Item | Value |
---|---|
geneid | 84466 |
ensemblid | ENSG00000145794.17 |
hgncid | 29634 |
symbol | MEGF10 |
name | multiple EGF like domains 10 |
refseq_nuc | NM_001256545.2 |
refseq_prot | NP_001243474.1 |
ensembl_nuc | ENST00000503335.7 |
ensembl_prot | ENSP00000423354.2 |
mane_status | MANE Select |
chr | chr5 |
start | 127290796 |
end | 127461222 |
strand | + |
ver | v1.2 |
region | chr5:127290796-127461222 |
region5000 | chr5:127285796-127466222 |
regionname0 | MEGF10_chr5_127290796_127461222 |
regionname5000 | MEGF10_chr5_127285796_127466222 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1140 | 220 | 67 | 42 | 77 | 8 | 24 | 54 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0002 | 0/0 | 1140 | 27 | 3 | 6 | 14 | 2 | 2 | 11 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0003 | 0/0 | 1140 | 12 | 3 | 4 | 5 | 0 | 0 | 3 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0004 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0005 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0006 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0007 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0008 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(542): Show |
chr5 | 127285796 | 127466222 |
a0009 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
a0010 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | MVISL others(1135): Show |
chr5 | 127285796 | 127466222 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3420 | 79 | 20 | 14 | 34 | 2 | 8 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0002 | 0/0 | 3420 | 65 | 9 | 18 | 25 | 4 | 9 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0004 | 0/0 | 3420 | 12 | 9 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0005 | 0/0 | 3420 | 11 | 0 | 0 | 6 | 1 | 4 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0006 | 0/0 | 3420 | 9 | 0 | 0 | 9 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0007 | 0/0 | 3420 | 9 | 9 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0008 | 0/0 | 3420 | 7 | 7 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0010 | 1/0 | 3420 | 5 | 1 | 2 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0012 | 0/0 | 3420 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0014 | 0/0 | 3420 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0015 | 0/0 | 3420 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0017 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0018 | 0/0 | 3420 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0020 | 0/0 | 3420 | 2 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0021 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0026 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0027 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0029 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0034 | 0/0 | 3420 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0035 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0001c0036 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0002c0003 | 0/0 | 3420 | 20 | 0 | 3 | 14 | 2 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0002c0011 | 0/0 | 3420 | 4 | 0 | 3 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0002c0016 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0002c0028 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0003c0009 | 0/0 | 3420 | 7 | 2 | 4 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0003c0013 | 0/0 | 3420 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0003c0024 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0003c0031 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0004c0022 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0005c0019 | 0/0 | 3420 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0006c0032 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0007c0023 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0008c0030 | 0/0 | 3455 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3450): Show |
chr5 | 127285796 | 127466222 | ||
a0009c0033 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 | ||
a0010c0025 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | ATGGT others(3415): Show |
chr5 | 127285796 | 127466222 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7606 | 58 | 15 | 10 | 24 | 2 | 6 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0004 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0005 | 0/0 | 7606 | 11 | 4 | 0 | 6 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0013 | 0/0 | 7604 | 3 | 0 | 1 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0021 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0032 | 0/0 | 7606 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0033 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0034 | 0/0 | 7606 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0035 | 0/0 | 7606 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0001t0036 | 0/0 | 7606 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0002 | 0/0 | 7604 | 39 | 3 | 7 | 21 | 1 | 7 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0003 | 0/0 | 7604 | 19 | 6 | 7 | 3 | 3 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0017 | 0/0 | 7604 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0025 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0026 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0027 | 0/0 | 7606 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0028 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0002t0038 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0004t0004 | 0/0 | 7606 | 12 | 9 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0005t0007 | 0/0 | 7606 | 10 | 0 | 0 | 6 | 1 | 3 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0005t0016 | 0/0 | 7606 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0006t0001 | 0/0 | 7606 | 8 | 0 | 0 | 8 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0006t0005 | 0/0 | 7606 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0007t0004 | 0/0 | 7606 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0007t0008 | 0/0 | 7606 | 5 | 5 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0007t0020 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0007t0029 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0008t0004 | 0/0 | 7606 | 5 | 5 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0008t0008 | 0/0 | 7606 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0010t0001 | 1/0 | 7606 | 5 | 1 | 2 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0012t0014 | 0/0 | 7604 | 3 | 2 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0012t0021 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0014t0001 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0014t0005 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0014t0023 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0015t0002 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0015t0003 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0017t0002 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0017t0003 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0018t0020 | 0/0 | 7604 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0018t0039 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0020t0001 | 0/0 | 7606 | 2 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0021t0003 | 0/0 | 7604 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0026t0016 | 0/0 | 7606 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0027t0004 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0029t0001 | 0/0 | 7606 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0034t0005 | 0/0 | 7606 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0001c0035t0002 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0001c0036t0002 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0002c0003t0006 | 0/0 | 7604 | 10 | 0 | 0 | 10 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0002c0003t0009 | 0/0 | 7604 | 7 | 0 | 2 | 3 | 2 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0002c0003t0015 | 0/0 | 7604 | 3 | 0 | 1 | 1 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0002c0011t0010 | 0/0 | 7602 | 4 | 0 | 3 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0002c0016t0019 | 0/0 | 7604 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0002c0028t0030 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0003c0009t0010 | 0/0 | 7602 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0009t0011 | 0/0 | 7602 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0009t0012 | 0/0 | 7602 | 4 | 1 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0009t0024 | 0/0 | 7602 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0013t0011 | 0/0 | 7602 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0013t0037 | 0/0 | 7602 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0024t0011 | 0/0 | 7602 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7597): Show |
chr5 | 127285796 | 127466222 |
a0003c0031t0040 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0004c0022t0022 | 0/0 | 7604 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0005c0019t0018 | 0/0 | 7606 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0006c0032t0031 | 0/0 | 7604 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0007c0023t0001 | 0/0 | 7606 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7601): Show |
chr5 | 127285796 | 127466222 |
a0008c0030t0005 | 0/0 | 7641 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7636): Show |
chr5 | 127285796 | 127466222 |
a0009c0033t0002 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
a0010c0025t0002 | 0/0 | 7604 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | AGACA others(7599): Show |
chr5 | 127285796 | 127466222 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0013g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0013g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0021g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0032g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0033g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0034g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0035g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0001t0036g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0017g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0017g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0025g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0026g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0027g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0028g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0002t0038g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0004t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0005t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0006t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0020g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0007t0029g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0008t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0010t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0010t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0010t0001g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0010t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0010t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0012t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0012t0014g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0012t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0012t0021g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0014t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0014t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0014t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0015t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0015t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0017t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0017t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0018t0020g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0018t0039g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0020t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0020t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0021t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0021t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0026t0016g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0027t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0029t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0034t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0035t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0001c0036t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0009g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0015g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0015g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0003t0015g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0011t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0011t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0011t0010g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0011t0010g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0016t0019g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0016t0019g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0002c0028t0030g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0010g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0012g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0012g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0009t0024g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0013t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0013t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0013t0037g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0024t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0003c0031t0040g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0004c0022t0022g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0004c0022t0022g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0005c0019t0018g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0005c0019t0018g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0006c0032t0031g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0007c0023t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0008c0030t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0009c0033t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
a0010c0025t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0009 | g0047 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00099 | hp2 | a0001 | c0010 | t0001 | g0011 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00140 | hp1 | a0001 | c0002 | t0003 | g0227 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0074 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00323 | hp1 | a0001 | c0005 | t0007 | g0025 | EUR | FIN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00408 | hp2 | a0002 | c0003 | t0006 | g0016 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00423 | hp1 | a0002 | c0003 | t0006 | g0015 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00438 | hp1 | a0001 | c0001 | t0013 | g0101 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00558 | hp2 | a0001 | c0006 | t0001 | g0026 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00639 | hp1 | a0001 | c0018 | t0020 | g0243 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00639 | hp2 | a0001 | c0002 | t0038 | g0226 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00642 | hp1 | a0001 | c0001 | t0013 | g0076 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG00642 | hp2 | a0003 | c0009 | t0012 | g0180 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01069 | hp1 | a0001 | c0002 | t0003 | g0197 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0004 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01070 | hp2 | a0002 | c0011 | t0010 | g0120 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01071 | hp1 | a0002 | c0011 | t0010 | g0121 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01071 | hp2 | a0001 | c0004 | t0004 | g0005 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01074 | hp2 | a0001 | c0002 | t0025 | g0045 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01106 | hp1 | a0002 | c0003 | t0015 | g0018 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01167 | hp1 | a0001 | c0020 | t0001 | g0178 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01167 | hp2 | a0003 | c0009 | t0012 | g0212 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01169 | hp2 | a0003 | c0009 | t0012 | g0213 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01192 | hp2 | a0001 | c0002 | t0026 | g0056 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01243 | hp1 | a0001 | c0001 | t0021 | g0193 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01243 | hp2 | a0001 | c0012 | t0014 | g0262 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01255 | hp1 | a0001 | c0010 | t0001 | g0192 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01255 | hp2 | a0003 | c0009 | t0010 | g0088 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01256 | hp1 | a0001 | c0021 | t0003 | g0173 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01256 | hp2 | a0001 | c0010 | t0001 | g0228 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01257 | hp2 | a0002 | c0003 | t0009 | g0109 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01258 | hp1 | a0001 | c0021 | t0003 | g0174 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01258 | hp2 | a0002 | c0003 | t0009 | g0110 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01361 | hp1 | a0001 | c0001 | t0036 | g0257 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01496 | hp1 | a0001 | c0004 | t0004 | g0137 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0149 | EUR | IBS | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01934 | hp1 | a0001 | c0002 | t0003 | g0150 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0168 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01981 | hp2 | a0002 | c0011 | t0010 | g0090 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02004 | hp2 | a0001 | c0001 | t0032 | g0218 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02040 | hp2 | a0001 | c0005 | t0007 | g0024 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02071 | hp2 | a0002 | c0003 | t0006 | g0012 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02083 | hp2 | a0001 | c0005 | t0007 | g0179 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02129 | hp1 | a0003 | c0024 | t0011 | g0075 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02135 | hp1 | a0003 | c0013 | t0011 | g0097 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02135 | hp2 | a0001 | c0015 | t0003 | g0033 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02145 | hp1 | a0001 | c0010 | t0001 | g0019 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02145 | hp2 | a0002 | c0028 | t0030 | g0114 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02148 | hp1 | a0001 | c0002 | t0028 | g0073 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02155 | hp2 | a0001 | c0005 | t0007 | g0030 | EAS | CDX | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02257 | hp1 | a0001 | c0036 | t0002 | g0050 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02257 | hp2 | a0001 | c0014 | t0001 | g0253 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02258 | hp1 | a0001 | c0007 | t0004 | g0254 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02258 | hp2 | a0001 | c0012 | t0021 | g0009 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02280 | hp2 | a0001 | c0004 | t0004 | g0240 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02451 | hp1 | a0001 | c0017 | t0003 | g0140 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02451 | hp2 | a0006 | c0032 | t0031 | g0099 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02615 | hp2 | a0001 | c0027 | t0004 | g0135 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02622 | hp1 | a0001 | c0004 | t0004 | g0265 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02622 | hp2 | a0001 | c0018 | t0039 | g0006 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02630 | hp1 | a0001 | c0008 | t0008 | g0072 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02647 | hp1 | a0004 | c0022 | t0022 | g0249 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0190 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02683 | hp2 | a0001 | c0005 | t0007 | g0021 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02717 | hp1 | a0001 | c0004 | t0004 | g0255 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02717 | hp2 | a0003 | c0009 | t0012 | g0260 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02738 | hp2 | a0002 | c0003 | t0015 | g0134 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02809 | hp2 | a0001 | c0014 | t0023 | g0039 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02818 | hp1 | a0001 | c0007 | t0008 | g0036 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0229 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02886 | hp1 | a0001 | c0004 | t0004 | g0177 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02886 | hp2 | a0001 | c0014 | t0005 | g0038 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02895 | hp1 | a0001 | c0007 | t0008 | g0002 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02897 | hp1 | a0001 | c0007 | t0008 | g0002 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02922 | hp2 | a0001 | c0012 | t0014 | g0263 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0175 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02970 | hp2 | a0001 | c0008 | t0004 | g0233 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02976 | hp2 | a0001 | c0007 | t0029 | g0124 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03041 | hp2 | a0002 | c0016 | t0019 | g0232 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03098 | hp1 | a0001 | c0008 | t0004 | g0236 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03139 | hp1 | a0001 | c0004 | t0004 | g0250 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03139 | hp2 | a0001 | c0008 | t0008 | g0089 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0258 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03209 | hp1 | a0002 | c0016 | t0019 | g0231 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03209 | hp2 | a0004 | c0022 | t0022 | g0248 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03225 | hp2 | a0001 | c0007 | t0008 | g0080 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03239 | hp1 | a0002 | c0011 | t0010 | g0122 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03453 | hp2 | a0001 | c0007 | t0008 | g0037 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03492 | hp1 | a0001 | c0005 | t0007 | g0027 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0064 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03516 | hp1 | a0001 | c0004 | t0004 | g0252 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03516 | hp2 | a0003 | c0031 | t0040 | g0170 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03540 | hp1 | a0001 | c0007 | t0020 | g0167 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03579 | hp1 | a0005 | c0019 | t0018 | g0007 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03579 | hp2 | a0001 | c0004 | t0004 | g0251 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03654 | hp1 | a0001 | c0020 | t0001 | g0196 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03654 | hp2 | a0001 | c0002 | t0017 | g0103 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03669 | hp1 | a0001 | c0002 | t0017 | g0102 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03669 | hp2 | a0001 | c0005 | t0007 | g0034 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03834 | hp2 | a0001 | c0005 | t0016 | g0083 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0042 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG03942 | hp2 | a0001 | c0001 | t0035 | g0237 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0068 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG04184 | hp2 | a0001 | c0034 | t0005 | g0115 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG04204 | hp1 | a0001 | c0026 | t0016 | g0081 | SAS | STU | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18522 | hp2 | a0001 | c0012 | t0014 | g0261 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18906 | hp1 | a0001 | c0029 | t0001 | g0244 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18906 | hp2 | a0001 | c0008 | t0004 | g0235 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18939 | hp1 | a0001 | c0006 | t0001 | g0221 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18939 | hp2 | a0002 | c0003 | t0015 | g0219 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18946 | hp1 | a0001 | c0006 | t0001 | g0224 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18949 | hp1 | a0001 | c0005 | t0007 | g0029 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18966 | hp2 | a0002 | c0003 | t0006 | g0001 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18970 | hp1 | a0002 | c0003 | t0009 | g0123 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18971 | hp1 | a0002 | c0003 | t0006 | g0014 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18974 | hp1 | a0002 | c0003 | t0009 | g0105 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18975 | hp1 | a0002 | c0003 | t0009 | g0126 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18975 | hp2 | a0001 | c0005 | t0007 | g0031 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18977 | hp2 | a0007 | c0023 | t0001 | g0028 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18981 | hp2 | a0001 | c0001 | t0034 | g0203 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18984 | hp1 | a0001 | c0006 | t0001 | g0223 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18986 | hp2 | a0002 | c0003 | t0006 | g0010 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18987 | hp1 | a0002 | c0003 | t0006 | g0156 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18987 | hp2 | a0001 | c0015 | t0002 | g0118 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18989 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18989 | hp2 | a0001 | c0006 | t0001 | g0032 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18994 | hp1 | a0001 | c0001 | t0013 | g0096 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18994 | hp2 | a0001 | c0006 | t0005 | g0119 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18995 | hp1 | a0003 | c0009 | t0011 | g0092 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19001 | hp2 | a0001 | c0006 | t0001 | g0222 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19002 | hp1 | a0001 | c0001 | t0033 | g0198 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19004 | hp1 | a0001 | c0006 | t0001 | g0022 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19004 | hp2 | a0003 | c0013 | t0011 | g0077 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19012 | hp2 | a0001 | c0005 | t0007 | g0023 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19043 | hp1 | a0001 | c0007 | t0004 | g0242 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19056 | hp1 | a0001 | c0006 | t0001 | g0035 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19056 | hp2 | a0002 | c0003 | t0006 | g0013 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19060 | hp1 | a0002 | c0003 | t0006 | g0017 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19062 | hp2 | a0003 | c0013 | t0037 | g0136 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19064 | hp1 | a0001 | c0002 | t0027 | g0117 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19068 | hp2 | a0002 | c0003 | t0006 | g0001 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19076 | hp1 | a0008 | c0030 | t0005 | g0084 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19076 | hp2 | a0009 | c0033 | t0002 | g0043 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19083 | hp1 | a0001 | c0035 | t0002 | g0129 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19086 | hp1 | a0010 | c0025 | t0002 | g0059 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ASW | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20129 | hp2 | a0001 | c0008 | t0004 | g0247 | AFR | ASW | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20752 | hp1 | a0002 | c0003 | t0009 | g0108 | EUR | TSI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0151 | EUR | TSI | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02109 | hp1 | a0001 | c0004 | t0004 | g0176 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02486 | hp1 | a0001 | c0008 | t0004 | g0238 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG02486 | hp2 | a0001 | c0017 | t0002 | g0060 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0171 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0138 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA21309 | hp1 | a0003 | c0009 | t0024 | g0085 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
NA21309 | hp2 | a0005 | c0019 | t0018 | g0008 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
homoSapiens | grch38p0 | a0001 | c0010 | t0001 | g0186 | REF | REF | MEGF10_chr5_127285796_127466222 | MEGF10 | chr5 | 127285796 | 127466222 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:127396735 | G | A | 2 | a0002 a0010 |
28 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(25): Show |
missense_variant | MODERATE | c.616G>A | p.Val206Ile | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/25 | 895/7606 | 616/3423 | 206/1140 | chr5 | 127396735 | |||
chr5:127398741 | A | G | 1 | a0007 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.725A>G | p.Asn242Ser | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/25 | 1004/7606 | 725/3423 | 242/1140 | chr5 | 127398741 | |||
chr5:127410517 | G | A | 1 | a0005 | 2 | HG03579.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1046G>A | p.Arg349His | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/25 | 1325/7606 | 1046/3423 | 349/1140 | chr5 | 127410517 | |||
chr5:127420126 | C | A | 1 | a0008 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.1509C>A | p.Asn503Lys | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/25 | 1788/7606 | 1509/3423 | 503/1140 | chr5 | 127420126 | |||
chr5:127420127 | G | GAGGAAAA others(28): Show |
1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1510_1511insAGGAAA others(29): Show |
p.Gly504fs | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/25 | 1790/7606 | 1511/3423 | 504/1140 | chr5 | 127420127 | |||
chr5:127420128 | G | C | 1 | a0008 | 1 | NA19076.hp1 | missense_variant | MODERATE | c.1511G>C | p.Gly504Ala | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/25 | 1790/7606 | 1511/3423 | 504/1140 | chr5 | 127420128 | |||
chr5:127438510 | G | A | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2176G>A | p.Ala726Thr | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/25 | 2455/7606 | 2176/3423 | 726/1140 | chr5 | 127438510 | |||
chr5:127445619 | G | A | 1 | a0004 | 2 | HG02647.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.2654G>A | p.Gly885Glu | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/25 | 2933/7606 | 2654/3423 | 885/1140 | chr5 | 127445619 | |||
chr5:127455590 | G | A | 2 | a0002 a0003 |
39 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(36): Show |
missense_variant | MODERATE | c.3215G>A | p.Arg1072Lys | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/25 | 3494/7606 | 3215/3423 | 1072/1140 | chr5 | 127455590 | |||
chr5:127457136 | G | A | 1 | a0009 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.3241G>A | p.Val1081Met | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3520/7606 | 3241/3423 | 1081/1140 | chr5 | 127457136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:127339177 | G | A | 4 | a0001c0005 a0001c0006 a0001c0015 others(1): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
synonymous_variant | LOW | c.174G>A | p.Thr58Thr | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/25 | 453/7606 | 174/3423 | 58/1140 | chr5 | 127339177 | |||
chr5:127396608 | C | T | 2 | a0001c0014 a0004c0022 |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.489C>T | p.Ile163Ile | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/25 | 768/7606 | 489/3423 | 163/1140 | chr5 | 127396608 | |||
chr5:127396641 | G | A | 1 | a0003c0024 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.522G>A | p.Arg174Arg | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/25 | 801/7606 | 522/3423 | 174/1140 | chr5 | 127396641 | |||
chr5:127396707 | G | A | 10 | a0001c0005 a0001c0008 a0001c0017 others(7): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
synonymous_variant | LOW | c.588G>A | p.Gln196Gln | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/25 | 867/7606 | 588/3423 | 196/1140 | chr5 | 127396707 | |||
chr5:127396728 | C | T | 1 | a0001c0036 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.609C>T | p.Cys203Cys | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/25 | 888/7606 | 609/3423 | 203/1140 | chr5 | 127396728 | |||
chr5:127410422 | C | T | 1 | a0001c0035 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.951C>T | p.Gly317Gly | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/25 | 1230/7606 | 951/3423 | 317/1140 | chr5 | 127410422 | |||
chr5:127410455 | C | T | 2 | a0001c0012 a0004c0022 |
6 | HG01243.hp2 HG02258.hp2 HG02647.hp1 others(3): Show |
synonymous_variant | LOW | c.984C>T | p.Asn328Asn | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/25 | 1263/7606 | 984/3423 | 328/1140 | chr5 | 127410455 | |||
chr5:127410512 | C | A | 1 | a0001c0029 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1041C>A | p.Gly347Gly | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/25 | 1320/7606 | 1041/3423 | 347/1140 | chr5 | 127410512 | |||
chr5:127410585 | C | T | 35 | a0001c0001 a0001c0002 a0001c0004 others(32): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
synonymous_variant | LOW | c.1114C>T | p.Leu372Leu | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/25 | 1393/7606 | 1114/3423 | 372/1140 | chr5 | 127410585 | |||
chr5:127420051 | C | T | 1 | a0001c0021 | 2 | HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.1434C>T | p.His478His | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/25 | 1713/7606 | 1434/3423 | 478/1140 | chr5 | 127420051 | |||
chr5:127420117 | G | A | 1 | a0004c0022 | 2 | HG02647.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.1500G>A | p.Gln500Gln | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/25 | 1779/7606 | 1500/3423 | 500/1140 | chr5 | 127420117 | |||
chr5:127433454 | T | C | 8 | a0001c0004 a0001c0005 a0001c0007 others(5): Show |
62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
synonymous_variant | LOW | c.1785T>C | p.Pro595Pro | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/25 | 2064/7606 | 1785/3423 | 595/1140 | chr5 | 127433454 | |||
chr5:127434772 | C | T | 1 | a0001c0034 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1926C>T | p.Thr642Thr | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 15/25 | 2205/7606 | 1926/3423 | 642/1140 | chr5 | 127434772 | |||
chr5:127435419 | C | T | 2 | a0003c0013 a0003c0024 |
4 | HG02129.hp1 HG02135.hp1 NA19004.hp2 others(1): Show |
synonymous_variant | LOW | c.2034C>T | p.Asn678Asn | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/25 | 2313/7606 | 2034/3423 | 678/1140 | chr5 | 127435419 | |||
chr5:127435461 | C | T | 2 | a0001c0004 a0001c0027 |
13 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(10): Show |
synonymous_variant | LOW | c.2076C>T | p.Pro692Pro | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/25 | 2355/7606 | 2076/3423 | 692/1140 | chr5 | 127435461 | |||
chr5:127438509 | C | T | 1 | a0001c0020 | 2 | HG01167.hp1 HG03654.hp1 |
synonymous_variant | LOW | c.2175C>T | p.Ser725Ser | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/25 | 2454/7606 | 2175/3423 | 725/1140 | chr5 | 127438509 | |||
chr5:127438533 | C | T | 4 | a0002c0011 a0003c0009 a0003c0013 others(1): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
synonymous_variant | LOW | c.2199C>T | p.Cys733Cys | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/25 | 2478/7606 | 2199/3423 | 733/1140 | chr5 | 127438533 | |||
chr5:127455537 | G | A | 5 | a0002c0011 a0002c0016 a0003c0009 others(2): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
synonymous_variant | LOW | c.3162G>A | p.Pro1054Pro | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/25 | 3441/7606 | 3162/3423 | 1054/1140 | chr5 | 127455537 | |||
chr5:127455564 | G | A | 2 | a0001c0005 a0001c0026 |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
synonymous_variant | LOW | c.3189G>A | p.Glu1063Glu | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/25 | 3468/7606 | 3189/3423 | 1063/1140 | chr5 | 127455564 | |||
chr5:127457282 | T | A | 8 | a0001c0002 a0001c0015 a0001c0017 others(5): Show |
75 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(72): Show |
synonymous_variant | LOW | c.3387T>A | p.Gly1129Gly | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3666/7606 | 3387/3423 | 1129/1140 | chr5 | 127457282 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:127290953 | G | A | 33 | a0001c0001t0005 a0001c0001t0013 a0001c0002t0002 others(30): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
5_prime_UTR_variant | MODIFIER | c.-122G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/25 | 40356 | chr5 | 127290953 | ||||||
chr5:127457322 | C | G | 1 | a0003c0031t0040 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 4 | chr5 | 127457322 | ||||||
chr5:127457370 | G | T | 1 | a0001c0002t0017 | 2 | HG03654.hp2 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*52G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 52 | chr5 | 127457370 | ||||||
chr5:127457388 | A | G | 1 | a0001c0018t0039 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 70 | chr5 | 127457388 | ||||||
chr5:127457430 | A | G | 1 | a0006c0032t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 112 | chr5 | 127457430 | ||||||
chr5:127457482 | G | A | 1 | a0001c0001t0032 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 164 | chr5 | 127457482 | ||||||
chr5:127457510 | A | T | 1 | a0004c0022t0022 | 2 | HG02647.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*192A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 192 | chr5 | 127457510 | ||||||
chr5:127457527 | C | G | 50 | a0001c0001t0004 a0001c0001t0021 a0001c0002t0002 others(47): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*209C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 209 | chr5 | 127457527 | ||||||
chr5:127457675 | T | G | 2 | a0002c0011t0010 a0003c0009t0010 |
5 | HG01070.hp2 HG01071.hp1 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*357T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 357 | chr5 | 127457675 | ||||||
chr5:127457744 | A | G | 1 | a0001c0001t0036 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 426 | chr5 | 127457744 | ||||||
chr5:127457825 | T | C | 1 | a0001c0018t0039 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 507 | chr5 | 127457825 | ||||||
chr5:127457852 | A | G | 3 | a0001c0005t0007 a0001c0005t0016 a0001c0026t0016 |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*534A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 534 | chr5 | 127457852 | ||||||
chr5:127457943 | A | G | 4 | a0002c0003t0006 a0002c0003t0009 a0002c0003t0015 others(1): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*625A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 625 | chr5 | 127457943 | ||||||
chr5:127458034 | CTGTT | C | 8 | a0002c0011t0010 a0003c0009t0010 a0003c0009t0011 others(5): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*722delTTTG | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 719 | INFO_REALIGN_3_PRIME | chr5 | 127458034 | |||||
chr5:127458251 | C | G | 3 | a0001c0001t0021 a0001c0012t0021 a0006c0032t0031 |
3 | HG01243.hp1 HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*933C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 933 | chr5 | 127458251 | ||||||
chr5:127458370 | C | A | 1 | a0003c0013t0037 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1052 | chr5 | 127458370 | ||||||
chr5:127458468 | T | C | 2 | a0001c0002t0025 a0001c0002t0038 |
2 | HG00639.hp2 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1150T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1150 | chr5 | 127458468 | ||||||
chr5:127458564 | C | T | 8 | a0001c0001t0004 a0001c0004t0004 a0001c0007t0004 others(5): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1246C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1246 | chr5 | 127458564 | ||||||
chr5:127458614 | T | A | 1 | a0003c0031t0040 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1296T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1296 | chr5 | 127458614 | ||||||
chr5:127458630 | G | A | 3 | a0001c0001t0013 a0001c0001t0033 a0005c0019t0018 |
6 | HG00438.hp1 HG00642.hp1 HG03579.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1312G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1312 | chr5 | 127458630 | ||||||
chr5:127458728 | G | T | 11 | a0001c0005t0007 a0001c0005t0016 a0001c0026t0016 others(8): Show |
27 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1410G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1410 | chr5 | 127458728 | ||||||
chr5:127458840 | C | A | 8 | a0002c0011t0010 a0003c0009t0010 a0003c0009t0011 others(5): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1522C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1522 | chr5 | 127458840 | ||||||
chr5:127459003 | G | T | 1 | a0002c0003t0006 | 10 | HG00408.hp2 HG00423.hp1 HG02071.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1685G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1685 | chr5 | 127459003 | ||||||
chr5:127459128 | C | T | 11 | a0001c0005t0007 a0001c0005t0016 a0001c0026t0016 others(8): Show |
27 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1810C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1810 | chr5 | 127459128 | ||||||
chr5:127459224 | C | T | 1 | a0001c0014t0023 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 1906 | chr5 | 127459224 | ||||||
chr5:127459384 | A | G | 1 | a0002c0028t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2066A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2066 | chr5 | 127459384 | ||||||
chr5:127459416 | G | A | 1 | a0005c0019t0018 | 2 | HG03579.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2098G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2098 | chr5 | 127459416 | ||||||
chr5:127459432 | T | C | 12 | a0001c0005t0007 a0001c0005t0016 a0001c0026t0016 others(9): Show |
28 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2114T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2114 | chr5 | 127459432 | ||||||
chr5:127459467 | G | A | 27 | a0001c0001t0004 a0001c0004t0004 a0001c0005t0007 others(24): Show |
82 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2149G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2149 | chr5 | 127459467 | ||||||
chr5:127459540 | A | G | 1 | a0001c0001t0035 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2222A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2222 | chr5 | 127459540 | ||||||
chr5:127459554 | C | A | 49 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0033 others(46): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2236 | chr5 | 127459554 | ||||||
chr5:127459558 | G | A | 3 | a0001c0005t0007 a0001c0005t0016 a0001c0026t0016 |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2240G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2240 | chr5 | 127459558 | ||||||
chr5:127459837 | G | A | 1 | a0001c0002t0026 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2519G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2519 | chr5 | 127459837 | ||||||
chr5:127459867 | G | C | 1 | a0002c0028t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 2549 | chr5 | 127459867 | ||||||
chr5:127460457 | C | A | 1 | a0002c0016t0019 | 2 | HG03041.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3139C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3139 | chr5 | 127460457 | ||||||
chr5:127460493 | G | A | 3 | a0001c0001t0021 a0001c0012t0021 a0006c0032t0031 |
3 | HG01243.hp1 HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3175G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3175 | chr5 | 127460493 | ||||||
chr5:127460509 | A | T | 1 | a0003c0009t0024 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3191A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3191 | chr5 | 127460509 | ||||||
chr5:127460839 | TCA | T | 32 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0033 others(29): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3524_*3525delCA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3524 | INFO_REALIGN_3_PRIME | chr5 | 127460839 | |||||
chr5:127460893 | T | G | 52 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0021 others(49): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3575T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3575 | chr5 | 127460893 | ||||||
chr5:127460933 | G | A | 1 | a0001c0002t0028 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3615G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3615 | chr5 | 127460933 | ||||||
chr5:127461055 | A | C | 1 | a0001c0007t0029 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3737A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3737 | chr5 | 127461055 | ||||||
chr5:127461067 | G | A | 1 | a0001c0001t0034 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3749G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 25/25 | 3749 | chr5 | 127461067 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:127291178 | G | A | 6 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0012t0021g0009 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+122G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291178 | |||||||
chr5:127291198 | G | A | 11 | a0001c0010t0001g0011 a0001c0010t0001g0019 a0002c0003t0006g0001 others(8): Show |
12 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+142G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291198 | |||||||
