Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1140 | 220 | 67 | 42 | 77 | 8 | 24 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002 | 0/0 | 1140 | 27 | 3 | 6 | 14 | 2 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003 | 0/0 | 1140 | 12 | 3 | 4 | 5 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0004 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0005 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0006 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0007 | 0/0 | 547 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0008 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0009 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0010 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3423 | 79 | 20 | 14 | 34 | 2 | 8 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0002 | 0/0 | 3423 | 65 | 9 | 18 | 25 | 4 | 9 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0003 | 0/0 | 3423 | 20 | 0 | 3 | 14 | 2 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0004 | 0/0 | 3423 | 12 | 9 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0005 | 0/0 | 3423 | 11 | 0 | 0 | 6 | 1 | 4 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0006 | 0/0 | 3423 | 9 | 0 | 0 | 9 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0007 | 0/0 | 3423 | 9 | 9 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0008 | 0/0 | 3423 | 7 | 7 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0009 | 0/0 | 3423 | 7 | 2 | 4 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0010 | 1/0 | 3423 | 5 | 1 | 2 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0011 | 0/0 | 3423 | 4 | 0 | 3 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0012 | 0/0 | 3423 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0013 | 0/0 | 3423 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0014 | 0/0 | 3423 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0015 | 0/0 | 3423 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0016 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0017 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0018 | 0/0 | 3423 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0019 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0020 | 0/0 | 3423 | 2 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0021 | 0/0 | 3423 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0022 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0023 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0024 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0025 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0026 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0027 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0028 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0029 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0030 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0031 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0032 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0033 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0034 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0035 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| c0036 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4184 | 76 | 18 | 13 | 33 | 3 | 7 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0002 | 0/0 | 4182 | 45 | 5 | 7 | 25 | 1 | 7 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0003 | 0/0 | 4182 | 23 | 7 | 9 | 4 | 3 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0004 | 0/0 | 4184 | 21 | 18 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0005 | 0/0 | 4184 | 15 | 5 | 0 | 8 | 0 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0006 | 0/0 | 4182 | 10 | 0 | 0 | 10 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0007 | 0/0 | 4184 | 10 | 0 | 0 | 6 | 1 | 3 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0008 | 0/0 | 4184 | 7 | 7 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0009 | 0/0 | 4182 | 7 | 0 | 2 | 3 | 2 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0010 | 0/0 | 4180 | 5 | 0 | 4 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0011 | 0/0 | 4180 | 4 | 0 | 0 | 4 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0012 | 0/0 | 4180 | 4 | 1 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0013 | 0/0 | 4182 | 3 | 0 | 1 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0014 | 0/0 | 4182 | 3 | 2 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0015 | 0/0 | 4182 | 3 | 0 | 1 | 1 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0016 | 0/0 | 4184 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0017 | 0/0 | 4182 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0018 | 0/0 | 4184 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0019 | 0/0 | 4182 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0020 | 0/0 | 4182 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0021 | 0/0 | 4182 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0022 | 0/0 | 4182 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0023 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0024 | 0/0 | 4180 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0025 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0026 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0027 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0028 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0029 | 0/0 | 4184 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0030 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0031 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0032 | 0/0 | 4184 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0033 | 0/0 | 4182 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0034 | 0/0 | 4184 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0035 | 0/0 | 4184 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0036 | 0/0 | 4184 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0037 | 0/0 | 4180 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0038 | 0/0 | 4182 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0039 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| t0040 | 0/0 | 4182 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/1 | 79 | 20 | 14 | 34 | 2 | 8 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 65 | 9 | 18 | 25 | 4 | 9 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 12 | 9 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 11 | 0 | 0 | 6 | 1 | 4 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0010 | a0001 | c0010 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0014 | a0001 | c0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0017 | a0001 | c0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0018 | a0001 | c0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0020 | a0001 | c0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0021 | a0001 | c0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0026 | a0001 | c0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0027 | a0001 | c0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0029 | a0001 | c0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0034 | a0001 | c0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0035 | a0001 | c0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0036 | a0001 | c0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 20 | 0 | 3 | 14 | 2 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0011 | a0002 | c0011 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0016 | a0002 | c0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0028 | a0002 | c0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0009 | a0003 | c0009 | 0/0 | 7 | 2 | 4 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0013 | a0003 | c0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0024 | a0003 | c0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0031 | a0003 | c0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0004c0019 | a0004 | c0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0005c0022 | a0005 | c0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0006c0025 | a0006 | c0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0007c0030 | a0007 | c0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0008c0033 | a0008 | c0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0009c0032 | a0009 | c0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0010c0023 | a0010 | c0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 58 | 15 | 10 | 24 | 2 | 6 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 11 | 4 | 0 | 6 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0001t0036 | a0001 | c0001 | t0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 39 | 3 | 7 | 21 | 1 | 7 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 19 | 6 | 7 | 3 | 3 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0017 | a0001 | c0002 | t0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0025 | a0001 | c0002 | t0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0026 | a0001 | c0002 | t0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0027 | a0001 | c0002 | t0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0028 | a0001 | c0002 | t0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0002t0038 | a0001 | c0002 | t0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0004t0004 | a0001 | c0004 | t0004 | 0/0 | 12 | 9 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0005t0007 | a0001 | c0005 | t0007 | 0/0 | 10 | 0 | 0 | 6 | 1 | 3 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0005t0016 | a0001 | c0005 | t0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0006t0005 | a0001 | c0006 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0007t0004 | a0001 | c0007 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0007t0008 | a0001 | c0007 | t0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0007t0020 | a0001 | c0007 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0007t0029 | a0001 | c0007 | t0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0008t0004 | a0001 | c0008 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0008t0008 | a0001 | c0008 | t0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0012t0014 | a0001 | c0012 | t0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0012t0021 | a0001 | c0012 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0014t0001 | a0001 | c0014 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0014t0005 | a0001 | c0014 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0014t0023 | a0001 | c0014 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0015t0002 | a0001 | c0015 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0015t0003 | a0001 | c0015 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0017t0002 | a0001 | c0017 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0017t0003 | a0001 | c0017 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0018t0020 | a0001 | c0018 | t0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0018t0039 | a0001 | c0018 | t0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0021t0003 | a0001 | c0021 | t0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0026t0016 | a0001 | c0026 | t0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0027t0004 | a0001 | c0027 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0029t0001 | a0001 | c0029 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0034t0005 | a0001 | c0034 | t0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0035t0002 | a0001 | c0035 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0001c0036t0002 | a0001 | c0036 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0003t0006 | a0002 | c0003 | t0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0003t0009 | a0002 | c0003 | t0009 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0003t0015 | a0002 | c0003 | t0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0011t0010 | a0002 | c0011 | t0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0016t0019 | a0002 | c0016 | t0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0002c0028t0030 | a0002 | c0028 | t0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0009t0010 | a0003 | c0009 | t0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0009t0011 | a0003 | c0009 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0009t0012 | a0003 | c0009 | t0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0009t0024 | a0003 | c0009 | t0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0013t0011 | a0003 | c0013 | t0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0013t0037 | a0003 | c0013 | t0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0024t0011 | a0003 | c0024 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0003c0031t0040 | a0003 | c0031 | t0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0004c0019t0018 | a0004 | c0019 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0005c0022t0022 | a0005 | c0022 | t0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0006c0025t0002 | a0006 | c0025 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0007c0030t0005 | a0007 | c0030 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0008c0033t0002 | a0008 | c0033 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0009c0032t0031 | a0009 | c0032 | t0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| a0010c0023t0001 | a0010 | c0023 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0004g0165 | a0001 | c0001 | t0004 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0049 | a0001 | c0001 | t0005 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0060 | a0001 | c0001 | t0005 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0065 | a0001 | c0001 | t0005 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0083 | a0001 | c0001 | t0005 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0094 | a0001 | c0001 | t0005 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0095 | a0001 | c0001 | t0005 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0108 | a0001 | c0001 | t0005 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0112 | a0001 | c0001 | t0005 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0113 | a0001 | c0001 | t0005 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0114 | a0001 | c0001 | t0005 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0005g0129 | a0001 | c0001 | t0005 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0013g0077 | a0001 | c0001 | t0013 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0013g0099 | a0001 | c0001 | t0013 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0013g0104 | a0001 | c0001 | t0013 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0021g0194 | a0001 | c0001 | t0021 | g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0032g0219 | a0001 | c0001 | t0032 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0033g0197 | a0001 | c0001 | t0033 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0034g0204 | a0001 | c0001 | t0034 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0035g0238 | a0001 | c0001 | t0035 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0001t0036g0258 | a0001 | c0001 | t0036 | g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0041 | a0001 | c0002 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0042 | a0001 | c0002 | t0002 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0043 | a0001 | c0002 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0045 | a0001 | c0002 | t0002 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0047 | a0001 | c0002 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0050 | a0001 | c0002 | t0002 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0052 | a0001 | c0002 | t0002 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0053 | a0001 | c0002 | t0002 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0055 | a0001 | c0002 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0056 | a0001 | c0002 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0057 | a0001 | c0002 | t0002 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0058 | a0001 | c0002 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0062 | a0001 | c0002 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0063 | a0001 | c0002 | t0002 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0064 | a0001 | c0002 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0066 | a0001 | c0002 | t0002 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0067 | a0001 | c0002 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0068 | a0001 | c0002 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0069 | a0001 | c0002 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0070 | a0001 | c0002 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0071 | a0001 | c0002 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0072 | a0001 | c0002 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0075 | a0001 | c0002 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0079 | a0001 | c0002 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0080 | a0001 | c0002 | t0002 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0087 | a0001 | c0002 | t0002 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0088 | a0001 | c0002 | t0002 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0092 | a0001 | c0002 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0097 | a0001 | c0002 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0098 | a0001 | c0002 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0103 | a0001 | c0002 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0105 | a0001 | c0002 | t0002 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0106 | a0001 | c0002 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0117 | a0001 | c0002 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0126 | a0001 | c0002 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0128 | a0001 | c0002 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0131 | a0001 | c0002 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0132 | a0001 | c0002 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0002g0257 | a0001 | c0002 | t0002 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0019 | a0001 | c0002 | t0003 | g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0139 | a0001 | c0002 | t0003 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0143 | a0001 | c0002 | t0003 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0150 | a0001 | c0002 | t0003 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0151 | a0001 | c0002 | t0003 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0152 | a0001 | c0002 | t0003 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0169 | a0001 | c0002 | t0003 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0170 | a0001 | c0002 | t0003 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0172 | a0001 | c0002 | t0003 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0173 | a0001 | c0002 | t0003 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0185 | a0001 | c0002 | t0003 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0191 | a0001 | c0002 | t0003 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0196 | a0001 | c0002 | t0003 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0215 | a0001 | c0002 | t0003 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0228 | a0001 | c0002 | t0003 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0230 | a0001 | c0002 | t0003 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0242 | a0001 | c0002 | t0003 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0259 | a0001 | c0002 | t0003 | g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0003g0260 | a0001 | c0002 | t0003 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0017g0100 | a0001 | c0002 | t0017 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0017g0101 | a0001 | c0002 | t0017 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0025g0046 | a0001 | c0002 | t0025 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0026g0054 | a0001 | c0002 | t0026 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0027g0118 | a0001 | c0002 | t0027 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0028g0074 | a0001 | c0002 | t0028 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0002t0038g0227 | a0001 | c0002 | t0038 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0003 | a0001 | c0004 | t0004 | g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0004 | a0001 | c0004 | t0004 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0138 | a0001 | c0004 | t0004 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0176 | a0001 | c0004 | t0004 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0177 | a0001 | c0004 | t0004 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0178 | a0001 | c0004 | t0004 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0241 | a0001 | c0004 | t0004 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0251 | a0001 | c0004 | t0004 | g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0252 | a0001 | c0004 | t0004 | g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0253 | a0001 | c0004 | t0004 | g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0256 | a0001 | c0004 | t0004 | g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0004t0004g0266 | a0001 | c0004 | t0004 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0020 | a0001 | c0005 | t0007 | g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0022 | a0001 | c0005 | t0007 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0023 | a0001 | c0005 | t0007 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0024 | a0001 | c0005 | t0007 | g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0025 | a0001 | c0005 | t0007 | g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0027 | a0001 | c0005 | t0007 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0029 | a0001 | c0005 | t0007 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0030 | a0001 | c0005 | t0007 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0033 | a0001 | c0005 | t0007 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0007g0180 | a0001 | c0005 | t0007 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0005t0016g0084 | a0001 | c0005 | t0016 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0021 | a0001 | c0006 | t0001 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0028 | a0001 | c0006 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0031 | a0001 | c0006 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0034 | a0001 | c0006 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0222 | a0001 | c0006 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0223 | a0001 | c0006 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0224 | a0001 | c0006 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0001g0225 | a0001 | c0006 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0006t0005g0120 | a0001 | c0006 | t0005 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0004g0243 | a0001 | c0007 | t0004 | g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0004g0255 | a0001 | c0007 | t0004 | g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0008g0035 | a0001 | c0007 | t0008 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0008g0036 | a0001 | c0007 | t0008 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0008g0037 | a0001 | c0007 | t0008 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0008g0038 | a0001 | c0007 | t0008 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0008g0081 | a0001 | c0007 | t0008 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0020g0168 | a0001 | c0007 | t0020 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0007t0029g0125 | a0001 | c0007 | t0029 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0004g0234 | a0001 | c0008 | t0004 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0004g0236 | a0001 | c0008 | t0004 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0004g0237 | a0001 | c0008 | t0004 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0004g0239 | a0001 | c0008 | t0004 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0004g0248 | a0001 | c0008 | t0004 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0008g0073 | a0001 | c0008 | t0008 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0008t0008g0090 | a0001 | c0008 | t0008 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0010t0001g0010 | a0001 | c0010 | t0001 | g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0010t0001g0018 | a0001 | c0010 | t0001 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0010t0001g0187 | a0001 | c0010 | t0001 | g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0010t0001g0193 | a0001 | c0010 | t0001 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0010t0001g0229 | a0001 | c0010 | t0001 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0012t0014g0262 | a0001 | c0012 | t0014 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0012t0014g0263 | a0001 | c0012 | t0014 | g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0012t0014g0264 | a0001 | c0012 | t0014 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0012t0021g0008 | a0001 | c0012 | t0021 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0014t0001g0254 | a0001 | c0014 | t0001 | g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0014t0005g0039 | a0001 | c0014 | t0005 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0014t0023g0040 | a0001 | c0014 | t0023 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0015t0002g0119 | a0001 | c0015 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0015t0003g0032 | a0001 | c0015 | t0003 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0017t0002g0061 | a0001 | c0017 | t0002 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0017t0003g0141 | a0001 | c0017 | t0003 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0018t0020g0244 | a0001 | c0018 | t0020 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0018t0039g0005 | a0001 | c0018 | t0039 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0020t0001g0179 | a0001 | c0020 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0020t0001g0203 | a0001 | c0020 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0021t0003g0174 | a0001 | c0021 | t0003 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0021t0003g0175 | a0001 | c0021 | t0003 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0026t0016g0082 | a0001 | c0026 | t0016 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0027t0004g0136 | a0001 | c0027 | t0004 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0029t0001g0245 | a0001 | c0029 | t0001 | g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0034t0005g0116 | a0001 | c0034 | t0005 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0035t0002g0130 | a0001 | c0035 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0001c0036t0002g0051 | a0001 | c0036 | t0002 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0001 | a0002 | c0003 | t0006 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0009 | a0002 | c0003 | t0006 | g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0011 | a0002 | c0003 | t0006 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0012 | a0002 | c0003 | t0006 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0013 | a0002 | c0003 | t0006 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0014 | a0002 | c0003 | t0006 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0015 | a0002 | c0003 | t0006 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0016 | a0002 | c0003 | t0006 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0006g0157 | a0002 | c0003 | t0006 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0048 | a0002 | c0003 | t0009 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0107 | a0002 | c0003 | t0009 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0109 | a0002 | c0003 | t0009 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0110 | a0002 | c0003 | t0009 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0111 | a0002 | c0003 | t0009 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0124 | a0002 | c0003 | t0009 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0009g0127 | a0002 | c0003 | t0009 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0015g0017 | a0002 | c0003 | t0015 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0015g0135 | a0002 | c0003 | t0015 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0003t0015g0220 | a0002 | c0003 | t0015 | g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0011t0010g0091 | a0002 | c0011 | t0010 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0011t0010g0121 | a0002 | c0011 | t0010 | g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0011t0010g0122 | a0002 | c0011 | t0010 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0011t0010g0123 | a0002 | c0011 | t0010 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0016t0019g0232 | a0002 | c0016 | t0019 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0016t0019g0233 | a0002 | c0016 | t0019 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0002c0028t0030g0115 | a0002 | c0028 | t0030 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0010g0089 | a0003 | c0009 | t0010 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0011g0093 | a0003 | c0009 | t0011 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0012g0181 | a0003 | c0009 | t0012 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0012g0213 | a0003 | c0009 | t0012 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0012g0214 | a0003 | c0009 | t0012 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0012g0261 | a0003 | c0009 | t0012 | g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0009t0024g0086 | a0003 | c0009 | t0024 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0013t0011g0078 | a0003 | c0013 | t0011 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0013t0011g0096 | a0003 | c0013 | t0011 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0013t0037g0137 | a0003 | c0013 | t0037 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0024t0011g0076 | a0003 | c0024 | t0011 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0003c0031t0040g0171 | a0003 | c0031 | t0040 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0004c0019t0018g0006 | a0004 | c0019 | t0018 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0004c0019t0018g0007 | a0004 | c0019 | t0018 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0005c0022t0022g0249 | a0005 | c0022 | t0022 | g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0005c0022t0022g0250 | a0005 | c0022 | t0022 | g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0006c0025t0002g0059 | a0006 | c0025 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0007c0030t0005g0085 | a0007 | c0030 | t0005 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0008c0033t0002g0044 | a0008 | c0033 | t0002 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0009c0032t0031g0102 | a0009 | c0032 | t0031 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| a0010c0023t0001g0026 | a0010 | c0023 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF10_chr5_127285796_127466222 | MEGF10 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0009 | g0048 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00099 | hp2 | a0001 | c0010 | t0001 | g0010 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0228 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | GBR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00323 | hp1 | a0001 | c0005 | t0007 | g0024 | EUR | FIN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00408 | hp2 | a0002 | c0003 | t0006 | g0015 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00423 | hp1 | a0002 | c0003 | t0006 | g0014 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00438 | hp1 | a0001 | c0001 | t0013 | g0104 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0028 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00639 | hp1 | a0001 | c0018 | t0020 | g0244 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00639 | hp2 | a0001 | c0002 | t0038 | g0227 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0077 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG00642 | hp2 | a0003 | c0009 | t0012 | g0181 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0196 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01069 | hp2 | a0001 | c0004 | t0004 | g0003 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01070 | hp2 | a0002 | c0011 | t0010 | g0121 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01071 | hp1 | a0002 | c0011 | t0010 | g0122 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01071 | hp2 | a0001 | c0004 | t0004 | g0004 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01074 | hp2 | a0001 | c0002 | t0025 | g0046 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01106 | hp1 | a0002 | c0003 | t0015 | g0017 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01167 | hp1 | a0001 | c0020 | t0001 | g0179 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01167 | hp2 | a0003 | c0009 | t0012 | g0213 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01169 | hp2 | a0003 | c0009 | t0012 | g0214 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01192 | hp2 | a0001 | c0002 | t0026 | g0054 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0194 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01243 | hp2 | a0001 | c0012 | t0014 | g0263 | AMR | PUR | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01255 | hp1 | a0001 | c0010 | t0001 | g0193 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01255 | hp2 | a0003 | c0009 | t0010 | g0089 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01256 | hp1 | a0001 | c0021 | t0003 | g0174 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01256 | hp2 | a0001 | c0010 | t0001 | g0229 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01257 | hp2 | a0002 | c0003 | t0009 | g0111 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01258 | hp1 | a0001 | c0021 | t0003 | g0175 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01258 | hp2 | a0002 | c0003 | t0009 | g0110 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01361 | hp1 | a0001 | c0001 | t0036 | g0258 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0257 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01496 | hp1 | a0001 | c0004 | t0004 | g0138 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0185 | AMR | CLM | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0150 | EUR | IBS | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0151 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0169 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0170 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01981 | hp2 | a0002 | c0011 | t0010 | g0091 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02004 | hp2 | a0001 | c0001 | t0032 | g0219 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02040 | hp2 | a0001 | c0005 | t0007 | g0023 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02071 | hp2 | a0002 | c0003 | t0006 | g0011 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02083 | hp2 | a0001 | c0005 | t0007 | g0180 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02129 | hp1 | a0003 | c0024 | t0011 | g0076 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02135 | hp1 | a0003 | c0013 | t0011 | g0096 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02135 | hp2 | a0001 | c0015 | t0003 | g0032 | EAS | KHV | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02145 | hp1 | a0001 | c0010 | t0001 | g0018 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02145 | hp2 | a0002 | c0028 | t0030 | g0115 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02148 | hp1 | a0001 | c0002 | t0028 | g0074 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02155 | hp2 | a0001 | c0005 | t0007 | g0029 | EAS | CDX | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02257 | hp1 | a0001 | c0036 | t0002 | g0051 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02257 | hp2 | a0001 | c0014 | t0001 | g0254 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02258 | hp1 | a0001 | c0007 | t0004 | g0255 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02258 | hp2 | a0001 | c0012 | t0021 | g0008 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02280 | hp2 | a0001 | c0004 | t0004 | g0241 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | PEL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02451 | hp1 | a0001 | c0017 | t0003 | g0141 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02451 | hp2 | a0009 | c0032 | t0031 | g0102 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02615 | hp2 | a0001 | c0027 | t0004 | g0136 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02622 | hp1 | a0001 | c0004 | t0004 | g0266 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02622 | hp2 | a0001 | c0018 | t0039 | g0005 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02630 | hp1 | a0001 | c0008 | t0008 | g0073 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02647 | hp1 | a0005 | c0022 | t0022 | g0250 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0191 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02683 | hp2 | a0001 | c0005 | t0007 | g0020 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02717 | hp1 | a0001 | c0004 | t0004 | g0256 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02717 | hp2 | a0003 | c0009 | t0012 | g0261 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0103 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02738 | hp2 | a0002 | c0003 | t0015 | g0135 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02809 | hp2 | a0001 | c0014 | t0023 | g0040 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02818 | hp1 | a0001 | c0007 | t0008 | g0035 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0230 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02886 | hp1 | a0001 | c0004 | t0004 | g0178 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02886 | hp2 | a0001 | c0014 | t0005 | g0039 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02895 | hp1 | a0001 | c0007 | t0008 | g0037 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02897 | hp1 | a0001 | c0007 | t0008 | g0036 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02922 | hp2 | a0001 | c0012 | t0014 | g0264 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0176 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02970 | hp2 | a0001 | c0008 | t0004 | g0234 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02976 | hp2 | a0001 | c0007 | t0029 | g0125 