 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.865+3117G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740236 | |||||||
| chr7:81740395 | G | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+2958C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740395 | |||||||
| chr7:81740435 | C | T | 3 | a0001c0001t0009g0133 a0001c0002t0004g0244 a0001c0002t0009g0245 |
3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.865+2918G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740435 | |||||||
| chr7:81740454 | T | C | 14 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+2899A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740454 | |||||||
| chr7:81740948 | G | T | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(198): Show |
209 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.865+2405C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81740948 | |||||||
| chr7:81741054 | A | T | 2 | a0001c0001t0003g0215 a0001c0001t0003g0217 |
2 | HG01192.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.865+2299T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741054 | |||||||
| chr7:81741135 | C | T | 1 | a0001c0002t0006g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.865+2218G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741135 | |||||||
| chr7:81741262 | G | A | 8 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0166 others(5): Show |
8 | HG00140.hp2 HG01175.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+2091C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741262 | |||||||
| chr7:81741286 | A | AT | 14 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.865+2066dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741286 | |||||||
| chr7:81741288 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0081 |
2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.865+2065A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741288 | |||||||
| chr7:81741384 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.865+1969A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741384 | |||||||
| chr7:81741458 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+1895C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741458 | |||||||
| chr7:81741526 | G | T | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+1827C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741526 | |||||||
| chr7:81741583 | C | CTG | 32 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0034 others(29): Show |
35 | HG00438.hp1 HG00544.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.865+1768_865+1769d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741583 | C | CTGTG | 20 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0066 others(17): Show |
22 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.865+1766_865+1769d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741583 | C | CTGTGTG | 10 | a0001c0001t0010g0178 a0001c0002t0003g0123 a0001c0002t0004g0248 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+1764_865+1769d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741583 | C | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.865+1770G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741583 | CTG | C | 7 | a0001c0001t0001g0048 a0001c0001t0009g0102 a0001c0001t0009g0103 others(4): Show |
7 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.865+1768_865+1769d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741583 | CTGTGTG | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG00140.hp2 HG01175.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+1764_865+1769d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741583 | |||||||
| chr7:81741720 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.865+1633G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741720 | |||||||
| chr7:81741744 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.865+1609C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741744 | |||||||
| chr7:81741922 | G | C | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.865+1431C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741922 | |||||||
| chr7:81741938 | C | CA | 169 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(166): Show |
177 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.865+1414dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | |||||||
| chr7:81741938 | C | CAA | 19 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0066 others(16): Show |
19 | HG00140.hp2 HG01069.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.865+1413_865+1414d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | |||||||
| chr7:81741938 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0009g0133 a0001c0002t0009g0245 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.865+1403_865+1414d others(14): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741938 | |||||||
| chr7:81741982 | CAT | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG01099.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+1369_865+1370d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81741982 | |||||||
| chr7:81742011 | C | T | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.865+1342G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742011 | |||||||
| chr7:81742026 | A | G | 1 | a0004c0010t0003g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.865+1327T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742026 | |||||||
| chr7:81742064 | T | C | 10 | a0001c0001t0007g0097 a0001c0001t0009g0133 a0001c0001t0014g0131 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.865+1289A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742064 | |||||||
| chr7:81742303 | T | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(210): Show |
221 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.865+1050A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742303 | |||||||
| chr7:81742615 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.865+738T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742615 | |||||||
| chr7:81742731 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742731 | |||||||
| chr7:81742763 | A | G | 6 | a0001c0001t0004g0134 a0001c0002t0004g0017 a0001c0002t0004g0248 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+590T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742763 | |||||||
| chr7:81742840 | A | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.865+513T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81742840 | |||||||
| chr7:81743008 | G | C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0169 a0001c0001t0001g0176 others(1): Show |
4 | HG02165.hp1 HG02523.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+345C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743008 | |||||||
| chr7:81743136 | A | G | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.865+217T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743136 | |||||||
| chr7:81743167 | T | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+186A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 7/17 | chr7 | 81743167 | |||||||
| chr7:81743685 | A | G | 2 | a0001c0005t0006g0007 a0001c0011t0006g0116 |
3 | HG02486.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.747-214T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81743685 | |||||||
| chr7:81744198 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(188): Show |