chr5:127291388 | T | A | 1 | a0001c0002t0003g0020 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-19+332T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291388 | |||||||
chr5:127291541 | C | T | 8 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(5): Show |
8 | HG01243.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+485C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291541 | |||||||
chr5:127291565 | T | G | 15 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(12): Show |
15 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+509T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291565 | |||||||
chr5:127291670 | T | A | 3 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0018t0039g0006 |
3 | HG01069.hp2 HG01071.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-19+614T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291670 | |||||||
chr5:127291896 | C | A | 15 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(12): Show |
15 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+840C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291896 | |||||||
chr5:127291917 | C | T | 1 | a0001c0001t0036g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-19+861C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291917 | |||||||
chr5:127291941 | C | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+885C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291941 | |||||||
chr5:127291959 | T | C | 8 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(5): Show |
8 | HG01243.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+903T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127291959 | |||||||
chr5:127292113 | A | G | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19+1057A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127292113 | |||||||
chr5:127292183 | T | G | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+1127T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127292183 | |||||||
chr5:127292406 | A | G | 144 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0005g0048 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.-19+1350A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127292406 | |||||||
chr5:127292567 | T | C | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19+1511T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127292567 | |||||||
chr5:127292892 | C | CT | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+1839dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127292892 | ||||||
chr5:127292975 | A | G | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-19+1919A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127292975 | |||||||
chr5:127293079 | G | T | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+2023G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293079 | |||||||
chr5:127293329 | T | C | 15 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(12): Show |
15 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+2273T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293329 | |||||||
chr5:127293420 | C | T | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+2364C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293420 | |||||||
chr5:127293478 | C | T | 123 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0005g0048 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-19+2422C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293478 | |||||||
chr5:127293598 | T | A | 5 | a0001c0007t0008g0002 a0001c0007t0008g0036 a0001c0007t0008g0037 others(2): Show |
6 | HG02809.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+2542T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293598 | |||||||
chr5:127293789 | G | A | 1 | a0001c0002t0002g0040 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-19+2733G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127293789 | |||||||
chr5:127294069 | C | T | 25 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0004t0004g0250 others(22): Show |
26 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+3013C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294069 | |||||||
chr5:127294264 | G | A | 1 | a0005c0019t0018g0007 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-19+3208G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294264 | |||||||
chr5:127294324 | C | T | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+3268C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294324 | |||||||
chr5:127294485 | A | G | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19+3429A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294485 | |||||||
chr5:127294610 | C | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+3554C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294610 | |||||||
chr5:127294635 | C | A | 19 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0007t0004g0242 others(16): Show |
20 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19+3579C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127294635 | |||||||
chr5:127294799 | A | AAAT | 21 | a0001c0001t0001g0230 a0001c0001t0001g0234 a0001c0001t0001g0245 others(18): Show |
21 | HG00408.hp2 HG00423.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+3779_-19+3781d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294799 | A | AAATAAT | 24 | a0001c0001t0001g0239 a0001c0001t0035g0237 a0001c0004t0004g0240 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19+3776_-19+3781d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294799 | A | AAATAATA others(2): Show |
6 | a0001c0001t0001g0264 a0001c0002t0002g0116 a0001c0004t0004g0255 others(3): Show |
6 | HG02135.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+3773_-19+3781d others(11): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294799 | A | AAATAATA others(8): Show |
5 | a0001c0001t0005g0128 a0001c0002t0002g0130 a0001c0002t0002g0131 others(2): Show |
5 | HG02132.hp2 NA18955.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+3767_-19+3781d others(17): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294799 | AAAT | A | 45 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0139 others(42): Show |
45 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.-19+3779_-19+3781d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294799 | AAATAATA others(8): Show |
A | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+3767_-19+3781d others(17): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294799 | ||||||
chr5:127294835 | T | TAATAAA | 5 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(2): Show |
5 | HG01361.hp2 HG01975.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+3781_-19+3782i others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(2): Show |
39 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19+3781_-19+3782i others(11): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(5): Show |
37 | a0001c0001t0005g0082 a0001c0001t0005g0093 a0001c0001t0005g0094 others(34): Show |
37 | HG00408.hp1 HG00438.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.-19+3781_-19+3782i others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(9): Show |
1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19+3781_-19+3782i others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(8): Show |
9 | a0001c0002t0002g0125 a0001c0006t0005g0119 a0001c0007t0029g0124 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+3781_-19+3782i others(17): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(9): Show |
1 | a0001c0002t0027g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-19+3781_-19+3782i others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127294835 | T | TAATAATA others(11): Show |
1 | a0001c0002t0002g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-19+3781_-19+3782i others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127294835 | ||||||
chr5:127295183 | A | AT | 25 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0004t0004g0250 others(22): Show |
26 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+4128dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127295183 | ||||||
chr5:127295252 | A | G | 1 | a0001c0010t0001g0228 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-19+4196A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127295252 | |||||||
chr5:127295256 | T | A | 98 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0064 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-19+4200T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127295256 | |||||||
chr5:127295758 | A | C | 8 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0012t0014g0261 others(5): Show |
8 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+4702A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127295758 | |||||||
chr5:127295825 | A | C | 1 | a0001c0007t0008g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19+4769A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127295825 | |||||||
chr5:127296010 | C | A | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+4954C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296010 | |||||||
chr5:127296044 | C | T | 25 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(22): Show |
27 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19+4988C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296044 | |||||||
chr5:127296099 | T | C | 28 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(25): Show |
30 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19+5043T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296099 | |||||||
chr5:127296149 | A | G | 116 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-19+5093A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296149 | |||||||
chr5:127296513 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-19+5457G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296513 | |||||||
chr5:127296558 | A | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+5502A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296558 | |||||||
chr5:127296586 | C | G | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+5530C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296586 | |||||||
chr5:127296610 | T | G | 1 | a0001c0020t0001g0178 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-19+5554T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296610 | |||||||
chr5:127296749 | T | G | 1 | a0001c0002t0025g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-19+5693T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296749 | |||||||
chr5:127296820 | A | C | 2 | a0002c0003t0006g0013 a0002c0003t0006g0014 |
2 | NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-19+5764A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296820 | |||||||
chr5:127296916 | A | T | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+5860A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296916 | |||||||
chr5:127296921 | A | G | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+5865A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127296921 | |||||||
chr5:127297129 | A | G | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+6073A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297129 | |||||||
chr5:127297156 | G | A | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+6100G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297156 | |||||||
chr5:127297273 | C | T | 1 | a0001c0002t0002g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-19+6217C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297273 | |||||||
chr5:127297373 | T | C | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+6317T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297373 | |||||||
chr5:127297700 | A | T | 1 | a0001c0002t0002g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-19+6644A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297700 | |||||||
chr5:127297712 | C | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+6656C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297712 | |||||||
chr5:127297744 | G | A | 160 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-19+6688G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297744 | |||||||
chr5:127297750 | G | A | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+6694G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127297750 | |||||||
chr5:127298047 | A | G | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-19+6991A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298047 | |||||||
chr5:127298135 | C | T | 105 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(102): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19+7079C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298135 | |||||||
chr5:127298181 | C | T | 1 | a0003c0013t0011g0077 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19+7125C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298181 | |||||||
chr5:127298262 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-19+7206C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298262 | |||||||
chr5:127298266 | C | T | 160 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-19+7210C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298266 | |||||||
chr5:127298343 | C | T | 1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-19+7287C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298343 | |||||||
chr5:127298739 | A | G | 1 | a0003c0013t0011g0077 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-19+7683A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298739 | |||||||
chr5:127298752 | C | G | 50 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(47): Show |
52 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-19+7696C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298752 | |||||||
chr5:127298801 | G | A | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+7745G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298801 | |||||||
chr5:127298851 | G | A | 12 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(9): Show |
12 | HG02280.hp2 HG02486.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+7795G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298851 | |||||||
chr5:127298978 | G | A | 2 | a0001c0001t0001g0239 a0001c0008t0004g0238 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-19+7922G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127298978 | |||||||
chr5:127299307 | G | T | 2 | a0001c0001t0013g0076 a0001c0007t0008g0080 |
2 | HG00642.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+8251G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299307 | |||||||
chr5:127299363 | C | A | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+8307C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299363 | |||||||
chr5:127299372 | AG | A | 3 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 |
3 | HG02109.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-19+8317delG | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299372 | |||||||
chr5:127299391 | C | T | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+8335C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299391 | |||||||
chr5:127299462 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-19+8406T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299462 | |||||||
chr5:127299691 | T | C | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+8635T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299691 | |||||||
chr5:127299745 | GT | G | 139 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19+8702delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127299745 | ||||||
chr5:127299975 | G | C | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+8919G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299975 | |||||||
chr5:127299999 | A | G | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-19+8943A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127299999 | |||||||
chr5:127300087 | C | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+9031C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300087 | |||||||
chr5:127300164 | G | T | 1 | a0001c0006t0001g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-19+9108G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300164 | |||||||
chr5:127300308 | C | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+9252C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300308 | |||||||
chr5:127300519 | C | T | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+9463C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300519 | |||||||
chr5:127300552 | T | C | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+9496T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300552 | |||||||
chr5:127300610 | T | A | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+9554T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127300610 | |||||||
chr5:127301090 | C | T | 30 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(27): Show |
32 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.-19+10034C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301090 | |||||||
chr5:127301238 | C | T | 4 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+10182C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301238 | |||||||
chr5:127301303 | G | A | 3 | a0001c0002t0002g0046 a0001c0002t0002g0079 a0008c0030t0005g0084 |
3 | NA18953.hp2 NA18955.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-19+10247G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301303 | |||||||
chr5:127301385 | G | T | 1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19+10329G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301385 | |||||||
chr5:127301390 | A | AT | 7 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0008t0004g0247 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+10344dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127301390 | ||||||
chr5:127301640 | C | T | 3 | a0001c0002t0003g0258 a0001c0002t0003g0259 a0003c0009t0012g0260 |
3 | HG02630.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+10584C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301640 | |||||||
chr5:127301854 | G | T | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+10798G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127301854 | |||||||
chr5:127302090 | G | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+11034G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302090 | |||||||
chr5:127302180 | T | C | 162 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19+11124T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302180 | |||||||
chr5:127302274 | A | T | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19+11218A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302274 | |||||||
chr5:127302374 | A | G | 5 | a0001c0001t0001g0239 a0001c0004t0004g0240 a0001c0008t0004g0235 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+11318A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302374 | |||||||
chr5:127302553 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+11497A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302553 | |||||||
chr5:127302767 | C | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+11711C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302767 | |||||||
chr5:127302839 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+11783C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302839 | |||||||
chr5:127302902 | A | G | 6 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0012t0021g0009 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+11846A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302902 | |||||||
chr5:127302984 | G | T | 1 | a0001c0002t0003g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-19+11928G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127302984 | |||||||
chr5:127303035 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-19+11979A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303035 | |||||||
chr5:127303099 | G | A | 7 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(4): Show |
8 | HG02630.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+12043G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303099 | |||||||
chr5:127303333 | G | C | 163 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-19+12277G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303333 | |||||||
chr5:127303335 | C | CA | 25 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0264 others(22): Show |
27 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19+12299dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127303335 | ||||||
chr5:127303335 | CA | C | 37 | a0001c0001t0001g0166 a0001c0002t0002g0074 a0001c0002t0028g0073 others(34): Show |
37 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-19+12299delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127303335 | ||||||
chr5:127303405 | A | G | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+12349A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303405 | |||||||
chr5:127303406 | C | T | 12 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(9): Show |
12 | HG02280.hp2 HG02486.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+12350C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303406 | |||||||
chr5:127303443 | T | C | 162 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19+12387T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303443 | |||||||
chr5:127303504 | A | G | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+12448A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303504 | |||||||
chr5:127303509 | G | T | 1 | a0001c0008t0004g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-19+12453G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303509 | |||||||
chr5:127303577 | G | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+12521G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303577 | |||||||
chr5:127303722 | T | C | 1 | a0001c0007t0008g0002 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+12666T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303722 | |||||||
chr5:127303740 | A | T | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+12684A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303740 | |||||||
chr5:127303797 | G | T | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19+12741G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303797 | |||||||
chr5:127303899 | G | T | 110 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-19+12843G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127303899 | |||||||
chr5:127304011 | C | T | 6 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0012t0021g0009 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+12955C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304011 | |||||||
chr5:127304030 | C | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+12974C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304030 | |||||||
chr5:127304109 | T | C | 162 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-19+13053T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304109 | |||||||
chr5:127304261 | T | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+13205T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304261 | |||||||
chr5:127304513 | G | A | 160 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-19+13457G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304513 | |||||||
chr5:127304538 | G | A | 3 | a0001c0008t0004g0233 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG02970.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-19+13482G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304538 | |||||||
chr5:127304554 | C | A | 137 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-19+13498C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304554 | |||||||
chr5:127304829 | T | C | 1 | a0002c0003t0006g0015 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-19+13773T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304829 | |||||||
chr5:127304884 | T | C | 145 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-19+13828T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304884 | |||||||
chr5:127304954 | A | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+13898A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127304954 | |||||||
chr5:127305152 | G | T | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+14096G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305152 | |||||||
chr5:127305279 | T | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+14223T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305279 | |||||||
chr5:127305410 | G | A | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+14354G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305410 | |||||||
chr5:127305604 | G | A | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+14548G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305604 | |||||||
chr5:127305851 | C | T | 3 | a0001c0008t0004g0233 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG02970.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-19+14795C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305851 | |||||||
chr5:127305879 | T | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+14823T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305879 | |||||||
chr5:127305962 | C | T | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-19+14906C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127305962 | |||||||
chr5:127306068 | A | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+15012A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306068 | |||||||
chr5:127306078 | G | A | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+15022G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306078 | |||||||
chr5:127306079 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+15023T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306079 | |||||||
chr5:127306117 | T | C | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-19+15061T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306117 | |||||||
chr5:127306188 | C | T | 1 | a0001c0001t0032g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-19+15132C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306188 | |||||||
chr5:127306264 | T | C | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+15208T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306264 | |||||||
chr5:127306295 | T | C | 1 | a0003c0009t0024g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+15239T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306295 | |||||||
chr5:127306456 | G | A | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+15400G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306456 | |||||||
chr5:127306465 | A | G | 2 | a0001c0007t0020g0167 a0001c0008t0004g0247 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+15409A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306465 | |||||||
chr5:127306665 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0215 others(5): Show |
9 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+15609C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306665 | |||||||
chr5:127306677 | C | T | 3 | a0002c0003t0009g0108 a0002c0003t0009g0109 a0002c0003t0009g0110 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+15621C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306677 | |||||||
chr5:127306854 | G | C | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+15798G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306854 | |||||||
chr5:127306871 | C | T | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+15815C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306871 | |||||||
chr5:127306983 | T | G | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+15927T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127306983 | |||||||
chr5:127307047 | T | G | 1 | a0001c0002t0003g0229 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+15991T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307047 | |||||||
chr5:127307109 | G | A | 3 | a0001c0002t0003g0258 a0001c0002t0003g0259 a0003c0009t0012g0260 |
3 | HG02630.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+16053G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307109 | |||||||
chr5:127307228 | A | G | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+16172A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307228 | |||||||
chr5:127307366 | G | A | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19+16310G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307366 | |||||||
chr5:127307375 | G | T | 1 | a0001c0001t0005g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-19+16319G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307375 | |||||||
chr5:127307396 | A | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+16340A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307396 | |||||||
chr5:127307742 | A | T | 2 | a0003c0013t0037g0136 a0003c0024t0011g0075 |
2 | HG02129.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-19+16686A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307742 | |||||||
chr5:127307841 | C | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+16785C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307841 | |||||||
chr5:127307842 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+16786C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307842 | |||||||
chr5:127307865 | A | G | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-19+16809A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307865 | |||||||
chr5:127307898 | A | T | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+16842A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127307898 | |||||||
chr5:127308450 | G | A | 3 | a0001c0008t0004g0233 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG02970.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-19+17394G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308450 | |||||||
chr5:127308469 | T | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+17413T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308469 | |||||||
chr5:127308517 | G | A | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+17461G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308517 | |||||||
chr5:127308607 | G | T | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-19+17551G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308607 | |||||||
chr5:127308614 | C | T | 18 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(15): Show |
20 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19+17558C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308614 | |||||||
chr5:127308704 | A | G | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+17648A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308704 | |||||||
chr5:127308709 | G | A | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-19+17653G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308709 | |||||||
chr5:127308719 | G | A | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-19+17663G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308719 | |||||||
chr5:127308860 | T | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+17804T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308860 | |||||||
chr5:127308940 | T | C | 16 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(13): Show |
16 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+17884T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308940 | |||||||
chr5:127308988 | C | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+17932C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308988 | |||||||
chr5:127308989 | G | A | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-19+17933G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127308989 | |||||||
chr5:127309058 | A | C | 1 | a0001c0002t0003g0214 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-19+18002A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309058 | |||||||
chr5:127309077 | G | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+18021G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309077 | |||||||
chr5:127309122 | G | T | 9 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+18066G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309122 | |||||||
chr5:127309392 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-19+18336C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309392 | |||||||
chr5:127309484 | T | A | 3 | a0001c0001t0001g0183 a0001c0002t0003g0020 a0001c0002t0003g0184 |
3 | HG01257.hp1 HG01496.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-19+18428T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309484 | |||||||
chr5:127309596 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+18540A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309596 | |||||||
chr5:127309642 | T | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+18586T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309642 | |||||||
chr5:127309651 | G | A | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+18595G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309651 | |||||||
chr5:127309924 | C | T | 1 | a0001c0012t0014g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19+18868C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309924 | |||||||
chr5:127309947 | C | CTCTT | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0032g0218 others(3): Show |
6 | HG00423.hp2 HG00438.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+18938_-19+1894 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCC others(1): Show |
13 | a0001c0001t0001g0183 a0001c0001t0013g0076 a0001c0002t0002g0041 others(10): Show |
13 | HG00642.hp1 HG01975.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCC others(5): Show |
21 | a0001c0002t0002g0040 a0001c0002t0002g0069 a0001c0002t0002g0074 others(18): Show |
22 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCC others(9): Show |
5 | a0001c0002t0002g0106 a0001c0002t0003g0172 a0001c0002t0003g0184 others(2): Show |
5 | HG01099.hp2 HG01496.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCC others(13): Show |
2 | a0001c0021t0003g0173 a0001c0021t0003g0174 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(1): Show |
14 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0143 others(11): Show |
14 | HG02040.hp1 HG02040.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19+18934_-19+1894 others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(5): Show |
15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
15 | HG01243.hp1 HG01255.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+18930_-19+1894 others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(9): Show |
40 | a0001c0001t0001g0132 a0001c0001t0001g0152 a0001c0001t0001g0153 others(37): Show |
40 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-19+18926_-19+1894 others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(13): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0133 a0001c0001t0001g0162 others(18): Show |
22 | HG01074.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+18922_-19+1894 others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(17): Show |
9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
9 | HG01099.hp1 HG01952.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+18918_-19+1894 others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(21): Show |
4 | a0001c0001t0001g0211 a0001c0001t0001g0220 a0003c0009t0012g0212 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+18914_-19+1894 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309947 | C | CTCTTTCT others(29): Show |
1 | a0001c0005t0007g0031 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-19+18906_-19+1894 others(40): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309947 | ||||||
chr5:127309950 | T | TTTCC | 41 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(38): Show |
42 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309950 | ||||||
chr5:127309950 | T | TTTCCTTC others(1): Show |
7 | a0001c0004t0004g0175 a0001c0004t0004g0177 a0001c0004t0004g0250 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+18897_-19+1889 others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309950 | ||||||
chr5:127309954 | T | C | 60 | a0001c0001t0005g0048 a0001c0001t0005g0064 a0001c0001t0005g0093 others(57): Show |
60 | HG00099.hp1 HG00438.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+18898T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309954 | |||||||
chr5:127309958 | T | C | 1 | a0001c0004t0004g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+18902T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309958 | |||||||
chr5:127309990 | T | C | 1 | a0001c0002t0002g0049 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-19+18934T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309990 | |||||||
chr5:127309994 | T | C | 2 | a0001c0002t0002g0049 a0001c0004t0004g0175 |
2 | HG02300.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-19+18938T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309994 | |||||||
chr5:127309994 | T | TTTCTTCT others(11): Show |
1 | a0001c0002t0002g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(22): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(13): Show |
1 | a0001c0004t0004g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(17): Show |
3 | a0001c0002t0002g0116 a0001c0008t0004g0247 a0004c0022t0022g0249 |
3 | HG02647.hp1 NA18950.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(21): Show |
2 | a0002c0011t0010g0120 a0002c0011t0010g0121 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(5): Show |
1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(17): Show |
3 | a0001c0008t0008g0089 a0001c0017t0002g0060 a0003c0031t0040g0170 |
3 | HG02486.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(21): Show |
3 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0003c0013t0011g0077 |
3 | HG02132.hp2 NA19004.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(25): Show |
1 | a0002c0003t0009g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(36): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(29): Show |
1 | a0001c0001t0005g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(40): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(37): Show |
2 | a0001c0014t0005g0038 a0003c0009t0010g0088 |
2 | HG01255.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(48): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(17): Show |
6 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0013g0101 others(3): Show |
6 | HG00438.hp1 HG01074.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(21): Show |
8 | a0001c0001t0005g0113 a0001c0002t0002g0046 a0001c0002t0002g0067 others(5): Show |
8 | HG01981.hp2 HG02451.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(25): Show |
5 | a0001c0001t0005g0093 a0001c0001t0005g0107 a0001c0002t0002g0065 others(2): Show |
5 | HG01070.hp1 HG02129.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(36): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(29): Show |
2 | a0001c0001t0005g0064 a0001c0002t0002g0063 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(40): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(33): Show |
2 | a0001c0002t0002g0066 a0003c0009t0024g0085 |
2 | HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(44): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(13): Show |
1 | a0001c0005t0007g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(17): Show |
2 | a0001c0002t0002g0125 a0001c0008t0008g0072 |
2 | HG02630.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(21): Show |
5 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0004t0004g0265 others(2): Show |
5 | HG02145.hp2 HG02622.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(25): Show |
2 | a0001c0002t0002g0104 a0002c0003t0009g0105 |
2 | HG03704.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-19+18941_-19+1894 others(36): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(29): Show |
1 | a0001c0001t0005g0094 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(40): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309994 | T | TTTCTTTC others(41): Show |
1 | a0001c0014t0023g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-19+18941_-19+1894 others(52): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127309994 | ||||||
chr5:127309998 | C | T | 10 | a0001c0002t0027g0117 a0001c0007t0008g0036 a0001c0007t0008g0037 others(7): Show |
10 | HG01106.hp1 HG01243.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+18942C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309998 | |||||||
chr5:127309999 | T | C | 2 | a0001c0001t0005g0064 a0001c0002t0002g0063 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-19+18943T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127309999 | |||||||
chr5:127310001 | C | T | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+18945C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310001 | |||||||
chr5:127310005 | C | T | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+18949C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310005 | |||||||
chr5:127310009 | C | T | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+18953C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310009 | |||||||
chr5:127310011 | T | TTCC | 17 | a0001c0001t0001g0264 a0001c0002t0002g0074 a0001c0002t0003g0020 others(14): Show |
18 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+18956_-19+1895 others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127310011 | ||||||
chr5:127310011 | T | TTCCTTCC | 10 | a0001c0002t0002g0051 a0001c0002t0002g0058 a0001c0002t0002g0062 others(7): Show |
10 | HG01099.hp2 HG01169.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+18956_-19+1895 others(11): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127310011 | ||||||
chr5:127310011 | T | TTCCTTCC others(4): Show |
3 | a0001c0002t0002g0057 a0001c0002t0026g0056 a0001c0002t0028g0073 |
3 | HG01192.hp2 HG02109.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-19+18956_-19+1895 others(15): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127310011 | ||||||
chr5:127310011 | T | TTCCTTCC others(8): Show |
2 | a0001c0002t0002g0256 a0003c0013t0011g0097 |
2 | HG01361.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-19+18956_-19+1895 others(19): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127310011 | ||||||
chr5:127310013 | T | C | 115 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(112): Show |
116 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-19+18957T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310013 | |||||||
chr5:127310015 | T | C | 32 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(29): Show |
33 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+18959T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310015 | |||||||
chr5:127310016 | T | TCC | 4 | a0001c0002t0002g0049 a0001c0004t0004g0251 a0001c0007t0004g0254 others(1): Show |
4 | HG02258.hp1 HG02300.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+18960_-19+1896 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310016 | |||||||
chr5:127310016 | T | TCCTTCC | 15 | a0001c0001t0001g0245 a0001c0001t0005g0055 a0001c0002t0002g0040 others(12): Show |
15 | HG01069.hp2 HG01071.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19+18960_-19+1896 others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310016 | |||||||
chr5:127310016 | T | TCCTTCCT others(3): Show |
10 | a0001c0001t0013g0076 a0001c0002t0002g0041 a0001c0002t0002g0054 others(7): Show |
10 | HG00558.hp1 HG00642.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+18960_-19+1896 others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310016 | |||||||
chr5:127310016 | T | TCCTTCCT others(7): Show |
5 | a0001c0001t0013g0096 a0001c0002t0002g0053 a0001c0002t0002g0086 others(2): Show |
5 | HG00621.hp1 HG02615.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+18960_-19+1896 others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310016 | |||||||
chr5:127310016 | T | TCCTTCCT others(11): Show |
1 | a0001c0036t0002g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19+18960_-19+1896 others(22): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310016 | |||||||
chr5:127310017 | T | C | 79 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0246 others(76): Show |
80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-19+18961T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310017 | |||||||
chr5:127310018 | T | C | 113 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0246 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.-19+18962T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310018 | |||||||
chr5:127310018 | T | TCC | 35 | a0001c0001t0001g0245 a0001c0001t0005g0055 a0001c0001t0013g0076 others(32): Show |
35 | HG00558.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19+18962_-19+1896 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310018 | |||||||
chr5:127310019 | T | C | 33 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+18963T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310019 | |||||||
chr5:127310021 | T | C | 112 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(109): Show |
113 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-19+18965T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310021 | |||||||
chr5:127310023 | T | C | 33 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+18967T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310023 | |||||||
chr5:127310025 | T | C | 102 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0246 others(99): Show |
103 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-19+18969T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310025 | |||||||
chr5:127310027 | T | C | 33 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+18971T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310027 | |||||||
chr5:127310029 | T | C | 81 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0005g0055 others(78): Show |
82 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-19+18973T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310029 | |||||||
chr5:127310031 | T | C | 33 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(30): Show |