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03041 | hp2 | a0002 | c0016 | t0019 | g0233 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03098 | hp1 | a0001 | c0008 | t0004 | g0237 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0114 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03139 | hp1 | a0001 | c0004 | t0004 | g0251 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03139 | hp2 | a0001 | c0008 | t0008 | g0090 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0260 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03209 | hp1 | a0002 | c0016 | t0019 | g0232 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03209 | hp2 | a0005 | c0022 | t0022 | g0249 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03225 | hp2 | a0001 | c0007 | t0008 | g0081 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03239 | hp1 | a0002 | c0011 | t0010 | g0123 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03453 | hp2 | a0001 | c0007 | t0008 | g0038 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03492 | hp1 | a0001 | c0005 | t0007 | g0025 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0065 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03516 | hp1 | a0001 | c0004 | t0004 | g0253 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03516 | hp2 | a0003 | c0031 | t0040 | g0171 | AFR | ESN | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03540 | hp1 | a0001 | c0007 | t0020 | g0168 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03579 | hp1 | a0004 | c0019 | t0018 | g0006 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03579 | hp2 | a0001 | c0004 | t0004 | g0252 | AFR | MSL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03654 | hp1 | a0001 | c0020 | t0001 | g0203 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03654 | hp2 | a0001 | c0002 | t0017 | g0101 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03669 | hp1 | a0001 | c0002 | t0017 | g0100 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03669 | hp2 | a0001 | c0005 | t0007 | g0033 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0072 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03834 | hp2 | a0001 | c0005 | t0016 | g0084 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0043 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG03942 | hp2 | a0001 | c0001 | t0035 | g0238 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG04184 | hp2 | a0001 | c0034 | t0005 | g0116 | SAS | BEB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG04204 | hp1 | a0001 | c0026 | t0016 | g0082 | SAS | STU | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18522 | hp2 | a0001 | c0012 | t0014 | g0262 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18906 | hp1 | a0001 | c0029 | t0001 | g0245 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18906 | hp2 | a0001 | c0008 | t0004 | g0236 | AFR | YRI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18939 | hp1 | a0001 | c0006 | t0001 | g0222 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18939 | hp2 | a0002 | c0003 | t0015 | g0220 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18946 | hp1 | a0001 | c0006 | t0001 | g0225 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18949 | hp1 | a0001 | c0005 | t0007 | g0027 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18966 | hp2 | a0002 | c0003 | t0006 | g0001 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18970 | hp1 | a0002 | c0003 | t0009 | g0124 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18971 | hp1 | a0002 | c0003 | t0006 | g0012 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18974 | hp1 | a0002 | c0003 | t0009 | g0107 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18975 | hp1 | a0002 | c0003 | t0009 | g0127 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18975 | hp2 | a0001 | c0005 | t0007 | g0030 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18977 | hp2 | a0010 | c0023 | t0001 | g0026 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18981 | hp2 | a0001 | c0001 | t0034 | g0204 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18984 | hp1 | a0001 | c0006 | t0001 | g0224 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18986 | hp2 | a0002 | c0003 | t0006 | g0009 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18987 | hp1 | a0002 | c0003 | t0006 | g0157 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18987 | hp2 | a0001 | c0015 | t0002 | g0119 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18989 | hp2 | a0001 | c0006 | t0001 | g0031 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0099 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18994 | hp2 | a0001 | c0006 | t0005 | g0120 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18995 | hp1 | a0003 | c0009 | t0011 | g0093 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0223 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19002 | hp1 | a0001 | c0001 | t0033 | g0197 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19004 | hp1 | a0001 | c0006 | t0001 | g0021 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19004 | hp2 | a0003 | c0013 | t0011 | g0078 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19012 | hp2 | a0001 | c0005 | t0007 | g0022 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19043 | hp1 | a0001 | c0007 | t0004 | g0243 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19056 | hp1 | a0001 | c0006 | t0001 | g0034 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19056 | hp2 | a0002 | c0003 | t0006 | g0013 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19060 | hp1 | a0002 | c0003 | t0006 | g0016 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19062 | hp2 | a0003 | c0013 | t0037 | g0137 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19064 | hp1 | a0001 | c0002 | t0027 | g0118 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19068 | hp2 | a0002 | c0003 | t0006 | g0001 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19076 | hp1 | a0007 | c0030 | t0005 | g0085 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19076 | hp2 | a0008 | c0033 | t0002 | g0044 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19083 | hp1 | a0001 | c0035 | t0002 | g0130 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19086 | hp1 | a0006 | c0025 | t0002 | g0059 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | ASW | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20129 | hp2 | a0001 | c0008 | t0004 | g0248 | AFR | ASW | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20752 | hp1 | a0002 | c0003 | t0009 | g0109 | EUR | TSI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0152 | EUR | TSI | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02109 | hp1 | a0001 | c0004 | t0004 | g0177 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02486 | hp1 | a0001 | c0008 | t0004 | g0239 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG02486 | hp2 | a0001 | c0017 | t0002 | g0061 | AFR | ACB | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | USA | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA21309 | hp1 | a0003 | c0009 | t0024 | g0086 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 |
| NA21309 | hp2 | a0004 | c0019 | t0018 | g0007 | AFR | LWK | MEGF10_chr5_127285796_127466222 | MEGF10 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | MEGF10_chr5_127285796_127466222 | MEGF10 |
| homoSapiens_grch38 | hp1 | a0001 | c0010 | t0001 | g0187 | REF | REF | MEGF10_chr5_127285796_127466222 | MEGF10 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:127396735
|
G | A | 2 | a0002a0006 | 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 | a0010 | 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 | a0004 | 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 | a0007 | 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 | a0007 | 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 | a0007 | 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 | a0009 | 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 | a0005 | 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 | a0002a0003 | 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 | a0008 | 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 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:127339177
|
G | A | 4 | a0001c0005a0001c0006a0001c0015others(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 | a0001c0014a0005c0022 | 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 | a0001c0005a0001c0008a0001c0017others(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 | a0001c0012a0005c0022 | 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 | a0001c0001a0001c0002a0001c0004others(32): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): 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 | a0005c0022 | 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 | a0001c0004a0001c0005a0001c0007others(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 | a0003c0013a0003c0024 | 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 | a0001c0004a0001c0027 | 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 | a0002c0011a0003c0009a0003c0013others(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 | a0002c0011a0002c0016a0003c0009others(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 | a0001c0005a0001c0026 | 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 | a0001c0002a0001c0015a0001c0017others(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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:127290953
|
G | A | 33 | a0001c0001t0005a0001c0001t0013a0001c0002t0002others(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 | a0009c0032t0031 | 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 | a0005c0022t0022 | 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 | a0001c0001t0004a0001c0001t0021a0001c0002t0002others(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 | a0002c0011t0010a0003c0009t0010 | 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 | a0001c0005t0007a0001c0005t0016a0001c0026t0016 | 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 | a0002c0003t0006a0002c0003t0009a0002c0003t0015others(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 | a0002c0011t0010a0003c0009t0010a0003c0009t0011others(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 | a0001c0001t0021a0001c0012t0021a0009c0032t0031 | 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 | a0001c0002t0025a0001c0002t0038 | 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 | a0001c0001t0004a0001c0004t0004a0001c0007t0004others(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 | a0001c0001t0013a0001c0001t0033a0004c0019t0018 | 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 | a0001c0005t0007a0001c0005t0016a0001c0026t0016others(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 | a0002c0011t0010a0003c0009t0010a0003c0009t0011others(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 | a0001c0005t0007a0001c0005t0016a0001c0026t0016others(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 | a0004c0019t0018 | 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 | a0001c0005t0007a0001c0005t0016a0001c0026t0016others(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 | a0001c0001t0004a0001c0004t0004a0001c0005t0007others(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 | a0001c0001t0004a0001c0001t0013a0001c0001t0033others(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 | a0001c0005t0007a0001c0005t0016a0001c0026t0016 | 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 | a0001c0001t0021a0001c0012t0021a0009c0032t0031 | 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 | a0001c0001t0013a0001c0001t0021a0001c0001t0033others(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 | a0001c0001t0004a0001c0001t0013a0001c0001t0021others(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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:127291178
|
G | A | 6 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0012t0021g0008others(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 | a0001c0010t0001g0010a0001c0010t0001g0018a0002c0003t0006g0001others(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 | a0001c0002t0003g0019 | 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 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0018t0039g0005 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0036g0258 | 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 | a0001c0004t0004g0266 | 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 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(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 | a0001c0002t0002g0257 | 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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | 145 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0005g0049others(142): 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 | a0001c0007t0004g0243 | 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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | a0001c0002t0003g0242 | 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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | 124 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0005g0049others(121): 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 | 6 | a0001c0007t0008g0035a0001c0007t0008g0036a0001c0007t0008g0037others(3): 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 | a0001c0002t0002g0041 | 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 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0004t0004g0251others(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 | a0004c0019t0018g0006 | 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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | a0001c0012t0021g0008 | 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 | a0001c0004t0004g0266 | 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 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0007t0004g0243others(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 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0246others(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 | a0001c0001t0001g0240a0001c0001t0035g0238a0001c0004t0004g0241others(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 | a0001c0001t0001g0265a0001c0002t0002g0117a0001c0004t0004g0256others(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 | a0001c0001t0005g0129a0001c0002t0002g0131a0001c0002t0002g0132others(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 | 46 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0140others(43): Show | 46 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(43): 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 | a0001c0004t0004g0266 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 |
40 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(37): 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 | a0001c0001t0005g0083a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0026t0016g0082 | 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 | a0001c0002t0002g0126a0001c0006t0005g0120a0001c0007t0029g0125others(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 | a0001c0002t0027g0118 | 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 | a0001c0002t0002g0128 | 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 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0004t0004g0251others(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 | a0001c0010t0001g0229 | 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 | 99 | a0001c0001t0005g0049a0001c0001t0005g0060a0001c0001t0005g0065others(96): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0012t0014g0262others(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 | a0001c0007t0008g0081 | 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 | a0001c0004t0004g0266 | 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 | 26 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(23): 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 | 29 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(26): 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 | 117 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(114): 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 | a0001c0001t0001g0226 | 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 | a0001c0004t0004g0266 | 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 | a0001c0034t0005g0116 | 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 | a0001c0020t0001g0179 | 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 | a0001c0002t0025g0046 | 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 | a0002c0003t0006g0012a0002c0003t0006g0013 | 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 | a0001c0029t0001g0245 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0002t0002g0080 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0079 | 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | 161 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(158): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0003c0013t0011g0078 | 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 | a0001c0001t0001g0221 | 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 | 161 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(158): 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 | a0001c0005t0007g0033 | 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 | a0003c0013t0011g0078 | 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 | 51 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(48): 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 | a0001c0029t0001g0245 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0001t0001g0240a0001c0008t0004g0239 | 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 | a0001c0001t0013g0077a0001c0007t0008g0081 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0001t0001g0133a0001c0001t0001g0134 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 140 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(137): 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0029t0001g0245 | 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 | a0001c0006t0001g0031 | 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 31 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(28): 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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114others(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 | a0001c0002t0002g0047a0001c0002t0002g0080a0007c0030t0005g0085 | 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 | a0001c0026t0016g0082 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0008t0004g0248others(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 | a0001c0002t0003g0259a0001c0002t0003g0260a0003c0009t0012g0261 | 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 | a0001c0034t0005g0116 | 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | 163 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(160): 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 | a0001c0002t0002g0257 | 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 | a0001c0001t0001g0240a0001c0004t0004g0241a0001c0008t0004g0236others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0012t0021g0008others(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 | a0001c0002t0003g0170 | 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 | a0001c0001t0001g0235 | 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 | 8 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(5): 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 | 164 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(161): 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 | 26 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0265others(23): 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 | a0001c0001t0001g0167a0001c0002t0002g0075a0001c0002t0028g0074others(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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | 163 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(160): 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | a0001c0008t0004g0234 | 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | 2 | a0001c0007t0008g0036a0001c0007t0008g0037 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0007t0004g0243 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0012t0021g0008others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 163 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(160): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 161 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(158): 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 | a0001c0008t0004g0234a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | 138 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(135): 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 | a0002c0003t0006g0014 | 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 | 146 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(143): 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 | a0001c0029t0001g0245 | 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 | a0001c0004t0004g0266 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0008t0004g0234a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0003c0031t0040g0171 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | a0001c0001t0032g0219 | 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 | a0001c0029t0001g0245 | 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 | a0003c0009t0024g0086 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0007t0020g0168a0001c0008t0004g0248 | 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 | a0001c0001t0001g0002a0001c0001t0001g0166a0001c0001t0001g0216others(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 | a0002c0003t0009g0109a0002c0003t0009g0110a0002c0003t0009g0111 | 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 | a0001c0004t0004g0266 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0002t0003g0230 | 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 | a0001c0002t0003g0259a0001c0002t0003g0260a0003c0009t0012g0261 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0012t0021g0008 | 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 | a0001c0001t0005g0108 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0003c0013t0037g0137a0003c0024t0011g0076 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0008t0004g0234a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0029t0001g0245 | 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 | a0001c0001t0035g0238 | 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 | 19 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(16): 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0004t0004g0266 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0003c0031t0040g0171 | 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0002t0003g0215 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0184a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0012t0014g0264 | 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 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0032g0219others(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 | a0001c0001t0001g0184a0001c0001t0013g0077a0001c0002t0002g0042others(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 |
22 | a0001c0002t0002g0041a0001c0002t0002g0070a0001c0002t0002g0075others(19): 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 | a0001c0002t0002g0105a0001c0002t0003g0173a0001c0002t0003g0185others(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 | a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0144others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(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 |
41 | a0001c0001t0001g0133a0001c0001t0001g0153a0001c0001t0001g0154others(38): Show | 41 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(38): 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 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0001t0001g0163others(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 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0001c0001t0001g0212a0001c0001t0001g0221a0003c0009t0012g0213others(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 | a0001c0005t0007g0030 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0004t0004g0176a0001c0004t0004g0178a0001c0004t0004g0251others(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 | a0001c0001t0005g0049a0001c0001t0005g0065a0001c0001t0005g0094others(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 | a0001c0004t0004g0177 | 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 | a0001c0002t0002g0050 | 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 | a0001c0002t0002g0050a0001c0004t0004g0176 | 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 | a0001c0002t0002g0053 | 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 | a0001c0004t0004g0177 | 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 | a0001c0002t0002g0117a0001c0008t0004g0248a0005c0022t0022g0250 | 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 | a0002c0011t0010g0121a0002c0011t0010g0122 | 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 | a0001c0005t0007g0033 | 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 | a0001c0008t0008g0090a0001c0017t0002g0061a0003c0031t0040g0171 | 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 | a0001c0002t0002g0131a0001c0002t0002g0132a0003c0013t0011g0078 | 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 | a0002c0003t0009g0048 | 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 | a0001c0001t0005g0049 | 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 | a0001c0014t0005g0039a0003c0009t0010g0089 | 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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0013g0104others(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 | a0001c0001t0005g0114a0001c0002t0002g0047a0001c0002t0002g0068others(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 | a0001c0001t0005g0094a0001c0001t0005g0108a0001c0002t0002g0066others(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 | a0001c0001t0005g0065a0001c0002t0002g0064 | 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 | a0001c0002t0002g0067a0003c0009t0024g0086 | 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 | a0001c0005t0007g0024 | 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 | a0001c0002t0002g0126a0001c0008t0008g0073 | 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 | a0001c0002t0002g0071a0001c0002t0002g0072a0001c0004t0004g0266others(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 | a0001c0002t0002g0106a0002c0003t0009g0107 | 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 | a0001c0001t0005g0095 | 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 | a0001c0014t0023g0040 | 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 | a0001c0002t0027g0118a0001c0007t0008g0035a0001c0007t0008g0038others(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 | a0001c0001t0005g0065a0001c0002t0002g0064 | 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 | a0001c0029t0001g0245 | 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 | a0001c0029t0001g0245 | 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 | a0001c0029t0001g0245 | 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 | a0001c0001t0001g0265a0001c0002t0002g0075a0001c0002t0003g0019others(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 | a0001c0002t0002g0052a0001c0002t0002g0057a0001c0002t0002g0062others(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 | a0001c0002t0002g0055a0001c0002t0026g0054a0001c0002t0028g0074 | 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 | a0001c0002t0002g0257a0003c0013t0011g0096 | 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 | 116 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(113): 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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | a0001c0002t0002g0050a0001c0004t0004g0252a0001c0007t0004g0255others(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 | a0001c0001t0001g0246a0001c0001t0005g0060a0001c0002t0002g0041others(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 | a0001c0001t0013g0077a0001c0002t0002g0042a0001c0002t0002g0058others(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 | a0001c0001t0013g0099a0001c0002t0002g0056a0001c0002t0002g0087others(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 | a0001c0036t0002g0051 | 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 | 80 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0247others(77): 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 | 114 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0247others(111): 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 | a0001c0001t0001g0246a0001c0001t0005g0060a0001c0001t0013g0077others(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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | 113 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(110): 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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | 103 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0247others(100): 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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | 82 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0005g0060others(79): 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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | 64 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0005g0060others(61): 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 | 116 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(113): 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 | 22 | a0001c0001t0001g0184a0001c0002t0002g0043a0001c0002t0003g0260others(19): 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 | a0001c0001t0001g0265a0001c0002t0002g0052a0001c0002t0002g0055others(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 | a0001c0002t0002g0105 | 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 | 27 | a0001c0001t0001g0265a0001c0002t0002g0043a0001c0002t0002g0052others(24): 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 | a0001c0008t0004g0234 | 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 | a0003c0013t0011g0096 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0002t0002g0128 | 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 | a0001c0027t0004g0136 | 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 | a0001c0029t0001g0245 | 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 | a0001c0001t0001g0140a0001c0002t0003g0150a0001c0002t0003g0151others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0020g0168others(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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0002c0003t0006g0016 | 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 | a0001c0001t0001g0184a0001c0001t0005g0060a0001c0001t0005g0065others(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 | a0001c0002t0003g0169 | 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 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(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 | a0001c0034t0005g0116 | 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 | a0001c0001t0001g0184a0001c0001t0005g0060a0001c0001t0005g0065others(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 | a0001c0029t0001g0245 | 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 | a0001c0029t0001g0245 | 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 | a0001c0029t0001g0245 | 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 | a0001c0001t0001g0209 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0012t0021g0008others(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 | a0001c0004t0004g0266 | 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 | 140 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(137): 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 | a0001c0008t0008g0073 | 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0029t0001g0245 | 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 | 263 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0134others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0035g0238 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0150 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0020g0168a0001c0008t0004g0248a0001c0012t0021g0008others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0182a0001c0001t0001g0231 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0029t0001g0245 | 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0007t0029g0125 | 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 | 140 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(137): 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 | a0001c0002t0003g0259a0001c0002t0003g0260a0003c0009t0012g0261 | 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | a0001c0017t0002g0061 | 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 | a0001c0002t0002g0257 | 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 | a0001c0001t0001g0240a0001c0001t0001g0246a0001c0001t0001g0247others(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 | a0001c0002t0002g0043 | 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 | a0001c0004t0004g0252 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0007t0020g0168a0001c0008t0004g0248a0001c0012t0021g0008others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0005t0007g0030 | 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 | a0001c0007t0020g0168a0001c0008t0004g0248a0001c0012t0021g0008others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | 172 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(169): 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 | a0001c0002t0002g0097 | 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 | a0002c0003t0006g0011 | 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 | a0001c0029t0001g0245 | 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0001t0001g0246a0001c0001t0001g0247 | 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 | 19 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(16): 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 | a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0001c0001t0005g0095 | 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 | 149 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(146): 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 | a0001c0002t0002g0079a0001c0008t0008g0073a0001c0017t0002g0061 | 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 | a0001c0029t0001g0245 | 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 | a0006c0025t0002g0059 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0246others(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 | a0001c0001t0001g0208 | 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 | a0001c0002t0002g0106 | 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 | a0001c0008t0004g0234a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | 30 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(27): 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0004t0004g0266a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0231others(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 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0231others(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 | a0001c0002t0002g0067 | 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 | a0001c0001t0013g0104a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0001t0001g0216 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0266 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0002t0002g0041others(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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0007t0029g0125 | 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 | a0001c0001t0013g0077 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0001t0001g0142a0001c0002t0003g0139a0001c0004t0004g0138others(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 | 166 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0265others(163): 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 | a0007c0030t0005g0085 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0167others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0008t0004g0248 | 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 | a0001c0001t0001g0216a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0002t0002g0097a0001c0002t0002g0105a0001c0002t0002g0117others(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 | a0001c0002t0002g0052 | 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 | a0001c0004t0004g0241a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0005t0007g0033 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0005t0007g0033 | 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 | a0001c0010t0001g0010a0001c0010t0001g0018a0002c0003t0006g0001others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0191a0001c0002t0003g0230 | 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 | a0001c0005t0007g0180 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0005t0007g0020 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0021g0194 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0002t0003g0172a0001c0002t0003g0173a0001c0021t0003g0174others(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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0012t0021g0008 | 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 | a0001c0001t0021g0194 | 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 | a0001c0012t0021g0008 | 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 | a0001c0004t0004g0251a0001c0004t0004g0252a0001c0004t0004g0253others(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 | a0001c0002t0003g0191 | 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 | a0001c0002t0038g0227 | 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 | a0002c0016t0019g0233 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0001t0001g0167 | 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 | a0001c0008t0004g0248 | 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 | a0001c0002t0003g0172a0001c0002t0003g0173a0001c0021t0003g0174others(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 | 147 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0265others(144): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0004t0004g0241others(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 | a0001c0020t0001g0179 | 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 | a0001c0001t0001g0142a0001c0001t0001g0156a0001c0002t0002g0043others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0006t0001g0031 | 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 | a0001c0004t0004g0004a0001c0012t0014g0262a0001c0012t0014g0263others(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 | a0001c0001t0005g0065a0001c0001t0013g0077a0001c0002t0002g0042others(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 | a0001c0007t0020g0168a0002c0011t0010g0091a0003c0009t0012g0213 | 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 | a0001c0001t0001g0202a0001c0001t0013g0104a0001c0002t0002g0257others(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 | a0001c0001t0001g0184a0001c0002t0002g0041a0001c0002t0002g0063others(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 | a0001c0007t0004g0243a0001c0007t0029g0125a0001c0012t0021g0008others(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 | 83 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0134others(80): Show | 84 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-18-5382delA | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | chr5 | 127325908 | ||||||