199 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.747-727C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744198 | |||||||
| chr7:81744303 | AT | A | 10 | a0001c0001t0007g0097 a0001c0001t0009g0133 a0001c0001t0014g0131 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+696delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | |||||||
| chr7:81744303 | ATT | A | 13 | a0001c0001t0001g0066 a0001c0001t0004g0134 a0001c0001t0010g0178 others(10): Show |
13 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.746+695_746+696del others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | |||||||
| chr7:81744303 | ATTT | A | 189 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(186): Show |
197 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.746+694_746+696del others(3): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744303 | |||||||
| chr7:81744364 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.746+636T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744364 | |||||||
| chr7:81744515 | C | G | 1 | a0001c0002t0004g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.746+485G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744515 | |||||||
| chr7:81744804 | C | G | 4 | a0001c0001t0009g0133 a0001c0002t0002g0246 a0001c0002t0004g0244 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.746+196G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744804 | |||||||
| chr7:81744895 | C | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | NA18969.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.746+105G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 6/17 | chr7 | 81744895 | |||||||
| chr7:81745184 | G | C | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(244): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.626-64C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745184 | |||||||
| chr7:81745503 | T | C | 24 | a0001c0001t0004g0134 a0001c0001t0007g0097 a0001c0001t0009g0102 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.626-383A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745503 | |||||||
| chr7:81745602 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.626-482A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745602 | |||||||
| chr7:81745649 | A | G | 14 | a0001c0001t0004g0134 a0001c0001t0009g0102 a0001c0001t0009g0103 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.626-529T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745649 | |||||||
| chr7:81745735 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.626-615C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745735 | |||||||
| chr7:81745771 | T | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0207 others(1): Show |
4 | HG00140.hp2 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-651A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745771 | |||||||
| chr7:81745801 | A | C | 10 | a0001c0001t0007g0097 a0001c0001t0009g0133 a0001c0001t0014g0131 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.626-681T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745801 | |||||||
| chr7:81745802 | G | A | 1 | a0001c0001t0007g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626-682C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745802 | |||||||
| chr7:81745881 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.626-761T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745881 | |||||||
| chr7:81745883 | A | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG01099.hp2 HG01433.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-763T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745883 | |||||||
| chr7:81745901 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.626-781A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81745901 | |||||||
| chr7:81746032 | G | T | 5 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-912C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746032 | |||||||
| chr7:81746132 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0207 others(1): Show |
4 | HG00140.hp2 HG03017.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.626-1012C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746132 | |||||||
| chr7:81746143 | T | C | 1 | a0004c0010t0003g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.626-1023A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746143 | |||||||
| chr7:81746266 | A | C | 12 | a0001c0001t0004g0134 a0001c0001t0007g0097 a0001c0001t0014g0131 others(9): Show |
12 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.626-1146T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746266 | |||||||
| chr7:81746341 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0204 a0001c0001t0003g0174 |
3 | HG00544.hp2 HG02040.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.626-1221C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746341 | |||||||
| chr7:81746354 | G | GTCCA | 6 | a0001c0001t0010g0178 a0001c0002t0003g0123 a0001c0002t0007g0122 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.626-1238_626-1235d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746354 | |||||||
| chr7:81746376 | G | C | 1 | a0001c0001t0002g0177 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.626-1256C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746376 | |||||||
| chr7:81746471 | G | T | 4 | a0001c0001t0009g0133 a0001c0002t0002g0246 a0001c0002t0004g0244 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1351C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746471 | |||||||
| chr7:81746538 | G | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(206): Show |
217 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.626-1418C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746538 | |||||||
| chr7:81746552 | C | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.626-1432G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746552 | |||||||
| chr7:81746613 | G | A | 216 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(213): Show |
224 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.626-1493C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746613 | |||||||
| chr7:81746628 | T | G | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(190): Show |
201 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.626-1508A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746628 | |||||||
| chr7:81746630 | G | C | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(190): Show |
201 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.626-1510C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746630 | |||||||
| chr7:81746631 | T | C | 4 | a0001c0001t0009g0133 a0001c0002t0002g0246 a0001c0002t0004g0244 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-1511A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81746631 | |||||||
| chr7:81747032 | T | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-1912A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747032 | |||||||
| chr7:81747043 | A | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(196): Show |
207 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.626-1923T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747043 | |||||||
| chr7:81747158 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.626-2038C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747158 | |||||||
| chr7:81747198 | G | A | 1 | a0002c0003t0001g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.626-2078C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747198 | |||||||
