Item | Value |
---|---|
geneid | 1954 |
ensemblid | ENSG00000105429.13 |
hgncid | 3233 |
symbol | MEGF8 |
name | multiple EGF like domains 8 |
refseq_nuc | NM_001271938.2 |
refseq_prot | NP_001258867.1 |
ensembl_nuc | ENST00000251268.11 |
ensembl_prot | ENSP00000251268.5 |
mane_status | MANE Select |
chr | chr19 |
start | 42325635 |
end | 42378765 |
strand | + |
ver | v1.2 |
region | chr19:42325635-42378765 |
region5000 | chr19:42320635-42383765 |
regionname0 | MEGF8_chr19_42325635_42378765 |
regionname5000 | MEGF8_chr19_42320635_42383765 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2845 | 122 | 46 | 34 | 20 | 6 | 14 | 7 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0002 | 0/0 | 2845 | 31 | 10 | 6 | 8 | 1 | 6 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0003 | 0/0 | 2845 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0004 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0005 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0006 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0007 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0008 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0009 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0010 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0011 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0012 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0013 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0014 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0015 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0016 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0017 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0018 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0019 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
a0020 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | MALGK others(2840): Show |
chr19 | 42320635 | 42383765 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 8535 | 88 | 20 | 32 | 15 | 6 | 13 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0003 | 0/0 | 8535 | 14 | 14 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0005 | 0/0 | 8535 | 5 | 4 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0007 | 0/0 | 8535 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0009 | 0/0 | 8535 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0010 | 0/0 | 8535 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0011 | 0/0 | 8535 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0022 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0030 | 0/0 | 8535 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0031 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0035 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0036 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0001c0037 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0002c0002 | 0/0 | 8535 | 18 | 0 | 5 | 8 | 1 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0002c0004 | 0/0 | 8535 | 7 | 6 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0002c0006 | 0/0 | 8535 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0002c0008 | 0/0 | 8535 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0002c0015 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0003c0012 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0003c0019 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0004c0026 | 0/0 | 8535 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0005c0032 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0006c0028 | 0/0 | 8535 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0007c0018 | 0/0 | 8535 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0008c0034 | 0/0 | 8535 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0009c0033 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0010c0017 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0011c0021 | 0/0 | 8535 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0012c0020 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0013c0014 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0014c0023 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0015c0016 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0016c0013 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0017c0025 | 0/0 | 8535 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0018c0027 | 0/0 | 8535 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0019c0029 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 | ||
a0020c0024 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | ATGGC others(8530): Show |
chr19 | 42320635 | 42383765 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 11137 | 55 | 14 | 24 | 10 | 1 | 5 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0002 | 0/1 | 11136 | 19 | 1 | 7 | 2 | 4 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0005 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0006 | 0/0 | 11137 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0007 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0011 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0013 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0015 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0017 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0018 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0019 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0001t0024 | 0/0 | 11137 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0003t0001 | 0/0 | 11137 | 14 | 14 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0005t0003 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0001c0005t0004 | 0/0 | 11136 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0001c0007t0001 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0009t0001 | 0/0 | 11137 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0010t0001 | 0/0 | 11137 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0011t0001 | 0/0 | 11137 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0022t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0030t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0031t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0035t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0036t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0001c0037t0005 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0002c0002t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0002c0002t0003 | 0/0 | 11136 | 14 | 0 | 5 | 5 | 1 | 3 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0002t0007 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0002c0002t0020 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0002t0021 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0004t0008 | 0/0 | 11136 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0004t0009 | 0/0 | 11136 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0004t0010 | 0/0 | 11136 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0004t0023 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0006t0001 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0002c0008t0003 | 0/0 | 11136 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0002c0015t0016 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0003c0012t0004 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0003c0019t0004 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0004c0026t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0005c0032t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0006c0028t0002 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0007c0018t0003 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0008c0034t0001 | 0/0 | 11137 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0009c0033t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0010c0017t0003 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0011c0021t0014 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0012c0020t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0013c0014t0012 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11131): Show |
chr19 | 42320635 | 42383765 |
a0014c0023t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0015c0016t0022 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0016c0013t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0017c0025t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0018c0027t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0019c0029t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
a0020c0024t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | GTCTC others(11132): Show |
chr19 | 42320635 | 42383765 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0008 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0015g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0017g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0019g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0024g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0009t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0009t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0010t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0010t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0011t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0022t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0030t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0031t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0035t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0036t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0037t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0020g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0021g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0023g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0008t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0008t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0015t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0003c0012t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0003c0019t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0004c0026t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0005c0032t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0006c0028t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0007c0018t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0008c0034t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0009c0033t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0010c0017t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0011c0021t0014g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0012c0020t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0013c0014t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0014c0023t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0015c0016t0022g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0016c0013t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0017c0025t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0018c0027t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0019c0029t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0020c0024t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0004 | c0026 | t0001 | g0109 | EUR | GBR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00609 | hp1 | a0005 | c0032 | t0001 | g0007 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00621 | hp1 | a0001 | c0009 | t0001 | g0133 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00738 | hp1 | a0001 | c0010 | t0001 | g0088 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0015 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0033 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01074 | hp1 | a0006 | c0028 | t0002 | g0092 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01175 | hp2 | a0007 | c0018 | t0003 | g0043 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01243 | hp1 | a0002 | c0004 | t0008 | g0029 