| chr5:127325909
|
A | T | 107 | a0001c0001t0001g0142a0001c0001t0001g0202a0001c0001t0005g0049others(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 | 22 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0153others(19): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0015g0017 | 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 | a0001c0002t0003g0260a0002c0003t0006g0014 | 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 | a0001c0006t0001g0034 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0004g0243others(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 | a0001c0008t0004g0248 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0142 | 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 | a0001c0002t0002g0075 | 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 | a0001c0018t0039g0005 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 23 | a0001c0001t0001g0145a0001c0001t0001g0265a0001c0001t0021g0194others(20): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0014a0002c0003t0006g0015a0002c0003t0006g0016 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0134others(195): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0142a0001c0004t0004g0138a0001c0017t0003g0141 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | 22 | a0001c0001t0001g0265a0001c0001t0021g0194a0001c0002t0003g0259others(19): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0053others(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 | a0001c0001t0001g0216a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0002t0003g0172a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0002t0002g0075a0001c0002t0028g0074 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0004g0243others(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 | a0005c0022t0022g0249 | 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 | a0001c0008t0008g0073 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0018t0020g0244a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0201 | 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 | a0001c0008t0004g0248 | 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 | a0001c0001t0013g0077 | 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 | a0001c0026t0016g0082 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0001t0001g0155 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0150a0001c0002t0003g0152 | 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 | 159 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0246others(156): 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 | a0001c0002t0002g0055a0001c0002t0026g0054 | 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 | a0003c0009t0012g0213a0003c0009t0012g0214 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0001t0001g0002a0001c0001t0001g0166a0001c0001t0001g0216others(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 | 156 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0001g0265others(153): 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 | 20 | a0001c0001t0001g0265a0001c0002t0003g0259a0001c0002t0003g0260others(17): 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0001t0001g0145a0001c0001t0005g0049a0001c0001t0005g0094others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0008t0004g0248 | 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 | a0001c0004t0004g0266 | 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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | a0001c0001t0021g0194a0001c0004t0004g0266 | 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 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0012g0181a0003c0009t0012g0213a0003c0009t0012g0214 | 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 | a0001c0004t0004g0251 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0001c0008t0004g0248 | 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 | a0001c0001t0035g0238 | 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 | a0001c0001t0001g0195 | 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 | a0001c0007t0004g0243 | 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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0004t0004g0178others(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 | a0003c0009t0024g0086 | 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 | a0001c0002t0003g0228a0001c0002t0038g0227 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0002c0003t0009g0107others(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 | a0001c0002t0003g0259a0001c0002t0003g0260 | 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 | 26 | a0001c0001t0001g0145a0001c0001t0001g0265a0001c0001t0021g0194others(23): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0022a0001c0005t0007g0023a0001c0005t0007g0027others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0008t0004g0248 | 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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114others(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 | a0001c0007t0004g0243 | 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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0008t0004g0234others(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 | a0001c0001t0013g0077 | 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 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0005g0065others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0002t0003g0151 | 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 | a0001c0001t0021g0194a0001c0004t0004g0266 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0004t0004g0176others(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 | a0001c0004t0004g0177 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | 26 | a0001c0001t0001g0145a0001c0001t0001g0265a0001c0001t0021g0194others(23): 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 | a0001c0001t0005g0094 | 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 | 25 | a0001c0001t0001g0265a0001c0001t0021g0194a0001c0002t0003g0259others(22): 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0008t0004g0248 | 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 | a0001c0001t0001g0145 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0007t0004g0243 | 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 | a0001c0018t0039g0005 | 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 | a0001c0001t0001g0186 | 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 | a0001c0002t0003g0151a0001c0002t0003g0196 | 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 | a0001c0018t0039g0005 | 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 | a0001c0002t0003g0242 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0004g0243 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0035g0238 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0147a0001c0001t0001g0184a0001c0001t0005g0065others(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 | a0001c0001t0001g0147a0001c0001t0001g0184a0001c0001t0005g0065others(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 | a0003c0009t0012g0261 | 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 | a0001c0001t0001g0182a0001c0001t0001g0231a0002c0003t0015g0220 | 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 | a0001c0001t0001g0207 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0170 | 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 | a0001c0006t0001g0031 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | 22 | a0001c0001t0001g0145a0001c0001t0021g0194a0001c0004t0004g0266others(19): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0020g0168others(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 | a0001c0008t0004g0236a0001c0008t0004g0237 | 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 | a0001c0001t0005g0108 | 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 | a0001c0001t0001g0148 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0001c0018t0039g0005a0001c0027t0004g0136 | 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 | 2 | a0001c0007t0008g0036a0001c0007t0008g0037 | 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 | a0001c0001t0005g0108 | 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 | a0001c0002t0026g0054 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0020g0168others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | 155 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(152): 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0004t0004g0178 | 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 | a0001c0001t0001g0184a0001c0001t0005g0049a0001c0001t0005g0065others(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 | a0006c0025t0002g0059 | 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0012g0181 | 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 | a0001c0007t0004g0243 | 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 | a0002c0003t0009g0109 | 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 | a0001c0001t0001g0161a0001c0001t0001g0167 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0008t0004g0234others(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 | a0001c0012t0021g0008 | 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 | 86 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0005g0065others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(83): 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 | a0001c0018t0039g0005a0001c0027t0004g0136 | 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 | a0001c0001t0021g0194a0001c0004t0004g0266a0004c0019t0018g0006others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0001t0013g0077 | 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 | a0001c0029t0001g0245 | 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 | a0001c0012t0021g0008 | 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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0008t0004g0234others(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 | a0002c0003t0015g0135 | 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 | a0001c0001t0001g0153a0001c0018t0020g0244 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0002c0003t0006g0011 | 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 | 168 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(165): 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 | a0001c0014t0001g0254 | 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 | a0001c0001t0005g0049 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0012g0261 | 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 | a0001c0002t0003g0259a0001c0002t0003g0260 | 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 | a0001c0018t0020g0244 | 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 | 167 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(164): 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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0002t0002g0097a0001c0002t0002g0105a0001c0002t0002g0117others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0035t0002g0130 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0003c0031t0040g0171 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0057 | 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 | a0001c0002t0003g0151a0001c0002t0003g0196 | 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 | a0001c0002t0002g0106 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0002c0003t0009g0107others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0002t0003g0151 | 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 | a0001c0020t0001g0203 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0002t0002g0056a0001c0002t0002g0068a0001c0002t0002g0070others(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 | a0001c0002t0002g0063 | 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 | a0001c0001t0001g0189 | 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 | a0001c0036t0002g0051 | 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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0004t0004g0266others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0235a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0008t0004g0239a0001c0008t0008g0073a0001c0008t0008g0090 | 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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0013g0099a0001c0001t0013g0104a0002c0003t0009g0107others(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 | a0001c0001t0001g0161 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 154 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(151): 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 | 53 | a0001c0001t0001g0133a0001c0001t0001g0142a0001c0001t0001g0144others(50): 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 | a0001c0001t0001g0134a0001c0001t0001g0153a0001c0001t0005g0049others(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 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(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 | a0002c0003t0006g0013a0003c0009t0012g0181a0009c0032t0031g0102 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0005g0083others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0004t0004g0003others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0002c0003t0009g0107a0002c0003t0009g0124a0002c0003t0009g0127 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0001t0001g0192 | 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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0032g0219 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | 154 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(151): 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 | a0001c0018t0039g0005 | 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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | 33 | a0001c0001t0001g0145a0001c0001t0021g0194a0001c0002t0003g0019others(30): 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 | a0001c0001t0001g0158a0001c0007t0004g0243 | 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 | a0001c0001t0001g0144a0001c0001t0005g0108 | 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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0149 | 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0147others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0070 | 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 | a0001c0004t0004g0266a0001c0012t0021g0008 | 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 | a0001c0007t0004g0243 | 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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | a0001c0001t0005g0083 | 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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0027g0118 | 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 | a0001c0002t0003g0151a0001c0002t0003g0196 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | a0001c0001t0001g0183a0001c0001t0005g0129 | 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 | a0001c0002t0002g0053a0001c0002t0002g0058a0001c0002t0002g0098others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0007t0029g0125others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0025 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0029g0125a0003c0031t0040g0171a0009c0032t0031g0102 | 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 | a0009c0032t0031g0102 | 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 | a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | 167 | a0001c0001t0001g0145a0001c0001t0001g0184a0001c0001t0005g0049others(164): 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 | a0001c0001t0005g0049a0001c0001t0005g0094a0001c0001t0005g0095others(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 | a0001c0002t0003g0173 | 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 | a0001c0001t0001g0002a0001c0001t0001g0144a0001c0001t0001g0147others(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 | 115 | a0001c0001t0001g0134a0001c0001t0001g0144a0001c0001t0001g0145others(112): 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 | a0001c0001t0013g0077a0001c0002t0002g0041a0001c0002t0002g0042others(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 | a0001c0001t0001g0002a0001c0001t0001g0166a0001c0001t0001g0183others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0010t0001g0229 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264others(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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0002c0016t0019g0232 | 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 | a0001c0015t0002g0119 | 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 | a0001c0002t0002g0043 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0010t0001g0010a0001c0010t0001g0018a0002c0003t0006g0001others(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 | a0001c0001t0001g0184a0001c0001t0005g0065a0001c0001t0013g0077others(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 | a0001c0002t0002g0075 | 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 | a0001c0002t0027g0118 | 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 | a0001c0002t0002g0132 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0003c0013t0011g0096 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0004t0004g0003others(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 | a0001c0001t0001g0186 | 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 | a0003c0009t0011g0093 | 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 | a0001c0002t0027g0118a0001c0026t0016g0082 | 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 | a0001c0002t0002g0041 | 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 | a0001c0001t0013g0077 | 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 | 52 | a0001c0001t0001g0145a0001c0001t0005g0049a0001c0001t0005g0094others(49): 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 | a0001c0001t0001g0146a0001c0001t0001g0164a0001c0001t0001g0240others(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 | a0001c0002t0002g0257 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0145 | 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 | 134 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0134others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0001c0007t0020g0168a0001c0012t0021g0008 | 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 | a0001c0001t0013g0077 | 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 | a0001c0002t0002g0043 | 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 | a0001c0015t0003g0032 | 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 | a0001c0001t0001g0145a0001c0001t0021g0194a0001c0007t0004g0243others(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 | a0001c0001t0001g0246a0001c0001t0001g0247 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088 | 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 | a0001c0002t0002g0075 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0004g0243 | 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 | a0001c0007t0004g0243 | 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 | a0001c0012t0014g0264 | 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 20 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(17): 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 | a0001c0017t0003g0141 | 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 | a0001c0007t0004g0243a0009c0032t0031g0102 | 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 | 20 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(17): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0012g0181 | 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 | a0001c0018t0020g0244 | 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 | a0001c0001t0021g0194 | 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 | a0002c0016t0019g0232 | 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 | a0008c0033t0002g0044 | 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 | a0001c0002t0003g0185 | 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 | a0005c0022t0022g0249 | 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 | a0001c0018t0020g0244 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0007t0029g0125 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | 89 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(86): 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 | a0001c0001t0013g0099a0001c0001t0013g0104 | 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 | a0001c0002t0002g0257 | 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 | a0001c0002t0003g0242 | 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 | a0001c0001t0001g0188a0001c0001t0001g0190 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0001t0001g0147a0001c0001t0001g0186a0001c0001t0001g0216others(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 | a0001c0001t0001g0002a0001c0001t0005g0049 | 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 | 24 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0153others(21): Show | 24 | HG00558.hp2 HG01074.hp1 HG01256.hp1 others(21): 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 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0240others(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 | a0001c0001t0001g0195a0001c0005t0007g0025a0001c0007t0029g0125 | 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 | a0001c0001t0001g0208a0001c0001t0005g0083a0001c0002t0003g0228others(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 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0156others(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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0146others(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 | 43 | a0001c0001t0001g0140a0001c0001t0001g0201a0001c0001t0001g0205others(40): 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 | a0001c0001t0021g0194a0001c0002t0002g0257a0001c0002t0003g0019others(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 | a0001c0001t0001g0199a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0005t0007g0030a0001c0008t0004g0239a0001c0008t0008g0073others(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 | a0002c0003t0006g0011a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0001t0001g0145a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0002c0003t0015g0135 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264others(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 | a0001c0001t0013g0077 | 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 | a0001c0002t0003g0191a0001c0002t0003g0230a0001c0017t0003g0141 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0002t0002g0079a0001c0017t0002g0061 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0198 | 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 | a0009c0032t0031g0102 | 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 | 82 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(79): 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 | a0001c0018t0020g0244 | 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 | a0002c0003t0015g0220 | 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 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0224others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0002t0002g0079 | 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 | a0001c0001t0001g0246 | 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 | a0003c0031t0040g0171 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0172a0001c0002t0003g0173a0001c0021t0003g0174others(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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | 88 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(85): 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 | a0001c0005t0007g0022a0001c0005t0007g0023a0001c0005t0007g0027 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0007t0029g0125 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 168 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0147others(165): 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 | a0001c0001t0001g0145a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104 | 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 | 21 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(18): 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 | a0001c0004t0004g0266 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0002t0002g0043 | 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 | a0001c0018t0020g0244 | 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 | a0004c0019t0018g0007 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0062others(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 | a0003c0031t0040g0171 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0007t0029g0125others(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 | a0001c0002t0002g0088 | 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 | 49 | a0001c0001t0001g0145a0001c0004t0004g0003a0001c0004t0004g0004others(46): 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 21 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(18): 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0018t0020g0244 | 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 | a0004c0019t0018g0007 | 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 | a0001c0001t0001g0145a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0001t0005g0049 | 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 | a0001c0004t0004g0176a0001c0004t0004g0177 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0001t0001g0161a0001c0001t0001g0167a0003c0009t0024g0086 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(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 | 85 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(82): 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 | a0001c0001t0005g0094a0001c0001t0005g0095 | 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 | a0001c0017t0002g0061 | 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 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0069others(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 | a0002c0003t0009g0109a0002c0003t0009g0110a0002c0003t0009g0111 | 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 | a0001c0002t0003g0191 | 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 | a0001c0001t0001g0145 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0002t0002g0257 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0218a0001c0007t0029g0125a0001c0008t0004g0234others(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 | a0001c0001t0001g0145a0001c0001t0001g0153a0001c0001t0001g0167others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(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 | a0001c0002t0003g0215 | 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 | a0001c0018t0039g0005 | 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 | a0001c0002t0025g0046a0001c0002t0038g0227 | 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 | a0001c0002t0003g0172a0001c0002t0003g0173a0001c0021t0003g0174others(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 | a0001c0001t0001g0198 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0004g0243a0001c0007t0029g0125a0001c0008t0004g0234others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0147a0001c0001t0001g0154a0001c0001t0001g0155others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0032g0219 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244 | 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 | a0001c0001t0001g0163a0001c0001t0001g0207a0001c0001t0005g0094others(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 | 77 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(74): 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 | a0001c0002t0002g0045 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 85 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(82): 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 | 82 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(79): 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 | a0001c0001t0032g0219 | 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 | a0001c0035t0002g0130 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0146 | 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 | a0001c0008t0004g0234a0001c0008t0004g0248 | 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 | a0001c0002t0003g0139a0001c0002t0003g0169a0001c0002t0003g0170others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0145 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0145a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0002t0002g0064a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0039g0005 | 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 | a0001c0018t0039g0005 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0005t0007g0020others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0005t0007g0020others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0007t0029g0125others(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 | 170 | a0001c0001t0001g0145a0001c0001t0001g0207a0001c0001t0005g0094others(167): 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 | a0001c0001t0001g0247 | 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 | a0001c0002t0002g0079 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0007t0008g0035 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0242 | 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 | 21 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(18): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0003c0024t0011g0076 | 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 | a0001c0001t0001g0142a0001c0001t0005g0060 | 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 | a0001c0007t0029g0125 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244 | 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 | a0009c0032t0031g0102 | 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 | 80 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(77): 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0001t0001g0198 | 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 | a0001c0002t0002g0106 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | a0001c0001t0001g0184a0001c0001t0005g0065 | 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 | a0001c0005t0007g0027 | 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 | a0001c0018t0020g0244 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0149 | 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 | a0001c0007t0029g0125 | 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 | a0001c0001t0005g0094a0001c0001t0005g0095 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | 21 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(18): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0009c0032t0031g0102 | 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 | a0009c0032t0031g0102 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0014t0023g0040 | 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 | a0001c0018t0039g0005 | 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 | 94 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(91): 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 | a0001c0001t0001g0154a0001c0001t0001g0155 | 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 | a0001c0002t0002g0064a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | 164 | a0001c0001t0001g0145a0001c0002t0002g0041a0001c0002t0002g0042others(161): 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 | a0001c0007t0029g0125 | 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 | a0001c0007t0029g0125 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0009c0032t0031g0102 | 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 | a0001c0001t0005g0060 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0007t0029g0125 | 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 | a0001c0004t0004g0256 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | 35 | a0001c0001t0001g0190a0001c0001t0001g0231a0001c0002t0002g0045others(32): 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0169others(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 | a0001c0001t0013g0099a0001c0001t0013g0104a0001c0002t0002g0041others(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 | a0001c0001t0005g0094a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0025a0001c0005t0016g0084others(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 | a0001c0035t0002g0130 | 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 | a0001c0001t0001g0206 | 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 | a0001c0018t0020g0244 | 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 | a0001c0001t0001g0145a0001c0014t0001g0254a0001c0014t0005g0039others(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 | a0007c0030t0005g0085 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0242 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0149 | 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 | a0001c0006t0001g0034 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(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 | a0003c0009t0010g0089 | 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0205others(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 | 163 | a0001c0001t0001g0145a0001c0001t0013g0077a0001c0001t0013g0099others(160): 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 | a0001c0018t0039g0005 | 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 | a0001c0018t0039g0005 | 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 | a0001c0001t0001g0145a0001c0014t0001g0254a0001c0014t0005g0039others(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 | a0001c0001t0001g0145a0001c0014t0001g0254a0001c0014t0005g0039others(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 | a0001c0010t0001g0193 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0009c0032t0031g0102 | 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 | 163 | a0001c0001t0001g0145a0001c0001t0013g0077a0001c0001t0013g0099others(160): 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 | a0001c0005t0007g0022a0001c0005t0007g0023a0001c0005t0007g0027 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | 21 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(18): 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0009c0032t0031g0102 | 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 | 15 | a0001c0001t0001g0201a0001c0001t0005g0083a0001c0005t0007g0020others(12): 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0002t0003g0150a0001c0002t0003g0152 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0002t0003g0196 | 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 | 85 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(82): 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 | a0001c0005t0007g0180 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0002t0002g0041a0001c0002t0002g0042 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0007t0029g0125 | 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 | a0001c0008t0004g0234a0001c0008t0004g0236a0001c0008t0004g0237others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0188others(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 | a0003c0009t0012g0213 | 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 | a0001c0001t0001g0144a0001c0001t0001g0155a0001c0001t0001g0183others(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 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0002g0097others(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 | a0003c0009t0012g0214 | 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 | a0001c0001t0001g0201 | 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 | a0001c0007t0029g0125 | 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 | a0001c0002t0002g0053a0001c0002t0002g0058a0001c0002t0002g0098others(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 | a0001c0002t0002g0047a0001c0002t0002g0057a0001c0002t0002g0064others(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 | a0001c0002t0002g0080a0001c0002t0002g0103a0001c0002t0002g0105others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0001c0002t0002g0063a0001c0002t0003g0242a0001c0002t0028g0074 | 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 | a0001c0002t0002g0079 | 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 | a0001c0002t0002g0056a0001c0002t0002g0068a0001c0002t0002g0070others(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 | a0001c0001t0001g0145a0001c0001t0001g0189a0001c0005t0007g0020others(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 | a0001c0002t0027g0118a0001c0002t0038g0227a0001c0012t0014g0262 | 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 | a0001c0002t0002g0257 | 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 | a0001c0002t0002g0131a0001c0002t0017g0100a0001c0002t0017g0101others(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 | a0001c0017t0003g0141 | 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 | a0001c0002t0003g0260a0003c0009t0012g0261a0004c0019t0018g0006others(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 | a0001c0001t0013g0104 | 