| chr7:81747263 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.626-2143G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747263 | |||||||
| chr7:81747296 | A | G | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2176T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747296 | |||||||
| chr7:81747318 | G | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2198C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747318 | |||||||
| chr7:81747333 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626-2213G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747333 | |||||||
| chr7:81747334 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0215 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-2214C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747334 | |||||||
| chr7:81747334 | G | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626-2214C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747334 | |||||||
| chr7:81747368 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.626-2248A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747368 | |||||||
| chr7:81747388 | A | G | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2268T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747388 | |||||||
| chr7:81747406 | T | C | 16 | a0001c0001t0004g0134 a0001c0001t0009g0133 a0001c0001t0010g0178 others(13): Show |
16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.626-2286A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747406 | |||||||
| chr7:81747578 | G | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2458C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747578 | |||||||
| chr7:81747724 | C | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(211): Show |
222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.626-2604G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747724 | |||||||
| chr7:81747815 | C | T | 2 | a0001c0001t0004g0134 a0001c0002t0004g0017 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.626-2695G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81747815 | |||||||
| chr7:81748041 | G | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-2921C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748041 | |||||||
| chr7:81748147 | T | C | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-3027A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748147 | |||||||
| chr7:81748302 | A | C | 22 | a0001c0001t0004g0134 a0001c0001t0007g0097 a0001c0001t0009g0133 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.626-3182T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748302 | |||||||
| chr7:81748347 | T | C | 5 | a0001c0001t0007g0097 a0001c0002t0007g0112 a0001c0002t0007g0114 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-3227A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748347 | |||||||
| chr7:81748506 | T | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.626-3386A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748506 | |||||||
| chr7:81748600 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.626-3480C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748600 | |||||||
| chr7:81748610 | G | A | 4 | a0001c0001t0009g0133 a0001c0002t0002g0246 a0001c0002t0004g0244 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-3490C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748610 | |||||||
| chr7:81748663 | T | TAAAAC | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(183): Show |
193 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.625+3452_625+3456d others(7): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748663 | |||||||
| chr7:81748663 | T | TAAAACAA others(3): Show |
15 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0071 others(12): Show |
16 | HG01074.hp1 HG01074.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.625+3447_625+3456d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748663 | |||||||
| chr7:81748777 | A | G | 1 | a0001c0009t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.625+3343T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81748777 | |||||||
| chr7:81749072 | C | G | 2 | a0001c0001t0009g0102 a0001c0001t0009g0103 |
2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.625+3048G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749072 | |||||||
| chr7:81749165 | G | GTCTT | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2951_625+2954d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749165 | |||||||
| chr7:81749182 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | NA18983.hp2 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.625+2938G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749182 | |||||||
| chr7:81749191 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.625+2929G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749191 | |||||||
| chr7:81749238 | T | G | 10 | a0001c0001t0003g0139 a0001c0001t0005g0098 a0001c0001t0005g0135 others(7): Show |
10 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.625+2882A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749238 | |||||||
| chr7:81749356 | G | A | 16 | a0001c0001t0004g0134 a0001c0001t0009g0133 a0001c0001t0010g0178 others(13): Show |
16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.625+2764C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749356 | |||||||
| chr7:81749432 | A | G | 10 | a0001c0001t0003g0139 a0001c0001t0005g0098 a0001c0001t0005g0135 others(7): Show |
10 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.625+2688T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749432 | |||||||
| chr7:81749518 | G | A | 6 | a0001c0001t0004g0134 a0001c0002t0004g0017 a0001c0002t0004g0248 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+2602C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749518 | |||||||
| chr7:81749617 | G | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2503C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749617 | |||||||
| chr7:81749626 | A | G | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2494T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749626 | |||||||
| chr7:81749699 | A | G | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2421T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749699 | |||||||
| chr7:81749713 | C | T | 1 | a0001c0001t0013g0042 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.625+2407G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749713 | |||||||
| chr7:81749751 | C | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+2369G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749751 | |||||||
| chr7:81749915 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.625+2205T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749915 | |||||||
| chr7:81749980 | C | A | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.625+2140G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81749980 | |||||||
| chr7:81750095 | A | G | 1 | a0001c0002t0006g0094 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.625+2025T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750095 | |||||||
| chr7:81750235 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0076 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.625+1885T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750235 | |||||||
