Search by Gene
| geneid | 9902 |
|---|---|
| ensemblid | ENSG00000011028.14 |
| hgncid | 16875 |
| symbol | MRC2 |
| name | mannose receptor C type 2 |
| refseq_nuc | NM_006039.5 |
| refseq_prot | NP_006030.2 |
| ensembl_nuc | ENST00000303375.10 |
| ensembl_prot | ENSP00000307513.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 62627670 |
| end | 62693597 |
| strand | + |
| ver | v1.2 |
| region | chr17:62627670-62693597 |
| region5000 | chr17:62622670-62698597 |
| regionname0 | MRC2_chr17_62627670_62693597 |
| regionname5000 | MRC2_chr17_62622670_62698597 |
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 | 0/0 | 1479 | 200 | 31 | 51 | 92 | 6 | 20 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002 | 1/0 | 1479 | 57 | 37 | 6 | 7 | 0 | 6 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003 | 0/1 | 1479 | 19 | 1 | 5 | 4 | 3 | 5 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0004 | 0/0 | 1479 | 8 | 0 | 6 | 1 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0005 | 0/0 | 1479 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0007 | 0/0 | 1479 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0008 | 0/0 | 1479 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0009 | 0/0 | 1479 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0010 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0011 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0012 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0013 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0014 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0015 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0016 | 0/0 | 1456 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0017 | 0/0 | 1479 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0018 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0019 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0020 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0021 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0022 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | 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 | 0/0 | 4440 | 105 | 25 | 28 | 42 | 3 | 7 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0002 | 0/0 | 4440 | 76 | 1 | 23 | 37 | 3 | 12 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0003 | 1/0 | 4440 | 31 | 23 | 3 | 2 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0004 | 0/0 | 4440 | 13 | 0 | 3 | 4 | 2 | 4 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0005 | 0/0 | 4440 | 8 | 0 | 6 | 1 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0006 | 0/0 | 4440 | 7 | 5 | 1 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0007 | 0/0 | 4440 | 6 | 6 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0008 | 0/0 | 4440 | 6 | 0 | 0 | 6 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0009 | 0/0 | 4440 | 6 | 0 | 1 | 3 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0010 | 0/0 | 4440 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0011 | 0/1 | 4440 | 3 | 1 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0012 | 0/0 | 4440 | 3 | 0 | 1 | 0 | 1 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0013 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0014 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0015 | 0/0 | 4440 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0016 | 0/0 | 4440 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0017 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0018 | 0/0 | 4440 | 2 | 2 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0019 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0020 | 0/0 | 4440 | 2 | 1 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0021 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0022 | 0/0 | 4440 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0023 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0024 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0025 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0026 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0027 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0028 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0029 | 0/0 | 4420 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0030 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0031 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0032 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0033 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0034 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0035 | 0/0 | 4440 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0036 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0037 | 0/0 | 4440 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0038 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0039 | 0/0 | 4440 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0040 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0041 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| c0042 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | 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 | 1280 | 275 | 63 | 63 | 106 | 9 | 32 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0002 | 0/0 | 1280 | 19 | 7 | 4 | 8 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0003 | 0/0 | 1280 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0004 | 0/0 | 1280 | 4 | 3 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0005 | 0/0 | 1280 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0006 | 0/0 | 1280 | 3 | 0 | 1 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0007 | 0/0 | 1280 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0008 | 0/0 | 1280 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| t0009 | 0/0 | 1280 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | 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 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| 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 | 0/0 | 105 | 25 | 28 | 42 | 3 | 7 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 76 | 1 | 23 | 37 | 3 | 12 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0017 | a0001 | c0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0019 | a0001 | c0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0020 | a0001 | c0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0025 | a0001 | c0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0031 | a0001 | c0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0036 | a0001 | c0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0041 | a0001 | c0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0003 | a0002 | c0003 | 1/0 | 31 | 23 | 3 | 2 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0006 | a0002 | c0006 | 0/0 | 7 | 5 | 1 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0007 | a0002 | c0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0009 | a0002 | c0009 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0015 | a0002 | c0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0021 | a0002 | c0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0034 | a0002 | c0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0039 | a0002 | c0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 13 | 0 | 3 | 4 | 2 | 4 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0011 | a0003 | c0011 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0012 | a0003 | c0012 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 8 | 0 | 6 | 1 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0005c0010 | a0005 | c0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006c0018 | a0006 | c0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006c0026 | a0006 | c0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0007c0014 | a0007 | c0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0008c0016 | a0008 | c0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0009c0022 | a0009 | c0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0010c0023 | a0010 | c0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0011c0042 | a0011 | c0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0012c0035 | a0012 | c0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0013c0027 | a0013 | c0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0014c0038 | a0014 | c0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0015c0028 | a0015 | c0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0016c0029 | a0016 | c0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0017c0032 | a0017 | c0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0018c0033 | a0018 | c0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0019c0030 | a0019 | c0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0020c0040 | a0020 | c0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0021c0037 | a0021 | c0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0022c0024 | a0022 | c0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | 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 | 0/0 | 97 | 21 | 26 | 40 | 3 | 7 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 66 | 1 | 20 | 30 | 3 | 12 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0017t0001 | a0001 | c0017 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0019t0001 | a0001 | c0019 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0025t0001 | a0001 | c0025 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0031t0001 | a0001 | c0031 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0036t0001 | a0001 | c0036 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0001c0041t0001 | a0001 | c0041 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 1/0 | 31 | 23 | 3 | 2 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0006t0001 | a0002 | c0006 | t0001 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0006t0002 | a0002 | c0006 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0006t0004 | a0002 | c0006 | t0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0007t0001 | a0002 | c0007 | t0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0009t0001 | a0002 | c0009 | t0001 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0015t0002 | a0002 | c0015 | t0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0021t0001 | a0002 | c0021 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0034t0002 | a0002 | c0034 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0002c0039t0001 | a0002 | c0039 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 13 | 0 | 3 | 4 | 2 | 4 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0011t0001 | a0003 | c0011 | t0001 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0003c0012t0001 | a0003 | c0012 | t0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0004c0005t0001 | a0004 | c0005 | t0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0004c0005t0008 | a0004 | c0005 | t0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0005c0010t0001 | a0005 | c0010 | t0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006c0018t0002 | a0006 | c0018 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006c0018t0009 | a0006 | c0018 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0006c0026t0002 | a0006 | c0026 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0007c0014t0005 | a0007 | c0014 | t0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0008c0016t0001 | a0008 | c0016 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0009c0022t0001 | a0009 | c0022 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0010c0023t0001 | a0010 | c0023 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0011c0042t0001 | a0011 | c0042 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0012c0035t0001 | a0012 | c0035 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0013c0027t0001 | a0013 | c0027 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0014c0038t0001 | a0014 | c0038 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0015c0028t0002 | a0015 | c0028 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0016c0029t0002 | a0016 | c0029 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0017c0032t0001 | a0017 | c0032 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0018c0033t0001 | a0018 | c0033 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0019c0030t0001 | a0019 | c0030 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0020c0040t0001 | a0020 | c0040 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0021c0037t0001 | a0021 | c0037 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | copy fasta |
| a0022c0024t0005 | a0022 | c0024 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0278 | a0001 | c0001 | t0001 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0279 | a0001 | c0001 | t0001 | g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0281 | a0001 | c0001 | t0001 | g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0283 | a0001 | c0001 | t0001 | g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0288 | a0001 | c0001 | t0001 | g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0295 | a0001 | c0001 | t0001 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0298 | a0001 | c0001 | t0001 | g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0299 | a0001 | c0001 | t0001 | g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0304 | a0001 | c0001 | t0001 | g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0305 | a0001 | c0001 | t0001 | g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0308 | a0001 | c0001 | t0001 | g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0001g0309 | a0001 | c0001 | t0001 | g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0003g0009 | a0001 | c0001 | t0003 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0003g0014 | a0001 | c0001 | t0003 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0003g0037 | a0001 | c0001 | t0003 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0006g0163 | a0001 | c0001 | t0006 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0006g0195 | a0001 | c0001 | t0006 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0006g0205 | a0001 | c0001 | t0006 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0001t0007g0224 | a0001 | c0001 | t0007 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0004 | a0001 | c0002 | t0001 | g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0005 | a0001 | c0002 | t0001 | g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0041 | a0001 | c0002 | t0001 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0042 | a0001 | c0002 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0047 | a0001 | c0002 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0051 | a0001 | c0002 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0055 | a0001 | c0002 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0057 | a0001 | c0002 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0061 | a0001 | c0002 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0064 | a0001 | c0002 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0065 | a0001 | c0002 | t0001 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0074 | a0001 | c0002 | t0001 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0076 | a0001 | c0002 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0078 | a0001 | c0002 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0079 | a0001 | c0002 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0082 | a0001 | c0002 | t0001 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0085 | a0001 | c0002 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0086 | a0001 | c0002 | t0001 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0087 | a0001 | c0002 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0089 | a0001 | c0002 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0090 | a0001 | c0002 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0091 | a0001 | c0002 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0092 | a0001 | c0002 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0093 | a0001 | c0002 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0094 | a0001 | c0002 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0095 | a0001 | c0002 | t0001 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0100 | a0001 | c0002 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0101 | a0001 | c0002 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0102 | a0001 | c0002 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0104 | a0001 | c0002 | t0001 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0105 | a0001 | c0002 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0141 | a0001 | c0002 | t0001 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0142 | a0001 | c0002 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0146 | a0001 | c0002 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0151 | a0001 | c0002 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0153 | a0001 | c0002 | t0001 | g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0158 | a0001 | c0002 | t0001 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0176 | a0001 | c0002 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0186 | a0001 | c0002 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0187 | a0001 | c0002 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0220 | a0001 | c0002 