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 | a0001c0001t0013g0077a0001c0001t0013g0099 | 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 | a0001c0002t0003g0191 | 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 | a0001c0001t0001g0146a0001c0001t0001g0164a0001c0001t0001g0240others(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 | a0001c0001t0001g0166a0001c0002t0002g0045a0001c0004t0004g0003others(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 | a0001c0001t0001g0159a0001c0001t0001g0265a0001c0007t0008g0081 | 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 | a0001c0004t0004g0241a0001c0004t0004g0252a0001c0004t0004g0266others(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 | a0001c0004t0004g0138a0001c0007t0004g0255a0001c0007t0008g0035others(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 | a0001c0001t0001g0002a0001c0001t0001g0154a0001c0001t0001g0156others(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 | a0001c0001t0001g0210 | 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 | 32 | a0001c0001t0001g0146a0001c0001t0001g0159a0001c0001t0001g0164others(29): 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 | 9 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0190others(6): Show | 9 | HG00423.hp2 HG02004.hp2 HG02132.hp1 others(6): 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 | a0001c0001t0001g0133a0001c0001t0001g0182a0001c0001t0005g0049others(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 | a0001c0001t0001g0184a0001c0001t0001g0206a0001c0001t0005g0065others(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 | a0003c0009t0010g0089 | 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 | a0001c0001t0001g0189a0001c0001t0005g0083a0001c0034t0005g0116others(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 | a0001c0001t0001g0142a0001c0001t0001g0201a0001c0002t0002g0088others(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 | a0001c0001t0001g0147a0001c0001t0021g0194a0010c0023t0001g0026 | 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 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0211others(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 | a0001c0001t0001g0134a0001c0001t0001g0205a0001c0001t0001g0209others(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 | a0001c0001t0035g0238 | 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 | a0001c0001t0001g0145a0001c0001t0001g0148a0001c0001t0001g0160others(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 | a0001c0005t0007g0027a0001c0008t0004g0234 | 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 | a0002c0003t0009g0109 | 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 | a0001c0005t0007g0027 | 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 | a0001c0005t0007g0027 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0145a0001c0001t0001g0199a0001c0001t0001g0211others(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 | a0001c0001t0001g0134a0001c0005t0007g0180a0001c0008t0004g0234others(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 | a0001c0018t0020g0244a0002c0003t0006g0014a0002c0003t0009g0109others(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 | a0001c0001t0035g0238a0001c0018t0020g0244 | 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 | a0001c0005t0007g0027 | 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 | a0001c0001t0035g0238a0001c0005t0007g0027a0001c0018t0020g0244 | 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 | a0001c0005t0007g0027a0001c0018t0020g0244 | 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 | a0001c0005t0007g0027 | 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 | a0001c0005t0007g0020a0001c0005t0007g0023a0001c0005t0007g0024 | 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 | a0001c0005t0007g0022a0001c0005t0007g0029a0001c0005t0007g0033others(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 | a0001c0005t0007g0030a0001c0014t0001g0254a0001c0014t0005g0039others(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 | a0002c0003t0006g0009a0002c0003t0006g0012a0002c0003t0006g0013others(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 | a0001c0001t0001g0145a0001c0007t0029g0125a0002c0003t0006g0001others(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 | a0002c0003t0009g0109a0002c0003t0009g0127a0002c0003t0015g0017others(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 | a0001c0002t0002g0047a0001c0002t0002g0050a0001c0002t0002g0052others(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 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0001t0001g0142a0001c0001t0005g0060a0001c0012t0021g0008 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | 23 | a0001c0001t0001g0206a0001c0001t0013g0099a0001c0004t0004g0003others(20): 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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0005t0007g0020others(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 | a0001c0006t0001g0031 | 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 | a0001c0001t0001g0231 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | 171 | a0001c0001t0001g0145a0001c0001t0001g0246a0001c0001t0001g0247others(168): 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 | a0009c0032t0031g0102 | 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 | a0001c0001t0033g0197a0001c0001t0034g0204a0001c0034t0005g0116 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0007t0029g0125a0001c0008t0004g0234a0001c0008t0004g0236others(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 | 84 | a0001c0001t0001g0145a0001c0002t0002g0087a0001c0002t0002g0088others(81): 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0002t0003g0260 | 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 | a0001c0001t0001g0145a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0149 | 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 | a0001c0002t0003g0242 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0002c0003t0009g0109a0002c0003t0009g0110a0002c0003t0009g0111 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0001t0001g0211a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0005t0007g0030 | 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 | a0001c0005t0007g0022a0001c0005t0007g0023a0001c0005t0007g0027 | 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0153others(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 | 103 | a0001c0001t0001g0149a0001c0001t0001g0210a0001c0001t0001g0265others(100): 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 | a0001c0002t0002g0257a0001c0002t0003g0150a0001c0002t0003g0173others(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 | a0001c0005t0007g0025a0001c0005t0016g0084a0001c0007t0029g0125others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0009c0032t0031g0102 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | 29 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(26): 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0029a0001c0005t0007g0030 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 165 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0013g0077others(162): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0006t0001g0028 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0003c0031t0040g0171 | 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 | 70 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(67): 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0002t0002g0097a0001c0002t0027g0118 | 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 | a0002c0003t0015g0135 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0149 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 70 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(67): 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0001g0198 | 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 | a0001c0002t0002g0050a0001c0002t0002g0052 | 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 | a0003c0031t0040g0171 | 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 | a0001c0001t0001g0184a0001c0001t0005g0065 | 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 | 70 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(67): 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | 70 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(67): 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 | a0002c0003t0009g0107 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0003c0009t0010g0089others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0009c0032t0031g0102 | 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 | a0001c0002t0002g0064a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0002c0028t0030g0115 | 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 | a0001c0001t0001g0002a0001c0001t0001g0166a0001c0001t0001g0183others(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 | a0001c0018t0020g0244a0001c0018t0039g0005a0009c0032t0031g0102 | 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 | a0001c0002t0003g0139a0001c0002t0003g0169a0001c0002t0003g0170others(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 | a0001c0017t0002g0061 | 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 | a0001c0001t0005g0094a0001c0001t0005g0095 | 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 | a0003c0031t0040g0171 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0005t0007g0033 | 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 | a0001c0018t0039g0005 | 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 | 88 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0003g0139others(85): 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 | 41 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(38): 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 | a0001c0005t0007g0180 | 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 | a0001c0001t0001g0207 | 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 | a0002c0003t0009g0107a0002c0003t0009g0124a0002c0003t0009g0127others(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 | a0001c0005t0016g0084 | 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 | a0001c0007t0029g0125 | 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 | a0001c0001t0001g0221 | 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 | 83 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(80): 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 | a0001c0002t0002g0053a0001c0002t0002g0058a0001c0002t0002g0098 | 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 | 83 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(80): 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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0020t0001g0203 | 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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0001t0034g0204 | 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 | a0001c0004t0004g0251 | 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 | a0001c0018t0039g0005 | 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 | a0001c0002t0002g0257 | 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 | a0001c0001t0001g0246a0001c0001t0001g0247 | 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 | a0002c0028t0030g0115 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0001c0002t0003g0172a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0001c0007t0004g0255a0001c0008t0004g0236a0001c0008t0004g0237others(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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0018t0020g0244others(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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0002c0003t0006g0011 | 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 | 60 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(57): 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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0010t0001g0018 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005a0009c0032t0031g0102 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0018t0020g0244 | 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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0001c0002t0002g0056a0001c0002t0002g0068a0001c0002t0002g0070others(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 | a0001c0018t0020g0244a0001c0018t0039g0005a0009c0032t0031g0102 | 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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0018t0020g0244others(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 | a0001c0005t0007g0020 | 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 | 62 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(59): 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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0153others(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 | 82 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(79): 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 | ||||||
| chr5:127405252
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0134others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.917+2570C>T | MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 8/24 | chr5 | 127405252 | ||||||
| chr5:127405457
|
C | T | 1 | a0009c0032t0031g0102 | 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 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0224others(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 | a0001c0002t0003g0172a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | a0001c0001t0005g0108 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0026t0016g0082 | 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 | a0001c0018t0020g0244 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0257 | 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 | a0001c0012t0021g0008 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0001t0013g0099 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040others(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 | a0001c0002t0017g0100a0001c0002t0017g0101 | 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 | a0001c0018t0039g0005 | 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 | a0001c0026t0016g0082 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0012t0021g0008 | 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 | a0001c0001t0035g0238 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0017g0100others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | 88 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(85): 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 | a0003c0031t0040g0171 | 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 | a0001c0002t0002g0087 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0018t0020g0244a0001c0018t0039g0005a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0182 | 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 | 79 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(76): 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 | a0009c0032t0031g0102 | 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 | a0002c0003t0015g0017 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0005t0007g0020others(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 | a0002c0003t0006g0016 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0002c0028t0030g0115 | 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 | a0001c0001t0001g0231 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0002t0002g0045 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0039g0005a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0001c0002t0002g0097a0001c0002t0002g0106a0001c0002t0027g0118others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0207 | 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 | a0009c0032t0031g0102 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0151a0001c0002t0003g0196a0001c0036t0002g0051 | 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 | a0001c0001t0001g0235 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0028t0030g0115 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264others(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 | a0001c0001t0013g0077 | 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 | a0001c0012t0014g0262a0001c0012t0014g0263a0001c0012t0014g0264others(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 | a0001c0002t0002g0075a0001c0002t0028g0074 | 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 | a0003c0031t0040g0171 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | a0002c0003t0006g0016 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(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 | a0001c0001t0013g0099 | 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 | a0001c0001t0001g0201 | 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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0004t0004g0178a0001c0004t0004g0241 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0006t0001g0222a0001c0006t0001g0223a0001c0006t0001g0224others(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 | a0001c0005t0007g0033 | 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 | a0001c0001t0005g0095 | 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 | a0001c0001t0001g0002 | 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(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 | a0001c0001t0021g0194 | 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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0108 | 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 | a0001c0001t0001g0145a0001c0001t0001g0155a0001c0002t0002g0087others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0047a0001c0002t0002g0257a0001c0005t0007g0020others(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 | a0001c0001t0001g0246a0001c0001t0036g0258a0001c0002t0002g0087others(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 | 30 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(27): 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | 44 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0004t0004g0003others(41): 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 | a0001c0001t0021g0194a0001c0002t0003g0172a0001c0005t0007g0020others(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 | 144 | a0001c0001t0001g0162a0001c0001t0013g0077a0001c0001t0013g0099others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): 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 | a0001c0001t0001g0183a0001c0001t0005g0129 | 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 | a0001c0007t0004g0255 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0023 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0103 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0007c0030t0005g0085 | 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 | a0002c0003t0009g0107a0002c0003t0009g0124a0002c0003t0009g0127others(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 | 20 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(17): 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 | a0001c0015t0003g0032 | 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 | a0001c0002t0003g0259a0001c0002t0003g0260a0003c0009t0012g0261 | 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 | a0009c0032t0031g0102 