34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+18975T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310031 | |||||||
chr5:127310033 | T | C | 63 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0005g0055 others(60): Show |
64 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-19+18977T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310033 | |||||||
chr5:127310035 | C | T | 115 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(112): Show |
116 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.-19+18979C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310035 | |||||||
chr5:127310037 | T | C | 21 | a0001c0001t0001g0183 a0001c0002t0002g0042 a0001c0002t0003g0258 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+18981T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310037 | |||||||
chr5:127310037 | T | TC | 31 | a0001c0001t0001g0264 a0001c0002t0002g0051 a0001c0002t0002g0057 others(28): Show |
32 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19+18982dupC | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127310037 | ||||||
chr5:127310039 | T | C | 1 | a0001c0002t0002g0106 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-19+18983T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310039 | |||||||
chr5:127310041 | T | C | 26 | a0001c0001t0001g0264 a0001c0002t0002g0042 a0001c0002t0002g0051 others(23): Show |
28 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19+18985T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310041 | |||||||
chr5:127310042 | C | A | 1 | a0001c0008t0004g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-19+18986C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310042 | |||||||
chr5:127310045 | T | C | 1 | a0003c0013t0011g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-19+18989T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310045 | |||||||
chr5:127310046 | A | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+18990A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310046 | |||||||
chr5:127310151 | C | G | 1 | a0001c0002t0002g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-19+19095C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310151 | |||||||
chr5:127310231 | A | G | 1 | a0001c0027t0004g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19+19175A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310231 | |||||||
chr5:127310240 | A | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19+19184A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310240 | |||||||
chr5:127310605 | G | C | 4 | a0001c0001t0001g0139 a0001c0002t0003g0149 a0001c0002t0003g0150 others(1): Show |
4 | HG01515.hp2 HG01934.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+19549G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310605 | |||||||
chr5:127310755 | C | G | 8 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0020g0167 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+19699C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310755 | |||||||
chr5:127310770 | G | C | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+19714G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310770 | |||||||
chr5:127310915 | C | T | 1 | a0002c0003t0006g0017 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19+19859C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127310915 | |||||||
chr5:127311172 | T | C | 60 | a0001c0001t0001g0183 a0001c0001t0005g0055 a0001c0001t0005g0064 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+20116T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127311172 | |||||||
chr5:127311925 | A | G | 1 | a0001c0002t0003g0168 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-18-19366A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127311925 | |||||||
chr5:127312249 | C | T | 107 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.-18-19042C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312249 | |||||||
chr5:127312371 | G | A | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18-18920G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312371 | |||||||
chr5:127312509 | G | A | 67 | a0001c0001t0001g0183 a0001c0001t0005g0055 a0001c0001t0005g0064 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-18-18782G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312509 | |||||||
chr5:127312858 | G | T | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-18433G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312858 | |||||||
chr5:127312859 | A | C | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-18432A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312859 | |||||||
chr5:127312861 | A | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-18430A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312861 | |||||||
chr5:127312896 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-18-18395T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127312896 | |||||||
chr5:127313713 | T | C | 6 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0012t0021g0009 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-17578T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127313713 | |||||||
chr5:127313882 | T | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18-17409T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127313882 | |||||||
chr5:127314490 | G | A | 139 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-18-16801G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314490 | |||||||
chr5:127314543 | G | C | 1 | a0001c0008t0008g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-18-16748G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314543 | |||||||
chr5:127314719 | T | C | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-16572T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314719 | |||||||
chr5:127314720 | G | A | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-16571G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314720 | |||||||
chr5:127314889 | A | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(258): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-18-16402A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314889 | |||||||
chr5:127314933 | T | C | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-18-16358T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314933 | |||||||
chr5:127314968 | A | G | 1 | a0001c0002t0002g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18-16323A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127314968 | |||||||
chr5:127315075 | G | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-16216G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315075 | |||||||
chr5:127315095 | T | G | 1 | a0001c0002t0003g0149 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-18-16196T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315095 | |||||||
chr5:127315100 | G | A | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18-16191G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315100 | |||||||
chr5:127315113 | A | G | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-16178A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315113 | |||||||
chr5:127315125 | G | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-16166G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315125 | |||||||
chr5:127315376 | T | C | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-15915T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315376 | |||||||
chr5:127315397 | T | G | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-15894T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315397 | |||||||
chr5:127315484 | A | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-15807A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315484 | |||||||
chr5:127315603 | C | T | 5 | a0001c0007t0020g0167 a0001c0008t0004g0247 a0001c0012t0021g0009 others(2): Show |
5 | HG02258.hp2 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-15688C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315603 | |||||||
chr5:127315781 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-15510C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315781 | |||||||
chr5:127315823 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0230 |
2 | NA19083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-18-15468C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315823 | |||||||
chr5:127315864 | A | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-15427A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127315864 | |||||||
chr5:127316119 | T | C | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-15172T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316119 | |||||||
chr5:127316246 | T | C | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-15045T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316246 | |||||||
chr5:127316289 | G | T | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-15002G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316289 | |||||||
chr5:127316290 | C | G | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-15001C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316290 | |||||||
chr5:127316715 | A | G | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-14576A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316715 | |||||||
chr5:127316800 | A | G | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-14491A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127316800 | |||||||
chr5:127317018 | G | C | 139 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-18-14273G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317018 | |||||||
chr5:127317018 | G | T | 3 | a0001c0002t0003g0258 a0001c0002t0003g0259 a0003c0009t0012g0260 |
3 | HG02630.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-14273G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317018 | |||||||
chr5:127317050 | C | T | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-18-14241C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317050 | |||||||
chr5:127317064 | G | T | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-14227G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317064 | |||||||
chr5:127317068 | G | T | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-14223G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317068 | |||||||
chr5:127317132 | A | C | 1 | a0001c0017t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-14159A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317132 | |||||||
chr5:127317167 | T | C | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-18-14124T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317167 | |||||||
chr5:127317200 | A | G | 24 | a0001c0001t0001g0239 a0001c0001t0001g0245 a0001c0001t0001g0246 others(21): Show |
24 | HG00438.hp1 HG02145.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-14091A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317200 | |||||||
chr5:127317273 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-14018G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317273 | |||||||
chr5:127317278 | C | T | 1 | a0001c0004t0004g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-14013C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317278 | |||||||
chr5:127317436 | G | A | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-13855G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317436 | |||||||
chr5:127317516 | C | T | 5 | a0001c0007t0020g0167 a0001c0008t0004g0247 a0001c0012t0021g0009 others(2): Show |
5 | HG02258.hp2 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-13775C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317516 | |||||||
chr5:127317620 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-13671A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317620 | |||||||
chr5:127317621 | A | G | 1 | a0001c0002t0002g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18-13670A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317621 | |||||||
chr5:127317650 | A | G | 9 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-13641A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317650 | |||||||
chr5:127317788 | A | C | 1 | a0001c0005t0007g0031 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-18-13503A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127317788 | |||||||
chr5:127317902 | T | TA | 5 | a0001c0007t0020g0167 a0001c0008t0004g0247 a0001c0012t0021g0009 others(2): Show |
5 | HG02258.hp2 HG03540.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-13380dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127317902 | ||||||
chr5:127317915 | AG | A | 11 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-13370delG | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127317915 | ||||||
chr5:127318117 | G | C | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-13174G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318117 | |||||||
chr5:127318258 | A | G | 171 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-18-13033A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318258 | |||||||
chr5:127318282 | G | A | 1 | a0001c0002t0002g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-18-13009G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318282 | |||||||
chr5:127318307 | C | T | 1 | a0002c0003t0006g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-18-12984C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318307 | |||||||
chr5:127318313 | C | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-12978C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318313 | |||||||
chr5:127318370 | T | C | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-12921T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318370 | |||||||
chr5:127318516 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-18-12775C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318516 | |||||||
chr5:127318614 | T | A | 18 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(15): Show |
20 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-12677T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318614 | |||||||
chr5:127318651 | A | C | 2 | a0001c0002t0003g0020 a0001c0002t0003g0184 |
2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-18-12640A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318651 | |||||||
chr5:127318729 | G | A | 1 | a0001c0001t0005g0094 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-18-12562G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318729 | |||||||
chr5:127318931 | T | C | 148 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-18-12360T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318931 | |||||||
chr5:127318932 | G | A | 3 | a0001c0002t0002g0078 a0001c0008t0008g0072 a0001c0017t0002g0060 |
3 | HG00558.hp1 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-18-12359G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318932 | |||||||
chr5:127318997 | C | G | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-18-12294C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127318997 | |||||||
chr5:127319060 | C | G | 1 | a0010c0025t0002g0059 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-18-12231C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319060 | |||||||
chr5:127319137 | A | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-12154A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319137 | |||||||
chr5:127319278 | G | A | 110 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0001g0245 others(107): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-18-12013G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319278 | |||||||
chr5:127319394 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-18-11897C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319394 | |||||||
chr5:127319442 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-18-11849C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319442 | |||||||
chr5:127319489 | G | A | 3 | a0001c0008t0004g0233 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG02970.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-18-11802G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319489 | |||||||
chr5:127319669 | C | T | 29 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(26): Show |
31 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18-11622C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319669 | |||||||
chr5:127319869 | G | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-18-11422G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319869 | |||||||
chr5:127319912 | T | C | 24 | a0001c0004t0004g0265 a0001c0005t0007g0021 a0001c0005t0007g0023 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-11379T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127319912 | |||||||
chr5:127320038 | G | C | 98 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0230 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-18-11253G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320038 | |||||||
chr5:127320057 | C | T | 98 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0230 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-18-11234C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320057 | |||||||
chr5:127320081 | G | T | 1 | a0001c0002t0002g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-18-11210G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320081 | |||||||
chr5:127320183 | G | A | 23 | a0001c0001t0013g0101 a0001c0005t0007g0021 a0001c0005t0007g0023 others(20): Show |
23 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-11108G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320183 | |||||||
chr5:127320235 | T | G | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-11056T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320235 | |||||||
chr5:127320263 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18-11028C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320263 | |||||||
chr5:127320462 | T | C | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-10829T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320462 | |||||||
chr5:127320464 | TAGATACC others(6): Show |
T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-10824_-18-1081 others(17): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127320464 | ||||||
chr5:127320615 | G | A | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18-10676G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320615 | |||||||
chr5:127320625 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-10666C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320625 | |||||||
chr5:127320632 | A | ATT | 55 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0002t0002g0040 others(52): Show |
55 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-18-10656_-18-1065 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127320632 | ||||||
chr5:127320808 | C | T | 76 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-18-10483C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320808 | |||||||
chr5:127320981 | G | C | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-10310G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127320981 | |||||||
chr5:127321069 | A | G | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-18-10222A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321069 | |||||||
chr5:127321306 | T | G | 128 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-18-9985T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321306 | |||||||
chr5:127321525 | G | T | 87 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-18-9766G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321525 | |||||||
chr5:127321568 | T | A | 4 | a0001c0001t0001g0141 a0001c0002t0003g0138 a0001c0004t0004g0137 others(1): Show |
4 | HG01496.hp1 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9723T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321568 | |||||||
chr5:127321740 | T | A | 165 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0001g0264 others(162): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18-9551T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321740 | |||||||
chr5:127321823 | C | G | 1 | a0008c0030t0005g0084 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-18-9468C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321823 | |||||||
chr5:127321851 | G | A | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-9440G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321851 | |||||||
chr5:127321887 | A | G | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18-9404A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127321887 | |||||||
chr5:127322074 | C | CA | 113 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0166 others(110): Show |
113 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18-9204dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127322074 | ||||||
chr5:127322074 | CA | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-9204delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127322074 | ||||||
chr5:127322092 | A | G | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-9199A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322092 | |||||||
chr5:127322109 | GA | G | 24 | a0001c0001t0001g0215 a0001c0005t0007g0021 a0001c0005t0007g0023 others(21): Show |
24 | HG00558.hp2 HG02040.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-9171delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127322109 | ||||||
chr5:127322168 | G | A | 12 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(9): Show |
12 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18-9123G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322168 | |||||||
chr5:127322227 | A | G | 7 | a0001c0002t0002g0098 a0001c0002t0002g0106 a0001c0002t0002g0116 others(4): Show |
7 | HG02015.hp2 HG02132.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-9064A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322227 | |||||||
chr5:127322330 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-18-8961C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322330 | |||||||
chr5:127322574 | C | T | 7 | a0001c0004t0004g0240 a0001c0008t0004g0233 a0001c0008t0004g0235 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-8717C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322574 | |||||||
chr5:127322692 | A | G | 1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-8599A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322692 | |||||||
chr5:127322751 | T | A | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-8540T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322751 | |||||||
chr5:127322808 | T | C | 131 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(128): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18-8483T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127322808 | |||||||
chr5:127323013 | CATATATA others(7): Show |
C | 1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-8271_-18-8258d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127323013 | ||||||
chr5:127323712 | G | A | 11 | a0001c0010t0001g0011 a0001c0010t0001g0019 a0002c0003t0006g0001 others(8): Show |
12 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18-7579G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127323712 | |||||||
chr5:127323816 | C | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-7475C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127323816 | |||||||
chr5:127323878 | G | A | 2 | a0001c0002t0003g0190 a0001c0002t0003g0229 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-18-7413G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127323878 | |||||||
chr5:127324122 | G | A | 1 | a0001c0005t0007g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18-7169G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324122 | |||||||
chr5:127324200 | C | CT | 134 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(131): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-18-7087dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127324200 | ||||||
chr5:127324284 | T | C | 1 | a0001c0005t0007g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18-7007T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324284 | |||||||
chr5:127324317 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-6974A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324317 | |||||||
chr5:127324491 | A | G | 1 | a0001c0001t0021g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18-6800A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324491 | |||||||
chr5:127324609 | A | G | 131 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(128): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18-6682A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324609 | |||||||
chr5:127324830 | A | G | 4 | a0001c0002t0003g0171 a0001c0002t0003g0172 a0001c0021t0003g0173 others(1): Show |
4 | HG01099.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-6461A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324830 | |||||||
chr5:127324920 | T | C | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-6371T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324920 | |||||||
chr5:127324968 | C | G | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18-6323C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127324968 | |||||||
chr5:127325134 | G | T | 1 | a0001c0001t0021g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18-6157G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325134 | |||||||
chr5:127325367 | T | C | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18-5924T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325367 | |||||||
chr5:127325423 | A | G | 5 | a0001c0004t0004g0250 a0001c0004t0004g0251 a0001c0004t0004g0252 others(2): Show |
5 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-5868A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325423 | |||||||
chr5:127325506 | A | G | 1 | a0001c0002t0003g0190 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-5785A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325506 | |||||||
chr5:127325579 | T | A | 1 | a0001c0002t0038g0226 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18-5712T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325579 | |||||||
chr5:127325585 | T | C | 1 | a0002c0016t0019g0232 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-18-5706T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325585 | |||||||
chr5:127325688 | G | A | 91 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(88): Show |
91 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-18-5603G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325688 | |||||||
chr5:127325782 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18-5509G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325782 | |||||||
chr5:127325794 | A | C | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-5497A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325794 | |||||||
chr5:127325826 | AGTATATA others(21): Show |
A | 4 | a0001c0002t0003g0171 a0001c0002t0003g0172 a0001c0021t0003g0173 others(1): Show |
4 | HG01099.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-5449_-18-5422d others(30): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325826 | ||||||
chr5:127325827 | GTA | G | 146 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0001g0264 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-18-5449_-18-5448d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325827 | ||||||
chr5:127325842 | T | C | 9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-5449T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325842 | |||||||
chr5:127325844 | C | T | 9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-5447C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325844 | |||||||
chr5:127325849 | A | G | 9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-5442A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325849 | |||||||
chr5:127325855 | G | A | 9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-5436G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325855 | |||||||
chr5:127325855 | GTA | G | 8 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-5423_-18-5422d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325855 | ||||||
chr5:127325868 | T | C | 17 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0004t0004g0240 others(14): Show |
17 | HG00438.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18-5423T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325868 | |||||||
chr5:127325877 | G | GTGTGTAT others(17): Show |
1 | a0001c0020t0001g0178 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-18-5409_-18-5408i others(26): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325877 | ||||||
chr5:127325887 | GTA | G | 21 | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0002t0002g0042 others(18): Show |
21 | HG00642.hp2 HG01496.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-5382_-18-5381d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325887 | ||||||
chr5:127325887 | GTATA | G | 26 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(23): Show |
26 | HG00099.hp1 HG01169.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-5384_-18-5381d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325887 | ||||||
chr5:127325889 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-5402A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325889 | |||||||
chr5:127325891 | A | G | 1 | a0001c0006t0001g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-18-5400A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325891 | |||||||
chr5:127325902 | TATATA | T | 4 | a0001c0004t0004g0005 a0001c0012t0014g0261 a0001c0012t0014g0262 others(1): Show |
4 | HG01071.hp2 HG01243.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-5388_-18-5384d others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325902 | |||||||
chr5:127325904 | TATA | T | 53 | a0001c0001t0005g0064 a0001c0001t0013g0076 a0001c0002t0002g0041 others(50): Show |
53 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-18-5386_-18-5384d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325904 | |||||||
chr5:127325904 | TATATA | T | 3 | a0001c0007t0020g0167 a0002c0011t0010g0090 a0003c0009t0012g0212 |
3 | HG01167.hp2 HG01981.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-18-5386_-18-5382d others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325904 | |||||||
chr5:127325906 | TA | T | 8 | a0001c0001t0001g0195 a0001c0001t0013g0101 a0001c0002t0002g0256 others(5): Show |
8 | HG00438.hp1 HG00621.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-5384delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325906 | |||||||
chr5:127325906 | TATA | T | 7 | a0001c0001t0001g0183 a0001c0002t0002g0040 a0001c0002t0002g0061 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-5384_-18-5382d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325906 | |||||||
chr5:127325907 | A | T | 8 | a0001c0007t0004g0242 a0001c0007t0029g0124 a0001c0012t0021g0009 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-5384A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325907 | |||||||
chr5:127325908 | TA | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
83 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-18-5382delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325908 | |||||||
chr5:127325909 | A | T | 107 | a0001c0001t0001g0141 a0001c0001t0001g0195 a0001c0001t0005g0048 others(104): Show |
107 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-18-5382A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325909 | |||||||
chr5:127325909 | AT | A | 21 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0153 others(18): Show |
23 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-5369delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325909 | ||||||
chr5:127325909 | ATT | A | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-5370_-18-5369d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127325909 | ||||||
chr5:127325911 | T | A | 1 | a0002c0003t0015g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-18-5380T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325911 | |||||||
chr5:127325912 | T | A | 2 | a0001c0002t0003g0258 a0002c0003t0006g0015 |
2 | HG00423.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-5379T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325912 | |||||||
chr5:127325913 | T | A | 1 | a0001c0006t0001g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-18-5378T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325913 | |||||||
chr5:127325994 | T | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-5297T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325994 | |||||||
chr5:127326082 | A | T | 63 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(60): Show |
63 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-18-5209A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326082 | |||||||
chr5:127326166 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-5125C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326166 | |||||||
chr5:127326167 | G | T | 12 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0004g0242 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-5124G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326167 | |||||||
chr5:127326400 | G | C | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-4891G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326400 | |||||||
chr5:127326422 | T | C | 79 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-18-4869T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326422 | |||||||
chr5:127326678 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-4613A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326678 | |||||||
chr5:127326683 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-4608T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326683 | |||||||
chr5:127326749 | A | C | 1 | a0001c0002t0002g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-4542A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127326749 | |||||||
chr5:127327023 | C | G | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18-4268C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327023 | |||||||
chr5:127327128 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-4163A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327128 | |||||||
chr5:127327411 | A | G | 22 | a0001c0001t0001g0144 a0001c0001t0001g0264 a0001c0001t0021g0193 others(19): Show |
24 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-3880A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327411 | |||||||
chr5:127327575 | CT | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-3713delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127327575 | ||||||
chr5:127327617 | C | A | 3 | a0002c0003t0006g0015 a0002c0003t0006g0016 a0002c0003t0006g0017 |
3 | HG00408.hp2 HG00423.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-18-3674C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327617 | |||||||
chr5:127327714 | CT | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-18-3560delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127327714 | ||||||
chr5:127327714 | CTT | C | 24 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-3561_-18-3560d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | 127327714 | ||||||
chr5:127327768 | G | T | 3 | a0001c0001t0001g0141 a0001c0004t0004g0137 a0001c0017t0003g0140 |
3 | HG01496.hp1 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-18-3523G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327768 | |||||||
chr5:127327894 | T | A | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18-3397T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327894 | |||||||
chr5:127327983 | C | G | 21 | a0001c0001t0001g0264 a0001c0001t0021g0193 a0001c0002t0003g0258 others(18): Show |
23 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-3308C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127327983 | |||||||
chr5:127328067 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-3224A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328067 | |||||||
chr5:127328128 | G | A | 4 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3163G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328128 | |||||||
chr5:127328218 | G | A | 7 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0052 others(4): Show |
7 | HG01975.hp2 HG03704.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-3073G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328218 | |||||||
chr5:127328322 | C | T | 24 | a0001c0001t0001g0215 a0001c0005t0007g0021 a0001c0005t0007g0023 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-2969C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328322 | |||||||
chr5:127328347 | A | G | 63 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(60): Show |
63 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-18-2944A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328347 | |||||||
chr5:127328392 | A | G | 3 | a0001c0002t0003g0171 a0001c0021t0003g0173 a0001c0021t0003g0174 |
3 | HG01256.hp1 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-2899A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328392 | |||||||
chr5:127328490 | C | A | 5 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-2801C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328490 | |||||||
chr5:127328770 | C | T | 2 | a0001c0002t0002g0074 a0001c0002t0028g0073 |
2 | HG00140.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-18-2521C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328770 | |||||||
chr5:127328884 | T | A | 12 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0004g0242 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-2407T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328884 | |||||||
chr5:127328903 | A | G | 1 | a0004c0022t0022g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-2388A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127328903 | |||||||
chr5:127329071 | G | A | 1 | a0001c0008t0008g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-18-2220G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329071 | |||||||
chr5:127329139 | C | T | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-2152C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329139 | |||||||
chr5:127329239 | T | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-2052T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329239 | |||||||
chr5:127329242 | A | G | 9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-2049A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329242 | |||||||
chr5:127329289 | T | C | 79 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-18-2002T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329289 | |||||||
chr5:127329689 | A | C | 3 | a0001c0018t0020g0243 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG00639.hp1 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-18-1602A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329689 | |||||||
chr5:127329734 | G | A | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-1557G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127329734 | |||||||
chr5:127330153 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18-1138C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330153 | |||||||
chr5:127330154 | G | A | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-1137G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330154 | |||||||
chr5:127330392 | C | A | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-18-899C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330392 | |||||||
chr5:127330400 | G | A | 1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18-891G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330400 | |||||||
chr5:127330445 | C | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-18-846C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330445 | |||||||
chr5:127330718 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-18-573A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330718 | |||||||
chr5:127330837 | A | T | 26 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(23): Show |
26 | HG00323.hp1 HG00558.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18-454A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127330837 | |||||||
chr5:127331112 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-179A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127331112 | |||||||
chr5:127331434 | T | C | 24 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(21): Show |
24 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.116+10T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127331434 | |||||||
chr5:127331576 | G | A | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+152G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127331576 | |||||||
chr5:127331587 | C | G | 2 | a0001c0002t0003g0149 a0001c0002t0003g0151 |
2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.116+163C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127331587 | |||||||
chr5:127331859 | C | G | 158 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0001g0245 others(155): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.116+435C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127331859 | |||||||
chr5:127332054 | C | T | 2 | a0001c0002t0002g0057 a0001c0002t0026g0056 |
2 | HG01192.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.116+630C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127332054 | |||||||
chr5:127332174 | A | T | 2 | a0003c0009t0012g0212 a0003c0009t0012g0213 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.116+750A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127332174 | |||||||
chr5:127332284 | G | GTTTAAAC others(5): Show |
23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+861_116+862ins others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr5 | 127332284 | ||||||
chr5:127332759 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.116+1335G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127332759 | |||||||
chr5:127332991 | G | A | 64 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(61): Show |
64 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.116+1567G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127332991 | |||||||
chr5:127333078 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0215 others(5): Show |
9 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.116+1654G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333078 | |||||||
chr5:127333312 | T | G | 155 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0001g0264 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.116+1888T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333312 | |||||||
chr5:127333510 | CA | C | 19 | a0001c0001t0001g0264 a0001c0002t0003g0258 a0001c0002t0003g0259 others(16): Show |
21 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.116+2094delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr5 | 127333510 | ||||||
chr5:127333517 | AAT | A | 83 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(80): Show |
83 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.116+2095_116+2096d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr5 | 127333517 | ||||||
chr5:127333518 | AT | A | 53 | a0001c0001t0001g0144 a0001c0001t0005g0048 a0001c0001t0005g0093 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.116+2095delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333518 | |||||||
chr5:127333519 | T | A | 14 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(11): Show |
14 | HG01243.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.116+2095T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333519 | |||||||
chr5:127333525 | T | A | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.116+2101T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333525 | |||||||
chr5:127333646 | A | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116+2222A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333646 | |||||||
chr5:127333817 | A | T | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.116+2393A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127333817 | |||||||
chr5:127334032 | T | G | 2 | a0001c0001t0021g0193 a0001c0004t0004g0265 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.116+2608T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127334032 | |||||||
chr5:127334142 | G | C | 21 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.116+2718G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127334142 | |||||||
chr5:127334430 | G | A | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+3006G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127334430 | |||||||
chr5:127334760 | G | A | 3 | a0003c0009t0012g0180 a0003c0009t0012g0212 a0003c0009t0012g0213 |
3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.116+3336G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127334760 | |||||||
chr5:127335081 | A | G | 1 | a0001c0004t0004g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.116+3657A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335081 | |||||||
chr5:127335163 | T | A | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.116+3739T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335163 | |||||||
chr5:127335376 | A | G | 9 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.117-3744A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335376 | |||||||
chr5:127335462 | G | A | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117-3658G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335462 | |||||||
chr5:127335608 | A | G | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.117-3512A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335608 | |||||||
chr5:127335708 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.117-3412T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127335708 | |||||||
chr5:127336348 | T | C | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-2772T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127336348 | |||||||