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0235 | a0001 | c0002 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0237 | a0001 | c0002 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0238 | a0001 | c0002 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0240 | a0001 | c0002 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0241 | a0001 | c0002 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0243 | a0001 | c0002 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0245 | a0001 | c0002 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0248 | a0001 | c0002 | t0001 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0249 | a0001 | c0002 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0252 | a0001 | c0002 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0253 | a0001 | c0002 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0254 | a0001 | c0002 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0255 | a0001 | c0002 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0256 | a0001 | c0002 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0257 | a0001 | c0002 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0260 | a0001 | c0002 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0261 | a0001 | c0002 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0266 | a0001 | c0002 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0268 | a0001 | c0002 | t0001 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0285 | a0001 | c0002 | t0001 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0289 | a0001 | c0002 | t0001 | g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0290 | a0001 | c0002 | t0001 | g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0001g0310 | a0001 | c0002 | t0001 | g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0083 | a0001 | c0002 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0160 | a0001 | c0002 | t0002 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0172 | a0001 | c0002 | t0002 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0239 | a0001 | c0002 | t0002 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0242 | a0001 | c0002 | t0002 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0259 | a0001 | c0002 | t0002 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0263 | a0001 | c0002 | t0002 | g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0267 | a0001 | c0002 | t0002 | g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0273 | a0001 | c0002 | t0002 | g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0002t0002g0275 | a0001 | c0002 | t0002 | g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0040 | a0001 | c0008 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0208 | a0001 | c0008 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0222 | a0001 | c0008 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0223 | a0001 | c0008 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0225 | a0001 | c0008 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0008t0001g0284 | a0001 | c0008 | t0001 | g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0013t0001g0043 | a0001 | c0013 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0013t0001g0098 | a0001 | c0013 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0013t0001g0099 | a0001 | c0013 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0017t0001g0106 | a0001 | c0017 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0017t0001g0307 | a0001 | c0017 | t0001 | g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0019t0001g0038 | a0001 | c0019 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0019t0001g0048 | a0001 | c0019 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0020t0001g0066 | a0001 | c0020 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0020t0001g0302 | a0001 | c0020 | t0001 | g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0025t0001g0164 | a0001 | c0025 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0031t0001g0156 | a0001 | c0031 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0036t0001g0297 | a0001 | c0036 | t0001 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0001c0041t0001g0287 | a0001 | c0041 | t0001 | g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0006 | a0002 | c0003 | t0001 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0015 | a0002 | c0003 | t0001 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0018 | a0002 | c0003 | t0001 | g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0019 | a0002 | c0003 | t0001 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0020 | a0002 | c0003 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0021 | a0002 | c0003 | t0001 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0022 | a0002 | c0003 | t0001 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0023 | a0002 | c0003 | t0001 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0024 | a0002 | c0003 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0025 | a0002 | c0003 | t0001 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0052 | a0002 | c0003 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0072 | a0002 | c0003 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0108 | a0002 | c0003 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0110 | a0002 | c0003 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0111 | a0002 | c0003 | t0001 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0113 | a0002 | c0003 | t0001 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0114 | a0002 | c0003 | t0001 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0115 | a0002 | c0003 | t0001 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0117 | a0002 | c0003 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0118 | a0002 | c0003 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0120 | a0002 | c0003 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0130 | a0002 | c0003 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0133 | a0002 | c0003 | t0001 | g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0138 | a0002 | c0003 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0139 | a0002 | c0003 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0140 | a0002 | c0003 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0154 | a0002 | c0003 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0155 | a0002 | c0003 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0231 | a0002 | c0003 | t0001 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0303 | a0002 | c0003 | t0001 | g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0003t0001g0311 | a0002 | c0003 | t0001 | g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0001g0135 | a0002 | c0006 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0001g0258 | a0002 | c0006 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0002g0152 | a0002 | c0006 | t0002 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0004g0007 | a0002 | c0006 | t0004 | g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0004g0012 | a0002 | c0006 | t0004 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0004g0109 | a0002 | c0006 | t0004 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0006t0004g0147 | a0002 | c0006 | t0004 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0035 | a0002 | c0007 | t0001 | g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0119 | a0002 | c0007 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0192 | a0002 | c0007 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0193 | a0002 | c0007 | t0001 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0229 | a0002 | c0007 | t0001 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0007t0001g0282 | a0002 | c0007 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0026 | a0002 | c0009 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0027 | a0002 | c0009 | t0001 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0062 | a0002 | c0009 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0088 | a0002 | c0009 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0179 | a0002 | c0009 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0009t0001g0277 | a0002 | c0009 | t0001 | g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0015t0002g0010 | a0002 | c0015 | t0002 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0015t0002g0017 | a0002 | c0015 | t0002 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0015t0002g0230 | a0002 | c0015 | t0002 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0021t0001g0276 | a0002 | c0021 | t0001 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0021t0001g0280 | a0002 | c0021 | t0001 | g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0034t0002g0150 | a0002 | c0034 | t0002 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0002c0039t0001g0028 | a0002 | c0039 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0053 | a0003 | c0004 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0126 | a0003 | c0004 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0157 | a0003 | c0004 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0167 | a0003 | c0004 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0171 | a0003 | c0004 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0207 | a0003 | c0004 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0215 | a0003 | c0004 | t0001 | g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0217 | a0003 | c0004 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0219 | a0003 | c0004 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0227 | a0003 | c0004 | t0001 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0228 | a0003 | c0004 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0292 | a0003 | c0004 | t0001 | g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0004t0001g0296 | a0003 | c0004 | t0001 | g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0011t0001g0214 | a0003 | c0011 | t0001 | g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0011t0001g0221 | a0003 | c0011 | t0001 | g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0011t0001g0291 | a0003 | c0011 | t0001 | g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0012t0001g0070 | a0003 | c0012 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0012t0001g0071 | a0003 | c0012 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0003c0012t0001g0182 | a0003 | c0012 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0039 | a0004 | c0005 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0045 | a0004 | c0005 | t0001 | g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0046 | a0004 | c0005 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0056 | a0004 | c0005 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0081 | a0004 | c0005 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0236 | a0004 | c0005 | t0001 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0001g0274 | a0004 | c0005 | t0001 | g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0004c0005t0008g0054 | a0004 | c0005 | t0008 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0005c0010t0001g0161 | a0005 | c0010 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0005c0010t0001g0246 | a0005 | c0010 | t0001 | g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0005c0010t0001g0270 | a0005 | c0010 | t0001 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0005c0010t0001g0272 | a0005 | c0010 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0006c0018t0002g0306 | a0006 | c0018 | t0002 | g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0006c0018t0009g0013 | a0006 | c0018 | t0009 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0006c0026t0002g0271 | a0006 | c0026 | t0002 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0007c0014t0005g0030 | a0007 | c0014 | t0005 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0007c0014t0005g0031 | a0007 | c0014 | t0005 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0007c0014t0005g0127 | a0007 | c0014 | t0005 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0008c0016t0001g0165 | a0008 | c0016 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0008c0016t0001g0293 | a0008 | c0016 | t0001 | g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0008c0016t0001g0300 | a0008 | c0016 | t0001 | g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0009c0022t0001g0218 | a0009 | c0022 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0009c0022t0001g0234 | a0009 | c0022 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0010c0023t0001g0097 | a0010 | c0023 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0011c0042t0001g0159 | a0011 | c0042 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0012c0035t0001g0036 | a0012 | c0035 | t0001 | g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0013c0027t0001g0044 | a0013 | c0027 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0014c0038t0001g0206 | a0014 | c0038 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0015c0028t0002g0262 | a0015 | c0028 | t0002 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0016c0029t0002g0016 | a0016 | c0029 | t0002 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0017c0032t0001g0265 | a0017 | c0032 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0018c0033t0001g0134 | a0018 | c0033 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0019c0030t0001g0244 | a0019 | c0030 | t0001 | g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0020c0040t0001g0032 | a0020 | c0040 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0021c0037t0001g0049 | a0021 | c0037 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| a0022c0024t0005g0301 | a0022 | c0024 | t0005 | g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRC2_chr17_62622670_62698597 | MRC2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0012 | t0001 | g0071 | EUR | GBR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00140 | hp2 | a0003 | c0004 | t0001 | g0228 | EUR | GBR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00280 | hp1 | a0004 | c0005 | t0008 | g0054 | EUR | FIN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00438 | hp1 | a0002 | c0009 | t0001 | g0027 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0130 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | CHS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0227 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0110 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0113 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01074 | hp1 | a0004 | c0005 | t0001 | g0056 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01081 | hp2 | a0003 | c0012 | t0001 | g0070 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01167 | hp1 | a0019 | c0030 | t0001 | g0244 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01168 | hp1 | a0002 | c0009 | t0001 | g0179 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01243 | hp1 | a0002 | c0034 | t0002 | g0150 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01258 | hp1 | a0003 | c0011 | t0001 | g0221 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0224 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01433 | hp1 | a0021 | c0037 | t0001 | g0049 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01496 | hp2 | a0003 | c0004 | t0001 | g0215 | AMR | CLM | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01515 | hp1 | a0003 | c0004 | t0001 | g0171 | EUR | IBS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0051 | EUR | IBS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0087 | EUR | IBS | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01884 | hp1 | a0006 | c0026 | t0002 | g0271 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01891 | hp1 | a0002 | c0006 | t0004 | g0109 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01928 | hp1 | a0004 | c0005 | t0001 | g0046 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01943 | hp2 | a0004 | c0005 | t0001 | g0236 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01952 | hp2 | a0002 | c0006 | t0004 | g0007 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0292 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0273 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02004 | hp1 | a0004 | c0005 | t0001 | g0081 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02040 | hp1 | a0002 | c0021 | t0001 | g0280 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02055 | hp1 | a0001 | c0025 | t0001 | g0164 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02055 | hp2 | a0007 | c0014 | t0005 | g0031 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02074 | hp1 | a0001 | c0008 | t0001 | g0208 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02083 | hp2 | a0001 | c0008 | t0001 | g0040 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02129 | hp2 | a0001 | c0008 | t0001 | g0284 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02135 | hp1 | a0001 | c0041 | t0001 | g0287 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0163 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02155 | hp1 | a0001 | c0008 | t0001 | g0223 | EAS | CDX | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02155 | hp2 | a0002 | c0021 | t0001 | g0276 | EAS | CDX | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02165 | hp1 | a0013 | c0027 | t0001 | g0044 | EAS | CDX | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0114 