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0139 | 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 | a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0035t0002g0130 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0001g0265 | 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 | a0003c0031t0040g0171 | 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 | a0001c0002t0002g0087 | 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 | a0001c0001t0001g0182 | 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 | a0001c0007t0029g0125 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0002c0011t0010g0091others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0069others(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 | a0001c0002t0002g0045 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0012g0213a0003c0009t0012g0214 | 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 | a0001c0001t0001g0200 | 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 | a0003c0031t0040g0171 | 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 | 48 | a0001c0001t0001g0186a0001c0001t0001g0200a0001c0001t0001g0211others(45): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0031t0040g0171 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0002t0002g0092 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0010c0023t0001g0026 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0007t0029g0125 | 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 | a0001c0001t0032g0219 | 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 | a0001c0001t0005g0114 | 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 | a0001c0002t0002g0056 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0028t0030g0115 | 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 | a0003c0031t0040g0171 | 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 | a0001c0001t0001g0202a0001c0006t0001g0021 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0001t0001g0159 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0001g0208 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0034t0005g0116 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0018t0020g0244 | 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 | 58 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(55): 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | 58 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(55): 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 | a0001c0002t0003g0230a0001c0017t0002g0061 | 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 | a0003c0031t0040g0171 | 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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | 58 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(55): 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0105a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0031t0040g0171 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084a0001c0007t0004g0243 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0002c0028t0030g0115 | 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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040 | 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 | a0003c0031t0040g0171 | 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 | a0001c0002t0003g0172a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0003c0031t0040g0171 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244 | 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 | 46 | a0001c0001t0001g0207a0001c0001t0001g0246a0001c0001t0001g0247others(43): 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 | a0001c0004t0004g0176a0001c0007t0004g0255a0001c0008t0004g0234others(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 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0217others(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 | a0001c0001t0013g0104a0001c0005t0007g0020a0001c0005t0007g0022others(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 | a0001c0002t0002g0105a0001c0002t0002g0117a0001c0002t0002g0126others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0143 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0153others(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 | a0001c0002t0002g0097a0001c0002t0027g0118 | 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 | a0003c0009t0024g0086 | 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 | a0003c0031t0040g0171 | 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 | a0001c0008t0004g0236a0001c0008t0004g0237 | 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 | a0001c0002t0003g0259a0001c0002t0003g0260 | 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 | 44 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(41): 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0021g0194a0009c0032t0031g0102 | 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 | a0001c0002t0003g0242 | 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 | a0001c0007t0029g0125 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0205 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0002t0002g0043 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114 | 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 | a0002c0003t0006g0011 | 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 | a0001c0004t0004g0252 | 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 | a0003c0009t0012g0213a0003c0009t0012g0214 | 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 | 62 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114others(59): 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 | a0001c0015t0003g0032 | 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 | a0001c0001t0021g0194a0009c0032t0031g0102 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0005t0007g0027 | 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 | a0001c0034t0005g0116 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 164 | a0001c0001t0021g0194a0001c0002t0002g0041a0001c0002t0002g0042others(161): 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 | a0001c0002t0002g0045 | 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 | a0001c0001t0021g0194a0001c0012t0014g0262a0001c0012t0014g0263others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0003t0015g0017 | 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 | a0001c0002t0002g0088 | 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 | a0001c0001t0005g0094a0001c0001t0005g0095 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0002c0028t0030g0115 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0003c0009t0012g0261 | 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 | a0001c0001t0034g0204 | 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 | 78 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(75): 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0018t0039g0005 | 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 | a0001c0018t0039g0005 | 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 | a0003c0031t0040g0171 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0002t0002g0050a0001c0002t0002g0052a0001c0002t0017g0100others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0001t0001g0140 | 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 | a0001c0005t0007g0025a0001c0005t0016g0084 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0001g0142a0001c0001t0005g0060 | 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 | a0001c0001t0001g0265a0001c0004t0004g0003a0001c0004t0004g0004others(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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005a0002c0011t0010g0091others(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 | 29 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(26): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0001t0021g0194a0001c0012t0014g0262a0001c0012t0014g0263others(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 | a0002c0028t0030g0115 | 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 | a0001c0007t0004g0243 | 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 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0014t0001g0254others(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 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0114 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0021g0194a0009c0032t0031g0102 | 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 | a0001c0001t0021g0194a0001c0002t0002g0041a0001c0002t0002g0042others(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 | a0001c0005t0007g0020 | 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 | a0001c0002t0002g0117a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0034t0005g0116 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0014t0023g0040 | 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 | 164 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104others(161): 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 | 28 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(25): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0005t0007g0020 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005a0002c0011t0010g0091others(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 | a0003c0009t0012g0181 | 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 | 62 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(59): 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0002t0003g0185 | 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 | a0001c0001t0013g0077a0001c0001t0013g0099a0001c0001t0013g0104others(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 | a0001c0001t0001g0231 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0014t0001g0254a0001c0014t0005g0039a0001c0014t0023g0040 | 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 | a0003c0031t0040g0171 | 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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | a0001c0002t0017g0100a0001c0002t0017g0101 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0021g0194a0001c0002t0002g0041a0001c0002t0002g0042others(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 | a0001c0001t0013g0077 | 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 | a0003c0009t0024g0086 | 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 | a0002c0003t0006g0012a0002c0003t0006g0013 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0001c0018t0039g0005 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | 43 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(40): 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0013g0099 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0021g0194a0009c0032t0031g0102 | 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 | a0001c0001t0001g0207 | 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 | a0001c0018t0020g0244a0001c0018t0039g0005 | 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 | 165 | a0001c0001t0004g0165a0001c0001t0021g0194a0001c0002t0002g0041others(162): 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 | a0002c0028t0030g0115 | 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 | a0001c0001t0001g0156 | 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 | a0001c0027t0004g0136 | 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 | 43 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(40): 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 | a0001c0005t0007g0180 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0018t0020g0244 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | a0003c0031t0040g0171 | 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 | a0003c0031t0040g0171 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0001t0001g0207 | 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 | a0001c0018t0020g0244 | 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 | a0001c0015t0002g0119a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0004t0004g0176a0001c0004t0004g0177a0001c0027t0004g0136 | 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 | a0001c0001t0021g0194a0001c0002t0002g0041a0001c0002t0002g0042others(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 | a0002c0028t0030g0115 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0015t0002g0119a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0002t0002g0105a0001c0002t0002g0128 | 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 | a0001c0015t0002g0119a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0002t0002g0057a0001c0002t0002g0064a0001c0002t0002g0105others(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 | a0003c0031t0040g0171 | 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 | a0001c0005t0007g0180 | 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 | 60 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(57): 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 | a0001c0015t0002g0119a0002c0003t0006g0001a0002c0003t0006g0009others(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 | a0001c0002t0002g0057 | 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 | a0001c0026t0016g0082 | 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 | a0001c0001t0001g0206 | 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 | a0003c0031t0040g0171 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0002t0002g0041a0001c0002t0002g0042a0001c0002t0002g0043others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0001c0012t0021g0008 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0001t0001g0210a0001c0006t0001g0222 | 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 | a0001c0010t0001g0193 | 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 | a0003c0031t0040g0171 | 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 | a0001c0002t0003g0172a0001c0021t0003g0174a0001c0021t0003g0175 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0002t0002g0088 | 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 | a0001c0001t0013g0099 | 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 | a0001c0012t0014g0263a0001c0012t0014g0264 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0012t0021g0008 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0002t0002g0069a0001c0002t0002g0080a0001c0002t0002g0098others(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 | a0001c0001t0001g0144 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0003t0009g0109a0002c0003t0009g0110a0002c0003t0009g0111 | 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 | 61 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(58): 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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | a0001c0004t0004g0266 | 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 | a0002c0028t0030g0115 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0003c0009t0010g0089 | 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 | 31 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(28): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138 | 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 | a0001c0001t0001g0246a0001c0001t0001g0247 | 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 | a0003c0031t0040g0171 | 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 | a0001c0002t0003g0230 | 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 | a0004c0019t0018g0006a0004c0019t0018g0007 | 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 | a0001c0001t0001g0161a0001c0001t0001g0167 | 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 | a0001c0001t0021g0194a0001c0012t0014g0262a0001c0012t0014g0263others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | 30 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(27): 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0001t0021g0194a0001c0012t0014g0262a0001c0012t0014g0263others(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 | a0010c0023t0001g0026 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0035t0002g0130 | 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 | a0001c0018t0020g0244 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0028t0030g0115 | 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 | a0001c0001t0001g0206 | 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 | a0003c0031t0040g0171 | 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 | a0003c0013t0037g0137 | 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 | a0001c0002t0002g0087a0001c0002t0002g0088a0001c0002t0002g0257 | 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 | a0001c0001t0001g0140 | 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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0156others(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 | a0001c0002t0002g0097a0001c0002t0027g0118 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0004t0004g0252 | 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 | a0001c0002t0003g0215 | 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 | a0001c0018t0020g0244 | 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 | 20 | a0001c0001t0004g0165a0001c0004t0004g0003a0001c0004t0004g0004others(17): 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 | a0001c0001t0001g0202 | 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 | a0001c0002t0002g0053 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0001g0182a0001c0001t0001g0199a0001c0001t0001g0200others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0005t0007g0025 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0001t0021g0194a0001c0012t0021g0008a0009c0032t0031g0102 | 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 | a0008c0033t0002g0044 | 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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0149 | 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 | a0001c0007t0004g0243a0001c0007t0004g0255a0001c0007t0029g0125others(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 |
28 | a0001c0001t0004g0165a0001c0004t0004g0176a0001c0004t0004g0177others(25): 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 | a0001c0004t0004g0003a0001c0004t0004g0004a0001c0004t0004g0138others(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 | a0002c0016t0019g0232a0002c0016t0019g0233 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0018t0020g0244 | 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 | a0005c0022t0022g0249a0005c0022t0022g0250 | 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 | a0001c0002t0002g0064a0001c0002t0003g0019a0001c0002t0003g0185 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0006t0001g0224 | 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 | a0001c0002t0002g0080 | 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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0002t0002g0097a0001c0002t0027g0118 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 | a0001c0005t0007g0020a0001c0005t0007g0022a0001c0005t0007g0023others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0002c0011t0010g0091a0002c0011t0010g0121a0002c0011t0010g0122others(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 | a0001c0002t0003g0151a0001c0002t0003g0196a0001c0036t0002g0051 | 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 | a0002c0003t0006g0001a0002c0003t0006g0009a0002c0003t0006g0011others(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 |