chr5:127336853 | T | C | 9 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0004t0004g0177 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.117-2267T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127336853 | |||||||
chr5:127336909 | G | A | 1 | a0003c0009t0024g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117-2211G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127336909 | |||||||
chr5:127336929 | A | T | 2 | a0001c0002t0003g0227 a0001c0002t0038g0226 |
2 | HG00140.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.117-2191A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127336929 | |||||||
chr5:127337018 | G | A | 16 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(13): Show |
16 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.117-2102G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337018 | |||||||
chr5:127337046 | A | G | 5 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0002c0003t0009g0105 others(2): Show |
5 | HG00438.hp1 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.117-2074A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337046 | |||||||
chr5:127337387 | T | C | 2 | a0001c0002t0003g0258 a0001c0002t0003g0259 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.117-1733T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337387 | |||||||
chr5:127337467 | T | C | 25 | a0001c0001t0001g0144 a0001c0001t0001g0264 a0001c0001t0021g0193 others(22): Show |
27 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.117-1653T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337467 | |||||||
chr5:127337468 | G | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.117-1652G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337468 | |||||||
chr5:127337550 | A | T | 4 | a0001c0005t0007g0023 a0001c0005t0007g0024 a0001c0005t0007g0029 others(1): Show |
4 | HG02040.hp2 NA18949.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-1570A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337550 | |||||||
chr5:127337650 | C | A | 16 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(13): Show |
16 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.117-1470C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337650 | |||||||
chr5:127337739 | A | G | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117-1381A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337739 | |||||||
chr5:127337879 | C | T | 4 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.117-1241C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127337879 | |||||||
chr5:127338541 | T | G | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117-579T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127338541 | |||||||
chr5:127338630 | C | G | 16 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0008t0004g0233 others(13): Show |
16 | HG00438.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.117-490C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127338630 | |||||||
chr5:127338688 | A | C | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117-432A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127338688 | |||||||
chr5:127338921 | A | G | 65 | a0001c0001t0001g0183 a0001c0001t0001g0239 a0001c0001t0005g0064 others(62): Show |
65 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.117-199A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127338921 | |||||||
chr5:127338948 | C | T | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.117-172C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 2/24 | chr5 | 127338948 | |||||||
chr5:127339238 | C | G | 1 | a0001c0002t0003g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.218+17C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339238 | |||||||
chr5:127339263 | G | A | 2 | a0001c0001t0021g0193 a0001c0004t0004g0265 |
2 | HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.218+42G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339263 | |||||||
chr5:127339376 | G | A | 16 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(13): Show |
16 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.218+155G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339376 | |||||||
chr5:127339409 | G | C | 14 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0004t0004g0175 others(11): Show |
14 | HG00438.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+188G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339409 | |||||||
chr5:127339455 | A | G | 1 | a0001c0004t0004g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+234A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339455 | |||||||
chr5:127339865 | G | A | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.218+644G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127339865 | |||||||
chr5:127340088 | T | A | 13 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(10): Show |
13 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-442T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127340088 | |||||||
chr5:127340196 | T | TGA | 25 | a0001c0001t0001g0144 a0001c0001t0001g0264 a0001c0001t0021g0193 others(22): Show |
27 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.219-331_219-330dup others(2): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr5 | 127340196 | ||||||
chr5:127340267 | T | C | 1 | a0001c0001t0005g0093 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.219-263T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 3/24 | chr5 | 127340267 | |||||||
chr5:127340836 | T | C | 24 | a0001c0001t0001g0264 a0001c0001t0021g0193 a0001c0002t0003g0258 others(21): Show |
26 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.319+206T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127340836 | |||||||
chr5:127340862 | A | G | 27 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(24): Show |
27 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.319+232A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127340862 | |||||||
chr5:127341738 | T | C | 1 | a0001c0008t0004g0247 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319+1108T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127341738 | |||||||
chr5:127341871 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.319+1241C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127341871 | |||||||
chr5:127342286 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.319+1656A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342286 | |||||||
chr5:127342336 | C | T | 17 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.319+1706C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342336 | |||||||
chr5:127342348 | A | G | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+1718A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342348 | |||||||
chr5:127342357 | C | A | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.319+1727C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342357 | |||||||
chr5:127342393 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.319+1763G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342393 | |||||||
chr5:127342421 | A | G | 2 | a0001c0002t0003g0150 a0001c0002t0003g0197 |
2 | HG01069.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.319+1791A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342421 | |||||||
chr5:127342466 | C | T | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.319+1836C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342466 | |||||||
chr5:127342543 | G | T | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319+1913G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342543 | |||||||
chr5:127342823 | CCT | C | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.319+2194_319+2195d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342823 | |||||||
chr5:127342837 | A | C | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+2207A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127342837 | |||||||
chr5:127343391 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.319+2761C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127343391 | |||||||
chr5:127343441 | A | C | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319+2811A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127343441 | |||||||
chr5:127343505 | C | T | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.319+2875C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127343505 | |||||||
chr5:127343667 | AG | A | 22 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(19): Show |
22 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.319+3040delG | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127343667 | ||||||
chr5:127343710 | G | A | 68 | a0001c0001t0001g0146 a0001c0001t0001g0183 a0001c0001t0005g0064 others(65): Show |
68 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.319+3080G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127343710 | |||||||
chr5:127344005 | T | C | 70 | a0001c0001t0001g0146 a0001c0001t0001g0183 a0001c0001t0005g0064 others(67): Show |
70 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.319+3375T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344005 | |||||||
chr5:127344234 | G | A | 1 | a0003c0009t0012g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.319+3604G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344234 | |||||||
chr5:127344372 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0230 a0002c0003t0015g0219 |
3 | NA18939.hp2 NA19083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.319+3742G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344372 | |||||||
chr5:127344624 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.319+3994A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344624 | |||||||
chr5:127344651 | A | C | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.319+4021A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344651 | |||||||
chr5:127344754 | G | A | 1 | a0001c0002t0003g0169 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.319+4124G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344754 | |||||||
chr5:127344873 | G | A | 1 | a0001c0006t0001g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.319+4243G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127344873 | |||||||
chr5:127345121 | G | C | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.319+4491G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345121 | |||||||
chr5:127345133 | T | C | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+4503T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345133 | |||||||
chr5:127345372 | T | C | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.319+4742T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345372 | |||||||
chr5:127345413 | G | A | 21 | a0001c0001t0001g0144 a0001c0001t0021g0193 a0001c0004t0004g0265 others(18): Show |
23 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+4783G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345413 | |||||||
chr5:127345562 | C | T | 8 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0020g0167 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4932C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345562 | |||||||
chr5:127345853 | C | T | 2 | a0001c0008t0004g0235 a0001c0008t0004g0236 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.319+5223C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345853 | |||||||
chr5:127345890 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.319+5260C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127345890 | |||||||
chr5:127346059 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.319+5429G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346059 | |||||||
chr5:127346299 | G | A | 2 | a0001c0002t0002g0086 a0001c0002t0002g0087 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.319+5669G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346299 | |||||||
chr5:127346347 | C | T | 83 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(80): Show |
83 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.319+5717C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346347 | |||||||
chr5:127346662 | A | G | 133 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(130): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.319+6032A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346662 | |||||||
chr5:127346845 | G | A | 2 | a0001c0018t0039g0006 a0001c0027t0004g0135 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.319+6215G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346845 | |||||||
chr5:127346928 | T | A | 1 | a0001c0007t0008g0002 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.319+6298T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127346928 | |||||||
chr5:127347157 | T | A | 1 | a0001c0001t0005g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.319+6527T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347157 | |||||||
chr5:127347225 | A | G | 1 | a0001c0002t0026g0056 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.319+6595A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347225 | |||||||
chr5:127347324 | A | G | 10 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0020g0167 others(7): Show |
10 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+6694A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347324 | |||||||
chr5:127347476 | C | T | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.319+6846C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347476 | |||||||
chr5:127347629 | G | C | 19 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.319+6999G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347629 | |||||||
chr5:127347681 | T | G | 19 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.319+7051T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347681 | |||||||
chr5:127347724 | T | C | 154 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.319+7094T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347724 | |||||||
chr5:127347823 | T | A | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.319+7193T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347823 | |||||||
chr5:127347898 | C | T | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.319+7268C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347898 | |||||||
chr5:127347923 | A | G | 1 | a0001c0004t0004g0177 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319+7293A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127347923 | |||||||
chr5:127348117 | G | A | 133 | a0001c0001t0001g0183 a0001c0001t0005g0048 a0001c0001t0005g0064 others(130): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.319+7487G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348117 | |||||||
chr5:127348151 | C | A | 1 | a0010c0025t0002g0059 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.319+7521C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348151 | |||||||
chr5:127348151 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.319+7521C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348151 | |||||||
chr5:127348191 | A | G | 83 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(80): Show |
83 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.319+7561A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348191 | |||||||
chr5:127348487 | G | A | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.319+7857G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348487 | |||||||
chr5:127348508 | C | T | 1 | a0003c0009t0012g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.319+7878C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348508 | |||||||
chr5:127348528 | G | A | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+7898G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348528 | |||||||
chr5:127348958 | C | T | 1 | a0002c0003t0009g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.319+8328C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127348958 | |||||||
chr5:127349114 | C | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0166 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.319+8484C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349114 | |||||||
chr5:127349186 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.319+8556G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349186 | |||||||
chr5:127349186 | G | T | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.319+8556G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349186 | |||||||
chr5:127349327 | C | A | 17 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0008t0004g0233 others(14): Show |
17 | HG00438.hp1 HG02257.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+8697C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349327 | |||||||
chr5:127349590 | A | G | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.319+8960A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349590 | |||||||
chr5:127349682 | C | CT | 85 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(82): Show |
85 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.319+9063dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127349682 | ||||||
chr5:127349689 | T | G | 2 | a0001c0018t0039g0006 a0001c0027t0004g0135 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.319+9059T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349689 | |||||||
chr5:127349690 | T | G | 4 | a0001c0001t0021g0193 a0001c0004t0004g0265 a0005c0019t0018g0007 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+9060T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349690 | |||||||
chr5:127349691 | T | G | 5 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+9061T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349691 | |||||||
chr5:127349694 | G | GT | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.319+9072dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127349694 | ||||||
chr5:127349806 | G | A | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.319+9176G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127349806 | |||||||
chr5:127350119 | T | C | 1 | a0001c0029t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.319+9489T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350119 | |||||||
chr5:127350156 | C | T | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.319+9526C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350156 | |||||||
chr5:127350411 | A | G | 4 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+9781A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350411 | |||||||
chr5:127350453 | C | T | 17 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0008t0004g0233 others(14): Show |
17 | HG00438.hp1 HG02257.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+9823C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350453 | |||||||
chr5:127350749 | A | G | 1 | a0002c0003t0015g0134 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.319+10119A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350749 | |||||||
chr5:127350783 | A | T | 2 | a0001c0001t0001g0153 a0001c0018t0020g0243 |
2 | HG00639.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+10153A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350783 | |||||||
chr5:127350891 | G | A | 29 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(26): Show |
29 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.319+10261G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127350891 | |||||||
chr5:127351023 | A | G | 1 | a0002c0003t0006g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.319+10393A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351023 | |||||||
chr5:127351064 | G | A | 167 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.319+10434G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351064 | |||||||
chr5:127351111 | T | C | 1 | a0001c0014t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.319+10481T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351111 | |||||||
chr5:127351412 | C | A | 1 | a0001c0001t0005g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.319+10782C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351412 | |||||||
chr5:127351590 | C | G | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.319+10960C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351590 | |||||||
chr5:127351591 | T | C | 1 | a0003c0009t0012g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.319+10961T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351591 | |||||||
chr5:127351702 | C | T | 2 | a0001c0002t0003g0258 a0001c0002t0003g0259 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.319+11072C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351702 | |||||||
chr5:127351937 | A | C | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.319+11307A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351937 | |||||||
chr5:127351995 | C | A | 166 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.319+11365C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127351995 | |||||||
chr5:127352097 | A | AAT | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.319+11476_319+1147 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127352097 | ||||||
chr5:127352130 | A | T | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.319+11500A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352130 | |||||||
chr5:127352415 | A | C | 7 | a0001c0002t0002g0098 a0001c0002t0002g0106 a0001c0002t0002g0116 others(4): Show |
7 | HG02015.hp2 HG02132.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+11785A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352415 | |||||||
chr5:127352708 | T | C | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.319+12078T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352708 | |||||||
chr5:127352758 | T | C | 1 | a0001c0035t0002g0129 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.319+12128T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352758 | |||||||
chr5:127352825 | G | A | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.319+12195G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352825 | |||||||
chr5:127352840 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.319+12210T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352840 | |||||||
chr5:127352854 | G | A | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.319+12224G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127352854 | |||||||
chr5:127353034 | C | T | 32 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(29): Show |
32 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.319+12404C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353034 | |||||||
chr5:127353061 | C | T | 1 | a0001c0002t0002g0058 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.319+12431C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353061 | |||||||
chr5:127353194 | G | A | 2 | a0001c0002t0003g0150 a0001c0002t0003g0197 |
2 | HG01069.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.319+12564G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353194 | |||||||
chr5:127353357 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.319+12727C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353357 | |||||||
chr5:127353469 | G | A | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.319+12839G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353469 | |||||||
chr5:127353577 | T | C | 32 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(29): Show |
32 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.319+12947T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353577 | |||||||
chr5:127353592 | C | T | 5 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0002c0003t0009g0105 others(2): Show |
5 | HG00438.hp1 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+12962C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353592 | |||||||
chr5:127353746 | ACT | A | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.319+13119_319+1312 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127353746 | ||||||
chr5:127353797 | T | A | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.319+13167T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353797 | |||||||
chr5:127353801 | A | G | 1 | a0001c0002t0003g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.319+13171A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353801 | |||||||
chr5:127353805 | G | T | 1 | a0001c0020t0001g0196 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.319+13175G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127353805 | |||||||
chr5:127354098 | C | T | 32 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(29): Show |
32 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.319+13468C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127354098 | |||||||
chr5:127354243 | C | T | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.319+13613C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127354243 | |||||||
chr5:127354278 | A | G | 6 | a0001c0002t0002g0053 a0001c0002t0002g0067 a0001c0002t0002g0069 others(3): Show |
6 | HG00621.hp1 NA18940.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+13648A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127354278 | |||||||
chr5:127354659 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.319+14029A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127354659 | |||||||
chr5:127354979 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.319+14349T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127354979 | |||||||
chr5:127355211 | G | A | 1 | a0001c0036t0002g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.319+14581G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127355211 | |||||||
chr5:127355314 | T | TA | 15 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0004t0004g0265 others(12): Show |
15 | HG00438.hp1 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.320-14586dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127355314 | ||||||
chr5:127355477 | T | G | 32 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(29): Show |
32 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.320-14433T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127355477 | |||||||
chr5:127355849 | AT | A | 18 | a0001c0001t0001g0234 a0001c0001t0013g0096 a0001c0001t0013g0101 others(15): Show |
18 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.320-14050delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127355849 | ||||||
chr5:127356314 | T | C | 3 | a0001c0008t0004g0238 a0001c0008t0008g0072 a0001c0008t0008g0089 |
3 | HG02486.hp1 HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.320-13596T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127356314 | |||||||
chr5:127356537 | A | T | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-13373A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127356537 | |||||||
chr5:127356591 | A | G | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-13319A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127356591 | |||||||
chr5:127356645 | A | G | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-13265A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127356645 | |||||||
chr5:127356870 | G | A | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-13040G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127356870 | |||||||
chr5:127357087 | G | A | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.320-12823G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357087 | |||||||
chr5:127357196 | C | T | 1 | a0001c0002t0003g0214 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.320-12714C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357196 | |||||||
chr5:127357225 | A | G | 5 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0002c0003t0009g0105 others(2): Show |
5 | HG00438.hp1 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-12685A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357225 | |||||||
chr5:127357321 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.320-12589G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357321 | |||||||
chr5:127357438 | C | T | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-12472C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357438 | |||||||
chr5:127357573 | A | G | 153 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.320-12337A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357573 | |||||||
chr5:127357588 | A | AAAAT | 52 | a0001c0001t0001g0132 a0001c0001t0001g0141 a0001c0001t0001g0143 others(49): Show |
53 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.320-12282_320-1227 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127357588 | ||||||
chr5:127357588 | A | AAAATAAA others(1): Show |
32 | a0001c0001t0001g0133 a0001c0001t0001g0153 a0001c0001t0005g0048 others(29): Show |
32 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.320-12286_320-1227 others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127357588 | ||||||
chr5:127357588 | A | AAAATAAA others(5): Show |
15 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(12): Show |
16 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-12290_320-1227 others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127357588 | ||||||
chr5:127357588 | A | AAAATAAA others(9): Show |
3 | a0002c0003t0006g0013 a0003c0009t0012g0180 a0006c0032t0031g0099 |
3 | HG00642.hp2 HG02451.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.320-12294_320-1227 others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127357588 | ||||||
chr5:127357588 | AAAAT | A | 80 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0005g0082 others(77): Show |
80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.320-12282_320-1227 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127357588 | ||||||
chr5:127357665 | C | T | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-12245C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357665 | |||||||
chr5:127357979 | C | T | 17 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0004t0004g0004 others(14): Show |
17 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.320-11931C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127357979 | |||||||
chr5:127358060 | A | G | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-11850A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358060 | |||||||
chr5:127358066 | G | A | 50 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(47): Show |
50 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-11844G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358066 | |||||||
chr5:127358121 | C | T | 3 | a0002c0003t0009g0105 a0002c0003t0009g0123 a0002c0003t0009g0126 |
3 | NA18970.hp1 NA18974.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.320-11789C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358121 | |||||||
chr5:127358130 | C | T | 2 | a0001c0004t0004g0004 a0001c0004t0004g0005 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.320-11780C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358130 | |||||||
chr5:127358282 | T | G | 5 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-11628T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358282 | |||||||
chr5:127358403 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.320-11507T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358403 | |||||||
chr5:127358503 | G | T | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-11407G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358503 | |||||||
chr5:127358508 | T | TC | 50 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(47): Show |
50 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-11402_320-1140 others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358508 | |||||||
chr5:127358687 | A | G | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-11223A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358687 | |||||||
chr5:127358700 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.320-11210C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358700 | |||||||
chr5:127358737 | G | A | 1 | a0001c0001t0032g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.320-11173G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358737 | |||||||
chr5:127358745 | A | T | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.320-11165A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358745 | |||||||
chr5:127358831 | T | A | 153 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.320-11079T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358831 | |||||||
chr5:127358858 | G | A | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.320-11052G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358858 | |||||||
chr5:127358902 | T | A | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.320-11008T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127358902 | |||||||
chr5:127359058 | G | GT | 32 | a0001c0001t0001g0144 a0001c0001t0021g0193 a0001c0002t0003g0020 others(29): Show |
34 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.320-10839dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127359058 | ||||||
chr5:127359058 | G | T | 2 | a0001c0001t0001g0157 a0001c0007t0004g0242 |
2 | HG00323.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.320-10852G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359058 | |||||||
chr5:127359063 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0005g0107 |
2 | NA19007.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.320-10847T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359063 | |||||||
chr5:127359071 | T | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 |
3 | HG02922.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.320-10839T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359071 | |||||||
chr5:127359281 | AT | A | 30 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(27): Show |
30 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-10618delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127359281 | ||||||
chr5:127359348 | G | GT | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-10553dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127359348 | ||||||
chr5:127359355 | T | TG | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-10555_320-1055 others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359355 | |||||||
chr5:127359435 | T | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0143 a0001c0001t0001g0146 others(15): Show |
19 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-10475T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359435 | |||||||
chr5:127359490 | A | G | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-10420A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359490 | |||||||
chr5:127359595 | T | C | 1 | a0001c0002t0002g0069 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.320-10315T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359595 | |||||||
chr5:127359664 | A | C | 2 | a0001c0004t0004g0265 a0001c0012t0021g0009 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.320-10246A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359664 | |||||||
chr5:127359757 | A | G | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-10153A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359757 | |||||||
chr5:127359866 | T | C | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.320-10044T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359866 | |||||||
chr5:127359883 | T | C | 1 | a0001c0001t0005g0082 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.320-10027T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359883 | |||||||
chr5:127359886 | G | C | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.320-10024G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127359886 | |||||||
chr5:127360015 | G | A | 3 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0027g0117 |
3 | HG01975.hp2 NA18974.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.320-9895G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360015 | |||||||
chr5:127360448 | T | G | 2 | a0001c0002t0003g0150 a0001c0002t0003g0197 |
2 | HG01069.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.320-9462T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360448 | |||||||
chr5:127360490 | A | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.320-9420A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360490 | |||||||
chr5:127360509 | G | C | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.320-9401G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360509 | |||||||
chr5:127360624 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0005g0128 |
2 | NA18955.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.320-9286G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360624 | |||||||
chr5:127360744 | T | A | 4 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0095 others(1): Show |
4 | NA18966.hp1 NA18977.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-9166T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360744 | |||||||
chr5:127360862 | G | GTATA | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-9047_320-9046i others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127360862 | ||||||
chr5:127360864 | G | A | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-9046G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360864 | |||||||
chr5:127360880 | G | A | 5 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0007t0029g0124 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-9030G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360880 | |||||||
chr5:127360915 | C | T | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-8995C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360915 | |||||||
chr5:127360923 | A | G | 1 | a0001c0005t0007g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.320-8987A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127360923 | |||||||
chr5:127361039 | G | A | 20 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(17): Show |
20 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.320-8871G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361039 | |||||||
chr5:127361267 | G | C | 3 | a0001c0007t0029g0124 a0003c0031t0040g0170 a0006c0032t0031g0099 |
3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.320-8643G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361267 | |||||||
chr5:127361338 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.320-8572G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361338 | |||||||
chr5:127361365 | A | G | 2 | a0001c0012t0014g0262 a0001c0012t0014g0263 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.320-8545A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361365 | |||||||
chr5:127361446 | G | A | 166 | a0001c0001t0001g0144 a0001c0001t0001g0183 a0001c0001t0005g0048 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.320-8464G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361446 | |||||||
chr5:127361912 | A | G | 18 | a0001c0001t0005g0048 a0001c0001t0005g0093 a0001c0001t0005g0094 others(15): Show |
18 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-7998A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361912 | |||||||
chr5:127361945 | T | A | 1 | a0001c0002t0003g0172 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.320-7965T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127361945 | |||||||
chr5:127362063 | ATCTTT | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0143 a0001c0001t0001g0146 others(15): Show |
19 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-7842_320-7838d others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127362063 | ||||||
chr5:127362331 | G | GT | 114 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0144 others(111): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.320-7564dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127362331 | ||||||
chr5:127362331 | G | GTT | 11 | a0001c0001t0013g0076 a0001c0002t0002g0040 a0001c0002t0002g0041 others(8): Show |
11 | HG00642.hp1 HG01106.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.320-7565_320-7564d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127362331 | ||||||
chr5:127362378 | T | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0182 others(6): Show |
10 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.320-7532T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362378 | |||||||
chr5:127362386 | T | C | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-7524T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362386 | |||||||
chr5:127362578 | A | G | 18 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(15): Show |
18 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.320-7332A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362578 | |||||||
chr5:127362611 | G | A | 1 | a0001c0010t0001g0228 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.320-7299G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362611 | |||||||
chr5:127362653 | C | G | 66 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.320-7257C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362653 | |||||||
chr5:127362659 | C | T | 5 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 others(2): Show |
5 | HG01243.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-7251C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127362659 | |||||||
chr5:127363083 | T | C | 12 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(9): Show |
12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-6827T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363083 | |||||||
chr5:127363146 | T | C | 1 | a0002c0016t0019g0231 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-6764T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363146 | |||||||
chr5:127363277 | T | G | 1 | a0001c0015t0002g0118 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.320-6633T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363277 | |||||||
chr5:127363400 | A | G | 1 | a0001c0002t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.320-6510A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363400 | |||||||
chr5:127363589 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.320-6321G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363589 | |||||||
chr5:127363590 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.320-6320A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363590 | |||||||
chr5:127363629 | T | C | 11 | a0001c0010t0001g0011 a0001c0010t0001g0019 a0002c0003t0006g0001 others(8): Show |
12 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-6281T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363629 | |||||||
chr5:127363655 | G | A | 115 | a0001c0001t0001g0183 a0001c0001t0005g0064 a0001c0001t0013g0076 others(112): Show |
115 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.320-6255G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127363655 | |||||||
chr5:127364108 | T | C | 1 | a0001c0002t0002g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.320-5802T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364108 | |||||||
chr5:127364229 | T | C | 1 | a0001c0002t0027g0117 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.320-5681T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364229 | |||||||
chr5:127364234 | A | G | 1 | a0001c0002t0002g0131 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.320-5676A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364234 | |||||||
chr5:127364249 | C | A | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.320-5661C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364249 | |||||||
chr5:127364265 | C | T | 1 | a0003c0013t0011g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.320-5645C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364265 | |||||||
chr5:127364309 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.320-5601T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364309 | |||||||
chr5:127364448 | C | T | 17 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0004t0004g0004 others(14): Show |
17 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.320-5462C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364448 | |||||||
chr5:127364795 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.320-5115A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364795 | |||||||
chr5:127364983 | T | C | 1 | a0001c0002t0002g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.320-4927T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127364983 | |||||||
chr5:127365007 | C | G | 1 | a0003c0009t0011g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.320-4903C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365007 | |||||||
chr5:127365111 | C | A | 2 | a0001c0002t0027g0117 a0001c0026t0016g0081 |
2 | HG04204.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.320-4799C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365111 | |||||||
chr5:127365221 | T | C | 1 | a0001c0002t0002g0040 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.320-4689T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365221 | |||||||
chr5:127365452 | C | G | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.320-4458C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365452 | |||||||
chr5:127365498 | G | A | 51 | a0001c0001t0001g0144 a0001c0001t0005g0048 a0001c0001t0005g0093 others(48): Show |
53 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.320-4412G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365498 | |||||||
chr5:127365565 | T | C | 5 | a0001c0001t0001g0145 a0001c0001t0001g0163 a0001c0001t0001g0239 others(2): Show |
5 | HG02895.hp2 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-4345T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365565 | |||||||
chr5:127365662 | C | A | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.320-4248C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365662 | |||||||
chr5:127365691 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.320-4219A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365691 | |||||||
chr5:127365895 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.320-4015G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365895 | |||||||