| chr7:81750317 | T | G | 1 | a0002c0003t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.625+1803A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750317 | |||||||
| chr7:81750405 | C | G | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+1715G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750405 | |||||||
| chr7:81750406 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0191 |
3 | HG00280.hp2 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.625+1714C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750406 | |||||||
| chr7:81750598 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.625+1522A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750598 | |||||||
| chr7:81750649 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.625+1471C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750649 | |||||||
| chr7:81750737 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.625+1383C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750737 | |||||||
| chr7:81750818 | G | GT | 210 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(207): Show |
218 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.625+1301dupA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750818 | |||||||
| chr7:81750861 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.625+1259C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750861 | |||||||
| chr7:81750968 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.625+1152A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81750968 | |||||||
| chr7:81751258 | C | T | 248 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(245): Show |
265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.625+862G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751258 | |||||||
| chr7:81751336 | G | A | 6 | a0001c0001t0007g0097 a0001c0001t0014g0131 a0001c0002t0007g0112 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.625+784C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751336 | |||||||
| chr7:81751368 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.625+752C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751368 | |||||||
| chr7:81751496 | TCCATAG | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(211): Show |
222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+618_625+623del others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751496 | |||||||
| chr7:81751503 | A | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(211): Show |
222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+617T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751503 | |||||||
| chr7:81751505 | A | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(211): Show |
222 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.625+615T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751505 | |||||||
| chr7:81751521 | TTGG | T | 22 | a0001c0001t0004g0134 a0001c0001t0007g0097 a0001c0001t0009g0133 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.625+596_625+598del others(3): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751521 | |||||||
| chr7:81751593 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.625+527T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751593 | |||||||
| chr7:81751725 | T | C | 6 | a0001c0001t0010g0178 a0001c0002t0003g0123 a0001c0002t0007g0122 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+395A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751725 | |||||||
| chr7:81751873 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.625+247G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751873 | |||||||
| chr7:81751879 | G | A | 6 | a0001c0001t0010g0178 a0001c0002t0003g0123 a0001c0002t0007g0122 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+241C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81751879 | |||||||
| chr7:81752010 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.625+110G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 5/17 | chr7 | 81752010 | |||||||
| chr7:81752340 | T | G | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-78A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752340 | |||||||
| chr7:81752343 | G | A | 2 | a0001c0002t0004g0005 a0001c0002t0004g0111 |
3 | HG02451.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.483-81C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752343 | |||||||
| chr7:81752415 | T | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.483-153A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752415 | |||||||
| chr7:81752596 | C | G | 4 | a0001c0001t0009g0133 a0001c0002t0002g0246 a0001c0002t0004g0244 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-334G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752596 | |||||||
| chr7:81752737 | G | A | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.483-475C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752737 | |||||||
| chr7:81752903 | A | T | 1 | a0001c0001t0009g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.483-641T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752903 | |||||||
| chr7:81752966 | C | T | 1 | a0001c0002t0004g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.483-704G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81752966 | |||||||
| chr7:81753279 | A | C | 2 | a0001c0001t0005g0098 a0001c0001t0005g0145 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.483-1017T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753279 | |||||||
| chr7:81753318 | ACAGGTAA others(3): Show |
A | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-1066_483-1057d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753318 | |||||||
| chr7:81753374 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(212): Show |
223 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.483-1112G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753374 | |||||||
| chr7:81753378 | T | C | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1116A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753378 | |||||||
| chr7:81753379 | G | A | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.483-1117C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753379 | |||||||
| chr7:81753458 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.483-1196C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753458 | |||||||
| chr7:81753467 | A | C | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-1205T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81753467 | |||||||
| chr7:81754028 | C | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01099.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.483-1766G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754028 | |||||||
| chr7:81754088 | G | T | 1 | a0001c0002t0004g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.483-1826C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754088 | |||||||
| chr7:81754100 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0076 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.483-1838A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754100 | |||||||
| chr7:81754296 | T | C | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.483-2034A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754296 | |||||||
| chr7:81754382 | AT | A | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2121delA | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754382 | |||||||
| chr7:81754390 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.483-2128T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754390 | |||||||