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02273 | hp2 | a0004 | c0005 | t0001 | g0045 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02280 | hp1 | a0005 | c0010 | t0001 | g0161 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02293 | hp1 | a0004 | c0005 | t0001 | g0274 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02451 | hp1 | a0002 | c0006 | t0002 | g0152 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02602 | hp2 | a0017 | c0032 | t0001 | g0265 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02615 | hp2 | a0001 | c0017 | t0001 | g0106 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02622 | hp2 | a0001 | c0020 | t0001 | g0302 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02683 | hp1 | a0003 | c0004 | t0001 | g0217 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0115 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02723 | hp1 | a0005 | c0010 | t0001 | g0246 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02723 | hp2 | a0002 | c0007 | t0001 | g0229 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0157 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02738 | hp2 | a0002 | c0039 | t0001 | g0028 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02809 | hp1 | a0006 | c0018 | t0009 | g0013 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0111 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0154 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02896 | hp2 | a0005 | c0010 | t0001 | g0270 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0155 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02897 | hp2 | a0016 | c0029 | t0002 | g0016 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0120 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02922 | hp2 | a0002 | c0007 | t0001 | g0192 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02965 | hp2 | a0002 | c0007 | t0001 | g0035 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0140 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03041 | hp2 | a0007 | c0014 | t0005 | g0127 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0303 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03130 | hp2 | a0002 | c0015 | t0002 | g0010 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0231 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03195 | hp1 | a0002 | c0006 | t0004 | g0147 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03195 | hp2 | a0005 | c0010 | t0001 | g0272 | AFR | ESN | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0023 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0117 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03225 | hp1 | a0022 | c0024 | t0005 | g0301 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03225 | hp2 | a0002 | c0006 | t0004 | g0012 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03239 | hp2 | a0003 | c0004 | t0001 | g0296 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03453 | hp1 | a0001 | c0017 | t0001 | g0307 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0022 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03486 | hp2 | a0002 | c0007 | t0001 | g0119 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03492 | hp1 | a0002 | c0009 | t0001 | g0277 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0138 | AFR | GWD | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03579 | hp1 | a0002 | c0007 | t0001 | g0193 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0118 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03654 | hp2 | a0003 | c0004 | t0001 | g0126 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03669 | hp1 | a0001 | c0020 | t0001 | g0066 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03669 | hp2 | a0002 | c0009 | t0001 | g0026 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03834 | hp1 | a0002 | c0006 | t0001 | g0258 | SAS | BEB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0261 | SAS | BEB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0266 | SAS | BEB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03942 | hp2 | a0003 | c0012 | t0001 | g0182 | SAS | BEB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | MRC2_chr17_62622670_62698597 | MRC2 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | STU | MRC2_chr17_62622670_62698597 | MRC2 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0052 | SAS | STU | MRC2_chr17_62622670_62698597 | MRC2 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | STU | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | CHB | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18906 | hp1 | a0006 | c0018 | t0002 | g0306 | AFR | YRI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18906 | hp2 | a0002 | c0006 | t0001 | g0135 | AFR | YRI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18942 | hp1 | a0003 | c0004 | t0001 | g0207 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18948 | hp1 | a0001 | c0013 | t0001 | g0098 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18952 | hp2 | a0003 | c0004 | t0001 | g0219 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18957 | hp1 | a0018 | c0033 | t0001 | g0134 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18957 | hp2 | a0009 | c0022 | t0001 | g0218 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0167 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18963 | hp1 | a0003 | c0004 | t0001 | g0053 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18965 | hp2 | a0020 | c0040 | t0001 | g0032 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18966 | hp2 | a0001 | c0013 | t0001 | g0099 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18973 | hp2 | a0008 | c0016 | t0001 | g0165 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18974 | hp1 | a0001 | c0013 | t0001 | g0043 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18977 | hp2 | a0008 | c0016 | t0001 | g0300 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18983 | hp2 | a0001 | c0036 | t0001 | g0297 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18984 | hp2 | a0001 | c0008 | t0001 | g0222 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18992 | hp1 | a0001 | c0019 | t0001 | g0038 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18994 | hp2 | a0008 | c0016 | t0001 | g0293 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19000 | hp2 | a0004 | c0005 | t0001 | g0039 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19004 | hp2 | a0009 | c0022 | t0001 | g0234 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19005 | hp1 | a0002 | c0009 | t0001 | g0062 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0108 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19030 | hp2 | a0001 | c0031 | t0001 | g0156 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19074 | hp2 | a0010 | c0023 | t0001 | g0097 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19079 | hp2 | a0002 | c0009 | t0001 | g0088 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19085 | hp1 | a0001 | c0008 | t0001 | g0225 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19085 | hp2 | a0015 | c0028 | t0002 | g0262 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19086 | hp1 | a0011 | c0042 | t0001 | g0159 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19088 | hp1 | a0014 | c0038 | t0001 | g0206 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19090 | hp1 | a0001 | c0019 | t0001 | g0048 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | YRI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | ASW | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0102 | EUR | TSI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0072 | SAS | GIH | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02109 | hp1 | a0002 | c0015 | t0002 | g0017 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02486 | hp1 | a0012 | c0035 | t0001 | g0036 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG02486 | hp2 | a0002 | c0015 | t0002 | g0230 | AFR | ACB | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG03471 | hp2 | a0007 | c0014 | t0005 | g0030 | AFR | MSL | MRC2_chr17_62622670_62698597 | MRC2 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | USA | MRC2_chr17_62622670_62698597 | MRC2 |
| HG06807 | hp2 | a0003 | c0011 | t0001 | g0291 | AFR | USA | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20300 | hp1 | a0002 | c0007 | t0001 | g0282 | AFR | USA | MRC2_chr17_62622670_62698597 | MRC2 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | MRC2_chr17_62622670_62698597 | MRC2 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | MRC2_chr17_62622670_62698597 | MRC2 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0011 | t0001 | g0214 | REF | REF | MRC2_chr17_62622670_62698597 | MRC2 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0133 | REF | REF | MRC2_chr17_62622670_62698597 | MRC2 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62664556