chr5:127365930 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.320-3980A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127365930 | |||||||
chr5:127366200 | G | A | 2 | a0001c0007t0020g0167 a0001c0012t0021g0009 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.320-3710G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366200 | |||||||
chr5:127366263 | T | G | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.320-3647T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366263 | |||||||
chr5:127366302 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.320-3608G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366302 | |||||||
chr5:127366550 | G | A | 1 | a0001c0015t0003g0033 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.320-3360G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366550 | |||||||
chr5:127366707 | T | A | 28 | a0001c0001t0001g0144 a0001c0001t0021g0193 a0001c0007t0004g0242 others(25): Show |
29 | HG00408.hp2 HG00423.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.320-3203T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366707 | |||||||
chr5:127366721 | A | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.320-3189A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366721 | |||||||
chr5:127366738 | G | A | 2 | a0001c0002t0002g0086 a0001c0002t0002g0087 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.320-3172G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366738 | |||||||
chr5:127366783 | G | A | 1 | a0001c0002t0002g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.320-3127G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366783 | |||||||
chr5:127366879 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.320-3031G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127366879 | |||||||
chr5:127367147 | C | A | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-2763C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367147 | |||||||
chr5:127367610 | A | G | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-2300A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367610 | |||||||
chr5:127367638 | G | A | 1 | a0001c0012t0014g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.320-2272G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367638 | |||||||
chr5:127367676 | T | C | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.320-2234T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367676 | |||||||
chr5:127367769 | G | T | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.320-2141G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367769 | |||||||
chr5:127367890 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-2020T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367890 | |||||||
chr5:127367926 | T | C | 14 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(11): Show |
14 | HG00099.hp1 HG00642.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.320-1984T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127367926 | |||||||
chr5:127368120 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-1790C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368120 | |||||||
chr5:127368357 | G | A | 19 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.320-1553G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368357 | |||||||
chr5:127368383 | T | C | 1 | a0001c0017t0003g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.320-1527T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368383 | |||||||
chr5:127368383 | T | G | 2 | a0001c0007t0004g0242 a0006c0032t0031g0099 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.320-1527T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368383 | |||||||
chr5:127368388 | G | A | 19 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.320-1522G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368388 | |||||||
chr5:127368597 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-1313T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368597 | |||||||
chr5:127368600 | T | C | 1 | a0003c0009t0012g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.320-1310T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368600 | |||||||
chr5:127368752 | G | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.320-1158G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368752 | |||||||
chr5:127368839 | C | T | 1 | a0001c0001t0021g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.320-1071C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368839 | |||||||
chr5:127368893 | G | A | 1 | a0002c0016t0019g0231 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-1017G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368893 | |||||||
chr5:127368991 | G | C | 1 | a0009c0033t0002g0043 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.320-919G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127368991 | |||||||
chr5:127369072 | C | A | 1 | a0001c0002t0003g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.320-838C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127369072 | |||||||
chr5:127369221 | T | C | 1 | a0004c0022t0022g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.320-689T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127369221 | |||||||
chr5:127369613 | G | C | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.320-297G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127369613 | |||||||
chr5:127369772 | AGGAAC | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.320-134_320-130del others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr5 | 127369772 | ||||||
chr5:127369814 | T | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.320-96T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 4/24 | chr5 | 127369814 | |||||||
chr5:127370129 | C | G | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+127C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370129 | |||||||
chr5:127370137 | G | T | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+135G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370137 | |||||||
chr5:127370228 | G | A | 88 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(85): Show |
90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.412+226G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370228 | |||||||
chr5:127370428 | G | A | 2 | a0001c0001t0013g0096 a0001c0001t0013g0101 |
2 | HG00438.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.412+426G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370428 | |||||||
chr5:127370772 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.412+770C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370772 | |||||||
chr5:127370895 | G | A | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.412+893G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370895 | |||||||
chr5:127370941 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0189 |
2 | HG00423.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.412+939G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370941 | |||||||
chr5:127370957 | T | G | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+955T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127370957 | |||||||
chr5:127371190 | A | AGT | 4 | a0001c0001t0001g0146 a0001c0001t0001g0185 a0001c0001t0001g0215 others(1): Show |
4 | HG02148.hp2 NA18959.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1188_412+1189i others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371190 | |||||||
chr5:127371190 | ACT | A | 2 | a0001c0001t0001g0003 a0001c0001t0005g0048 |
3 | HG01106.hp2 HG01192.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.412+1189_412+1190d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371190 | |||||||
chr5:127371191 | C | CTG | 23 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0153 others(20): Show |
23 | HG00558.hp2 HG01074.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.412+1243_412+1244d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | C | CTGTG | 10 | a0001c0001t0001g0152 a0001c0001t0001g0158 a0001c0001t0001g0239 others(7): Show |
10 | HG01074.hp2 HG02300.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.412+1241_412+1244d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | C | CTGTGTG | 3 | a0001c0001t0001g0194 a0001c0005t0007g0027 a0001c0007t0029g0124 |
3 | HG02976.hp2 HG03492.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.412+1239_412+1244d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0207 a0001c0001t0005g0082 a0001c0002t0003g0227 others(1): Show |
4 | HG00140.hp1 HG00408.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1237_412+1244d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | C | G | 13 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0155 others(10): Show |
13 | HG01099.hp1 HG01361.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+1189C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371191 | |||||||
chr5:127371191 | CTG | C | 48 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0145 others(45): Show |
48 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.412+1243_412+1244d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTG | C | 42 | a0001c0001t0001g0139 a0001c0001t0001g0202 a0001c0001t0001g0204 others(39): Show |
43 | HG01167.hp1 HG01255.hp2 HG01952.hp1 others(40): Show |
intron_variant | MODIFIER | c.412+1241_412+1244d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTG | C | 17 | a0001c0001t0021g0193 a0001c0002t0002g0256 a0001c0002t0003g0020 others(14): Show |
17 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.412+1239_412+1244d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(1): Show |
C | 11 | a0001c0001t0001g0200 a0001c0001t0013g0096 a0001c0001t0013g0101 others(8): Show |
11 | HG00438.hp1 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+1237_412+1244d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(3): Show |
C | 4 | a0001c0005t0007g0031 a0001c0008t0004g0238 a0001c0008t0008g0072 others(1): Show |
4 | HG02486.hp1 HG02630.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+1235_412+1244d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(5): Show |
C | 3 | a0002c0003t0006g0012 a0002c0016t0019g0231 a0002c0016t0019g0232 |
3 | HG02071.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412+1233_412+1244d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(7): Show |
C | 23 | a0001c0001t0001g0144 a0002c0003t0006g0001 a0002c0003t0006g0010 others(20): Show |
24 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.412+1231_412+1244d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(9): Show |
C | 1 | a0002c0003t0015g0134 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.412+1229_412+1244d others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(11): Show |
C | 5 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 others(2): Show |
5 | HG00639.hp1 HG01243.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+1227_412+1244d others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371191 | CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.412+1223_412+1244d others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127371191 | ||||||
chr5:127371392 | T | A | 3 | a0001c0002t0003g0190 a0001c0002t0003g0229 a0001c0017t0003g0140 |
3 | HG02451.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.412+1390T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371392 | |||||||
chr5:127371527 | C | T | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+1525C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371527 | |||||||
chr5:127371528 | G | A | 2 | a0001c0002t0002g0078 a0001c0017t0002g0060 |
2 | HG00558.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.412+1526G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371528 | |||||||
chr5:127371593 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.412+1591T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371593 | |||||||
chr5:127371800 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.412+1798C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371800 | |||||||
chr5:127371894 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412+1892G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127371894 | |||||||
chr5:127372158 | T | C | 81 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.412+2156T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127372158 | |||||||
chr5:127372158 | T | G | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.412+2156T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127372158 | |||||||
chr5:127372380 | C | G | 1 | a0002c0003t0015g0219 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.412+2378C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127372380 | |||||||
chr5:127372752 | C | T | 4 | a0001c0006t0001g0221 a0001c0006t0001g0222 a0001c0006t0001g0223 others(1): Show |
4 | NA18939.hp1 NA18946.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+2750C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127372752 | |||||||
chr5:127373086 | G | A | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.412+3084G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373086 | |||||||
chr5:127373202 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.412+3200G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373202 | |||||||
chr5:127373340 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.412+3338C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373340 | |||||||
chr5:127373462 | C | T | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.412+3460C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373462 | |||||||
chr5:127373673 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+3671A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373673 | |||||||
chr5:127373740 | C | T | 4 | a0001c0002t0003g0171 a0001c0002t0003g0172 a0001c0021t0003g0173 others(1): Show |
4 | HG01099.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+3738C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373740 | |||||||
chr5:127373936 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412+3934G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127373936 | |||||||
chr5:127374202 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+4200C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374202 | |||||||
chr5:127374236 | C | T | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+4234C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374236 | |||||||
chr5:127374448 | C | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412+4446C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374448 | |||||||
chr5:127374453 | A | C | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.412+4451A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374453 | |||||||
chr5:127374512 | TA | T | 87 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(84): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.412+4518delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127374512 | ||||||
chr5:127374520 | A | G | 3 | a0001c0005t0007g0023 a0001c0005t0007g0024 a0001c0005t0007g0029 |
3 | HG02040.hp2 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.412+4518A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374520 | |||||||
chr5:127374626 | T | A | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+4624T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127374626 | |||||||
chr5:127375018 | C | A | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+5016C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375018 | |||||||
chr5:127375045 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+5043T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375045 | |||||||
chr5:127375223 | CT | C | 167 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0146 others(164): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.412+5231delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127375223 | ||||||
chr5:127375264 | C | T | 25 | a0001c0001t0001g0144 a0002c0003t0006g0001 a0002c0003t0006g0010 others(22): Show |
26 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.412+5262C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375264 | |||||||
chr5:127375289 | C | T | 3 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 |
3 | HG00438.hp1 HG00642.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.412+5287C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375289 | |||||||
chr5:127375464 | C | A | 20 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.412+5462C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375464 | |||||||
chr5:127375487 | G | C | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.412+5485G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375487 | |||||||
chr5:127375504 | T | A | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.412+5502T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375504 | |||||||
chr5:127375665 | C | T | 1 | a0001c0002t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.412+5663C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375665 | |||||||
chr5:127375835 | C | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.412+5833C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375835 | |||||||
chr5:127375894 | T | C | 1 | a0005c0019t0018g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412+5892T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375894 | |||||||
chr5:127375947 | A | G | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+5945A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127375947 | |||||||
chr5:127376033 | G | T | 4 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0062 others(1): Show |
4 | HG01975.hp2 HG02040.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+6031G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376033 | |||||||
chr5:127376614 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.412+6612T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376614 | |||||||
chr5:127376624 | G | A | 18 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0007t0029g0124 others(15): Show |
18 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+6622G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376624 | |||||||
chr5:127376627 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.412+6625G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376627 | |||||||
chr5:127376628 | G | T | 48 | a0001c0001t0001g0144 a0001c0004t0004g0004 a0001c0004t0004g0005 others(45): Show |
50 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.412+6626G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376628 | |||||||
chr5:127376752 | A | C | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+6750A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376752 | |||||||
chr5:127376797 | G | A | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+6795G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376797 | |||||||
chr5:127376895 | C | T | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+6893C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376895 | |||||||
chr5:127376896 | G | A | 20 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.412+6894G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376896 | |||||||
chr5:127376911 | C | T | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.412+6909C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376911 | |||||||
chr5:127376912 | G | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.412+6910G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376912 | |||||||
chr5:127376935 | G | A | 1 | a0005c0019t0018g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412+6933G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376935 | |||||||
chr5:127376981 | CA | C | 27 | a0001c0001t0001g0144 a0002c0003t0006g0001 a0002c0003t0006g0010 others(24): Show |
28 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.412+6980delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127376981 | |||||||
chr5:127377050 | A | G | 1 | a0001c0001t0005g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.412+7048A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377050 | |||||||
chr5:127377102 | T | C | 2 | a0001c0004t0004g0175 a0001c0004t0004g0176 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.412+7100T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377102 | |||||||
chr5:127377179 | T | C | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+7177T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377179 | |||||||
chr5:127377390 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0003c0009t0024g0085 |
3 | HG01074.hp1 HG01515.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.412+7388G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377390 | |||||||
chr5:127377448 | TC | T | 9 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 others(6): Show |
9 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.412+7447delC | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377448 | |||||||
chr5:127377512 | A | G | 13 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(10): Show |
13 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+7510A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377512 | |||||||
chr5:127377914 | A | G | 84 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(81): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.412+7912A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127377914 | |||||||
chr5:127378132 | A | G | 2 | a0001c0001t0005g0093 a0001c0001t0005g0094 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.412+8130A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378132 | |||||||
chr5:127378224 | T | C | 1 | a0001c0017t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.412+8222T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378224 | |||||||
chr5:127378286 | T | C | 5 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0068 others(2): Show |
5 | HG01070.hp1 HG02257.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+8284T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378286 | |||||||
chr5:127378302 | TA | T | 3 | a0002c0003t0009g0108 a0002c0003t0009g0109 a0002c0003t0009g0110 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.412+8302delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127378302 | ||||||
chr5:127378316 | T | C | 1 | a0001c0002t0003g0190 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.412+8314T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378316 | |||||||
chr5:127378360 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.412+8358C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378360 | |||||||
chr5:127378572 | C | A | 10 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(7): Show |
10 | HG02486.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.412+8570C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378572 | |||||||
chr5:127378851 | T | G | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.412+8849T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127378851 | |||||||
chr5:127378857 | GT | G | 15 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(12): Show |
15 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+8867delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127378857 | ||||||
chr5:127379064 | C | CT | 14 | a0001c0001t0001g0217 a0001c0007t0029g0124 a0001c0008t0004g0233 others(11): Show |
14 | HG01243.hp2 HG01952.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.412+9080dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379064 | ||||||
chr5:127379064 | CT | C | 99 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0166 others(96): Show |
99 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.412+9080delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379064 | ||||||
chr5:127379064 | CTT | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+9079_412+9080d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379064 | ||||||
chr5:127379081 | TTG | T | 19 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.412+9080_412+9081d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379081 | |||||||
chr5:127379313 | T | A | 1 | a0001c0002t0003g0214 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.412+9311T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379313 | |||||||
chr5:127379351 | C | T | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412+9349C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379351 | |||||||
chr5:127379459 | A | G | 2 | a0001c0002t0025g0045 a0001c0002t0038g0226 |
2 | HG00639.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.412+9457A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379459 | |||||||
chr5:127379514 | G | A | 4 | a0001c0002t0003g0171 a0001c0002t0003g0172 a0001c0021t0003g0173 others(1): Show |
4 | HG01099.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+9512G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379514 | |||||||
chr5:127379552 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.412+9550C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379552 | |||||||
chr5:127379565 | A | G | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+9563A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379565 | |||||||
chr5:127379594 | C | CT | 10 | a0001c0007t0004g0242 a0001c0007t0029g0124 a0001c0008t0004g0233 others(7): Show |
10 | HG02615.hp2 HG02630.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.412+9615dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379594 | ||||||
chr5:127379594 | C | CTT | 11 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(8): Show |
11 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+9614_412+9615d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379594 | ||||||
chr5:127379594 | CT | C | 64 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0001c0001t0001g0154 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.412+9615delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127379594 | ||||||
chr5:127379672 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+9670C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379672 | |||||||
chr5:127379692 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+9690C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379692 | |||||||
chr5:127379907 | G | A | 1 | a0001c0001t0032g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.412+9905G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379907 | |||||||
chr5:127379943 | C | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.412+9941C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379943 | |||||||
chr5:127379969 | A | C | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.412+9967A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127379969 | |||||||
chr5:127380061 | T | C | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.412+10059T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380061 | |||||||
chr5:127380067 | G | GT | 94 | a0001c0001t0001g0162 a0001c0001t0001g0206 a0001c0001t0005g0093 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.412+10077dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127380067 | ||||||
chr5:127380067 | G | GTT | 76 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(73): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.412+10076_412+1007 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127380067 | ||||||
chr5:127380166 | T | C | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.412+10164T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380166 | |||||||
chr5:127380231 | C | T | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+10229C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380231 | |||||||
chr5:127380340 | G | A | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+10338G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380340 | |||||||
chr5:127380368 | A | G | 84 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(81): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.412+10366A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380368 | |||||||
chr5:127380523 | CT | C | 81 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.412+10533delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127380523 | ||||||
chr5:127380548 | C | T | 1 | a0001c0001t0032g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.412+10546C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380548 | |||||||
chr5:127380554 | G | A | 1 | a0001c0035t0002g0129 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.412+10552G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380554 | |||||||
chr5:127380619 | A | G | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+10617A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380619 | |||||||
chr5:127380674 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.412+10672C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380674 | |||||||
chr5:127380738 | C | T | 2 | a0001c0008t0004g0233 a0001c0008t0004g0247 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412+10736C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380738 | |||||||
chr5:127380759 | C | T | 4 | a0001c0002t0003g0138 a0001c0002t0003g0168 a0001c0002t0003g0169 others(1): Show |
4 | HG01952.hp2 HG01981.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+10757C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380759 | |||||||
chr5:127380760 | G | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412+10758G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380760 | |||||||
chr5:127380787 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412+10785G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380787 | |||||||
chr5:127380871 | C | A | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+10869C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380871 | |||||||
chr5:127380878 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.412+10876G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380878 | |||||||
chr5:127380963 | A | T | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+10961A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380963 | |||||||
chr5:127380981 | A | G | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+10979A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127380981 | |||||||
chr5:127381278 | G | T | 27 | a0001c0001t0001g0144 a0002c0003t0006g0001 a0002c0003t0006g0010 others(24): Show |
28 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.412+11276G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381278 | |||||||
chr5:127381366 | C | A | 3 | a0001c0002t0002g0063 a0001c0002t0003g0020 a0001c0002t0003g0184 |
3 | HG01257.hp1 HG01496.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.412+11364C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381366 | |||||||
chr5:127381368 | GA | G | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+11369delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127381368 | ||||||
chr5:127381457 | T | C | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+11455T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381457 | |||||||
chr5:127381535 | C | T | 23 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(20): Show |
23 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+11533C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381535 | |||||||
chr5:127381544 | G | T | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412+11542G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381544 | |||||||
chr5:127381545 | C | T | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412+11543C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381545 | |||||||
chr5:127381646 | G | T | 31 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0005t0007g0021 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.412+11644G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381646 | |||||||
chr5:127381859 | T | C | 31 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0005t0007g0021 others(28): Show |
31 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.412+11857T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381859 | |||||||
chr5:127381998 | G | A | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+11996G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127381998 | |||||||
chr5:127382188 | A | G | 18 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0007t0029g0124 others(15): Show |
18 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+12186A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382188 | |||||||
chr5:127382292 | A | G | 169 | a0001c0001t0001g0144 a0001c0001t0001g0206 a0001c0001t0005g0093 others(166): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.412+12290A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382292 | |||||||
chr5:127382372 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.412+12370T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382372 | |||||||
chr5:127382561 | G | T | 1 | a0001c0002t0002g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.412+12559G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382561 | |||||||
chr5:127382750 | A | G | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+12748A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382750 | |||||||
chr5:127382810 | G | A | 1 | a0001c0007t0008g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.412+12808G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382810 | |||||||
chr5:127382811 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+12809C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382811 | |||||||
chr5:127382812 | G | A | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.412+12810G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382812 | |||||||
chr5:127382904 | C | T | 20 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.412+12902C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127382904 | |||||||
chr5:127383102 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+13100A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383102 | |||||||
chr5:127383235 | A | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.412+13233A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383235 | |||||||
chr5:127383303 | G | A | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.413-13229G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383303 | |||||||
chr5:127383409 | A | C | 1 | a0003c0024t0011g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.413-13123A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383409 | |||||||
chr5:127383805 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0005g0055 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413-12727G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383805 | |||||||
chr5:127383848 | C | T | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-12684C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383848 | |||||||
chr5:127383849 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.413-12683G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127383849 | |||||||
chr5:127384077 | C | G | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.413-12455C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384077 | |||||||
chr5:127384129 | C | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-12403C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384129 | |||||||
chr5:127384153 | C | T | 79 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(76): Show |
81 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.413-12379C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384153 | |||||||
chr5:127384278 | A | T | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.413-12254A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384278 | |||||||
chr5:127384283 | C | T | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-12249C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384283 | |||||||
chr5:127384284 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.413-12248G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384284 | |||||||
chr5:127384303 | A | C | 1 | a0001c0002t0002g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.413-12229A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384303 | |||||||
chr5:127384327 | A | G | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-12205A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384327 | |||||||
chr5:127384414 | C | G | 13 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(10): Show |
13 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.413-12118C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384414 | |||||||
chr5:127384565 | A | G | 11 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(8): Show |
11 | HG00639.hp1 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.413-11967A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384565 | |||||||
chr5:127384706 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0005g0064 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.413-11826G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384706 | |||||||
chr5:127384714 | C | T | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413-11818C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384714 | |||||||
chr5:127384721 | C | T | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.413-11811C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384721 | |||||||
chr5:127384723 | T | C | 13 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(10): Show |
13 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.413-11809T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384723 | |||||||
chr5:127384844 | T | C | 24 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(21): Show |
24 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.413-11688T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127384844 | |||||||
chr5:127385418 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.413-11114A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385418 | |||||||
chr5:127385493 | A | T | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-11039A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385493 | |||||||
chr5:127385544 | A | G | 2 | a0001c0001t0005g0093 a0001c0001t0005g0094 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.413-10988A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385544 | |||||||
chr5:127385553 | A | C | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.413-10979A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385553 | |||||||
chr5:127385718 | T | G | 20 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.413-10814T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385718 | |||||||
chr5:127385847 | A | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-10685A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385847 | |||||||
chr5:127385884 | T | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-10648T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127385884 | |||||||
chr5:127386065 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-10467G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127386065 | |||||||
chr5:127386161 | C | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-10371C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127386161 | |||||||
chr5:127386694 | G | T | 1 | a0001c0014t0023g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.413-9838G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127386694 | |||||||
chr5:127387146 | A | G | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413-9386A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387146 | |||||||
chr5:127387167 | A | G | 93 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(90): Show |
95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.413-9365A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387167 | |||||||
chr5:127387209 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0154 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.413-9323C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387209 | |||||||
chr5:127387383 | G | A | 3 | a0001c0002t0002g0063 a0001c0002t0003g0020 a0001c0002t0003g0184 |
3 | HG01257.hp1 HG01496.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.413-9149G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387383 | |||||||
chr5:127387629 | T | G | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-8903T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387629 | |||||||
chr5:127387852 | C | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.413-8680C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387852 | |||||||
chr5:127387870 | G | A | 163 | a0001c0001t0001g0144 a0001c0002t0002g0040 a0001c0002t0002g0041 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.413-8662G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387870 | |||||||
chr5:127387893 | G | C | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-8639G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387893 | |||||||
chr5:127387997 | A | G | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-8535A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127387997 | |||||||
chr5:127388071 | G | A | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-8461G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388071 | |||||||
chr5:127388104 | A | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-8428A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388104 | |||||||
chr5:127388165 | T | G | 1 | a0001c0001t0005g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.413-8367T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388165 | |||||||
chr5:127388208 | G | A | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-8324G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388208 | |||||||
chr5:127388263 | C | T | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-8269C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388263 | |||||||
chr5:127388345 | C | T | 1 | a0001c0004t0004g0255 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.413-8187C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388345 | |||||||
chr5:127388465 | C | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-8067C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388465 | |||||||
chr5:127388517 | T | TTTTA | 34 | a0001c0001t0001g0189 a0001c0001t0001g0230 a0001c0002t0002g0044 others(31): Show |
35 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.413-7975_413-7972d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388517 | ||||||
chr5:127388517 | T | TTTTATTT others(1): Show |
7 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0168 others(4): Show |
7 | HG01952.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-7979_413-7972d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388517 | ||||||
chr5:127388517 | TTTTA | T | 68 | a0001c0001t0013g0096 a0001c0001t0013g0101 a0001c0002t0002g0040 others(65): Show |
68 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.413-7975_413-7972d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388517 | ||||||
chr5:127388517 | TTTTATTT others(1): Show |
T | 14 | a0001c0001t0005g0093 a0001c0005t0007g0021 a0001c0005t0007g0023 others(11): Show |
14 | HG00323.hp1 HG00639.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.413-7979_413-7972d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388517 | ||||||
chr5:127388517 | TTTTATTT others(5): Show |
T | 43 | a0001c0001t0001g0144 a0001c0005t0007g0027 a0001c0005t0016g0083 others(40): Show |
44 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.413-7983_413-7972d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388517 | ||||||
chr5:127388580 | C | G | 1 | a0001c0035t0002g0129 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.413-7952C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388580 | |||||||
chr5:127388585 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.413-7947G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388585 | |||||||
chr5:127388653 | C | T | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.413-7879C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388653 | |||||||
chr5:127388694 | C | T | 34 | a0001c0001t0001g0144 a0001c0014t0001g0253 a0001c0014t0005g0038 others(31): Show |
35 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.413-7838C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388694 | |||||||
chr5:127388730 | A | G | 1 | a0008c0030t0005g0084 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.413-7802A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388730 | |||||||
chr5:127388735 | CAG | C | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-7794_413-7793d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127388735 | ||||||
chr5:127388767 | G | A | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.413-7765G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388767 | |||||||
chr5:127388781 | G | A | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-7751G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388781 | |||||||
chr5:127388888 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 |
3 | HG02922.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.413-7644G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388888 | |||||||
chr5:127388934 | A | G | 1 | a0001c0006t0001g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.413-7598A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388934 | |||||||
chr5:127388937 | C | T | 13 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(10): Show |
13 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.413-7595C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127388937 | |||||||
chr5:127389013 | G | T | 1 | a0003c0009t0010g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.413-7519G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389013 | |||||||
chr5:127389129 | G | A | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0204 others(3): Show |
6 | HG02015.hp1 HG02083.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-7403G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389129 | |||||||
chr5:127389362 | T | C | 162 | a0001c0001t0001g0144 a0001c0001t0013g0076 a0001c0001t0013g0096 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413-7170T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389362 | |||||||