| chr7:81754483 | C | A | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2221G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754483 | |||||||
| chr7:81754513 | T | C | 1 | a0001c0002t0009g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.483-2251A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754513 | |||||||
| chr7:81754545 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.483-2283G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754545 | |||||||
| chr7:81754554 | T | C | 4 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(1): Show |
4 | HG00558.hp2 HG02559.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2292A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754554 | |||||||
| chr7:81754626 | T | C | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2364A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754626 | |||||||
| chr7:81754707 | T | C | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-2445A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754707 | |||||||
| chr7:81754880 | C | G | 1 | a0001c0002t0009g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.482+2309G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81754880 | |||||||
| chr7:81755142 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.482+2047T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755142 | |||||||
| chr7:81755155 | G | C | 1 | a0001c0001t0002g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.482+2034C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755155 | |||||||
| chr7:81755183 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG02015.hp1 HG02074.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+2006G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755183 | |||||||
| chr7:81755222 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.482+1967T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755222 | |||||||
| chr7:81755267 | C | G | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+1922G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755267 | |||||||
| chr7:81755398 | A | C | 2 | a0001c0002t0002g0246 a0001c0002t0004g0017 |
2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.482+1791T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755398 | |||||||
| chr7:81755406 | A | AAGGGATT others(2): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1774_482+1782d others(11): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755406 | |||||||
| chr7:81755437 | G | A | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+1752C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755437 | |||||||
| chr7:81755515 | A | C | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.482+1674T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755515 | |||||||
| chr7:81755618 | G | A | 4 | a0001c0001t0008g0028 a0001c0001t0008g0077 a0001c0001t0008g0078 others(1): Show |
4 | HG02965.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1571C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755618 | |||||||
| chr7:81755685 | T | C | 1 | a0001c0002t0004g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.482+1504A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755685 | |||||||
| chr7:81755864 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+1325T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755864 | |||||||
| chr7:81755914 | T | G | 1 | a0001c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+1275A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81755914 | |||||||
| chr7:81756229 | T | A | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+960A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756229 | |||||||
| chr7:81756229 | T | G | 4 | a0001c0002t0003g0123 a0001c0002t0007g0122 a0001c0002t0010g0124 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+960A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756229 | |||||||
| chr7:81756276 | G | C | 6 | a0001c0002t0002g0246 a0001c0002t0003g0096 a0001c0002t0004g0017 others(3): Show |
6 | HG01069.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+913C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756276 | |||||||
| chr7:81756546 | T | C | 3 | a0001c0001t0005g0098 a0001c0001t0005g0145 a0001c0001t0005g0146 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.482+643A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756546 | |||||||
| chr7:81756579 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.482+610G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756579 | |||||||
| chr7:81756620 | C | A | 1 | a0001c0002t0001g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.482+569G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756620 | |||||||
| chr7:81756660 | C | CA | 8 | a0001c0002t0003g0123 a0001c0002t0004g0248 a0001c0002t0004g0249 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.482+528dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756660 | |||||||
| chr7:81756749 | C | T | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+440G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756749 | |||||||
| chr7:81756886 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.482+303C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756886 | |||||||
| chr7:81756901 | C | CAGAAAG | 30 | a0001c0002t0001g0110 a0001c0002t0001g0240 a0001c0002t0001g0252 others(27): Show |
31 | HG00558.hp2 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.482+287_482+288ins others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756901 | |||||||
| chr7:81756902 | A | AGAAAGG | 3 | a0001c0002t0006g0093 a0001c0002t0006g0094 a0001c0002t0006g0095 |
3 | HG01069.hp1 HG02615.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.482+286_482+287ins others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756902 | |||||||
| chr7:81756952 | C | G | 1 | a0001c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+237G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756952 | |||||||
| chr7:81756981 | A | G | 1 | a0001c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.482+208T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81756981 | |||||||
| chr7:81757056 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0003g0237 a0001c0001t0003g0238 |
3 | HG00639.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.482+133G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757056 | |||||||
| chr7:81757063 | G | A | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+126C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757063 | |||||||
| chr7:81757128 | T | A | 1 | a0001c0001t0002g0003 | 3 | HG01123.hp1 HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482+61A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757128 | |||||||
| chr7:81757167 | C | T | 4 | a0001c0002t0003g0123 a0001c0002t0007g0122 a0001c0002t0010g0124 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+22G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 4/17 | chr7 | 81757167 | |||||||
| chr7:81757550 | G | T | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-247C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757550 | |||||||
| chr7:81757553 | G | A | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.368-250C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757553 | |||||||
| chr7:81757769 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.368-466C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757769 | |||||||