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01346 | hp2 | a0001 | c0001 | t0024 | g0149 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01891 | hp1 | a0001 | c0005 | t0004 | g0131 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01975 | hp2 | a0008 | c0034 | t0001 | g0107 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01993 | hp1 | a0002 | c0002 | t0003 | g0032 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02074 | hp2 | a0002 | c0002 | t0021 | g0105 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02080 | hp1 | a0001 | c0009 | t0001 | g0007 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02132 | hp2 | a0009 | c0033 | t0001 | g0009 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02135 | hp1 | a0002 | c0002 | t0003 | g0042 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02155 | hp1 | a0010 | c0017 | t0003 | g0038 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0036 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02257 | hp1 | a0001 | c0001 | t0019 | g0113 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0034 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0116 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02280 | hp2 | a0002 | c0015 | t0016 | g0124 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02300 | hp2 | a0011 | c0021 | t0014 | g0056 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02615 | hp1 | a0002 | c0004 | t0009 | g0024 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02630 | hp1 | a0002 | c0004 | t0023 | g0069 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02630 | hp2 | a0002 | c0006 | t0001 | g0023 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02683 | hp1 | a0001 | c0001 | t0017 | g0080 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0045 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02723 | hp1 | a0001 | c0037 | t0005 | g0058 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02723 | hp2 | a0002 | c0004 | t0008 | g0028 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02735 | hp1 | a0002 | c0002 | t0007 | g0041 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02735 | hp2 | a0001 | c0001 | t0015 | g0148 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02809 | hp2 | a0012 | c0020 | t0001 | g0121 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02818 | hp1 | a0013 | c0014 | t0012 | g0104 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02886 | hp1 | a0002 | c0006 | t0001 | g0022 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0097 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02922 | hp2 | a0001 | c0005 | t0004 | g0130 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02970 | hp1 | a0014 | c0023 | t0001 | g0125 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02976 | hp1 | a0001 | c0007 | t0001 | g0071 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02976 | hp2 | a0015 | c0016 | t0022 | g0103 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03041 | hp2 | a0016 | c0013 | t0001 | g0087 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03098 | hp2 | a0001 | c0010 | t0001 | g0083 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03139 | hp1 | a0001 | c0035 | t0001 | g0102 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03139 | hp2 | a0002 | c0004 | t0010 | g0027 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03225 | hp2 | a0001 | c0031 | t0001 | g0094 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03453 | hp2 | a0002 | c0006 | t0001 | g0021 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0135 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0115 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03540 | hp2 | a0001 | c0022 | t0001 | g0066 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03669 | hp2 | a0017 | c0025 | t0001 | g0114 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0100 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03704 | hp1 | a0018 | c0027 | t0001 | g0054 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03704 | hp2 | a0001 | c0030 | t0001 | g0074 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03710 | hp1 | a0002 | c0008 | t0003 | g0044 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03927 | hp2 | a0002 | c0002 | t0003 | g0030 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG04228 | hp2 | a0002 | c0008 | t0003 | g0040 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18906 | hp1 | a0001 | c0007 | t0001 | g0050 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18906 | hp2 | a0001 | c0005 | t0003 | g0126 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18966 | hp2 | a0001 | c0036 | t0001 | g0082 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18981 | hp1 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18981 | hp2 | a0001 | c0011 | t0001 | g0068 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18983 | hp2 | a0001 | c0011 | t0001 | g0067 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | LWK | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19057 | hp1 | a0019 | c0029 | t0001 | g0134 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19057 | hp2 | a0002 | c0002 | t0020 | g0106 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0158 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19088 | hp1 | a0002 | c0002 | t0003 | g0159 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19240 | hp1 | a0020 | c0024 | t0001 | g0098 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19240 | hp2 | a0002 | c0004 | t0010 | g0026 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20129 | hp2 | a0001 | c0005 | t0004 | g0129 | AFR | ASW | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20805 | hp1 | a0001 | c0001 | t0013 | g0063 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0039 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01123 | hp1 | a0001 | c0005 | t0004 | g0127 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02109 | hp1 | a0003 | c0012 | t0004 | g0128 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02109 | hp2 | a0002 | c0004 | t0009 | g0025 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02559 | hp1 | a0003 | c0019 | t0004 | g0123 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0070 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0051 | REF | REF | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42336021 | G | A | 1 | a0016 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.919G>A | p.Val307Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/42 | 1528/11137 | 919/8538 | 307/2845 | chr19 | 42336021 | |||
chr19:42349650 | A | G | 1 | a0008 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2450A>G | p.His817Arg | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/42 | 3059/11137 | 2450/8538 | 817/2845 | chr19 | 42349650 | |||
chr19:42351538 | G | A | 1 | a0011 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2965G>A | p.Gly989Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 17/42 | 3574/11137 | 2965/8538 | 989/2845 | chr19 | 42351538 | |||
chr19:42353032 | C | T | 1 | a0015 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.3455C>T | p.Pro1152Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4064/11137 | 3455/8538 | 1152/2845 | chr19 | 42353032 | |||
chr19:42353539 | C | T | 1 | a0009 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.3625C>T | p.Arg1209Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 21/42 | 4234/11137 | 3625/8538 | 1209/2845 | chr19 | 42353539 | |||
chr19:42353674 | C | T | 1 | a0005 | 1 | HG00609.hp1 | missense_variant&splice_region_variant | MODERATE | c.3760C>T | p.Arg1254Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 21/42 | 4369/11137 | 3760/8538 | 1254/2845 | chr19 | 42353674 | |||
chr19:42356890 | C | T | 1 | a0019 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.4739C>T | p.Ala1580Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/42 | 5348/11137 | 4739/8538 | 1580/2845 | chr19 | 42356890 | |||
chr19:42358820 | C | T | 1 | a0012 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.5209C>T | p.Arg1737Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5818/11137 | 5209/8538 | 1737/2845 | chr19 | 42358820 | |||
chr19:42358883 | A | G | 5 | a0002 a0007 a0010 others(2): Show |
35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
missense_variant | MODERATE | c.5272A>G | p.Lys1758Glu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5881/11137 | 5272/8538 | 1758/2845 | chr19 | 42358883 | |||
chr19:42358931 | G | C | 1 | a0013 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.5320G>C | p.Glu1774Gln | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5929/11137 | 5320/8538 | 1774/2845 | chr19 | 42358931 | |||
chr19:42362149 | G | A | 1 | a0014 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.5780G>A | p.Arg1927His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 33/42 | 6389/11137 | 5780/8538 | 1927/2845 | chr19 | 42362149 | |||
chr19:42368650 | G | A | 1 | a0010 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.6469G>A | p.Gly2157Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/42 | 7078/11137 | 6469/8538 | 2157/2845 | chr19 | 42368650 | |||
chr19:42369710 | G | A | 1 | a0020 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6821G>A | p.Arg2274His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/42 | 7430/11137 | 6821/8538 | 2274/2845 | chr19 | 42369710 | |||
chr19:42370265 | C | A | 1 | a0017 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.6911C>A | p.Ala2304Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/42 | 7520/11137 | 6911/8538 | 2304/2845 | chr19 | 42370265 | |||
chr19:42370749 | G | A | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.7054G>A | p.Val2352Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/42 | 7663/11137 | 7054/8538 | 2352/2845 | chr19 | 42370749 | |||
chr19:42375910 | C | T | 2 | a0006 a0007 |
2 | HG01074.hp1 HG01175.hp2 |
missense_variant | MODERATE | c.7673C>T | p.Pro2558Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8282/11137 | 7673/8538 | 2558/2845 | chr19 | 42375910 | |||
chr19:42375999 | G | A | 1 | a0013 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.7762G>A | p.Val2588Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8371/11137 | 7762/8538 | 2588/2845 | chr19 | 42375999 | |||
chr19:42376377 | G | A | 1 | a0018 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.8140G>A | p.Ala2714Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8749/11137 | 8140/8538 | 2714/2845 | chr19 | 42376377 | |||
chr19:42376663 | G | A | 1 | a0003 | 2 | HG02109.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.8426G>A | p.Arg2809Lys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9035/11137 | 8426/8538 | 2809/2845 | chr19 | 42376663 | |||
chr19:42376704 | A | G | 1 | a0013 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.8467A>G | p.Ser2823Gly | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9076/11137 | 8467/8538 | 2823/2845 | chr19 | 42376704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326250 | C | T | 1 | a0001c0037 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.7C>T | p.Leu3Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 616/11137 | 7/8538 | 3/2845 | chr19 | 42326250 | |||
chr19:42334012 | G | A | 1 | a0003c0012 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.357G>A | p.Leu119Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/42 | 966/11137 | 357/8538 | 119/2845 | chr19 | 42334012 | |||
chr19:42334057 | C | T | 1 | a0001c0036 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.402C>T | p.Asn134Asn | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/42 | 1011/11137 | 402/8538 | 134/2845 | chr19 | 42334057 | |||
chr19:42336020 | C | T | 1 | a0001c0035 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.918C>T | p.Asp306Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/42 | 1527/11137 | 918/8538 | 306/2845 | chr19 | 42336020 | |||