chr5:127389420 | G | T | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413-7112G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389420 | |||||||
chr5:127389560 | T | C | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413-6972T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389560 | |||||||
chr5:127389584 | G | A | 34 | a0001c0001t0001g0144 a0001c0014t0001g0253 a0001c0014t0005g0038 others(31): Show |
35 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.413-6948G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389584 | |||||||
chr5:127389585 | C | A | 34 | a0001c0001t0001g0144 a0001c0014t0001g0253 a0001c0014t0005g0038 others(31): Show |
35 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.413-6947C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389585 | |||||||
chr5:127389720 | C | T | 1 | a0001c0010t0001g0192 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.413-6812C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389720 | |||||||
chr5:127389725 | A | G | 13 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(10): Show |
13 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.413-6807A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389725 | |||||||
chr5:127389837 | TG | T | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-6692delG | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127389837 | ||||||
chr5:127389870 | A | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-6662A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389870 | |||||||
chr5:127389876 | T | C | 162 | a0001c0001t0001g0144 a0001c0001t0013g0076 a0001c0001t0013g0096 others(159): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413-6656T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389876 | |||||||
chr5:127389899 | C | T | 3 | a0001c0005t0007g0023 a0001c0005t0007g0024 a0001c0005t0007g0029 |
3 | HG02040.hp2 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.413-6633C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389899 | |||||||
chr5:127389949 | A | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-6583A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127389949 | |||||||
chr5:127389972 | GC | G | 20 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.413-6557delC | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127389972 | ||||||
chr5:127390010 | G | T | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.413-6522G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390010 | |||||||
chr5:127390194 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-6338G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390194 | |||||||
chr5:127390295 | C | CT | 14 | a0001c0001t0001g0202 a0001c0001t0005g0082 a0001c0005t0007g0021 others(11): Show |
15 | HG00323.hp1 HG00408.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.413-6225dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127390295 | ||||||
chr5:127390308 | G | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-6224G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390308 | |||||||
chr5:127390348 | A | G | 2 | a0001c0002t0003g0149 a0001c0002t0003g0151 |
2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.413-6184A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390348 | |||||||
chr5:127390381 | C | T | 55 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(52): Show |
56 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-6151C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390381 | |||||||
chr5:127390443 | G | C | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-6089G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390443 | |||||||
chr5:127390596 | A | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-5936A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390596 | |||||||
chr5:127390970 | C | G | 1 | a0001c0002t0003g0197 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.413-5562C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390970 | |||||||
chr5:127390977 | G | A | 84 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(81): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.413-5555G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390977 | |||||||
chr5:127390994 | C | T | 1 | a0001c0005t0007g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.413-5538C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390994 | |||||||
chr5:127390995 | T | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-5537T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127390995 | |||||||
chr5:127391046 | C | T | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-5486C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391046 | |||||||
chr5:127391054 | G | A | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG01975.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.413-5478G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391054 | |||||||
chr5:127391071 | TACATACA others(51): Show |
T | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.413-5457_413-5400d others(60): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391071 | ||||||
chr5:127391080 | ACACACAT others(3): Show |
A | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-5450_413-5441d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391080 | ||||||
chr5:127391082 | A | G | 8 | a0001c0008t0004g0233 a0001c0008t0004g0235 a0001c0008t0004g0236 others(5): Show |
8 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.413-5450A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391082 | |||||||
chr5:127391085 | C | T | 52 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(49): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.413-5447C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391085 | |||||||
chr5:127391086 | A | G | 52 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(49): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.413-5446A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391086 | |||||||
chr5:127391087 | T | TGC | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0187 others(3): Show |
6 | HG01255.hp1 HG02155.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-5430_413-5429d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391087 | ||||||
chr5:127391087 | T | TGCGCGCG others(3): Show |
1 | a0003c0009t0012g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.413-5438_413-5429d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391087 | ||||||
chr5:127391087 | TGC | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0154 a0001c0001t0001g0182 others(5): Show |
8 | HG02809.hp1 HG02886.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-5430_413-5429d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391087 | ||||||
chr5:127391087 | TGCGCGC | T | 4 | a0001c0002t0002g0049 a0001c0002t0002g0051 a0001c0002t0002g0098 others(1): Show |
4 | HG02004.hp1 HG02015.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-5434_413-5429d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391087 | ||||||
chr5:127391089 | C | CGCGCGCA others(5): Show |
1 | a0003c0009t0012g0213 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.413-5437_413-5436i others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391089 | ||||||
chr5:127391092 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.413-5440G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391092 | |||||||
chr5:127391094 | G | A | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-5438G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391094 | |||||||
chr5:127391094 | GCGCGCGC others(5): Show |
G | 9 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0095 others(6): Show |
9 | HG01099.hp2 HG01952.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.413-5436_413-5425d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(7): Show |
G | 11 | a0001c0002t0002g0046 a0001c0002t0002g0058 a0001c0002t0002g0063 others(8): Show |
11 | HG00140.hp1 HG01169.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-5436_413-5423d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(9): Show |
G | 10 | a0001c0002t0002g0079 a0001c0002t0002g0100 a0001c0002t0002g0104 others(7): Show |
10 | HG01192.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.413-5436_413-5421d others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(17): Show |
G | 15 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(12): Show |
15 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-5436_413-5413d others(26): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(19): Show |
G | 3 | a0001c0002t0002g0061 a0001c0002t0003g0241 a0001c0002t0028g0073 |
3 | HG01993.hp1 HG02148.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.413-5436_413-5411d others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(21): Show |
G | 1 | a0001c0002t0002g0078 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.413-5436_413-5409d others(30): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(23): Show |
G | 1 | a0001c0002t0002g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.413-5436_413-5407d others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(25): Show |
G | 4 | a0001c0002t0002g0053 a0001c0002t0002g0067 a0001c0002t0002g0069 others(1): Show |
4 | HG00621.hp1 NA18940.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5436_413-5405d others(34): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391094 | GCGCGCGC others(29): Show |
G | 1 | a0001c0002t0002g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413-5436_413-5401d others(38): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391094 | ||||||
chr5:127391095 | C | T | 53 | a0001c0001t0001g0144 a0001c0001t0001g0188 a0001c0005t0007g0021 others(50): Show |
54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.413-5437C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391095 | |||||||
chr5:127391096 | GCGCGCGC others(1): Show |
G | 3 | a0001c0002t0027g0117 a0001c0002t0038g0226 a0001c0012t0014g0261 |
3 | HG00639.hp2 NA18522.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.413-5434_413-5427d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(3): Show |
G | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.413-5434_413-5425d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(5): Show |
G | 4 | a0001c0002t0002g0130 a0001c0002t0017g0102 a0001c0002t0017g0103 others(1): Show |
4 | HG01074.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5434_413-5423d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(7): Show |
G | 1 | a0001c0017t0003g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413-5434_413-5421d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(9): Show |
G | 4 | a0001c0002t0003g0258 a0003c0009t0012g0260 a0005c0019t0018g0007 others(1): Show |
4 | HG02717.hp2 HG03195.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5434_413-5419d others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(11): Show |
G | 1 | a0001c0001t0013g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.413-5434_413-5417d others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(13): Show |
G | 2 | a0001c0001t0013g0076 a0001c0001t0013g0096 |
2 | HG00642.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.413-5434_413-5415d others(22): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391096 | GCGCGCGC others(19): Show |
G | 1 | a0001c0002t0003g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413-5434_413-5409d others(28): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391096 | ||||||
chr5:127391098 | GCGCGCAC others(3): Show |
G | 1 | a0001c0002t0003g0190 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.413-5432_413-5423d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391098 | ||||||
chr5:127391100 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0163 a0001c0001t0001g0239 others(2): Show |
5 | HG02895.hp2 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-5432G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391100 | |||||||
chr5:127391100 | G | GCA | 7 | a0001c0001t0001g0165 a0001c0002t0002g0044 a0001c0004t0004g0004 others(4): Show |
7 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-5431_413-5430i others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391100 | G | GCACA | 3 | a0001c0001t0001g0158 a0001c0001t0001g0264 a0001c0007t0008g0080 |
3 | HG02965.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.413-5431_413-5430i others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391100 | G | GCACACA | 5 | a0001c0004t0004g0240 a0001c0004t0004g0251 a0001c0004t0004g0265 others(2): Show |
5 | HG00558.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-5431_413-5430i others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391100 | G | GCACACAC others(3): Show |
4 | a0001c0004t0004g0137 a0001c0007t0004g0254 a0001c0007t0008g0002 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5431_413-5430i others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391100 | GCGCA | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0152 a0001c0001t0001g0155 others(13): Show |
17 | HG01074.hp1 HG01099.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-5430_413-5427d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391100 | GCGCACAC others(5): Show |
G | 1 | a0001c0001t0001g0209 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.413-5430_413-5419d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391100 | ||||||
chr5:127391102 | G | A | 31 | a0001c0001t0001g0145 a0001c0001t0001g0158 a0001c0001t0001g0163 others(28): Show |
32 | HG00099.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.413-5430G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391102 | |||||||
chr5:127391102 | G | GCA | 8 | a0001c0001t0001g0162 a0001c0001t0001g0189 a0001c0001t0001g0207 others(5): Show |
8 | HG00423.hp2 HG02004.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.413-5379_413-5378d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | G | GCACA | 4 | a0001c0001t0001g0132 a0001c0001t0001g0181 a0001c0001t0005g0048 others(1): Show |
4 | HG02071.hp1 NA18522.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-5381_413-5378d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0183 a0001c0001t0001g0205 a0001c0001t0005g0064 others(1): Show |
4 | HG02056.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-5385_413-5378d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | G | GCGCGCGC others(5): Show |
1 | a0003c0009t0010g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.413-5429_413-5428i others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCA | G | 4 | a0001c0001t0001g0188 a0001c0001t0005g0082 a0001c0034t0005g0115 others(1): Show |
4 | HG00408.hp1 HG00438.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5379_413-5378d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCACA | G | 4 | a0001c0001t0001g0141 a0001c0001t0001g0202 a0001c0002t0002g0087 others(1): Show |
4 | HG02280.hp1 HG03195.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-5381_413-5378d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCACACA | G | 3 | a0001c0001t0001g0146 a0001c0001t0021g0193 a0007c0023t0001g0028 |
3 | HG01243.hp1 NA18959.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.413-5383_413-5378d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCACACAC others(1): Show |
G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0210 others(1): Show |
4 | HG02083.hp1 NA18940.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-5385_413-5378d others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCACACAC others(3): Show |
G | 7 | a0001c0001t0001g0133 a0001c0001t0001g0204 a0001c0001t0001g0208 others(4): Show |
7 | HG01167.hp1 HG01952.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-5387_413-5378d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391102 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.413-5391_413-5378d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391102 | ||||||
chr5:127391104 | A | G | 57 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0001g0159 others(54): Show |
58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.413-5428A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391104 | |||||||
chr5:127391104 | A | T | 2 | a0001c0005t0007g0029 a0001c0008t0004g0233 |
2 | HG02970.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.413-5428A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391104 | |||||||
chr5:127391105 | C | A | 1 | a0002c0003t0009g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.413-5427C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391105 | |||||||
chr5:127391105 | C | G | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413-5427C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391105 | |||||||
chr5:127391106 | A | C | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413-5426A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391106 | |||||||
chr5:127391106 | A | G | 50 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-5426A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391106 | |||||||
chr5:127391108 | A | G | 50 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-5424A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391108 | |||||||
chr5:127391110 | A | G | 47 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(44): Show |
48 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.413-5422A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391110 | |||||||
chr5:127391112 | A | G | 43 | a0001c0001t0001g0144 a0001c0001t0001g0200 a0001c0001t0001g0210 others(40): Show |
44 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.413-5420A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391112 | |||||||
chr5:127391114 | A | G | 21 | a0001c0001t0001g0133 a0001c0005t0007g0179 a0001c0008t0004g0233 others(18): Show |
22 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.413-5418A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391114 | |||||||
chr5:127391116 | A | G | 4 | a0001c0018t0020g0243 a0002c0003t0006g0015 a0002c0003t0009g0108 others(1): Show |
4 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-5416A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391116 | |||||||
chr5:127391118 | A | G | 2 | a0001c0001t0035g0237 a0001c0018t0020g0243 |
2 | HG00639.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.413-5414A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391118 | |||||||
chr5:127391119 | C | G | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413-5413C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391119 | |||||||
chr5:127391120 | A | G | 3 | a0001c0001t0035g0237 a0001c0005t0007g0029 a0001c0018t0020g0243 |
3 | HG00639.hp1 HG03942.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.413-5412A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391120 | |||||||
chr5:127391122 | A | G | 2 | a0001c0005t0007g0029 a0001c0018t0020g0243 |
2 | HG00639.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.413-5410A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391122 | |||||||
chr5:127391124 | A | G | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413-5408A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391124 | |||||||
chr5:127391139 | CACACACA others(13): Show |
C | 3 | a0001c0005t0007g0021 a0001c0005t0007g0024 a0001c0005t0007g0025 |
3 | HG00323.hp1 HG02040.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.413-5392_413-5373d others(22): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391139 | |||||||
chr5:127391141 | CACACACA others(11): Show |
C | 6 | a0001c0005t0007g0023 a0001c0005t0007g0030 a0001c0005t0007g0034 others(3): Show |
6 | HG02083.hp2 HG02155.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-5390_413-5373d others(20): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391141 | |||||||
chr5:127391143 | CACACACA others(9): Show |
C | 7 | a0001c0005t0007g0031 a0001c0014t0001g0253 a0001c0014t0005g0038 others(4): Show |
7 | HG01258.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-5388_413-5373d others(18): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391143 | |||||||
chr5:127391145 | CACACACA others(7): Show |
C | 7 | a0002c0003t0006g0010 a0002c0003t0006g0013 a0002c0003t0006g0014 others(4): Show |
7 | HG01257.hp2 HG03041.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-5386_413-5373d others(16): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391145 | |||||||
chr5:127391147 | CACACACA others(5): Show |
C | 12 | a0001c0001t0001g0144 a0001c0007t0029g0124 a0002c0003t0006g0001 others(9): Show |
13 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(10): Show |
intron_variant | MODIFIER | c.413-5384_413-5373d others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391147 | |||||||
chr5:127391149 | CACACATA others(3): Show |
C | 6 | a0002c0003t0009g0108 a0002c0003t0009g0126 a0002c0003t0015g0018 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-5382_413-5373d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391149 | |||||||
chr5:127391153 | CATACAT | C | 49 | a0001c0002t0002g0046 a0001c0002t0002g0049 a0001c0002t0002g0051 others(46): Show |
49 | HG00140.hp1 HG00639.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.413-5378_413-5373d others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391153 | |||||||
chr5:127391155 | T | C | 37 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(34): Show |
37 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.413-5377T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391155 | |||||||
chr5:127391159 | T | C | 32 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(29): Show |
32 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-5373T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391159 | |||||||
chr5:127391316 | C | T | 73 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(70): Show |
73 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.413-5216C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391316 | |||||||
chr5:127391328 | C | T | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.413-5204C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391328 | |||||||
chr5:127391348 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0005g0055 a0001c0012t0021g0009 |
3 | HG02258.hp2 HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413-5184C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391348 | |||||||
chr5:127391517 | T | C | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-5015T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391517 | |||||||
chr5:127391573 | T | TA | 22 | a0001c0001t0001g0205 a0001c0001t0013g0096 a0001c0004t0004g0004 others(19): Show |
23 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.413-4944dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391573 | ||||||
chr5:127391573 | TA | T | 56 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0005t0007g0021 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-4944delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127391573 | ||||||
chr5:127391578 | A | T | 1 | a0001c0006t0001g0032 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.413-4954A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391578 | |||||||
chr5:127391623 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413-4909C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391623 | |||||||
chr5:127391670 | A | G | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-4862A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391670 | |||||||
chr5:127391726 | C | T | 170 | a0001c0001t0001g0144 a0001c0001t0001g0245 a0001c0001t0001g0246 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.413-4806C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391726 | |||||||
chr5:127391781 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-4751G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391781 | |||||||
chr5:127391871 | T | A | 3 | a0001c0001t0033g0198 a0001c0001t0034g0203 a0001c0034t0005g0115 |
3 | HG04184.hp2 NA18981.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.413-4661T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127391871 | |||||||
chr5:127392047 | C | A | 56 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.413-4485C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392047 | |||||||
chr5:127392102 | G | A | 9 | a0001c0007t0029g0124 a0001c0008t0004g0233 a0001c0008t0004g0235 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-4430G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392102 | |||||||
chr5:127392277 | G | C | 83 | a0001c0001t0001g0144 a0001c0002t0002g0086 a0001c0002t0002g0087 others(80): Show |
85 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.413-4255G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392277 | |||||||
chr5:127392648 | T | C | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.413-3884T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392648 | |||||||
chr5:127392695 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-3837G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392695 | |||||||
chr5:127392814 | A | C | 21 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(18): Show |
21 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-3718A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392814 | |||||||
chr5:127392960 | C | T | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-3572C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127392960 | |||||||
chr5:127393005 | G | T | 51 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(48): Show |
52 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.413-3527G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393005 | |||||||
chr5:127393060 | T | A | 1 | a0001c0002t0003g0258 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.413-3472T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393060 | |||||||
chr5:127393119 | T | G | 51 | a0001c0001t0001g0144 a0001c0005t0007g0021 a0001c0005t0007g0023 others(48): Show |
52 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.413-3413T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393119 | |||||||
chr5:127393258 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.413-3274T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393258 | |||||||
chr5:127393501 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 |
3 | HG02922.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.413-3031C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393501 | |||||||
chr5:127393592 | A | T | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.413-2940A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393592 | |||||||
chr5:127393702 | A | G | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.413-2830A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393702 | |||||||
chr5:127393758 | G | C | 3 | a0002c0003t0009g0108 a0002c0003t0009g0109 a0002c0003t0009g0110 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.413-2774G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393758 | |||||||
chr5:127393777 | A | G | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-2755A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393777 | |||||||
chr5:127393810 | G | GT | 49 | a0001c0001t0001g0210 a0001c0005t0007g0021 a0001c0005t0007g0023 others(46): Show |
50 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.413-2711dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127393810 | ||||||
chr5:127393822 | C | T | 1 | a0001c0005t0007g0031 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.413-2710C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393822 | |||||||
chr5:127393836 | C | A | 3 | a0001c0005t0007g0023 a0001c0005t0007g0024 a0001c0005t0007g0029 |
3 | HG02040.hp2 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.413-2696C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393836 | |||||||
chr5:127393964 | C | T | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-2568C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127393964 | |||||||
chr5:127394007 | G | A | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-2525G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127394007 | |||||||
chr5:127394066 | C | G | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-2466C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127394066 | |||||||
chr5:127394292 | A | G | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-2240A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127394292 | |||||||
chr5:127394455 | A | G | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-2077A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127394455 | |||||||
chr5:127394841 | T | G | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-1691T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127394841 | |||||||
chr5:127395013 | C | T | 55 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(52): Show |
56 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-1519C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395013 | |||||||
chr5:127395145 | C | T | 8 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(5): Show |
8 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-1387C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395145 | |||||||
chr5:127395295 | G | A | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.413-1237G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395295 | |||||||
chr5:127395444 | A | G | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-1088A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395444 | |||||||
chr5:127395536 | C | CT | 15 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0152 others(12): Show |
15 | HG00438.hp2 HG02071.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.413-970dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395536 | CT | C | 102 | a0001c0001t0001g0148 a0001c0001t0001g0209 a0001c0001t0001g0264 others(99): Show |
103 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.413-970delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395536 | CTT | C | 19 | a0001c0002t0002g0256 a0001c0002t0003g0149 a0001c0002t0003g0172 others(16): Show |
19 | HG00323.hp1 HG01099.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-971_413-970del others(2): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395536 | CTTT | C | 35 | a0001c0005t0007g0027 a0001c0005t0016g0083 a0001c0007t0029g0124 others(32): Show |
36 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.413-972_413-970del others(3): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395536 | CTTTT | C | 7 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(4): Show |
7 | HG01070.hp2 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-973_413-970del others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395536 | CTTTTTTT others(3): Show |
C | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.413-979_413-970del others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr5 | 127395536 | ||||||
chr5:127395567 | C | T | 68 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(65): Show |
68 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.413-965C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395567 | |||||||
chr5:127395693 | C | T | 28 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(25): Show |
29 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-839C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395693 | |||||||
chr5:127395718 | G | C | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.413-814G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395718 | |||||||
chr5:127395734 | T | C | 55 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(52): Show |
56 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-798T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395734 | |||||||
chr5:127395791 | G | A | 2 | a0001c0005t0007g0030 a0001c0005t0007g0031 |
2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.413-741G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127395791 | |||||||
chr5:127396022 | T | G | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-510T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396022 | |||||||
chr5:127396029 | G | A | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-503G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396029 | |||||||
chr5:127396094 | A | G | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-438A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396094 | |||||||
chr5:127396139 | T | A | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.413-393T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396139 | |||||||
chr5:127396157 | GC | G | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.413-374delC | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396157 | |||||||
chr5:127396184 | G | C | 164 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0013g0076 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.413-348G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396184 | |||||||
chr5:127396204 | C | G | 7 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-328C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396204 | |||||||
chr5:127396265 | A | G | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.413-267A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 5/24 | chr5 | 127396265 | |||||||
chr5:127396835 | C | T | 1 | a0001c0006t0001g0026 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.659+57C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127396835 | |||||||
chr5:127396931 | A | C | 3 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 |
3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.659+153A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127396931 | |||||||
chr5:127397043 | A | G | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.659+265A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397043 | |||||||
chr5:127397080 | T | G | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.659+302T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397080 | |||||||
chr5:127397085 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.659+307G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397085 | |||||||
chr5:127397120 | A | T | 69 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(66): Show |
71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.659+342A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397120 | |||||||
chr5:127397159 | C | G | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.659+381C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397159 | |||||||
chr5:127397202 | T | C | 2 | a0001c0002t0002g0098 a0001c0002t0027g0117 |
2 | HG02015.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.659+424T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397202 | |||||||
chr5:127397335 | T | C | 1 | a0002c0003t0015g0134 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.659+557T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397335 | |||||||
chr5:127397612 | G | A | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.659+834G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397612 | |||||||
chr5:127397631 | G | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 |
3 | HG02922.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.659+853G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397631 | |||||||
chr5:127397703 | A | G | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.659+925A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397703 | |||||||
chr5:127397707 | G | A | 69 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(66): Show |
71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.659+929G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397707 | |||||||
chr5:127397708 | T | C | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.659+930T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397708 | |||||||
chr5:127397711 | A | G | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.659+933A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397711 | |||||||
chr5:127397820 | A | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.660-856A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397820 | |||||||
chr5:127397823 | C | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.660-853C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397823 | |||||||
chr5:127397982 | G | A | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.660-694G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127397982 | |||||||
chr5:127398056 | G | A | 24 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(21): Show |
25 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.660-620G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398056 | |||||||
chr5:127398074 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.660-602G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398074 | |||||||
chr5:127398232 | T | A | 2 | a0001c0002t0002g0049 a0001c0002t0002g0051 |
2 | HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.660-444T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398232 | |||||||
chr5:127398277 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.660-399G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398277 | |||||||
chr5:127398453 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0005g0064 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.660-223C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398453 | |||||||
chr5:127398575 | A | G | 69 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(66): Show |
71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.660-101A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398575 | |||||||
chr5:127398603 | C | T | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.660-73C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398603 | |||||||
chr5:127398673 | C | T | 69 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(66): Show |
71 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.660-3C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 6/24 | chr5 | 127398673 | |||||||
chr5:127398904 | T | C | 1 | a0002c0003t0009g0105 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.780+108T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127398904 | |||||||
chr5:127399020 | C | T | 12 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0003c0009t0010g0088 others(9): Show |
12 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.780+224C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399020 | |||||||
chr5:127399036 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.780+240G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399036 | |||||||
chr5:127399142 | T | C | 26 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(23): Show |
27 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+346T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399142 | |||||||
chr5:127399252 | C | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.780+456C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399252 | |||||||
chr5:127399340 | G | A | 3 | a0001c0002t0002g0063 a0001c0002t0003g0020 a0001c0002t0003g0184 |
3 | HG01257.hp1 HG01496.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.780+544G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399340 | |||||||
chr5:127399588 | T | C | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.780+792T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399588 | |||||||
chr5:127399642 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0165 a0001c0001t0001g0182 others(5): Show |
9 | HG01099.hp1 HG01106.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.780+846G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399642 | |||||||
chr5:127399689 | C | T | 3 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0006c0032t0031g0099 |
3 | HG00639.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.780+893C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399689 | |||||||
chr5:127399703 | T | A | 5 | a0001c0002t0003g0138 a0001c0002t0003g0168 a0001c0002t0003g0169 others(2): Show |
5 | HG01952.hp2 HG01981.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+907T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399703 | |||||||
chr5:127399737 | C | T | 1 | a0001c0017t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.780+941C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399737 | |||||||
chr5:127399738 | G | A | 2 | a0001c0001t0005g0093 a0001c0001t0005g0094 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.780+942G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399738 | |||||||
chr5:127399976 | C | T | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.780+1180C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399976 | |||||||
chr5:127399988 | G | A | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.780+1192G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127399988 | |||||||
chr5:127400089 | T | C | 1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.780+1293T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400089 | |||||||
chr5:127400165 | A | G | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.780+1369A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400165 | |||||||
chr5:127400179 | T | C | 87 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0003g0138 others(84): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.780+1383T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400179 | |||||||
chr5:127400453 | A | G | 40 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(37): Show |
41 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.780+1657A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400453 | |||||||
chr5:127400456 | C | G | 1 | a0001c0005t0007g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.780+1660C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400456 | |||||||
chr5:127400698 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.781-1848G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400698 | |||||||
chr5:127400793 | G | A | 4 | a0002c0003t0009g0105 a0002c0003t0009g0123 a0002c0003t0009g0126 others(1): Show |
4 | NA18939.hp2 NA18970.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1753G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400793 | |||||||
chr5:127400918 | T | C | 1 | a0001c0005t0016g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.781-1628T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400918 | |||||||
chr5:127400997 | C | T | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.781-1549C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400997 | |||||||
chr5:127400998 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.781-1548G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127400998 | |||||||
chr5:127401140 | T | G | 82 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(79): Show |
84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.781-1406T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401140 | |||||||
chr5:127401340 | T | A | 3 | a0001c0002t0002g0052 a0001c0002t0002g0054 a0001c0002t0002g0095 |
3 | NA18966.hp1 NA18977.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.781-1206T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401340 | |||||||
chr5:127401494 | G | A | 82 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(79): Show |
84 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.781-1052G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401494 | |||||||
chr5:127401752 | T | C | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.781-794T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401752 | |||||||
chr5:127401809 | G | A | 1 | a0001c0020t0001g0196 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.781-737G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401809 | |||||||
chr5:127401858 | C | A | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.781-688C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127401858 | |||||||
chr5:127402178 | C | T | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.781-368C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127402178 | |||||||
chr5:127402349 | A | C | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.781-197A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 7/24 | chr5 | 127402349 | |||||||
chr5:127402710 | C | G | 1 | a0001c0001t0034g0203 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.917+28C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127402710 | |||||||
chr5:127402748 | G | A | 1 | a0001c0004t0004g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.917+66G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127402748 | |||||||
chr5:127403017 | A | C | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.917+335A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403017 | |||||||
chr5:127403121 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.917+439C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403121 | |||||||
chr5:127403192 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.917+510C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403192 | |||||||
chr5:127403256 | C | T | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.917+574C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403256 | |||||||
chr5:127403393 | G | A | 74 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.917+711G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403393 | |||||||
chr5:127403689 | G | A | 3 | a0001c0002t0003g0171 a0001c0021t0003g0173 a0001c0021t0003g0174 |
3 | HG01256.hp1 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.917+1007G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403689 | |||||||
chr5:127403722 | AT | A | 7 | a0001c0007t0004g0254 a0001c0008t0004g0235 a0001c0008t0004g0236 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.917+1043delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr5 | 127403722 | ||||||
chr5:127403735 | A | G | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+1053A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403735 | |||||||
chr5:127403796 | G | A | 20 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0018t0020g0243 others(17): Show |
20 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.917+1114G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127403796 | |||||||