|
G | A | 2 | a0003a0010 | 20 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(17): Show |
missense_variant | MODERATE | c.127G>A | p.Val43Ile | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/30 | 260/5719 | 127/4440 | 43/1479 | chr17 | 62664556 | ||
| chr17:62664626
|
C | T | 1 | a0011 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.197C>T | p.Pro66Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/30 | 330/5719 | 197/4440 | 66/1479 | chr17 | 62664626 | ||
| chr17:62664893
|
G | C | 1 | a0022 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.464G>C | p.Ser155Thr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/30 | 597/5719 | 464/4440 | 155/1479 | chr17 | 62664893 | ||
| chr17:62664946
|
C | T | 1 | a0021 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.517C>T | p.His173Tyr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/30 | 650/5719 | 517/4440 | 173/1479 | chr17 | 62664946 | ||
| chr17:62671678
|
G | A | 1 | a0009 | 2 | NA18957.hp2 NA19004.hp2 |
missense_variant | MODERATE | c.1147G>A | p.Glu383Lys | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 7/30 | 1280/5719 | 1147/4440 | 383/1479 | chr17 | 62671678 | ||
| chr17:62672151
|
C | T | 1 | a0012 | 1 | HG02486.hp1 | missense_variant&splice_region_variant | MODERATE | c.1460C>T | p.Pro487Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/30 | 1593/5719 | 1460/4440 | 487/1479 | chr17 | 62672151 | ||
| chr17:62676394
|
C | G | 1 | a0020 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.1697C>G | p.Ala566Gly | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/30 | 1830/5719 | 1697/4440 | 566/1479 | chr17 | 62676394 | ||
| chr17:62680935
|
A | C | 1 | a0004 | 8 | HG00280.hp1 HG01074.hp1 HG01928.hp1 others(5): Show |
missense_variant | MODERATE | c.2609A>C | p.Asp870Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 17/30 | 2742/5719 | 2609/4440 | 870/1479 | chr17 | 62680935 | ||
| chr17:62688311
|
A | G | 1 | a0019 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.2969A>G | p.Glu990Gly | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 21/30 | 3102/5719 | 2969/4440 | 990/1479 | chr17 | 62688311 | ||
| chr17:62688862
|
C | T | 1 | a0008 | 3 | NA18973.hp2 NA18977.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.3236C>T | p.Ala1079Val | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/30 | 3369/5719 | 3236/4440 | 1079/1479 | chr17 | 62688862 | ||
| chr17:62688922
|
C | T | 1 | a0010 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.3296C>T | p.Thr1099Met | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/30 | 3429/5719 | 3296/4440 | 1099/1479 | chr17 | 62688922 | ||
| chr17:62689536
|
C | G | 1 | a0005 | 4 | HG02280.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.3349C>G | p.Pro1117Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/30 | 3482/5719 | 3349/4440 | 1117/1479 | chr17 | 62689536 | ||
| chr17:62689560
|
G | C | 1 | a0018 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.3373G>C | p.Ala1125Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/30 | 3506/5719 | 3373/4440 | 1125/1479 | chr17 | 62689560 | ||
| chr17:62689654
|
G | A | 14 | a0001a0003a0004others(11): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
missense_variant | MODERATE | c.3467G>A | p.Arg1156His | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/30 | 3600/5719 | 3467/4440 | 1156/1479 | chr17 | 62689654 | ||
| chr17:62689942
|
G | A | 1 | a0006 | 3 | HG01884.hp1 HG02809.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.3622G>A | p.Gly1208Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 25/30 | 3755/5719 | 3622/4440 | 1208/1479 | chr17 | 62689942 | ||
| chr17:62690186
|
A | T | 1 | a0015 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.3773A>T | p.His1258Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/30 | 3906/5719 | 3773/4440 | 1258/1479 | chr17 | 62690186 | ||
| chr17:62690642
|
C | T | 1 | a0014 | 1 | NA19088.hp1 | missense_variant&splice_region_variant | MODERATE | c.3893C>T | p.Ala1298Val | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 27/30 | 4026/5719 | 3893/4440 | 1298/1479 | chr17 | 62690642 | ||
| chr17:62692240
|
A | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4229A>C | p.Glu1410Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4362/5719 | 4229/4440 | 1410/1479 | chr17 | 62692240 | ||
| chr17:62692242
|
A | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4231A>T | p.Asn1411Tyr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4364/5719 | 4231/4440 | 1411/1479 | chr17 | 62692242 | ||
| chr17:62692243
|
A | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4232A>G | p.Asn1411Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4365/5719 | 4232/4440 | 1411/1479 | chr17 | 62692243 | ||
| chr17:62692246
|
C | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4235C>A | p.Pro1412Gln | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4368/5719 | 4235/4440 | 1412/1479 | chr17 | 62692246 | ||
| chr17:62692249
|
C | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4238C>G | p.Ala1413Gly | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4371/5719 | 4238/4440 | 1413/1479 | chr17 | 62692249 | ||
| chr17:62692252
|
C | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4241C>A | p.Ala1414Asp | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4374/5719 | 4241/4440 | 1414/1479 | chr17 | 62692252 | ||
| chr17:62692260
|
G | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4249G>A | p.Val1417Met | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4382/5719 | 4249/4440 | 1417/1479 | chr17 | 62692260 | ||
| chr17:62692261
|
T | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4250T>A | p.Val1417Glu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4383/5719 | 4250/4440 | 1417/1479 | chr17 | 62692261 | ||
| chr17:62692264
|
T | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4253T>C | p.Val1418Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4386/5719 | 4253/4440 | 1418/1479 | chr17 | 62692264 | ||
| chr17:62692267
|
T | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4256T>A | p.Leu1419Gln | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4389/5719 | 4256/4440 | 1419/1479 | chr17 | 62692267 | ||
| chr17:62692269
|
A | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4258A>T | p.Met1420Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4391/5719 | 4258/4440 | 1420/1479 | chr17 | 62692269 | ||
| chr17:62692270
|
T | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4259T>G | p.Met1420Arg | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4392/5719 | 4259/4440 | 1420/1479 | chr17 | 62692270 | ||
| chr17:62692275
|
G | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4264G>T | p.Val1422Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4397/5719 | 4264/4440 | 1422/1479 | chr17 | 62692275 | ||
| chr17:62692279
|
T | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4268T>A | p.Leu1423Gln | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4401/5719 | 4268/4440 | 1423/1479 | chr17 | 62692279 | ||
| chr17:62692294
|
T | A | 1 | a0016 | 1 | HG02897.hp2 | stop_gained | HIGH | c.4283T>A | p.Leu1428* | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4416/5719 | 4283/4440 | 1428/1479 | chr17 | 62692294 | ||
| chr17:62692295
|
G | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4284G>C | p.Leu1428Phe | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4417/5719 | 4284/4440 | 1428/1479 | chr17 | 62692295 | ||
| chr17:62692299
|
A | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4288A>G | p.Thr1430Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4421/5719 | 4288/4440 | 1430/1479 | chr17 | 62692299 | ||
| chr17:62692300
|
C | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4289C>G | p.Thr1430Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4422/5719 | 4289/4440 | 1430/1479 | chr17 | 62692300 | ||
| chr17:62692302
|
G | A | 2 | a0007a0022 | 4 | HG02055.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.4291G>A | p.Ala1431Thr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4424/5719 | 4291/4440 | 1431/1479 | chr17 | 62692302 | ||
| chr17:62692311
|
A | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4300A>T | p.Ile1434Phe | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4433/5719 | 4300/4440 | 1434/1479 | chr17 | 62692311 | ||
| chr17:62692314
|
C | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4303C>A | p.Leu1435Ile | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4436/5719 | 4303/4440 | 1435/1479 | chr17 | 62692314 | ||