| chr7:81757834 | T | A | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-531A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757834 | |||||||
| chr7:81757854 | T | C | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-551A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757854 | |||||||
| chr7:81757925 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.368-622T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81757925 | |||||||
| chr7:81758025 | CTA | C | 3 | a0001c0001t0005g0098 a0001c0001t0005g0145 a0001c0001t0005g0146 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.367+665_367+666del others(2): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758025 | |||||||
| chr7:81758060 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.367+632A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758060 | |||||||
| chr7:81758476 | A | C | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.367+216T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758476 | |||||||
| chr7:81758516 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.367+176T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 3/17 | chr7 | 81758516 | |||||||
| chr7:81759494 | A | G | 1 | a0001c0001t0008g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.255-690T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759494 | |||||||
| chr7:81759598 | G | A | 1 | a0001c0002t0001g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.255-794C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759598 | |||||||
| chr7:81759630 | G | A | 3 | a0001c0002t0004g0249 a0001c0002t0004g0250 a0001c0002t0004g0251 |
3 | HG02257.hp1 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.255-826C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759630 | |||||||
| chr7:81759736 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.255-932G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759736 | |||||||
| chr7:81759741 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0003g0198 |
2 | NA18993.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.255-937A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759741 | |||||||
| chr7:81759768 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255-964A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759768 | |||||||
| chr7:81759891 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.255-1087C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759891 | |||||||
| chr7:81759945 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0003g0096 |
3 | HG01243.hp1 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.255-1141G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759945 | |||||||
| chr7:81759954 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1150T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759954 | |||||||
| chr7:81759996 | G | A | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1192C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81759996 | |||||||
| chr7:81760411 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.255-1607A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760411 | |||||||
| chr7:81760498 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.255-1694A>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760498 | |||||||
| chr7:81760658 | CAT | C | 2 | a0001c0001t0006g0012 a0001c0001t0008g0202 |
3 | HG03209.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.255-1856_255-1855d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760658 | |||||||
| chr7:81760676 | CGTGCGTG others(13): Show |
C | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255-1892_255-1873d others(22): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760676 | |||||||
| chr7:81760680 | C | CGT | 16 | a0001c0001t0001g0069 a0001c0001t0001g0241 a0001c0001t0001g0242 others(13): Show |
16 | HG00438.hp2 HG02027.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.255-1878_255-1877d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGT | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0034 others(39): Show |
48 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.255-1878_255-1877d others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGTGT | C | 107 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0018 others(104): Show |
109 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.255-1880_255-1877d others(6): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGTGTGT | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(54): Show |
61 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.255-1882_255-1877d others(8): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0154 a0001c0001t0001g0156 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-1884_255-1877d others(10): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0206 a0001c0001t0007g0097 |
3 | HG02735.hp1 NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.255-1886_255-1877d others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760680 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0003g0013 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.255-1894_255-1877d others(20): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760680 | |||||||
| chr7:81760682 | T | TGC | 8 | a0001c0002t0003g0123 a0001c0002t0004g0248 a0001c0002t0004g0249 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-1879_255-1878i others(4): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760682 | |||||||
| chr7:81760686 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.255-1882A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760686 | |||||||
| chr7:81760690 | T | C | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-1886A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760690 | |||||||
| chr7:81760796 | G | A | 3 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0009g0245 |
3 | HG02145.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.254+1911C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760796 | |||||||
| chr7:81760847 | T | C | 2 | a0001c0002t0004g0244 a0001c0002t0010g0243 |
2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.254+1860A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760847 | |||||||
| chr7:81760921 | T | C | 1 | a0001c0002t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254+1786A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760921 | |||||||
| chr7:81760971 | G | A | 3 | a0001c0001t0006g0012 a0001c0001t0008g0202 a0001c0001t0009g0133 |
4 | HG01884.hp1 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.254+1736C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81760971 | |||||||
| chr7:81761061 | G | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0140 a0001c0001t0001g0141 others(8): Show |
12 | HG01433.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.254+1646C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761061 | |||||||
| chr7:81761165 | A | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0132 |
3 | HG00280.hp1 HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.254+1542T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761165 | |||||||
| chr7:81761166 | C | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254+1541G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761166 | |||||||
| chr7:81761210 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.254+1497A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761210 | |||||||