chr5:127404077 | G | C | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+1395G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404077 | |||||||
chr5:127404312 | A | G | 1 | a0002c0003t0006g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.917+1630A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404312 | |||||||
chr5:127404346 | T | TTA | 59 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(56): Show |
61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.917+1670_917+1671d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr5 | 127404346 | ||||||
chr5:127404360 | C | T | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+1678C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404360 | |||||||
chr5:127404409 | G | A | 1 | a0001c0010t0001g0019 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.917+1727G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404409 | |||||||
chr5:127404537 | T | G | 3 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0006c0032t0031g0099 |
3 | HG00639.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.917+1855T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404537 | |||||||
chr5:127404542 | A | G | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.917+1860A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404542 | |||||||
chr5:127404568 | T | C | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.917+1886T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404568 | |||||||
chr5:127404624 | G | A | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+1942G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404624 | |||||||
chr5:127404801 | C | T | 5 | a0001c0002t0002g0053 a0001c0002t0002g0067 a0001c0002t0002g0069 others(2): Show |
5 | HG00621.hp1 NA18940.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.917+2119C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404801 | |||||||
chr5:127404808 | C | T | 3 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0006c0032t0031g0099 |
3 | HG00639.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.917+2126C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404808 | |||||||
chr5:127404809 | A | G | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+2127A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404809 | |||||||
chr5:127404860 | C | T | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.917+2178C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404860 | |||||||
chr5:127404936 | G | A | 20 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0018t0020g0243 others(17): Show |
20 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.917+2254G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404936 | |||||||
chr5:127404957 | C | G | 1 | a0001c0005t0007g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.917+2275C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127404957 | |||||||
chr5:127405108 | C | CAATATT | 61 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(58): Show |
63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.917+2427_917+2428i others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr5 | 127405108 | ||||||
chr5:127405136 | A | G | 10 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0152 others(7): Show |
10 | HG02809.hp1 HG02895.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.917+2454A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405136 | |||||||
chr5:127405143 | A | G | 81 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.917+2461A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405143 | |||||||
chr5:127405457 | C | T | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.917+2775C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405457 | |||||||
chr5:127405831 | G | A | 4 | a0001c0006t0001g0221 a0001c0006t0001g0222 a0001c0006t0001g0223 others(1): Show |
4 | NA18939.hp1 NA18946.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.917+3149G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405831 | |||||||
chr5:127405833 | C | T | 3 | a0001c0002t0003g0171 a0001c0021t0003g0173 a0001c0021t0003g0174 |
3 | HG01256.hp1 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.917+3151C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405833 | |||||||
chr5:127405894 | T | C | 16 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(13): Show |
16 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.917+3212T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405894 | |||||||
chr5:127406331 | G | A | 1 | a0001c0001t0005g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.917+3649G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406331 | |||||||
chr5:127406428 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.917+3746G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406428 | |||||||
chr5:127406515 | C | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.917+3833C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406515 | |||||||
chr5:127406567 | G | A | 1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.918-3822G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406567 | |||||||
chr5:127406716 | T | G | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.918-3673T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406716 | |||||||
chr5:127406791 | T | A | 17 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.918-3598T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406791 | |||||||
chr5:127406853 | A | G | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.918-3536A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406853 | |||||||
chr5:127406881 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-3508C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127406881 | |||||||
chr5:127407004 | C | A | 1 | a0001c0002t0002g0256 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.918-3385C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407004 | |||||||
chr5:127407211 | G | A | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.918-3178G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407211 | |||||||
chr5:127407239 | G | A | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.918-3150G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407239 | |||||||
chr5:127407265 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-3124T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407265 | |||||||
chr5:127407384 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-3005A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407384 | |||||||
chr5:127407553 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-2836G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407553 | |||||||
chr5:127407886 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-2503G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407886 | |||||||
chr5:127407891 | T | C | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.918-2498T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127407891 | |||||||
chr5:127408410 | G | A | 1 | a0001c0001t0013g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.918-1979G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408410 | |||||||
chr5:127408444 | C | T | 5 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 others(2): Show |
5 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.918-1945C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408444 | |||||||
chr5:127408593 | G | A | 2 | a0001c0002t0017g0102 a0001c0002t0017g0103 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.918-1796G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408593 | |||||||
chr5:127408609 | A | G | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.918-1780A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408609 | |||||||
chr5:127408721 | A | G | 1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.918-1668A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408721 | |||||||
chr5:127408793 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-1596A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127408793 | |||||||
chr5:127409017 | C | T | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.918-1372C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409017 | |||||||
chr5:127409038 | C | A | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.918-1351C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409038 | |||||||
chr5:127409155 | T | A | 1 | a0001c0001t0035g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.918-1234T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409155 | |||||||
chr5:127409186 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-1203A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409186 | |||||||
chr5:127409264 | G | T | 6 | a0001c0002t0002g0049 a0001c0002t0002g0051 a0001c0002t0017g0102 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.918-1125G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409264 | |||||||
chr5:127409273 | C | T | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.918-1116C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409273 | |||||||
chr5:127409296 | C | A | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.918-1093C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409296 | |||||||
chr5:127409516 | C | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-873C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409516 | |||||||
chr5:127409517 | G | A | 15 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.918-872G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409517 | |||||||
chr5:127409538 | T | A | 87 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(84): Show |
89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.918-851T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409538 | |||||||
chr5:127409624 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.918-765T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409624 | |||||||
chr5:127409725 | T | A | 1 | a0001c0002t0002g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918-664T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409725 | |||||||
chr5:127409786 | C | T | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.918-603C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127409786 | |||||||
chr5:127410087 | G | C | 3 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0006c0032t0031g0099 |
3 | HG00639.hp1 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.918-302G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127410087 | |||||||
chr5:127410241 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-148T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127410241 | |||||||
chr5:127410248 | G | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-141G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127410248 | |||||||
chr5:127410309 | C | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.918-80C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127410309 | |||||||
chr5:127410738 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1130+137C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127410738 | |||||||
chr5:127410742 | G | A | 78 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(75): Show |
80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1130+141G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127410742 | |||||||
chr5:127410807 | A | G | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1130+206A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127410807 | |||||||
chr5:127410932 | T | G | 1 | a0002c0003t0015g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1130+331T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127410932 | |||||||
chr5:127411013 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+412G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411013 | |||||||
chr5:127411031 | GA | G | 29 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0005t0007g0021 others(26): Show |
29 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1130+439delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127411031 | ||||||
chr5:127411040 | A | G | 1 | a0002c0003t0006g0017 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1130+439A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411040 | |||||||
chr5:127411199 | A | G | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1130+598A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411199 | |||||||
chr5:127411200 | C | T | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1130+599C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411200 | |||||||
chr5:127411345 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1130+744A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411345 | |||||||
chr5:127411389 | C | T | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.1130+788C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411389 | |||||||
chr5:127411398 | C | A | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1130+797C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411398 | |||||||
chr5:127411474 | T | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+873T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411474 | |||||||
chr5:127411550 | C | CTG | 12 | a0001c0018t0039g0006 a0002c0003t0006g0001 a0002c0003t0006g0010 others(9): Show |
13 | HG00408.hp2 HG00423.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1130+968_1130+969d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127411550 | ||||||
chr5:127411550 | CTGTG | C | 3 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 |
3 | HG01243.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1130+966_1130+969d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127411550 | ||||||
chr5:127411569 | T | C | 6 | a0001c0002t0002g0098 a0001c0002t0002g0104 a0001c0002t0027g0117 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130+968T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411569 | |||||||
chr5:127411569 | T | TGCGC | 8 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(5): Show |
8 | HG02040.hp2 HG02083.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1130+971_1130+974d others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127411569 | ||||||
chr5:127411571 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1130+970C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411571 | |||||||
chr5:127411571 | C | T | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1130+970C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411571 | |||||||
chr5:127411587 | G | A | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1130+986G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411587 | |||||||
chr5:127411697 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+1096T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411697 | |||||||
chr5:127411726 | T | A | 3 | a0001c0002t0003g0150 a0001c0002t0003g0197 a0001c0036t0002g0050 |
3 | HG01069.hp1 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1130+1125T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411726 | |||||||
chr5:127411736 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1130+1135A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411736 | |||||||
chr5:127411891 | T | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+1290T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411891 | |||||||
chr5:127411911 | G | A | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1130+1310G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127411911 | |||||||
chr5:127412122 | A | G | 6 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130+1521A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412122 | |||||||
chr5:127412138 | G | T | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1130+1537G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412138 | |||||||
chr5:127412284 | G | A | 4 | a0001c0012t0014g0261 a0001c0012t0014g0262 a0001c0012t0014g0263 others(1): Show |
4 | HG01243.hp2 HG02258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1130+1683G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412284 | |||||||
chr5:127412373 | T | C | 2 | a0001c0002t0002g0074 a0001c0002t0028g0073 |
2 | HG00140.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1130+1772T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412373 | |||||||
chr5:127412437 | T | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1130+1836T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412437 | |||||||
chr5:127412496 | G | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1130+1895G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412496 | |||||||
chr5:127412574 | T | C | 17 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1130+1973T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412574 | |||||||
chr5:127412631 | A | C | 1 | a0002c0003t0006g0017 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1130+2030A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412631 | |||||||
chr5:127412681 | A | AAAAC | 12 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(9): Show |
12 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1130+2100_1130+210 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127412681 | ||||||
chr5:127412701 | C | A | 1 | a0001c0001t0013g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1130+2100C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412701 | |||||||
chr5:127412726 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1130+2125A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412726 | |||||||
chr5:127412851 | T | A | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1130+2250T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412851 | |||||||
chr5:127412899 | C | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+2298C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412899 | |||||||
chr5:127412932 | G | A | 2 | a0001c0004t0004g0177 a0001c0004t0004g0240 |
2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1130+2331G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127412932 | |||||||
chr5:127413051 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1130+2450A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413051 | |||||||
chr5:127413095 | G | A | 4 | a0001c0006t0001g0221 a0001c0006t0001g0222 a0001c0006t0001g0223 others(1): Show |
4 | NA18939.hp1 NA18946.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130+2494G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413095 | |||||||
chr5:127413110 | A | G | 1 | a0001c0005t0007g0034 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1130+2509A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413110 | |||||||
chr5:127413457 | G | T | 1 | a0001c0001t0005g0094 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1130+2856G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413457 | |||||||
chr5:127413549 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1130+2948A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413549 | |||||||
chr5:127413726 | G | C | 8 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1130+3125G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413726 | |||||||
chr5:127413859 | G | A | 1 | a0001c0001t0021g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1130+3258G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127413859 | |||||||
chr5:127414257 | A | G | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1131-3381A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127414257 | |||||||
chr5:127414462 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-3176G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127414462 | |||||||
chr5:127414482 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-3156C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127414482 | |||||||
chr5:127414821 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-2817A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127414821 | |||||||
chr5:127414987 | A | G | 1 | a0001c0001t0005g0107 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1131-2651A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127414987 | |||||||
chr5:127415072 | GA | G | 22 | a0001c0001t0001g0144 a0001c0001t0001g0154 a0001c0002t0002g0086 others(19): Show |
22 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1131-2555delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127415072 | ||||||
chr5:127415072 | GAA | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-2556_1131-255 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127415072 | ||||||
chr5:127415343 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-2295T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127415343 | |||||||
chr5:127415896 | C | CA | 12 | a0001c0002t0002g0046 a0001c0002t0002g0256 a0001c0005t0007g0021 others(9): Show |
12 | HG00323.hp1 HG01361.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-1721dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127415896 | ||||||
chr5:127415896 | CA | C | 40 | a0001c0001t0001g0245 a0001c0001t0036g0257 a0001c0002t0002g0086 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1131-1721delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127415896 | ||||||
chr5:127415896 | CAA | C | 29 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.1131-1722_1131-172 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127415896 | ||||||
chr5:127415918 | G | A | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1131-1720G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127415918 | |||||||
chr5:127415980 | G | C | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1131-1658G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127415980 | |||||||
chr5:127416010 | A | AGTTTTT | 43 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0004t0004g0004 others(40): Show |
44 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1131-1608_1131-160 others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127416010 | ||||||
chr5:127416030 | TTTTTGG | T | 21 | a0001c0001t0021g0193 a0001c0002t0003g0171 a0001c0005t0007g0021 others(18): Show |
21 | HG00323.hp1 HG00639.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131-1602_1131-159 others(10): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr5 | 127416030 | ||||||
chr5:127416036 | G | T | 142 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(139): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1131-1602G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416036 | |||||||
chr5:127416088 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0005g0128 |
2 | NA18955.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1131-1550C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416088 | |||||||
chr5:127416188 | C | T | 1 | a0001c0007t0004g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1131-1450C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416188 | |||||||
chr5:127416246 | T | C | 16 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(13): Show |
16 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1131-1392T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416246 | |||||||
chr5:127416270 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-1368C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416270 | |||||||
chr5:127416337 | A | G | 1 | a0001c0005t0007g0024 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1131-1301A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416337 | |||||||
chr5:127416462 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-1176C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416462 | |||||||
chr5:127416598 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1131-1040G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416598 | |||||||
chr5:127416823 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1131-815C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127416823 | |||||||
chr5:127417096 | C | T | 4 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(1): Show |
4 | HG00438.hp1 HG00642.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131-542C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417096 | |||||||
chr5:127417272 | A | G | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1131-366A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417272 | |||||||
chr5:127417325 | CATAGAGT others(29): Show |
C | 1 | a0008c0030t0005g0084 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1131-312_1131-277d others(38): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417325 | |||||||
chr5:127417333 | T | G | 4 | a0002c0003t0009g0105 a0002c0003t0009g0123 a0002c0003t0009g0126 others(1): Show |
4 | NA18939.hp2 NA18970.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131-305T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417333 | |||||||
chr5:127417358 | C | A | 19 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1131-280C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417358 | |||||||
chr5:127417614 | A | T | 1 | a0001c0015t0003g0033 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1131-24A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 9/24 | chr5 | 127417614 | |||||||
chr5:127417923 | C | G | 3 | a0001c0002t0003g0258 a0001c0002t0003g0259 a0003c0009t0012g0260 |
3 | HG02630.hp2 HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1305+111C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127417923 | |||||||
chr5:127417978 | G | A | 1 | a0006c0032t0031g0099 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1305+166G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127417978 | |||||||
chr5:127418049 | CAT | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1305+238_1305+239d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127418049 | |||||||
chr5:127418473 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1306-647G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127418473 | |||||||
chr5:127418564 | C | T | 1 | a0001c0002t0003g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1306-556C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127418564 | |||||||
chr5:127418618 | C | A | 1 | a0001c0005t0016g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1306-502C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127418618 | |||||||
chr5:127418618 | C | G | 11 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(8): Show |
11 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306-502C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | chr5 | 127418618 | |||||||
chr5:127418840 | G | GT | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1306-278dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr5 | 127418840 | ||||||
chr5:127419245 | G | T | 1 | a0001c0035t0002g0129 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.1426+5G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419245 | |||||||
chr5:127419364 | G | A | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1426+124G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419364 | |||||||
chr5:127419647 | G | A | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1427-397G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419647 | |||||||
chr5:127419668 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1427-376T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419668 | |||||||
chr5:127419847 | T | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1427-197T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419847 | |||||||
chr5:127419898 | A | G | 1 | a0001c0002t0002g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1427-146A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419898 | |||||||
chr5:127419952 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1427-92G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 11/24 | chr5 | 127419952 | |||||||
chr5:127420321 | G | A | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1590+114G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420321 | |||||||
chr5:127420469 | T | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1590+262T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420469 | |||||||
chr5:127420503 | G | C | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1590+296G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420503 | |||||||
chr5:127420581 | T | C | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1590+374T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420581 | |||||||
chr5:127420814 | A | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1590+607A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420814 | |||||||
chr5:127420910 | T | C | 17 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0002c0011t0010g0090 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1590+703T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420910 | |||||||
chr5:127420967 | G | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1590+760G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127420967 | |||||||
chr5:127421088 | C | A | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1590+881C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421088 | |||||||
chr5:127421110 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1590+903T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421110 | |||||||
chr5:127421276 | CAA | C | 4 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0001c0002t0002g0068 others(1): Show |
4 | HG01070.hp1 HG03239.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1590+1072_1590+107 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr5 | 127421276 | ||||||
chr5:127421352 | C | G | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1590+1145C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421352 | |||||||
chr5:127421407 | C | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1590+1200C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421407 | |||||||
chr5:127421733 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1591-937G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421733 | |||||||
chr5:127421771 | A | G | 2 | a0003c0009t0012g0212 a0003c0009t0012g0213 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1591-899A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421771 | |||||||
chr5:127421844 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1591-826A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421844 | |||||||
chr5:127421853 | T | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1591-817T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127421853 | |||||||
chr5:127421988 | C | CA | 47 | a0001c0001t0001g0185 a0001c0001t0001g0201 a0001c0001t0001g0210 others(44): Show |
48 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1591-662dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr5 | 127421988 | ||||||
chr5:127421988 | CAA | C | 11 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(8): Show |
11 | HG00323.hp1 HG02040.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1591-663_1591-662d others(4): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr5 | 127421988 | ||||||
chr5:127422019 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1591-651C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127422019 | |||||||
chr5:127422449 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1591-221G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127422449 | |||||||
chr5:127422581 | A | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1591-89A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 12/24 | chr5 | 127422581 | |||||||
chr5:127422953 | G | A | 13 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(10): Show |
13 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1693+181G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127422953 | |||||||
chr5:127422968 | T | C | 1 | a0001c0002t0002g0091 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1693+196T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127422968 | |||||||
chr5:127423101 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+329C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423101 | |||||||
chr5:127423168 | C | T | 1 | a0007c0023t0001g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1693+396C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423168 | |||||||
chr5:127423171 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+399A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423171 | |||||||
chr5:127423243 | C | T | 9 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(6): Show |
10 | HG00408.hp2 HG00423.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693+471C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423243 | |||||||
chr5:127423312 | G | A | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1693+540G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423312 | |||||||
chr5:127423319 | A | C | 1 | a0001c0001t0032g0218 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1693+547A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423319 | |||||||
chr5:127423461 | A | G | 1 | a0001c0001t0005g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1693+689A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423461 | |||||||
chr5:127423688 | A | G | 1 | a0001c0002t0002g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1693+916A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423688 | |||||||
chr5:127423728 | G | A | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1693+956G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423728 | |||||||
chr5:127423744 | A | G | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1693+972A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423744 | |||||||
chr5:127423749 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1693+977G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423749 | |||||||
chr5:127423942 | A | G | 2 | a0001c0001t0001g0195 a0001c0006t0001g0022 |
2 | HG00621.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1693+1170A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127423942 | |||||||
chr5:127424090 | G | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1693+1318G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424090 | |||||||
chr5:127424092 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1693+1320C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424092 | |||||||
chr5:127424125 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+1353G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424125 | |||||||
chr5:127424255 | C | T | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1693+1483C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424255 | |||||||
chr5:127424682 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1693+1910A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424682 | |||||||
chr5:127424715 | A | C | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1693+1943A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424715 | |||||||
chr5:127424718 | C | A | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1693+1946C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424718 | |||||||
chr5:127424863 | T | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+2091T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424863 | |||||||
chr5:127424917 | C | T | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1693+2145C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424917 | |||||||
chr5:127424922 | A | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1693+2150A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127424922 | |||||||
chr5:127425125 | C | G | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1693+2353C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425125 | |||||||
chr5:127425130 | A | G | 57 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(54): Show |
58 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1693+2358A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425130 | |||||||
chr5:127425174 | G | A | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1693+2402G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425174 | |||||||
chr5:127425236 | A | G | 57 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(54): Show |
58 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1693+2464A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425236 | |||||||
chr5:127425289 | A | C | 2 | a0001c0002t0003g0229 a0001c0017t0002g0060 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1693+2517A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425289 | |||||||
chr5:127425362 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1693+2590T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425362 | |||||||
chr5:127425394 | G | T | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1693+2622G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425394 | |||||||
chr5:127425395 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+2623T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425395 | |||||||
chr5:127425681 | T | A | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1693+2909T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425681 | |||||||
chr5:127425682 | C | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1693+2910C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425682 | |||||||
chr5:127425694 | G | A | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1693+2922G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425694 | |||||||
chr5:127425801 | C | G | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1693+3029C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425801 | |||||||
chr5:127425844 | T | C | 57 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(54): Show |
58 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.1693+3072T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425844 | |||||||
chr5:127425890 | C | A | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1693+3118C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127425890 | |||||||
chr5:127426077 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+3305A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426077 | |||||||
chr5:127426191 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+3419C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426191 | |||||||
chr5:127426200 | A | C | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1693+3428A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426200 | |||||||
chr5:127426317 | C | T | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1693+3545C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426317 | |||||||
chr5:127426458 | C | T | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1693+3686C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426458 | |||||||
chr5:127426579 | ACT | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+3822_1693+382 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127426579 | ||||||
chr5:127426581 | T | A | 3 | a0001c0002t0002g0106 a0004c0022t0022g0248 a0004c0022t0022g0249 |
3 | HG02647.hp1 HG03209.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1693+3809T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426581 | |||||||
chr5:127426583 | T | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1693+3811T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426583 | |||||||
chr5:127426588 | C | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1693+3816C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426588 | |||||||
chr5:127426613 | G | A | 3 | a0001c0005t0007g0027 a0001c0005t0016g0083 a0001c0007t0004g0242 |
3 | HG03492.hp1 HG03834.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1693+3841G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426613 | |||||||
chr5:127426708 | G | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1693+3936G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426708 | |||||||
chr5:127426821 | C | T | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1693+4049C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127426821 | |||||||
chr5:127427005 | T | A | 3 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 |
3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1693+4233T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427005 | |||||||
chr5:127427093 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1693+4321G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427093 | |||||||
chr5:127427395 | A | G | 3 | a0001c0002t0003g0171 a0001c0021t0003g0173 a0001c0021t0003g0174 |
3 | HG01256.hp1 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1693+4623A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427395 | |||||||
chr5:127427555 | T | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+4783T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427555 | |||||||
chr5:127427644 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+4872A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427644 | |||||||
chr5:127427704 | A | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1693+4932A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427704 | |||||||
chr5:127427711 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1693+4939G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427711 | |||||||
chr5:127427850 | C | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+5078C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127427850 | |||||||
chr5:127428036 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1693+5264A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428036 | |||||||
chr5:127428105 | T | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1694-5258T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428105 | |||||||
chr5:127428141 | A | AT | 45 | a0001c0001t0001g0206 a0001c0001t0001g0245 a0001c0001t0001g0246 others(42): Show |
47 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1694-5199dupT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127428141 | ||||||
chr5:127428141 | A | ATT | 9 | a0001c0004t0004g0175 a0001c0007t0004g0254 a0001c0008t0004g0233 others(6): Show |
9 | HG02258.hp1 HG02615.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-5200_1694-519 others(6): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127428141 | ||||||
chr5:127428141 | AT | A | 69 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0216 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1694-5199delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127428141 | ||||||
chr5:127428141 | ATTTTTTT | A | 16 | a0001c0001t0013g0101 a0001c0005t0007g0021 a0001c0005t0007g0023 others(13): Show |
16 | HG00323.hp1 HG00438.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1694-5205_1694-519 others(11): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127428141 | ||||||
chr5:127428141 | ATTTTTTT others(3): Show |
A | 6 | a0001c0002t0002g0106 a0001c0002t0002g0116 a0001c0002t0002g0125 others(3): Show |
6 | HG02132.hp2 NA18946.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1694-5208_1694-519 others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127428141 | ||||||
chr5:127428398 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1694-4965A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428398 | |||||||
chr5:127428408 | A | G | 1 | a0001c0002t0003g0142 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1694-4955A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428408 | |||||||
chr5:127428503 | C | T | 5 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-4860C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428503 | |||||||
chr5:127428588 | A | G | 10 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0152 others(7): Show |
10 | HG02809.hp1 HG02895.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1694-4775A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428588 | |||||||
chr5:127428640 | C | G | 2 | a0001c0002t0002g0098 a0001c0002t0027g0117 |
2 | HG02015.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1694-4723C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428640 | |||||||
chr5:127428704 | T | G | 1 | a0003c0009t0024g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1694-4659T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428704 | |||||||
chr5:127428883 | C | T | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1694-4480C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428883 | |||||||
chr5:127428884 | G | A | 2 | a0001c0008t0004g0235 a0001c0008t0004g0236 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1694-4479G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428884 | |||||||
chr5:127428900 | A | G | 2 | a0001c0002t0003g0258 a0001c0002t0003g0259 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1694-4463A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127428900 | |||||||
chr5:127429006 | T | C | 43 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(40): Show |
44 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1694-4357T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127429006 | |||||||
chr5:127429024 | C | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1694-4339C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127429024 | |||||||
chr5:127429248 | A | G | 14 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(11): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1694-4115A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127429248 | |||||||
chr5:127429394 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1694-3969G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127429394 | |||||||
chr5:127429926 | G | A | 2 | a0001c0001t0021g0193 a0006c0032t0031g0099 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1694-3437G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127429926 | |||||||
chr5:127430046 | T | C | 1 | a0001c0002t0003g0241 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1694-3317T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430046 | |||||||
chr5:127430254 | T | C | 1 | a0001c0007t0029g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1694-3109T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430254 | |||||||
chr5:127430278 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1694-3085A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430278 | |||||||