| chr17:62692315
|
T | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4304T>C | p.Leu1435Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4437/5719 | 4304/4440 | 1435/1479 | chr17 | 62692315 | ||
| chr17:62692317
|
T | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4306T>C | p.Tyr1436His | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4439/5719 | 4306/4440 | 1436/1479 | chr17 | 62692317 | ||
| chr17:62692321
|
G | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4310G>T | p.Arg1437Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4443/5719 | 4310/4440 | 1437/1479 | chr17 | 62692321 | ||
| chr17:62692324
|
G | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4313G>T | p.Arg1438Met | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4446/5719 | 4313/4440 | 1438/1479 | chr17 | 62692324 | ||
| chr17:62692329
|
C | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4318C>G | p.Gln1440Glu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4451/5719 | 4318/4440 | 1440/1479 | chr17 | 62692329 | ||
| chr17:62692335
|
ATCGAGCG others(13): Show |
A | 1 | a0016 | 1 | HG02897.hp2 | frameshift_variant | HIGH | c.4325_4344delTCGAGC others(14): Show |
p.Ile1442fs | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4458/5719 | 4325/4440 | 1442/1479 | chr17 | 62692335 | ||
| chr17:62692344
|
G | A | 1 | a0017 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.4333G>A | p.Gly1445Arg | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4466/5719 | 4333/4440 | 1445/1479 | chr17 | 62692344 | ||
| chr17:62692357
|
G | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4346G>C | p.Gly1449Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4479/5719 | 4346/4440 | 1449/1479 | chr17 | 62692357 | ||
| chr17:62692362
|
C | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4351C>T | p.Arg1451Cys | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4484/5719 | 4351/4440 | 1451/1479 | chr17 | 62692362 | ||
| chr17:62692365
|
T | C | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4354T>C | p.Tyr1452His | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4487/5719 | 4354/4440 | 1452/1479 | chr17 | 62692365 | ||
| chr17:62692366
|
A | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4355A>T | p.Tyr1452Phe | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4488/5719 | 4355/4440 | 1452/1479 | chr17 | 62692366 | ||
| chr17:62692371
|
C | T | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4360C>T | p.Arg1454Cys | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4493/5719 | 4360/4440 | 1454/1479 | chr17 | 62692371 | ||
| chr17:62692374
|
A | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4363A>G | p.Ser1455Gly | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4496/5719 | 4363/4440 | 1455/1479 | chr17 | 62692374 | ||
| chr17:62692378
|
G | T | 1 | a0013 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.4367G>T | p.Ser1456Ile | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4500/5719 | 4367/4440 | 1456/1479 | chr17 | 62692378 | ||
| chr17:62692380
|
T | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4369T>A | p.Ser1457Thr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4502/5719 | 4369/4440 | 1457/1479 | chr17 | 62692380 | ||
| chr17:62692381
|
C | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4370C>A | p.Ser1457Tyr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4503/5719 | 4370/4440 | 1457/1479 | chr17 | 62692381 | ||
| chr17:62692386
|
C | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4375C>G | p.Pro1459Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4508/5719 | 4375/4440 | 1459/1479 | chr17 | 62692386 | ||
| chr17:62692387
|
C | A | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4376C>A | p.Pro1459His | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4509/5719 | 4376/4440 | 1459/1479 | chr17 | 62692387 | ||
| chr17:62692389
|
A | G | 1 | a0016 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.4378A>G | p.Thr1460Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4511/5719 | 4378/4440 | 1460/1479 | chr17 | 62692389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62664918
|
C | T | 7 | a0001c0008a0001c0041a0002c0009others(4): Show | 18 | HG00438.hp1 HG01168.hp1 HG02074.hp1 others(15): Show |
synonymous_variant | LOW | c.489C>T | p.Ser163Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/30 | 622/5719 | 489/4440 | 163/1479 | chr17 | 62664918 | ||
| chr17:62666143
|
C | T | 1 | a0001c0036 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.570C>T | p.Pro190Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 3/30 | 703/5719 | 570/4440 | 190/1479 | chr17 | 62666143 | ||
| chr17:62671725
|
C | T | 1 | a0002c0021 | 2 | HG02040.hp1 HG02155.hp2 |
synonymous_variant | LOW | c.1194C>T | p.Ala398Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 7/30 | 1327/5719 | 1194/4440 | 398/1479 | chr17 | 62671725 | ||
| chr17:62671776
|
C | G | 1 | a0001c0041 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1245C>G | p.Gly415Gly | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 7/30 | 1378/5719 | 1245/4440 | 415/1479 | chr17 | 62671776 | ||
| chr17:62671803
|
G | A | 1 | a0001c0017 | 2 | HG02615.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1272G>A | p.Ala424Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 7/30 | 1405/5719 | 1272/4440 | 424/1479 | chr17 | 62671803 | ||
| chr17:62672011
|
G | A | 1 | a0001c0025 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1320G>A | p.Leu440Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/30 | 1453/5719 | 1320/4440 | 440/1479 | chr17 | 62672011 | ||
| chr17:62675798
|
G | A | 2 | a0005c0010a0006c0026 | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
synonymous_variant | LOW | c.1578G>A | p.Thr526Thr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 10/30 | 1711/5719 | 1578/4440 | 526/1479 | chr17 | 62675798 | ||
| chr17:62680912
|
G | C | 29 | a0001c0001a0001c0002a0001c0008others(26): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
synonymous_variant | LOW | c.2586G>C | p.Ser862Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 17/30 | 2719/5719 | 2586/4440 | 862/1479 | chr17 | 62680912 | ||
| chr17:62688863
|
A | G | 33 | a0001c0001a0001c0002a0001c0008others(30): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
synonymous_variant | LOW | c.3237A>G | p.Ala1079Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/30 | 3370/5719 | 3237/4440 | 1079/1479 | chr17 | 62688863 | ||
| chr17:62688908
|
C | T | 1 | a0003c0012 | 3 | HG00140.hp1 HG01081.hp2 HG03942.hp2 |
synonymous_variant | LOW | c.3282C>T | p.Asp1094Asp | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/30 | 3415/5719 | 3282/4440 | 1094/1479 | chr17 | 62688908 | ||
| chr17:62689526
|
C | T | 1 | a0001c0019 | 2 | NA18992.hp1 NA19090.hp1 |
synonymous_variant | LOW | c.3339C>T | p.Pro1113Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/30 | 3472/5719 | 3339/4440 | 1113/1479 | chr17 | 62689526 | ||
| chr17:62689559
|
C | G | 1 | a0018c0033 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.3372C>G | p.Pro1124Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/30 | 3505/5719 | 3372/4440 | 1124/1479 | chr17 | 62689559 | ||
| chr17:62692250
|
G | C | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4239G>C | p.Ala1413Ala | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4372/5719 | 4239/4440 | 1413/1479 | chr17 | 62692250 | ||
| chr17:62692265
|
G | C | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4254G>C | p.Val1418Val | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4387/5719 | 4254/4440 | 1418/1479 | chr17 | 62692265 | ||
| chr17:62692293
|
T | C | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4282T>C | p.Leu1428Leu | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4415/5719 | 4282/4440 | 1428/1479 | chr17 | 62692293 | ||
| chr17:62692301
|
C | G | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4290C>G | p.Thr1430Thr | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4423/5719 | 4290/4440 | 1430/1479 | chr17 | 62692301 | ||
| chr17:62692373
|
C | T | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4362C>T | p.Arg1454Arg | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4495/5719 | 4362/4440 | 1454/1479 | chr17 | 62692373 | ||
| chr17:62692382
|
C | G | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4371C>G | p.Ser1457Ser | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4504/5719 | 4371/4440 | 1457/1479 | chr17 | 62692382 | ||
| chr17:62692388
|