| chr7:81761246 | A | G | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.254+1461T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761246 | |||||||
| chr7:81761310 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.254+1397C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761310 | |||||||
| chr7:81761341 | A | T | 2 | a0001c0002t0003g0123 a0001c0002t0007g0122 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.254+1366T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761341 | |||||||
| chr7:81761555 | T | TA | 21 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0105 others(18): Show |
21 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.254+1151dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761555 | |||||||
| chr7:81761555 | TA | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0132 a0001c0001t0003g0214 others(4): Show |
7 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.254+1151delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761555 | |||||||
| chr7:81761659 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.254+1048G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761659 | |||||||
| chr7:81761665 | G | A | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254+1042C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761665 | |||||||
| chr7:81761709 | T | C | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.254+998A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81761709 | |||||||
| chr7:81762322 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.254+385C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762322 | |||||||
| chr7:81762355 | C | T | 1 | a0001c0001t0014g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.254+352G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762355 | |||||||
| chr7:81762397 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.254+310T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762397 | |||||||
| chr7:81762519 | C | T | 11 | a0001c0002t0001g0110 a0001c0002t0003g0117 a0001c0002t0003g0118 others(8): Show |
12 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.254+188G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 2/17 | chr7 | 81762519 | |||||||
| chr7:81762894 | A | T | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-22T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81762894 | |||||||
| chr7:81763105 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.89-233A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763105 | |||||||
| chr7:81763310 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.89-438C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763310 | |||||||
| chr7:81763556 | C | G | 2 | a0001c0002t0003g0247 a0001c0002t0009g0245 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.89-684G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763556 | |||||||
| chr7:81763729 | G | A | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.89-857C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763729 | |||||||
| chr7:81763812 | C | T | 6 | a0001c0002t0003g0247 a0001c0002t0004g0248 a0001c0002t0004g0249 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-940G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81763812 | |||||||
| chr7:81764069 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.89-1197G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764069 | |||||||
| chr7:81764152 | T | C | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-1280A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764152 | |||||||
| chr7:81764320 | C | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01891.hp1 HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.89-1448G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764320 | |||||||
| chr7:81764327 | A | G | 1 | a0001c0002t0007g0122 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.89-1455T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764327 | |||||||
| chr7:81764457 | T | C | 5 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-1585A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764457 | |||||||
| chr7:81764895 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.89-2023G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764895 | |||||||
| chr7:81764989 | A | G | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-2117T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81764989 | |||||||
| chr7:81765018 | G | A | 7 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0004g0248 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2146C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765018 | |||||||
| chr7:81765047 | T | C | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2175A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765047 | |||||||
| chr7:81765058 | A | G | 4 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(1): Show |
4 | NA18942.hp2 NA18977.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2186T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765058 | |||||||
| chr7:81765081 | T | C | 4 | a0001c0002t0003g0123 a0001c0002t0007g0122 a0001c0002t0010g0124 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2209A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765081 | |||||||
| chr7:81765183 | G | C | 5 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2311C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765183 | |||||||
| chr7:81765300 | A | C | 4 | a0001c0002t0003g0123 a0001c0002t0007g0122 a0001c0002t0010g0124 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2428T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765300 | |||||||
| chr7:81765364 | A | C | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2492T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765364 | |||||||
| chr7:81765462 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01952.hp1 HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.89-2590G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765462 | |||||||
| chr7:81765479 | A | G | 7 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0004g0248 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2607T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765479 | |||||||
| chr7:81765510 | C | T | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2638G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765510 | |||||||
| chr7:81765511 | A | G | 7 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0004g0248 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2639T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765511 | |||||||
| chr7:81765547 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.89-2675G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765547 | |||||||
| chr7:81765588 | T | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0003g0210 |
3 | HG02129.hp1 NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.89-2716A>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765588 | |||||||
| chr7:81765644 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.89-2772T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765644 | |||||||
| chr7:81765777 | C | T | 16 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(13): Show |
16 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-2905G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765777 | |||||||
| chr7:81765787 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.89-2915T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765787 | |||||||