chr19:42348328 | G | A | 9 | a0002c0002 a0002c0004 a0002c0006 others(6): Show |
35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.2154G>A | p.Val718Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/42 | 2763/11137 | 2154/8538 | 718/2845 | chr19 | 42348328 | |||
chr19:42348397 | C | T | 4 | a0002c0002 a0002c0008 a0007c0018 others(1): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.2223C>T | p.Asp741Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/42 | 2832/11137 | 2223/8538 | 741/2845 | chr19 | 42348397 | |||
chr19:42349630 | T | C | 14 | a0001c0003 a0001c0005 a0002c0002 others(11): Show |
57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
synonymous_variant | LOW | c.2430T>C | p.Asn810Asn | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/42 | 3039/11137 | 2430/8538 | 810/2845 | chr19 | 42349630 | |||
chr19:42351717 | C | T | 1 | a0001c0011 | 2 | NA18981.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.3057C>T | p.His1019His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 18/42 | 3666/11137 | 3057/8538 | 1019/2845 | chr19 | 42351717 | |||
chr19:42353010 | C | T | 1 | a0001c0007 | 3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.3433C>T | p.Leu1145Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4042/11137 | 3433/8538 | 1145/2845 | chr19 | 42353010 | |||
chr19:42353027 | C | T | 4 | a0002c0002 a0002c0008 a0007c0018 others(1): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.3450C>T | p.Pro1150Pro | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4059/11137 | 3450/8538 | 1150/2845 | chr19 | 42353027 | |||
chr19:42354596 | C | T | 3 | a0001c0003 a0003c0019 a0012c0020 |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.4020C>T | p.Tyr1340Tyr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4629/11137 | 4020/8538 | 1340/2845 | chr19 | 42354596 | |||
chr19:42354617 | C | T | 1 | a0001c0031 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.4041C>T | p.Phe1347Phe | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4650/11137 | 4041/8538 | 1347/2845 | chr19 | 42354617 | |||
chr19:42354641 | T | C | 4 | a0002c0002 a0002c0008 a0007c0018 others(1): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.4065T>C | p.Val1355Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4674/11137 | 4065/8538 | 1355/2845 | chr19 | 42354641 | |||
chr19:42355972 | C | T | 1 | a0001c0030 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4359C>T | p.Cys1453Cys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 24/42 | 4968/11137 | 4359/8538 | 1453/2845 | chr19 | 42355972 | |||
chr19:42356864 | C | T | 1 | a0002c0008 | 2 | HG03710.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.4713C>T | p.Ala1571Ala | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/42 | 5322/11137 | 4713/8538 | 1571/2845 | chr19 | 42356864 | |||
chr19:42357415 | C | T | 1 | a0001c0010 | 2 | HG00738.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.4842C>T | p.Thr1614Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/42 | 5451/11137 | 4842/8538 | 1614/2845 | chr19 | 42357415 | |||
chr19:42358927 | G | A | 1 | a0003c0012 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.5316G>A | p.Leu1772Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5925/11137 | 5316/8538 | 1772/2845 | chr19 | 42358927 | |||
chr19:42359166 | G | A | 1 | a0001c0022 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.5412G>A | p.Ser1804Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/42 | 6021/11137 | 5412/8538 | 1804/2845 | chr19 | 42359166 | |||
chr19:42359229 | G | A | 3 | a0001c0003 a0003c0019 a0012c0020 |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.5475G>A | p.Leu1825Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/42 | 6084/11137 | 5475/8538 | 1825/2845 | chr19 | 42359229 | |||
chr19:42368937 | G | A | 2 | a0002c0004 a0002c0015 |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
synonymous_variant | LOW | c.6576G>A | p.Thr2192Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/42 | 7185/11137 | 6576/8538 | 2192/2845 | chr19 | 42368937 | |||
chr19:42370748 | C | T | 1 | a0002c0004 | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.7053C>T | p.Cys2351Cys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/42 | 7662/11137 | 7053/8538 | 2351/2845 | chr19 | 42370748 | |||
chr19:42375968 | C | T | 1 | a0001c0009 | 2 | HG00621.hp1 HG02080.hp1 |
synonymous_variant | LOW | c.7731C>T | p.Tyr2577Tyr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8340/11137 | 7731/8538 | 2577/2845 | chr19 | 42375968 | |||
chr19:42375974 | G | A | 3 | a0002c0015 a0013c0014 a0015c0016 |
3 | HG02280.hp2 HG02818.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.7737G>A | p.Thr2579Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8346/11137 | 7737/8538 | 2579/2845 | chr19 | 42375974 | |||
chr19:42376703 | C | A | 1 | a0013c0014 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.8466C>A | p.Gly2822Gly | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9075/11137 | 8466/8538 | 2822/2845 | chr19 | 42376703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326085 | A | T | 3 | a0002c0004t0008 a0002c0004t0009 a0002c0004t0010 |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-159A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 159 | chr19 | 42326085 | ||||||
chr19:42326117 | C | T | 1 | a0001c0001t0024 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 127 | chr19 | 42326117 | ||||||
chr19:42376987 | C | T | 1 | a0001c0001t0006 | 3 | HG00597.hp1 HG00609.hp2 HG00621.hp2 |
3_prime_UTR_variant | MODIFIER | c.*212C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 212 | chr19 | 42376987 | ||||||
chr19:42377079 | C | T | 3 | a0002c0004t0009 a0002c0004t0010 a0002c0004t0023 |
5 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 304 | chr19 | 42377079 | ||||||
chr19:42377181 | G | A | 1 | a0001c0001t0011 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 406 | chr19 | 42377181 | ||||||
chr19:42377680 | G | A | 1 | a0013c0014t0012 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 905 | chr19 | 42377680 | ||||||
chr19:42377753 | C | T | 1 | a0015c0016t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*978C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 978 | chr19 | 42377753 | ||||||
chr19:42377803 | T | A | 2 | a0001c0001t0005 a0001c0037t0005 |
4 | HG01884.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1028T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1028 | chr19 | 42377803 | ||||||
chr19:42377840 | C | T | 2 | a0002c0002t0020 a0002c0002t0021 |
2 | HG02074.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1065C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1065 | chr19 | 42377840 | ||||||
chr19:42377940 | G | A | 1 | a0001c0001t0013 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1165 | chr19 | 42377940 | ||||||
chr19:42377943 | G | A | 7 | a0001c0005t0003 a0002c0002t0003 a0002c0002t0020 others(4): Show |
21 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1168G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1168 | chr19 | 42377943 | ||||||
chr19:42378052 | C | A | 1 | a0011c0021t0014 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1277 | chr19 | 42378052 | ||||||
chr19:42378221 | C | T | 3 | a0001c0001t0019 a0002c0004t0008 a0002c0004t0010 |
5 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1446C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1446 | chr19 | 42378221 | ||||||
chr19:42378393 | A | G | 1 | a0002c0002t0021 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1618 | chr19 | 42378393 | ||||||
chr19:42378397 | G | A | 2 | a0001c0001t0015 a0001c0001t0024 |
2 | HG01346.hp2 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1622G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1622 | chr19 | 42378397 | ||||||
chr19:42378424 | C | T | 5 | a0001c0001t0018 a0002c0004t0008 a0002c0004t0009 others(2): Show |
8 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1649C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1649 | chr19 | 42378424 | ||||||
chr19:42378493 | G | A | 2 | a0001c0001t0007 a0002c0002t0007 |
2 | HG02735.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1718G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1718 | chr19 | 42378493 | ||||||
chr19:42378514 | C | T | 1 | a0001c0001t0017 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1739C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1739 | chr19 | 42378514 | ||||||
chr19:42378627 | G | C | 3 | a0002c0004t0009 a0002c0004t0023 a0013c0014t0012 |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1852G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1852 | chr19 | 42378627 | ||||||
chr19:42378677 | TA | T | 18 | a0001c0001t0002 a0001c0005t0003 a0001c0005t0004 others(15): Show |
55 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1903delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1903 | chr19 | 42378677 | ||||||
chr19:42378701 | T | C | 14 | a0001c0005t0003 a0001c0005t0004 a0002c0002t0003 others(11): Show |
33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1926T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1926 | chr19 | 42378701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326739 | CT | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(110): Show |
120 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.187+329delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42326739 | ||||||
chr19:42326739 | CTT | C | 6 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(3): Show |
6 | HG01069.hp1 HG01993.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+328_187+329del others(2): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42326739 | ||||||
chr19:42326751 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01069.hp2 HG01934.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+321T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326751 | |||||||
chr19:42326909 | C | T | 6 | a0001c0005t0003g0126 a0001c0005t0004g0127 a0001c0005t0004g0129 others(3): Show |
6 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+479C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326909 | |||||||
chr19:42326931 | T | C | 26 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(23): Show |
26 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+501T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326931 | |||||||
chr19:42327033 | A | G | 21 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(18): Show |
26 | HG00140.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+603A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327033 | |||||||
chr19:42327044 | T | C | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.187+614T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327044 | |||||||
chr19:42327562 | C | G | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1132C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327562 | |||||||
chr19:42327664 | G | A | 6 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+1234G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327664 | |||||||
chr19:42327670 | C | T | 2 | a0002c0015t0016g0124 a0014c0023t0001g0125 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.187+1240C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327670 | |||||||
chr19:42328209 | A | G | 28 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(25): Show |
28 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.187+1779A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328209 | |||||||
chr19:42328405 | T | A | 22 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.187+1975T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328405 | |||||||
chr19:42328567 | A | AGT | 45 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0001t0001g0077 others(42): Show |