chr5:127430449 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1694-2914G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430449 | |||||||
chr5:127430509 | A | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1694-2854A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430509 | |||||||
chr5:127430586 | T | C | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1694-2777T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430586 | |||||||
chr5:127430589 | A | T | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1694-2774A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430589 | |||||||
chr5:127430669 | C | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1694-2694C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430669 | |||||||
chr5:127430758 | C | G | 1 | a0001c0002t0002g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1694-2605C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430758 | |||||||
chr5:127430884 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-2479G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430884 | |||||||
chr5:127430890 | G | T | 3 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 |
3 | HG02965.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1694-2473G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430890 | |||||||
chr5:127430989 | T | G | 1 | a0002c0003t0006g0012 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1694-2374T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127430989 | |||||||
chr5:127431113 | A | G | 1 | a0001c0004t0004g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1694-2250A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431113 | |||||||
chr5:127431143 | T | A | 2 | a0003c0009t0012g0212 a0003c0009t0012g0213 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1694-2220T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431143 | |||||||
chr5:127431211 | A | G | 61 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 others(58): Show |
62 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.1694-2152A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431211 | |||||||
chr5:127431599 | T | G | 1 | a0001c0015t0003g0033 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1694-1764T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431599 | |||||||
chr5:127431648 | G | A | 2 | a0001c0001t0021g0193 a0006c0032t0031g0099 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1694-1715G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431648 | |||||||
chr5:127431746 | C | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1694-1617C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127431746 | |||||||
chr5:127432010 | G | T | 1 | a0001c0005t0007g0029 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1694-1353G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432010 | |||||||
chr5:127432053 | G | T | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1694-1310G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432053 | |||||||
chr5:127432095 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1694-1268G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432095 | |||||||
chr5:127432250 | G | A | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1694-1113G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432250 | |||||||
chr5:127432269 | A | G | 163 | a0001c0001t0021g0193 a0001c0002t0002g0040 a0001c0002t0002g0041 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1694-1094A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432269 | |||||||
chr5:127432509 | T | C | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1694-854T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432509 | |||||||
chr5:127432524 | C | T | 8 | a0001c0001t0021g0193 a0001c0012t0014g0261 a0001c0012t0014g0262 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1694-839C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432524 | |||||||
chr5:127432535 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1694-828G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432535 | |||||||
chr5:127432649 | T | C | 1 | a0002c0003t0015g0018 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1694-714T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432649 | |||||||
chr5:127432669 | C | T | 1 | a0001c0002t0002g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1694-694C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432669 | |||||||
chr5:127432701 | C | T | 2 | a0001c0001t0005g0093 a0001c0001t0005g0094 |
2 | HG02129.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1694-662C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432701 | |||||||
chr5:127432898 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1694-465G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127432898 | |||||||
chr5:127433002 | CA | C | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1694-358delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr5 | 127433002 | ||||||
chr5:127433012 | G | A | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1694-351G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127433012 | |||||||
chr5:127433020 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1694-343G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127433020 | |||||||
chr5:127433053 | T | C | 1 | a0003c0009t0012g0260 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1694-310T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 13/24 | chr5 | 127433053 | |||||||
chr5:127433634 | T | A | 1 | a0001c0001t0034g0203 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1840+125T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127433634 | |||||||
chr5:127433854 | G | A | 77 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(74): Show |
79 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1840+345G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127433854 | |||||||
chr5:127434019 | A | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1840+510A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434019 | |||||||
chr5:127434058 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1840+549A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434058 | |||||||
chr5:127434072 | A | C | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1840+563A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434072 | |||||||
chr5:127434073 | T | G | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1840+564T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434073 | |||||||
chr5:127434113 | C | T | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1841-574C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434113 | |||||||
chr5:127434125 | A | G | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1841-562A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434125 | |||||||
chr5:127434182 | G | A | 6 | a0001c0002t0002g0049 a0001c0002t0002g0051 a0001c0002t0017g0102 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1841-505G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434182 | |||||||
chr5:127434258 | C | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1841-429C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434258 | |||||||
chr5:127434404 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1841-283T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434404 | |||||||
chr5:127434520 | T | G | 2 | a0001c0005t0007g0027 a0001c0005t0016g0083 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1841-167T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434520 | |||||||
chr5:127434667 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1841-20G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 14/24 | chr5 | 127434667 | |||||||
chr5:127434864 | C | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.1975+43C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 15/24 | chr5 | 127434864 | |||||||
chr5:127434881 | C | T | 3 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 |
3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1975+60C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 15/24 | chr5 | 127434881 | |||||||
chr5:127434912 | CATGTTTT others(16): Show |
C | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.1975+96_1975+118de others(24): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr5 | 127434912 | ||||||
chr5:127435081 | C | A | 2 | a0001c0001t0001g0141 a0001c0001t0005g0055 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1975+260C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 15/24 | chr5 | 127435081 | |||||||
chr5:127435641 | CT | C | 11 | a0001c0001t0001g0264 a0001c0004t0004g0004 a0001c0004t0004g0005 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.2104+163delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr5 | 127435641 | ||||||
chr5:127435741 | C | T | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2104+252C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127435741 | |||||||
chr5:127436118 | G | A | 17 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0002c0011t0010g0090 others(14): Show |
17 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.2104+629G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436118 | |||||||
chr5:127436243 | T | A | 28 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(25): Show |
29 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.2104+754T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436243 | |||||||
chr5:127436307 | T | C | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2104+818T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436307 | |||||||
chr5:127436330 | A | G | 8 | a0001c0001t0021g0193 a0001c0012t0014g0261 a0001c0012t0014g0262 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+841A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436330 | |||||||
chr5:127436549 | G | A | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2104+1060G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436549 | |||||||
chr5:127436554 | G | T | 1 | a0001c0007t0004g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2104+1065G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436554 | |||||||
chr5:127436646 | T | C | 5 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0014t0001g0253 others(2): Show |
5 | HG02129.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104+1157T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436646 | |||||||
chr5:127436786 | G | A | 3 | a0001c0001t0005g0111 a0001c0001t0005g0112 a0001c0001t0005g0113 |
3 | HG02965.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2104+1297G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127436786 | |||||||
chr5:127437022 | A | G | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2105-1417A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437022 | |||||||
chr5:127437056 | C | G | 75 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2105-1383C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437056 | |||||||
chr5:127437138 | T | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2105-1301T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437138 | |||||||
chr5:127437187 | C | T | 2 | a0001c0001t0021g0193 a0006c0032t0031g0099 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2105-1252C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437187 | |||||||
chr5:127437372 | G | A | 82 | a0001c0001t0021g0193 a0001c0002t0002g0040 a0001c0002t0002g0041 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.2105-1067G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437372 | |||||||
chr5:127437402 | C | A | 1 | a0001c0005t0007g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2105-1037C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437402 | |||||||
chr5:127437402 | C | G | 31 | a0001c0002t0002g0116 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2105-1037C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437402 | |||||||
chr5:127437406 | C | T | 1 | a0001c0034t0005g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2105-1033C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437406 | |||||||
chr5:127437414 | C | CAAAA | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2105-1024_2105-102 others(8): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr5 | 127437414 | ||||||
chr5:127437416 | T | C | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2105-1023T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437416 | |||||||
chr5:127437460 | C | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2105-979C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437460 | |||||||
chr5:127437468 | G | A | 1 | a0001c0014t0023g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2105-971G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437468 | |||||||
chr5:127437488 | A | T | 163 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2105-951A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437488 | |||||||
chr5:127437613 | T | C | 27 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(24): Show |
28 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.2105-826T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437613 | |||||||
chr5:127437623 | C | T | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2105-816C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437623 | |||||||
chr5:127437678 | A | G | 31 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.2105-761A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437678 | |||||||
chr5:127437760 | G | A | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2105-679G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437760 | |||||||
chr5:127437821 | G | C | 1 | a0001c0005t0007g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2105-618G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437821 | |||||||
chr5:127437898 | T | C | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2105-541T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127437898 | |||||||
chr5:127438117 | G | T | 18 | a0001c0018t0020g0243 a0001c0018t0039g0006 a0002c0011t0010g0090 others(15): Show |
18 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.2105-322G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127438117 | |||||||
chr5:127438148 | G | A | 1 | a0003c0009t0012g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2105-291G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127438148 | |||||||
chr5:127438167 | A | C | 61 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(58): Show |
63 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2105-272A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127438167 | |||||||
chr5:127438336 | C | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2105-103C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 16/24 | chr5 | 127438336 | |||||||
chr5:127438802 | A | G | 1 | a0001c0002t0003g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2233+235A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127438802 | |||||||
chr5:127438947 | C | T | 6 | a0001c0001t0013g0076 a0001c0001t0013g0096 a0001c0001t0013g0101 others(3): Show |
6 | HG00438.hp1 HG00642.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2233+380C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127438947 | |||||||
chr5:127438967 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2233+400T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127438967 | |||||||
chr5:127438971 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2233+404G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127438971 | |||||||
chr5:127439051 | C | T | 3 | a0001c0014t0001g0253 a0001c0014t0005g0038 a0001c0014t0023g0039 |
3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2233+484C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439051 | |||||||
chr5:127439119 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2233+552G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439119 | |||||||
chr5:127439220 | A | G | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2233+653A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439220 | |||||||
chr5:127439248 | G | A | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2233+681G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439248 | |||||||
chr5:127439264 | G | A | 2 | a0001c0002t0017g0102 a0001c0002t0017g0103 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2233+697G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439264 | |||||||
chr5:127439397 | G | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.2233+830G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439397 | |||||||
chr5:127439421 | TTAA | T | 83 | a0001c0001t0021g0193 a0001c0002t0002g0040 a0001c0002t0002g0041 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.2233+857_2233+859d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr5 | 127439421 | ||||||
chr5:127439485 | A | T | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2233+918A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439485 | |||||||
chr5:127439513 | A | T | 1 | a0003c0009t0024g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2233+946A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439513 | |||||||
chr5:127439600 | A | G | 2 | a0002c0003t0006g0013 a0002c0003t0006g0014 |
2 | NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2233+1033A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439600 | |||||||
chr5:127439698 | C | T | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.2234-1041C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439698 | |||||||
chr5:127439770 | A | G | 75 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2234-969A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439770 | |||||||
chr5:127439978 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2234-761G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127439978 | |||||||
chr5:127440047 | C | T | 76 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.2234-692C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127440047 | |||||||
chr5:127440136 | G | A | 1 | a0001c0018t0039g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2234-603G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127440136 | |||||||
chr5:127440230 | T | C | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2234-509T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127440230 | |||||||
chr5:127440615 | T | C | 42 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(39): Show |
43 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.2234-124T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 17/24 | chr5 | 127440615 | |||||||
chr5:127440931 | T | G | 19 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(16): Show |
20 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.2362+64T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127440931 | |||||||
chr5:127441026 | C | T | 1 | a0001c0001t0013g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2362+159C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441026 | |||||||
chr5:127441341 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2362+474C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441341 | |||||||
chr5:127441379 | T | C | 2 | a0001c0001t0021g0193 a0006c0032t0031g0099 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2362+512T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441379 | |||||||
chr5:127441412 | A | T | 1 | a0001c0002t0003g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2362+545A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441412 | |||||||
chr5:127441459 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2362+592G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441459 | |||||||
chr5:127441466 | T | TTAC | 2 | a0001c0018t0020g0243 a0001c0018t0039g0006 |
2 | HG00639.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2362+601_2362+603d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr5 | 127441466 | ||||||
chr5:127441670 | G | A | 164 | a0001c0001t0004g0164 a0001c0001t0021g0193 a0001c0002t0002g0040 others(161): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2362+803G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127441670 | |||||||
chr5:127442174 | A | G | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2363-824A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127442174 | |||||||
chr5:127442398 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2363-600C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127442398 | |||||||
chr5:127442430 | A | G | 1 | a0001c0027t0004g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2363-568A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127442430 | |||||||
chr5:127442553 | G | A | 42 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(39): Show |
43 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.2363-445G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127442553 | |||||||
chr5:127442577 | A | G | 1 | a0001c0005t0007g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2363-421A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 18/24 | chr5 | 127442577 | |||||||
chr5:127443149 | G | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2491+23G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443149 | |||||||
chr5:127443158 | C | T | 30 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(27): Show |
30 | HG00323.hp1 HG00642.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2491+32C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443158 | |||||||
chr5:127443221 | A | C | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2491+95A>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443221 | |||||||
chr5:127443336 | T | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2491+210T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443336 | |||||||
chr5:127443429 | A | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2491+303A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443429 | |||||||
chr5:127443477 | C | CA | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.2491+352dupA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr5 | 127443477 | ||||||
chr5:127443510 | C | T | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2491+384C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443510 | |||||||
chr5:127443589 | A | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2491+463A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443589 | |||||||
chr5:127443595 | A | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2491+469A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443595 | |||||||
chr5:127443604 | T | A | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2491+478T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127443604 | |||||||
chr5:127444290 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2491+1164A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444290 | |||||||
chr5:127444309 | C | T | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2492-1148C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444309 | |||||||
chr5:127444370 | C | T | 20 | a0001c0015t0002g0118 a0002c0003t0006g0001 a0002c0003t0006g0010 others(17): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.2492-1087C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444370 | |||||||
chr5:127444484 | G | A | 3 | a0001c0004t0004g0175 a0001c0004t0004g0176 a0001c0027t0004g0135 |
3 | HG02109.hp1 HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2492-973G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444484 | |||||||
chr5:127444520 | G | A | 81 | a0001c0001t0021g0193 a0001c0002t0002g0040 a0001c0002t0002g0041 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2492-937G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444520 | |||||||
chr5:127444605 | G | T | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2492-852G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444605 | |||||||
chr5:127444652 | C | T | 72 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2492-805C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444652 | |||||||
chr5:127444681 | C | G | 15 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(12): Show |
15 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2492-776C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444681 | |||||||
chr5:127444703 | G | T | 20 | a0001c0015t0002g0118 a0002c0003t0006g0001 a0002c0003t0006g0010 others(17): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.2492-754G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127444703 | |||||||
chr5:127445019 | C | G | 2 | a0001c0002t0002g0106 a0001c0002t0002g0127 |
2 | NA18946.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2492-438C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127445019 | |||||||
chr5:127445043 | A | G | 20 | a0001c0015t0002g0118 a0002c0003t0006g0001 a0002c0003t0006g0010 others(17): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.2492-414A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127445043 | |||||||
chr5:127445064 | G | A | 12 | a0001c0002t0002g0058 a0001c0002t0002g0063 a0001c0002t0002g0106 others(9): Show |
12 | HG00140.hp1 HG01169.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2492-393G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127445064 | |||||||
chr5:127445079 | G | A | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2492-378G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127445079 | |||||||
chr5:127445204 | C | G | 1 | a0001c0005t0007g0179 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2492-253C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 19/24 | chr5 | 127445204 | |||||||
chr5:127445754 | T | C | 59 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(56): Show |
60 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2728+61T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127445754 | |||||||
chr5:127445876 | G | A | 20 | a0001c0015t0002g0118 a0002c0003t0006g0001 a0002c0003t0006g0010 others(17): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.2728+183G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127445876 | |||||||
chr5:127445886 | G | T | 1 | a0001c0002t0002g0058 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2728+193G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127445886 | |||||||
chr5:127445946 | T | A | 1 | a0001c0026t0016g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2728+253T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127445946 | |||||||
chr5:127446190 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2728+497G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446190 | |||||||
chr5:127446207 | T | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2728+514T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446207 | |||||||
chr5:127446330 | G | T | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2728+637G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446330 | |||||||
chr5:127446619 | G | C | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2728+926G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446619 | |||||||
chr5:127446633 | T | A | 74 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2729-924T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446633 | |||||||
chr5:127446650 | G | T | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2729-907G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446650 | |||||||
chr5:127446690 | G | C | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2729-867G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446690 | |||||||
chr5:127446810 | G | A | 10 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(7): Show |
10 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.2729-747G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446810 | |||||||
chr5:127446867 | G | A | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2729-690G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446867 | |||||||
chr5:127446958 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2729-599G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127446958 | |||||||
chr5:127447070 | G | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2729-487G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447070 | |||||||
chr5:127447127 | G | T | 2 | a0001c0001t0001g0209 a0001c0006t0001g0221 |
2 | NA18939.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2729-430G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447127 | |||||||
chr5:127447153 | C | T | 1 | a0001c0010t0001g0192 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2729-404C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447153 | |||||||
chr5:127447180 | T | C | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2729-377T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447180 | |||||||
chr5:127447278 | C | A | 3 | a0001c0002t0003g0171 a0001c0021t0003g0173 a0001c0021t0003g0174 |
3 | HG01256.hp1 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2729-279C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447278 | |||||||
chr5:127447278 | C | T | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2729-279C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447278 | |||||||
chr5:127447321 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2729-236G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447321 | |||||||
chr5:127447456 | C | T | 1 | a0001c0001t0013g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2729-101C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447456 | |||||||
chr5:127447475 | C | G | 2 | a0001c0012t0014g0262 a0001c0012t0014g0263 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2729-82C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447475 | |||||||
chr5:127447495 | C | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2729-62C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 20/24 | chr5 | 127447495 | |||||||
chr5:127447865 | C | A | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2856+181C>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 21/24 | chr5 | 127447865 | |||||||
chr5:127448369 | T | C | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2856+685T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 21/24 | chr5 | 127448369 | |||||||
chr5:127448451 | T | C | 1 | a0001c0012t0021g0009 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2857-648T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 21/24 | chr5 | 127448451 | |||||||
chr5:127448770 | A | G | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2857-329A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 21/24 | chr5 | 127448770 | |||||||
chr5:127448790 | CT | C | 18 | a0001c0002t0002g0068 a0001c0002t0002g0079 a0001c0002t0002g0095 others(15): Show |
18 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2857-292delT | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr5 | 127448790 | ||||||
chr5:127449453 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2980+231T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449453 | |||||||
chr5:127449471 | G | C | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.2980+249G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449471 | |||||||
chr5:127449613 | C | T | 3 | a0002c0003t0009g0108 a0002c0003t0009g0109 a0002c0003t0009g0110 |
3 | HG01257.hp2 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2980+391C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449613 | |||||||
chr5:127449618 | G | A | 60 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(57): Show |
61 | HG00323.hp1 HG00642.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2980+396G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449618 | |||||||
chr5:127449646 | T | A | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2980+424T>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449646 | |||||||
chr5:127449862 | A | G | 1 | a0001c0004t0004g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2980+640A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449862 | |||||||
chr5:127449924 | T | C | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2980+702T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127449924 | |||||||
chr5:127449932 | TTTAAA | T | 14 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(11): Show |
14 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.2980+715_2980+719d others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr5 | 127449932 | ||||||
chr5:127450193 | C | T | 1 | a0003c0009t0010g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2980+971C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450193 | |||||||
chr5:127450199 | ATAT | A | 30 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(27): Show |
31 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.2980+979_2980+981d others(5): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr5 | 127450199 | ||||||
chr5:127450354 | ATATATAT others(3): Show |
A | 3 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 |
3 | HG01069.hp2 HG01071.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2980+1140_2980+114 others(14): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr5 | 127450354 | ||||||
chr5:127450463 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2980+1241C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450463 | |||||||
chr5:127450529 | C | G | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2980+1307C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450529 | |||||||
chr5:127450558 | C | T | 1 | a0001c0002t0003g0229 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2980+1336C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450558 | |||||||
chr5:127450594 | G | A | 2 | a0005c0019t0018g0007 a0005c0019t0018g0008 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2980+1372G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450594 | |||||||
chr5:127450878 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0166 |
2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2980+1656C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127450878 | |||||||
chr5:127451202 | T | C | 6 | a0001c0001t0021g0193 a0001c0012t0014g0261 a0001c0012t0014g0262 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2980+1980T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451202 | |||||||
chr5:127451221 | C | T | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2980+1999C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451221 | |||||||
chr5:127451594 | G | A | 29 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(26): Show |
30 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2980+2372G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451594 | |||||||
chr5:127451669 | G | C | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2980+2447G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451669 | |||||||
chr5:127451696 | G | A | 8 | a0001c0001t0021g0193 a0001c0012t0014g0261 a0001c0012t0014g0262 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2980+2474G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451696 | |||||||
chr5:127451829 | G | T | 1 | a0007c0023t0001g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2980+2607G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451829 | |||||||
chr5:127451978 | C | T | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2981-2588C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127451978 | |||||||
chr5:127452217 | C | T | 1 | a0001c0035t0002g0129 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2981-2349C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452217 | |||||||
chr5:127452417 | G | A | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2981-2149G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452417 | |||||||
chr5:127452485 | G | A | 15 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2981-2081G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452485 | |||||||
chr5:127452526 | G | A | 1 | a0002c0028t0030g0114 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2981-2040G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452526 | |||||||
chr5:127452577 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2981-1989G>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452577 | |||||||
chr5:127452644 | C | T | 1 | a0003c0031t0040g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2981-1922C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452644 | |||||||
chr5:127452713 | A | G | 1 | a0003c0013t0037g0136 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2981-1853A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452713 | |||||||
chr5:127452773 | A | G | 3 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0002g0256 |
3 | HG01361.hp2 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2981-1793A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452773 | |||||||
chr5:127452907 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2981-1659T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452907 | |||||||
chr5:127452965 | G | T | 2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2981-1601G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127452965 | |||||||
chr5:127453081 | G | A | 11 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0155 others(8): Show |
11 | HG02071.hp1 HG02897.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.2981-1485G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453081 | |||||||
chr5:127453126 | G | A | 2 | a0001c0002t0002g0098 a0001c0002t0027g0117 |
2 | HG02015.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2981-1440G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453126 | |||||||
chr5:127453301 | C | T | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2981-1265C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453301 | |||||||
chr5:127453362 | T | C | 1 | a0001c0004t0004g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2981-1204T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453362 | |||||||
chr5:127453645 | T | G | 1 | a0001c0002t0003g0214 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2981-921T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453645 | |||||||
chr5:127453658 | T | C | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2981-908T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453658 | |||||||
chr5:127453669 | A | G | 19 | a0001c0001t0004g0164 a0001c0004t0004g0004 a0001c0004t0004g0005 others(16): Show |
20 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2981-897A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453669 | |||||||
chr5:127453747 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2981-819C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453747 | |||||||
chr5:127453839 | A | G | 1 | a0001c0002t0002g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2981-727A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127453839 | |||||||
chr5:127454139 | T | C | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2981-427T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127454139 | |||||||
chr5:127454294 | A | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0200 a0001c0001t0001g0201 others(9): Show |
12 | HG01167.hp1 HG01952.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.2981-272A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127454294 | |||||||
chr5:127454401 | G | A | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2981-165G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127454401 | |||||||
chr5:127454410 | G | T | 1 | a0001c0005t0007g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2981-156G>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127454410 | |||||||
chr5:127454478 | A | G | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2981-88A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 22/24 | chr5 | 127454478 | |||||||
chr5:127454863 | A | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3025+253A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127454863 | |||||||
chr5:127454935 | A | T | 3 | a0001c0001t0021g0193 a0001c0012t0021g0009 a0006c0032t0031g0099 |
3 | HG01243.hp1 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3025+325A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127454935 | |||||||
chr5:127455024 | C | T | 1 | a0009c0033t0002g0043 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3026-377C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127455024 | |||||||
chr5:127455122 | TAAAAC | T | 12 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(9): Show |
12 | HG00323.hp1 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.3026-273_3026-269d others(7): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr5 | 127455122 | ||||||
chr5:127455129 | A | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3026-272A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127455129 | |||||||
chr5:127455149 | T | G | 37 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(34): Show |
38 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.3026-252T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127455149 | |||||||
chr5:127455276 | A | T | 20 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(17): Show |
21 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(18): Show |
intron_variant | MODIFIER | c.3026-125A>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | chr5 | 127455276 | |||||||
chr5:127455365 | ACAGCATT others(8): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3026-34_3026-20del others(15): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr5 | 127455365 | ||||||
chr5:127455647 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 |
3 | HG02922.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3232+40T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127455647 | |||||||
chr5:127455723 | G | GTATTTTA others(3): Show |
7 | a0001c0007t0004g0242 a0001c0007t0004g0254 a0001c0007t0029g0124 others(4): Show |
7 | HG02258.hp1 HG02486.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3232+135_3232+144d others(12): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr5 | 127455723 | ||||||
chr5:127455723 | G | GTATTTTA others(8): Show |
27 | a0001c0001t0004g0164 a0001c0004t0004g0175 a0001c0004t0004g0176 others(24): Show |
28 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3232+130_3232+144d others(17): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr5 | 127455723 | ||||||
chr5:127455723 | G | GTATTTTA others(13): Show |
9 | a0001c0004t0004g0004 a0001c0004t0004g0005 a0001c0004t0004g0137 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3232+125_3232+144d others(22): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr5 | 127455723 | ||||||
chr5:127455723 | G | GTATTTTA others(23): Show |
2 | a0002c0016t0019g0231 a0002c0016t0019g0232 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3232+144_3232+145i others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr5 | 127455723 | ||||||
chr5:127455827 | C | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3232+220C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127455827 | |||||||
chr5:127455832 | C | T | 1 | a0001c0018t0020g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3232+225C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127455832 | |||||||
chr5:127455987 | T | G | 2 | a0004c0022t0022g0248 a0004c0022t0022g0249 |
2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3232+380T>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127455987 | |||||||
chr5:127456156 | C | T | 3 | a0001c0002t0002g0063 a0001c0002t0003g0020 a0001c0002t0003g0184 |
3 | HG01257.hp1 HG01496.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.3232+549C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456156 | |||||||
chr5:127456157 | G | A | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3232+550G>A | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456157 | |||||||
chr5:127456391 | C | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3233-737C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456391 | |||||||
chr5:127456415 | A | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3233-713A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456415 | |||||||
chr5:127456425 | C | T | 1 | a0001c0006t0001g0223 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3233-703C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456425 | |||||||
chr5:127456429 | C | G | 1 | a0001c0002t0002g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3233-699C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456429 | |||||||
chr5:127456552 | A | G | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3233-576A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456552 | |||||||
chr5:127456579 | T | C | 2 | a0001c0002t0002g0098 a0001c0002t0027g0117 |
2 | HG02015.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3233-549T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456579 | |||||||
chr5:127456657 | A | G | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.3233-471A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456657 | |||||||
chr5:127456739 | C | G | 50 | a0001c0005t0007g0021 a0001c0005t0007g0023 a0001c0005t0007g0024 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.3233-389C>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456739 | |||||||
chr5:127456774 | C | T | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3233-354C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456774 | |||||||
chr5:127456829 | C | T | 17 | a0002c0011t0010g0090 a0002c0011t0010g0120 a0002c0011t0010g0121 others(14): Show |
17 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3233-299C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456829 | |||||||
chr5:127456952 | A | G | 3 | a0001c0002t0003g0150 a0001c0002t0003g0197 a0001c0036t0002g0050 |
3 | HG01069.hp1 HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3233-176A>G | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127456952 | |||||||
chr5:127457070 | T | C | 21 | a0002c0003t0006g0001 a0002c0003t0006g0010 a0002c0003t0006g0012 others(18): Show |
22 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.3233-58T>C | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 24/24 | chr5 | 127457070 |