| chr7:81765894 | C | T | 5 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
5 | HG00558.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3022G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765894 | |||||||
| chr7:81765901 | G | C | 4 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0004g0250 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-3029C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81765901 | |||||||
| chr7:81766129 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.89-3257C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766129 | |||||||
| chr7:81766269 | T | C | 28 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0233 others(25): Show |
30 | HG00609.hp1 HG00733.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-3397A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766269 | |||||||
| chr7:81766406 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+3478C>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766406 | |||||||
| chr7:81766407 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88+3477T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766407 | |||||||
| chr7:81766484 | G | A | 1 | a0001c0002t0003g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.88+3400C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766484 | |||||||
| chr7:81766591 | A | G | 1 | a0001c0002t0002g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.88+3293T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81766591 | |||||||
| chr7:81767156 | A | G | 11 | a0001c0002t0001g0110 a0001c0002t0003g0117 a0001c0002t0003g0118 others(8): Show |
12 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+2728T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767156 | |||||||
| chr7:81767230 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.88+2654T>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767230 | |||||||
| chr7:81767249 | A | G | 12 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(9): Show |
12 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+2635T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767249 | |||||||
| chr7:81767295 | GA | G | 16 | a0001c0001t0001g0021 a0001c0001t0001g0099 a0001c0001t0001g0101 others(13): Show |
16 | HG00639.hp1 HG00639.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+2588delT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767295 | |||||||
| chr7:81767718 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02148.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+2166T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767718 | |||||||
| chr7:81767761 | G | T | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.88+2123C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767761 | |||||||
| chr7:81767792 | A | T | 1 | a0001c0001t0007g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.88+2092T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767792 | |||||||
| chr7:81767798 | T | C | 1 | a0001c0002t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+2086A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767798 | |||||||
| chr7:81767875 | C | A | 1 | a0001c0002t0007g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88+2009G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767875 | |||||||
| chr7:81767928 | A | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02056.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.88+1956T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81767928 | |||||||
| chr7:81768357 | A | G | 4 | a0001c0002t0003g0096 a0001c0002t0006g0093 a0001c0002t0006g0094 others(1): Show |
4 | HG01069.hp1 HG01243.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1527T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768357 | |||||||
| chr7:81768386 | C | T | 32 | a0001c0002t0001g0110 a0001c0002t0001g0240 a0001c0002t0001g0252 others(29): Show |
32 | HG00558.hp2 HG01069.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+1498G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768386 | |||||||
| chr7:81768444 | A | G | 4 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | NA18974.hp1 NA18987.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+1440T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768444 | |||||||
| chr7:81768600 | C | G | 3 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0009g0245 |
3 | HG02145.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.88+1284G>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768600 | |||||||
| chr7:81768601 | A | G | 7 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0004g0248 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+1283T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768601 | |||||||
| chr7:81768614 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(74): Show |
78 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.88+1270G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768614 | |||||||
| chr7:81768781 | G | A | 7 | a0001c0002t0002g0246 a0001c0002t0003g0247 a0001c0002t0004g0248 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+1103C>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768781 | |||||||
| chr7:81768784 | T | C | 1 | a0001c0002t0001g0240 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.88+1100A>G | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768784 | |||||||
| chr7:81768986 | G | T | 1 | a0001c0002t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+898C>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81768986 | |||||||
| chr7:81769017 | GTTCCCAC others(7): Show |
G | 1 | a0001c0002t0009g0245 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88+853_88+866delTA others(12): Show |
HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769017 | |||||||
| chr7:81769040 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(75): Show |
79 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.88+844G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769040 | |||||||
| chr7:81769178 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.88+706T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769178 | |||||||
| chr7:81769199 | A | T | 1 | a0001c0002t0004g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88+685T>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769199 | |||||||
| chr7:81769250 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.88+634G>A | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769250 | |||||||
| chr7:81769328 | C | A | 3 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 |
3 | HG00558.hp2 HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.88+556G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769328 | |||||||
| chr7:81769412 | A | G | 1 | a0002c0003t0001g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.88+472T>C | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769412 | |||||||
| chr7:81769573 | C | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00438.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.88+311G>T | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769573 | |||||||
| chr7:81769724 | C | CA | 12 | a0001c0002t0001g0252 a0001c0002t0001g0253 a0001c0002t0001g0254 others(9): Show |
12 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+159dupT | HGF | ENSG00000019991.18 | transcript | ENST00000222390.11 | protein_coding | 1/17 | chr7 | 81769724 |