51 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.187+2159_187+2160d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGT | 2 | a0001c0001t0005g0101 a0001c0035t0001g0102 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.187+2157_187+2160d others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(11): Show |
2 | a0001c0005t0004g0127 a0002c0004t0009g0024 |
2 | HG01123.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.187+2143_187+2160d others(20): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(13): Show |
1 | a0002c0004t0009g0025 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.187+2141_187+2160d others(22): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(15): Show |
5 | a0002c0002t0003g0030 a0002c0004t0008g0028 a0002c0004t0008g0029 others(2): Show |
5 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2139_187+2160d others(24): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(17): Show |
3 | a0002c0002t0003g0031 a0002c0002t0003g0032 a0002c0006t0001g0021 |
3 | HG01993.hp1 HG03453.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.187+2160_187+2161i others(26): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(19): Show |
12 | a0001c0005t0003g0126 a0002c0002t0001g0037 a0002c0002t0003g0015 others(9): Show |
12 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(28): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(21): Show |
1 | a0002c0002t0003g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.187+2160_187+2161i others(30): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(23): Show |
7 | a0001c0005t0004g0129 a0002c0002t0003g0042 a0002c0002t0007g0041 others(4): Show |
7 | HG01175.hp2 HG02135.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(32): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328567 | A | AGTGTGTG others(25): Show |
5 | a0001c0005t0004g0130 a0001c0005t0004g0131 a0002c0002t0003g0045 others(2): Show |
5 | HG01891.hp1 HG02683.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(34): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | ||||||
chr19:42328674 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+2244G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328674 | |||||||
chr19:42329015 | G | C | 1 | a0001c0030t0001g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.187+2585G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329015 | |||||||
chr19:42329127 | C | T | 1 | a0007c0018t0003g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.187+2697C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329127 | |||||||
chr19:42329198 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0002g0075 |
3 | HG01258.hp1 HG01516.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.187+2768G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329198 | |||||||
chr19:42329389 | T | C | 1 | a0002c0002t0003g0031 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.187+2959T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329389 | |||||||
chr19:42329452 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+3022G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329452 | |||||||
chr19:42329498 | G | A | 6 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3068G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329498 | |||||||
chr19:42329763 | C | T | 6 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3333C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329763 | |||||||
chr19:42329828 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.187+3398C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329828 | |||||||
chr19:42329854 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3424A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329854 | |||||||
chr19:42329948 | A | C | 1 | a0003c0019t0004g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.187+3518A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329948 | |||||||
chr19:42329982 | G | C | 1 | a0002c0008t0003g0044 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+3552G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329982 | |||||||
chr19:42329991 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.187+3561G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329991 | |||||||
chr19:42330178 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.188-3427A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330178 | |||||||
chr19:42330556 | T | C | 6 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(3): Show |
6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-3049T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330556 | |||||||
chr19:42330570 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.188-3035G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330570 | |||||||
chr19:42330599 | A | G | 60 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(57): Show |
65 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.188-3006A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330599 | |||||||
chr19:42330790 | T | C | 1 | a0002c0008t0003g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188-2815T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330790 | |||||||
chr19:42330937 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.188-2668C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330937 | |||||||
chr19:42331540 | T | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
162 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(159): Show |
intron_variant | MODIFIER | c.188-2065T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331540 | |||||||
chr19:42331545 | G | A | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.188-2060G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331545 | |||||||
chr19:42331849 | C | T | 3 | a0001c0001t0011g0100 a0013c0014t0012g0104 a0015c0016t0022g0103 |
3 | HG02818.hp1 HG02976.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.188-1756C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331849 | |||||||
chr19:42331939 | A | C | 4 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0010g0026 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-1666A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331939 | |||||||
chr19:42332164 | C | T | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.188-1441C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332164 | |||||||
chr19:42332398 | G | A | 11 | a0001c0003t0001g0001 a0001c0003t0001g0020 a0001c0003t0001g0115 others(8): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-1207G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332398 | |||||||
chr19:42332494 | A | G | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.188-1111A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332494 | |||||||
chr19:42333112 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-493G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333112 | |||||||
chr19:42333253 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.188-352G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333253 | |||||||
chr19:42333494 | A | G | 2 | a0001c0007t0001g0070 a0001c0007t0001g0071 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.188-111A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333494 | |||||||
chr19:42333504 | A | G | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-101A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333504 | |||||||
chr19:42333769 | G | T | 1 | a0002c0002t0003g0045 | 1 | HG02683.hp2 | splice_donor_variant&intron_variant | HIGH | c.351+1G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 2/41 | chr19 | 42333769 | |||||||
chr19:42334003 | G | A | 4 | a0002c0002t0003g0015 a0002c0002t0003g0032 a0002c0002t0003g0033 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.352-4G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 2/41 | chr19 | 42334003 | |||||||
chr19:42334265 | G | C | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.558+52G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334265 | |||||||
chr19:42334359 | C | G | 2 | a0001c0011t0001g0067 a0001c0011t0001g0068 |
2 | NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.558+146C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334359 | |||||||
chr19:42334733 | C | T | 1 | a0001c0022t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.559-302C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334733 | |||||||
chr19:42335254 | G | A | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.739+39G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 4/41 | chr19 | 42335254 | |||||||
chr19:42335445 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.828+60C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335445 | |||||||
chr19:42335755 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.829-176C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335755 | |||||||
chr19:42335867 | G | A | 1 | a0008c0034t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.829-64G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335867 | |||||||
chr19:42336546 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1244+200C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/41 | chr19 | 42336546 | |||||||
chr19:42336734 | G | A | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1245-73G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/41 | chr19 | 42336734 | |||||||
chr19:42337405 | T | C | 22 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1513+199T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337405 | |||||||
chr19:42337501 | C | G | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513+295C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337501 | |||||||
chr19:42337506 | C | CT | 7 | a0001c0001t0001g0019 a0001c0001t0018g0097 a0002c0002t0003g0030 others(4): Show |
7 | HG01175.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513+319dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42337506 | ||||||
chr19:42337631 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+425T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337631 | |||||||
chr19:42337660 | C | T | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1513+454C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337660 | |||||||
chr19:42337802 | G | A | 1 | a0001c0009t0001g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1513+596G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337802 | |||||||
chr19:42337811 | T | C | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1513+605T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337811 | |||||||
chr19:42338256 | T | G | 2 | a0001c0003t0001g0115 a0001c0003t0001g0116 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1513+1050T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338256 | |||||||
chr19:42338328 | C | T | 1 | a0002c0002t0003g0032 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513+1122C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338328 | |||||||
chr19:42338450 | A | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+1244A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338450 | |||||||
chr19:42338642 | T | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+1436T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338642 | |||||||
chr19:42338825 | A | AT | 12 | a0001c0001t0001g0065 a0001c0001t0001g0096 a0001c0001t0001g0132 others(9): Show |
12 | HG00597.hp1 HG01175.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1513+1646dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | ||||||
chr19:42338825 | A | T | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1513+1619A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338825 | |||||||
chr19:42338825 | AT | A | 29 | a0001c0001t0001g0047 a0001c0001t0001g0079 a0001c0001t0002g0016 others(26): Show |
29 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1513+1646delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | ||||||
chr19:42338825 | ATT | A | 5 | a0001c0001t0001g0019 a0002c0002t0003g0035 a0002c0006t0001g0021 others(2): Show |
5 | HG00639.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1513+1645_1513+164 others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | ||||||
chr19:42338825 | ATTTTTTT others(8): Show |
A | 3 | a0001c0007t0001g0050 a0001c0007t0001g0070 a0001c0007t0001g0071 |
3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1513+1632_1513+164 others(19): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | ||||||
chr19:42338858 | G | A | 1 | a0008c0034t0001g0107 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1513+1652G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338858 | |||||||
chr19:42339013 | T | C | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1513+1807T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42339013 | |||||||
chr19:42339724 | C | T | 1 | a0001c0003t0001g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1513+2518C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42339724 | |||||||
chr19:42340139 | T | C | 1 | a0001c0001t0005g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1513+2933T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340139 | |||||||
chr19:42340375 | G | A | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514-3102G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340375 | |||||||
chr19:42340576 | T | G | 1 | a0001c0001t0002g0136 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1514-2901T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340576 | |||||||
chr19:42340723 | G | A | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1514-2754G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340723 | |||||||
chr19:42340852 | G | C | 2 | a0001c0001t0001g0108 a0001c0001t0019g0113 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1514-2625G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340852 | |||||||
chr19:42340962 | C | G | 1 | a0001c0005t0003g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1514-2515C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340962 | |||||||
chr19:42341242 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1514-2235T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341242 | |||||||
chr19:42341259 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1514-2218G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341259 | |||||||
chr19:42341429 | C | CA | 24 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0053 others(21): Show |
24 | HG00621.hp2 HG01175.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1514-2027dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341429 | ||||||
chr19:42341429 | CA | C | 34 | a0001c0001t0001g0151 a0001c0003t0001g0119 a0001c0005t0004g0129 others(31): Show |
34 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1514-2027delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341429 | ||||||
chr19:42341450 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1514-2027A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341450 | |||||||
chr19:42341727 | G | C | 2 | a0002c0015t0016g0124 a0013c0014t0012g0104 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1514-1750G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341727 | |||||||
chr19:42341832 | C | T | 2 | a0002c0015t0016g0124 a0013c0014t0012g0104 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1514-1645C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341832 | |||||||
chr19:42341835 | TA | T | 5 | a0001c0003t0001g0115 a0001c0003t0001g0116 a0001c0003t0001g0118 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1514-1639delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341835 | ||||||
chr19:42341899 | C | T | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1514-1578C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341899 | |||||||
chr19:42341912 | C | T | 1 | a0001c0001t0013g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1514-1565C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341912 | |||||||
chr19:42341922 | C | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-1555C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341922 | |||||||
chr19:42342434 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1514-1043C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342434 | |||||||
chr19:42342567 | A | G | 9 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1514-910A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342567 | |||||||
chr19:42342599 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1514-878G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342599 | |||||||
chr19:42342599 | G | T | 34 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(31): Show |
34 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1514-878G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342599 | |||||||
chr19:42342636 | C | CA | 9 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1514-827dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42342636 | ||||||
chr19:42343082 | G | A | 1 | a0001c0001t0011g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1514-395G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343082 | |||||||
chr19:42343241 | T | C | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-236T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343241 | |||||||
chr19:42343302 | C | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-175C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343302 | |||||||
chr19:42343714 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1668+83G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 9/41 | chr19 | 42343714 | |||||||
chr19:42343841 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0031t0001g0094 |
3 | HG02145.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1669-113C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 9/41 | chr19 | 42343841 | |||||||
chr19:42344191 | G | C | 1 | a0001c0001t0011g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1788+118G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 10/41 | chr19 | 42344191 | |||||||
chr19:42344292 | G | A | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1789-149G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 10/41 | chr19 | 42344292 | |||||||
chr19:42344598 | A | G | 7 | a0002c0002t0003g0015 a0002c0002t0003g0032 a0002c0002t0003g0033 others(4): Show |
7 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1933+13A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344598 | |||||||
chr19:42344612 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(142): Show |
155 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.1933+27A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344612 | |||||||
chr19:42344663 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1934-7T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344663 | |||||||
chr19:42345291 | G | T | 3 | a0002c0004t0009g0024 a0002c0004t0009g0025 a0002c0004t0023g0069 |
3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2097+458G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42345291 | |||||||
chr19:42345969 | T | C | 52 | a0001c0003t0001g0001 a0001c0003t0001g0020 a0001c0003t0001g0115 others(49): Show |
57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2097+1136T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42345969 | |||||||
chr19:42346101 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2097+1268T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346101 | |||||||
chr19:42346398 | C | T | 1 | a0014c0023t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2097+1565C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346398 | |||||||
chr19:42346402 | C | T | 1 | a0007c0018t0003g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2097+1569C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346402 | |||||||
chr19:42346611 | A | C | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098-1661A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346611 | |||||||
chr19:42346800 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0002g0062 |
2 | HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2098-1472C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346800 | |||||||
chr19:42346984 | C | CA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0142 a0001c0001t0002g0075 others(3): Show |
6 | HG01516.hp2 HG01978.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2098-1267dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | ||||||
chr19:42346984 | CA | C | 34 | a0001c0001t0001g0150 a0001c0001t0002g0016 a0001c0001t0006g0145 others(31): Show |
34 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.2098-1267delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | ||||||
chr19:42346984 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0061 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2098-1277_2098-126 others(15): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | ||||||
chr19:42346999 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2098-1273A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346999 | |||||||
chr19:42347059 | C | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0142 others(5): Show |
10 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.2098-1213C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347059 | |||||||
chr19:42347071 | C | A | 1 | a0019c0029t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1201C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347071 | |||||||
chr19:42347072 | T | C | 1 | a0019c0029t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1200T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347072 | |||||||
chr19:42347074 | A | T | 1 | a0019c0029t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1198A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347074 | |||||||
chr19:42347081 | C | T | 1 | a0019c0029t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1191C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347081 | |||||||
chr19:42347218 | T | G | 1 | a0011c0021t0014g0056 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2098-1054T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347218 | |||||||
chr19:42347585 | C | T | 1 | a0001c0035t0001g0102 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2098-687C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347585 | |||||||
chr19:42347760 | C | G | 52 | a0001c0003t0001g0001 a0001c0003t0001g0020 a0001c0003t0001g0115 others(49): Show |
57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2098-512C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347760 | |||||||
chr19:42347908 | A | G | 3 | a0002c0004t0009g0024 a0002c0004t0009g0025 a0002c0004t0023g0069 |
3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2098-364A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347908 | |||||||
chr19:42348011 | G | A | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098-261G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348011 | |||||||
chr19:42348126 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2098-146C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348126 | |||||||
chr19:42348186 | G | A | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2098-86G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348186 | |||||||
chr19:42348691 | C | T | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2298+219C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | chr19 | 42348691 | |||||||
chr19:42349300 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2299-199A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | chr19 | 42349300 | |||||||
chr19:42349302 | GA | G | 19 | a0001c0003t0001g0001 a0001c0003t0001g0020 a0001c0003t0001g0115 others(16): Show |
24 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2299-179delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | INFO_REALIGN_3_PRIME | chr19 | 42349302 | ||||||
chr19:42349849 | T | G | 26 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(23): Show |
26 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2499+150T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/41 | chr19 | 42349849 | |||||||
chr19:42349930 | C | G | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2500-218C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/41 | chr19 | 42349930 | |||||||
chr19:42350453 | G | A | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2736+69G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350453 | |||||||
chr19:42350464 | G | T | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2736+80G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350464 | |||||||
chr19:42350608 | T | C | 1 | a0001c0003t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2736+224T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350608 | |||||||
chr19:42350839 | A | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0059 others(15): Show |
20 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.2737-377A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350839 | |||||||
chr19:42350943 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2737-273C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350943 | |||||||
chr19:42350988 | G | A | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2737-228G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350988 | |||||||
chr19:42351015 | T | C | 35 | a0001c0001t0001g0081 a0002c0002t0001g0037 a0002c0002t0003g0015 others(32): Show |
35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2737-201T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42351015 | |||||||
chr19:42351038 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01258.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2737-178C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42351038 | |||||||
chr19:42352146 | G | A | 1 | a0017c0025t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3102-62G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 18/41 | chr19 | 42352146 | |||||||
chr19:42352925 | C | T | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3351-3C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 19/41 | chr19 | 42352925 | |||||||
chr19:42353245 | C | T | 22 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3550+118C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353245 | |||||||
chr19:42353293 | A | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.3550+166A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353293 | |||||||
chr19:42353360 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3551-105C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353360 | |||||||
chr19:42354118 | GT | G | 36 | a0001c0001t0019g0113 a0002c0002t0001g0037 a0002c0002t0003g0015 others(33): Show |
36 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.4011+107delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr19 | 42354118 | ||||||
chr19:42354171 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4011+147C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354171 | |||||||
chr19:42354239 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4011+215G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354239 | |||||||
chr19:42354516 | C | G | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.4012-72C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354516 | |||||||
chr19:42355084 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0019g0113 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4144+364G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | chr19 | 42355084 | |||||||
chr19:42355255 | CAT | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.4145-489_4145-488d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | INFO_REALIGN_3_PRIME | chr19 | 42355255 | ||||||
chr19:42355375 | G | A | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4145-383G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | chr19 | 42355375 | |||||||
chr19:42356497 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4622+44G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 26/41 | chr19 | 42356497 | |||||||
chr19:42356712 | G | A | 1 | a0002c0002t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4623-62G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 26/41 | chr19 | 42356712 | |||||||
chr19:42357068 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4830+87C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357068 | |||||||
chr19:42357141 | G | A | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.4830+160G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357141 | |||||||
chr19:42357323 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0147 a0001c0001t0001g0150 others(1): Show |
4 | HG00639.hp1 HG01074.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.4831-81G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357323 | |||||||
chr19:42357599 | C | T | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5011+15C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357599 | |||||||
chr19:42357700 | A | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5011+116A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357700 | |||||||
chr19:42357766 | C | T | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5011+182C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357766 | |||||||
chr19:42357807 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5011+223C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357807 | |||||||
chr19:42358749 | G | A | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5176-38G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 29/41 | chr19 | 42358749 | |||||||
chr19:42359084 | C | T | 1 | a0001c0035t0001g0102 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5344-14C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/41 | chr19 | 42359084 | |||||||
chr19:42359254 | T | C | 1 | a0013c0014t0012g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5488+12T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359254 | |||||||
chr19:42359380 | T | C | 1 | a0002c0002t0020g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5488+138T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359380 | |||||||
chr19:42359405 | CT | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5488+173delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359405 | ||||||
chr19:42359684 | T | C | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5488+442T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359684 | |||||||
chr19:42359795 | C | G | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.5488+553C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359795 | |||||||
chr19:42359853 | A | AT | 31 | a0001c0001t0001g0065 a0001c0001t0001g0152 a0001c0001t0001g0156 others(28): Show |
31 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.5488+633dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | ||||||
chr19:42359853 | A | ATT | 7 | a0002c0004t0008g0029 a0002c0004t0009g0024 a0002c0004t0009g0025 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.5488+632_5488+633d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | ||||||
chr19:42359853 | AT | A | 5 | a0001c0001t0002g0075 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01516.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5488+633delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | ||||||
chr19:42359900 | G | T | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5488+658G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359900 | |||||||
chr19:42360150 | C | CA | 14 | a0001c0001t0002g0017 a0001c0001t0002g0057 a0001c0003t0001g0001 others(11): Show |
19 | HG01884.hp1 HG01891.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.5489-608dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360150 | ||||||
chr19:42360150 | CAAAA | C | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.5489-611_5489-608d others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360150 | ||||||
chr19:42360345 | G | GT | 9 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0152 others(6): Show |
9 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.5489-413dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360345 | ||||||
chr19:42360410 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5489-365A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360410 | |||||||
chr19:42360426 | A | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5489-349A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360426 | |||||||
chr19:42360482 | G | C | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5489-293G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360482 | |||||||
chr19:42361044 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5720+38G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361044 | |||||||
chr19:42361131 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0076 others(13): Show |
18 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.5720+125G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361131 | |||||||
chr19:42361324 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5720+318C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361324 | |||||||
chr19:42361357 | A | G | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5720+351A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361357 | |||||||
chr19:42361901 | G | A | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5721-189G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361901 | |||||||
chr19:42362718 | C | G | 1 | a0002c0002t0007g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6058+121C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362718 | |||||||
chr19:42362867 | C | T | 11 | a0001c0003t0001g0001 a0001c0003t0001g0020 a0001c0003t0001g0115 others(8): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.6059-181C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362867 | |||||||
chr19:42362869 | G | A | 1 | a0002c0002t0003g0036 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6059-179G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362869 | |||||||
chr19:42363394 | C | T | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6273+132C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363394 | |||||||
chr19:42363395 | G | T | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+133G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363395 | |||||||
chr19:42363601 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.6273+339G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363601 | |||||||
chr19:42363736 | C | T | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6273+474C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363736 | |||||||
chr19:42363845 | C | T | 1 | a0001c0022t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6273+583C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363845 | |||||||
chr19:42363873 | C | T | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6273+611C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363873 | |||||||
chr19:42363917 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+655T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363917 | |||||||
chr19:42363929 | T | C | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6273+667T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363929 | |||||||
chr19:42364028 | C | A | 1 | a0001c0001t0002g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6273+766C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364028 | |||||||
chr19:42364065 | G | A | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6273+803G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364065 | |||||||
chr19:42364126 | T | C | 1 | a0012c0020t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6273+864T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364126 | |||||||
chr19:42364446 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.6273+1184A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364446 | |||||||
chr19:42364598 | C | T | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6273+1336C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364598 | |||||||
chr19:42365272 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+2010T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42365272 | |||||||
chr19:42365404 | T | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+2142T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42365404 | |||||||
chr19:42365772 | T | TA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0061 others(8): Show |
12 | HG00741.hp1 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.6273+2536dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | ||||||
chr19:42365772 | TA | T | 22 | a0001c0001t0001g0072 a0001c0001t0001g0144 a0001c0001t0002g0016 others(19): Show |
27 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.6273+2536delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | ||||||
chr19:42365772 | TAAAA | T | 31 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(28): Show |
31 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.6273+2533_6273+253 others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | ||||||
chr19:42366232 | G | A | 1 | a0002c0002t0003g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6274-2223G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42366232 | |||||||
chr19:42366721 | A | C | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6274-1734A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42366721 | |||||||
chr19:42367144 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(117): Show |
127 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.6274-1311G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367144 | |||||||
chr19:42367290 | C | CT | 5 | a0001c0001t0001g0089 a0001c0001t0001g0153 a0001c0001t0001g0155 others(2): Show |
5 | HG01261.hp2 HG02683.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.6274-1149dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42367290 | ||||||
chr19:42367290 | CT | C | 5 | a0001c0001t0001g0076 a0002c0002t0003g0015 a0002c0006t0001g0021 others(2): Show |
5 | HG01069.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6274-1149delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42367290 | ||||||
chr19:42367294 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6274-1161T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367294 | |||||||
chr19:42367375 | A | G | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6274-1080A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367375 | |||||||
chr19:42367416 | G | A | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6274-1039G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367416 | |||||||
chr19:42367445 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6274-1010C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367445 | |||||||
chr19:42367540 | G | A | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6274-915G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367540 | |||||||
chr19:42367560 | T | C | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6274-895T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367560 | |||||||
chr19:42367596 | C | T | 1 | a0014c0023t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6274-859C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367596 | |||||||
chr19:42367854 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6274-601G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367854 | |||||||
chr19:42368115 | A | G | 3 | a0002c0002t0003g0157 a0002c0002t0003g0158 a0002c0002t0003g0159 |
3 | NA18981.hp1 NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.6274-340A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368115 | |||||||
chr19:42368198 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6274-257G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368198 | |||||||
chr19:42368407 | TC | T | 25 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(22): Show |
25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6274-44delC | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42368407 | ||||||
chr19:42368446 | C | G | 1 | a0001c0001t0006g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.6274-9C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368446 | |||||||
chr19:42368673 | T | G | 1 | a0014c0023t0001g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6481+11T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/41 | chr19 | 42368673 | |||||||
chr19:42368827 | A | G | 1 | a0002c0008t0003g0044 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6482-16A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/41 | chr19 | 42368827 | |||||||
chr19:42369011 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0019g0113 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6641+9G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369011 | |||||||
chr19:42369218 | G | C | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6641+216G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369218 | |||||||
chr19:42369245 | C | T | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6641+243C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369245 | |||||||
chr19:42369487 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6642-44G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369487 | |||||||
chr19:42369930 | G | C | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6834+207G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42369930 | |||||||
chr19:42370069 | C | G | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6835-120C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370069 | |||||||
chr19:42370115 | C | G | 2 | a0001c0011t0001g0067 a0001c0011t0001g0068 |
2 | NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6835-74C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370115 | |||||||
chr19:42370130 | C | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6835-59C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370130 | |||||||
chr19:42370131 | G | A | 3 | a0001c0007t0001g0050 a0001c0007t0001g0070 a0001c0007t0001g0071 |
3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6835-58G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370131 | |||||||
chr19:42370150 | C | T | 2 | a0001c0001t0005g0084 a0001c0001t0005g0090 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6835-39C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370150 | |||||||
chr19:42370587 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-114A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370587 | |||||||
chr19:42370588 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-113G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370588 | |||||||
chr19:42370664 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-37A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370664 | |||||||
chr19:42370666 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-35G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370666 | |||||||
chr19:42370842 | CCGGGGG | C | 4 | a0001c0001t0001g0014 a0002c0002t0020g0106 a0002c0002t0021g0105 others(1): Show |
4 | HG01069.hp2 HG02074.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.7136+12_7136+17del others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | |||||||
chr19:42370842 | CCGGGGGG | C | 3 | a0002c0002t0003g0015 a0002c0002t0003g0034 a0002c0002t0003g0042 |
3 | HG01069.hp1 HG02135.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.7136+12_7136+18del others(7): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | |||||||
chr19:42370842 | CCGGGGGG others(1): Show |
C | 5 | a0002c0002t0003g0035 a0002c0002t0003g0158 a0002c0002t0003g0159 others(2): Show |
5 | HG00639.hp2 HG02155.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.7136+12_7136+19del others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | |||||||
chr19:42370842 | CCGGGGGG others(2): Show |
C | 7 | a0002c0002t0001g0037 a0002c0002t0003g0030 a0002c0002t0003g0032 others(4): Show |
7 | HG00597.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.7136+12_7136+20del others(9): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | |||||||
chr19:42370842 | CCGGGGGG others(3): Show |
C | 3 | a0002c0002t0003g0031 a0002c0002t0003g0036 a0002c0002t0003g0045 |
3 | HG02165.hp2 HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.7136+12_7136+21del others(10): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | |||||||
chr19:42370843 | CG | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0048 others(16): Show |
20 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.7136+41delG | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGG | C | 15 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0150 others(12): Show |
15 | HG00140.hp2 HG01074.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.7136+40_7136+41del others(2): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGG | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0059 others(11): Show |
17 | HG00597.hp1 HG00741.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.7136+39_7136+41del others(3): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGGG | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0064 a0001c0001t0001g0077 others(16): Show |
19 | HG00621.hp1 HG00621.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.7136+38_7136+41del others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGGGGGG others(6): Show |
C | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7136+29_7136+41del others(13): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGGGGGG others(10): Show |
C | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7136+25_7136+41del others(17): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGGGGGG others(12): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7136+23_7136+41del others(19): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370843 | CGGGGGGG others(13): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7136+22_7136+41del others(20): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | ||||||
chr19:42370847 | G | T | 1 | a0002c0002t0003g0157 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.7136+16G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370847 | |||||||
chr19:42370849 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7136+18G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370849 | |||||||
chr19:42370849 | G | T | 3 | a0002c0002t0020g0106 a0002c0002t0021g0105 a0002c0008t0003g0044 |
3 | HG02074.hp2 HG03710.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.7136+18G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370849 | |||||||
chr19:42370850 | G | T | 3 | a0002c0002t0003g0015 a0002c0002t0003g0034 a0002c0002t0003g0042 |
3 | HG01069.hp1 HG02135.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.7136+19G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370850 | |||||||
chr19:42370851 | G | C | 1 | a0006c0028t0002g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7136+20G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370851 | |||||||
chr19:42370851 | G | T | 5 | a0002c0002t0003g0035 a0002c0002t0003g0158 a0002c0002t0003g0159 others(2): Show |
5 | HG00639.hp2 HG02155.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.7136+20G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370851 | |||||||
chr19:42370852 | G | T | 7 | a0002c0002t0001g0037 a0002c0002t0003g0030 a0002c0002t0003g0032 others(4): Show |
7 | HG00597.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.7136+21G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370852 | |||||||
chr19:42370853 | G | T | 4 | a0001c0001t0005g0084 a0002c0002t0003g0031 a0002c0002t0003g0036 others(1): Show |
4 | HG02165.hp2 HG02683.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7136+22G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370853 | |||||||
chr19:42370854 | G | GT | 2 | a0001c0010t0001g0083 a0001c0010t0001g0088 |
2 | HG00738.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.7136+23_7136+24ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370854 | |||||||
chr19:42370854 | G | T | 2 | a0001c0001t0001g0111 a0002c0006t0001g0023 |
2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.7136+23G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370854 | |||||||
chr19:42370857 | G | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7136+26G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370857 | |||||||
chr19:42370860 | G | C | 1 | a0001c0022t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7136+29G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370860 | |||||||
chr19:42370863 | G | GT | 2 | a0001c0001t0001g0011 a0001c0001t0002g0057 |
2 | HG01978.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.7136+32_7136+33ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370863 | |||||||
chr19:42370863 | G | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0099 others(3): Show |
6 | HG01261.hp1 HG01934.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.7136+32G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370863 | |||||||
chr19:42370864 | G | GT | 4 | a0001c0001t0001g0089 a0001c0003t0001g0118 a0001c0005t0004g0129 others(1): Show |
4 | HG01884.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.7136+33_7136+34ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370864 | |||||||
chr19:42370864 | G | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0048 others(68): Show |
78 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.7136+33G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370864 | |||||||
chr19:42370865 | G | T | 2 | a0001c0001t0001g0059 a0011c0021t0014g0056 |
2 | HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.7136+34G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370865 | |||||||
chr19:42370866 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7136+35G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370866 | |||||||
chr19:42371064 | G | GCA | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7136+234_7136+235i others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42371064 | ||||||
chr19:42371064 | G | GCCC | 22 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.7136+235_7136+237d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42371064 | ||||||
chr19:42371068 | C | T | 7 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7136+237C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42371068 | |||||||
chr19:42371070 | T | A | 1 | a0002c0002t0003g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.7136+239T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42371070 | |||||||
chr19:42371809 | A | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+327A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42371809 | |||||||
chr19:42372039 | A | AAAC | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(88): Show |
97 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.7269+590_7269+592d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | ||||||
chr19:42372039 | A | AAACAAC | 5 | a0001c0001t0001g0089 a0001c0001t0001g0155 a0001c0001t0005g0090 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+587_7269+592d others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | ||||||
chr19:42372039 | A | AAACAACA others(5): Show |
3 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0031t0001g0094 |
3 | HG02145.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7269+581_7269+592d others(14): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | ||||||
chr19:42372039 | AAAC | A | 5 | a0001c0005t0004g0127 a0001c0005t0004g0129 a0001c0005t0004g0130 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+590_7269+592d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | ||||||
chr19:42372039 | AAACAAC | A | 22 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(19): Show |
22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.7269+587_7269+592d others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | ||||||
chr19:42372067 | AAC | A | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+587_7269+588d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372067 | ||||||
chr19:42372072 | C | A | 1 | a0002c0015t0016g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7269+590C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372072 | |||||||
chr19:42372074 | A | AAAAC | 4 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0010g0026 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.7269+593_7269+594i others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372074 | ||||||
chr19:42372074 | A | ACAAAAAC | 3 | a0002c0004t0009g0024 a0002c0004t0009g0025 a0002c0004t0023g0069 |
3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7269+592_7269+593i others(9): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | |||||||
chr19:42372074 | A | ACAAAC | 5 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG00140.hp1 HG01243.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+592_7269+593i others(7): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | |||||||
chr19:42372074 | A | C | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+592A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | |||||||
chr19:42372074 | AAC | A | 2 | a0013c0014t0012g0104 a0015c0016t0022g0103 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7269+616_7269+617d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372074 | ||||||
chr19:42372142 | T | C | 33 | a0002c0002t0001g0037 a0002c0002t0003g0015 a0002c0002t0003g0030 others(30): Show |
33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.7269+660T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372142 | |||||||
chr19:42372470 | C | A | 3 | a0002c0006t0001g0021 a0002c0006t0001g0022 a0002c0006t0001g0023 |
3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+988C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372470 | |||||||
chr19:42372490 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7269+1008A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372490 | |||||||
chr19:42372585 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.7269+1103G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372585 | |||||||
chr19:42372836 | C | T | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+1354C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372836 | |||||||
chr19:42373153 | C | T | 1 | a0001c0003t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7269+1671C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373153 | |||||||
chr19:42373167 | A | G | 1 | a0001c0010t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7269+1685A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373167 | |||||||
chr19:42373179 | G | A | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+1697G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373179 | |||||||
chr19:42373240 | G | A | 35 | a0001c0003t0001g0001 a0001c0003t0001g0115 a0001c0003t0001g0116 others(32): Show |
40 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.7269+1758G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373240 | |||||||
chr19:42373255 | G | C | 1 | a0001c0001t0005g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7269+1773G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373255 | |||||||
chr19:42373389 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7269+1907C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373389 | |||||||
chr19:42373477 | T | C | 1 | a0009c0033t0001g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7269+1995T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373477 | |||||||
chr19:42373576 | T | TG | 8 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7270-1931_7270-193 others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373576 | |||||||
chr19:42373625 | A | G | 1 | a0006c0028t0002g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7270-1882A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373625 | |||||||
chr19:42373706 | G | GT | 47 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(44): Show |
48 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.7270-1776dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | ||||||
chr19:42373706 | G | GTT | 10 | a0002c0002t0003g0031 a0002c0002t0003g0042 a0002c0002t0003g0157 others(7): Show |
10 | HG01175.hp2 HG02074.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.7270-1777_7270-177 others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | ||||||
chr19:42373706 | GTTTTTTT others(6): Show |
G | 3 | a0002c0004t0009g0024 a0002c0004t0009g0025 a0002c0004t0023g0069 |
3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7270-1788_7270-177 others(17): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | ||||||
chr19:42373718 | T | G | 10 | a0001c0003t0001g0001 a0001c0003t0001g0115 a0001c0003t0001g0116 others(7): Show |
15 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.7270-1789T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373718 | |||||||
chr19:42373952 | G | T | 3 | a0002c0004t0009g0024 a0002c0004t0009g0025 a0002c0004t0023g0069 |
3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7270-1555G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373952 | |||||||
chr19:42374385 | C | T | 9 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.7270-1122C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374385 | |||||||
chr19:42374388 | T | C | 9 | a0002c0004t0008g0028 a0002c0004t0008g0029 a0002c0004t0009g0024 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.7270-1119T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374388 | |||||||
chr19:42374470 | C | CA | 7 | a0001c0001t0001g0132 a0001c0001t0002g0017 a0001c0001t0002g0057 others(4): Show |
7 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.7270-1015dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42374470 | ||||||
chr19:42374470 | CA | C | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0061 others(21): Show |
24 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.7270-1015delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42374470 | ||||||
chr19:42374807 | T | C | 4 | a0002c0002t0003g0015 a0002c0002t0003g0032 a0002c0002t0003g0033 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.7270-700T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374807 | |||||||
chr19:42375043 | G | A | 1 | a0015c0016t0022g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7270-464G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375043 | |||||||
chr19:42375201 | G | A | 9 | a0001c0003t0001g0001 a0001c0003t0001g0115 a0001c0003t0001g0116 others(6): Show |
14 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.7270-306G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375201 | |||||||
chr19:42375219 | C | T | 1 | a0009c0033t0001g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7270-288C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375219 | |||||||
chr19:42375230 | C | T | 34 | a0001c0005t0003g0126 a0001c0005t0004g0127 a0001c0005t0004g0129 others(31): Show |
34 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.7270-277C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375230 | |||||||
chr19:42375314 | C | T | 19 | a0002c0002t0003g0015 a0002c0002t0003g0030 a0002c0002t0003g0031 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.7270-193C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375314 | |||||||
chr19:42375346 | G | T | 3 | a0001c0001t0001g0081 a0001c0036t0001g0082 a0002c0002t0001g0037 |
3 | HG00597.hp2 HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.7270-161G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375346 |