C | G | 1 | a0016c0029 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.4377C>G | p.Pro1459Pro | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4510/5719 | 4377/4440 | 1459/1479 | chr17 | 62692388 | ||
| chr17:62692442
|
A | G | 15 | a0001c0002a0001c0013a0001c0017others(12): Show | 108 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(105): Show |
synonymous_variant | LOW | c.4431A>G | p.Gln1477Gln | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 4564/5719 | 4431/4440 | 1477/1479 | chr17 | 62692442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62692580
|
G | A | 1 | a0001c0001t0003 | 4 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 129 | chr17 | 62692580 | |||||
| chr17:62692582
|
C | T | 2 | a0007c0014t0005a0022c0024t0005 | 4 | HG02055.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*131C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 131 | chr17 | 62692582 | |||||
| chr17:62692681
|
G | T | 1 | a0002c0006t0004 | 4 | HG01891.hp1 HG01952.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*230G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 230 | chr17 | 62692681 | |||||
| chr17:62692709
|
C | T | 2 | a0002c0006t0004a0006c0018t0009 | 5 | HG01891.hp1 HG01952.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*258C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 258 | chr17 | 62692709 | |||||
| chr17:62692959
|
T | C | 1 | a0001c0001t0006 | 3 | HG02040.hp2 HG02148.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*508T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 508 | chr17 | 62692959 | |||||
| chr17:62693189
|
C | T | 1 | a0004c0005t0008 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 738 | chr17 | 62693189 | |||||
| chr17:62693284
|
A | G | 12 | a0001c0002t0002a0002c0006t0002a0002c0006t0004others(9): Show | 28 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*833A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 833 | chr17 | 62693284 | |||||
| chr17:62693561
|
A | G | 1 | a0001c0001t0007 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 30/30 | 1110 | chr17 | 62693561 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62627960
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.118+40G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62627960 | ||||||
| chr17:62627987
|
C | G | 1 | a0002c0003t0001g0311 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.118+67C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62627987 | ||||||
| chr17:62628284
|
C | T | 3 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0002t0001g0310 | 3 | HG00639.hp1 HG01071.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.118+364C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62628284 | ||||||
| chr17:62628290
|
C | T | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118+370C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62628290 | ||||||
| chr17:62628322
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.118+402C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62628322 | ||||||
| chr17:62628886
|
T | C | 1 | a0001c0001t0001g0003 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118+966T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62628886 | ||||||
| chr17:62628964
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118+1044C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62628964 | ||||||
| chr17:62629625
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.118+1705C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62629625 | ||||||
| chr17:62629726
|
G | A | 2 | a0001c0002t0001g0004a0001c0002t0001g0005 | 2 | NA18959.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.118+1806G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62629726 | ||||||
| chr17:62629771
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118+1851G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62629771 | ||||||
| chr17:62629811
|
A | G | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118+1891A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62629811 | ||||||
| chr17:62630018
|
C | T | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.118+2098C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630018 | ||||||
| chr17:62630032
|
C | CTGGA | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0143others(9): Show | 12 | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+2113_118+2116d others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62630032 | |||||
| chr17:62630068
|
G | A | 1 | a0002c0006t0004g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118+2148G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630068 | ||||||
| chr17:62630202
|
C | T | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118+2282C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630202 | ||||||
| chr17:62630285
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.118+2365T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630285 | ||||||
| chr17:62630398
|
T | C | 1 | a0002c0003t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118+2478T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630398 | ||||||
| chr17:62630542
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+2622C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630542 | ||||||
| chr17:62630600
|
C | T | 1 | a0007c0014t0005g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.118+2680C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630600 | ||||||
| chr17:62630613
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.118+2693G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630613 | ||||||
| chr17:62630678
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118+2758G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62630678 | ||||||
| chr17:62631216
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.118+3296C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62631216 | ||||||
| chr17:62631520
|
T | C | 1 | a0002c0006t0004g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.118+3600T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62631520 | ||||||
| chr17:62631560
|
C | T | 1 | a0002c0006t0004g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118+3640C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62631560 | ||||||
| chr17:62631916
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.118+3996A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62631916 | ||||||
| chr17:62632192
|
C | A | 8 | a0001c0001t0001g0011a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+4272C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632192 | ||||||
| chr17:62632211
|
C | T | 1 | a0002c0006t0004g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118+4291C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632211 | ||||||
| chr17:62632383
|
C | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(38): Show | 41 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.118+4463C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632383 | ||||||
| chr17:62632492
|
G | A | 2 | a0001c0002t0001g0153a0002c0006t0002g0152 | 2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118+4572G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632492 | ||||||
| chr17:62632677
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 234 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.118+4757G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632677 | ||||||
| chr17:62632762
|
C | CAGATTGG others(8): Show |
1 | a0001c0019t0001g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.118+4843_118+4857d others(17): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62632762 | |||||
| chr17:62632994
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.118+5074C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62632994 | ||||||
| chr17:62633273
|
C | T | 1 | a0012c0035t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118+5353C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633273 | ||||||
| chr17:62633502
|
C | CA | 14 | a0001c0001t0001g0128a0001c0002t0001g0041a0001c0002t0001g0042others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+5602dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633502 | |||||
| chr17:62633502
|
CA | C | 34 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(31): Show | 34 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.118+5602delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633502 | |||||
| chr17:62633502
|
CAA | C | 16 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0288others(13): Show | 16 | HG00280.hp2 HG00408.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.118+5601_118+5602d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633502 | |||||
| chr17:62633521
|
A | G | 3 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0105 | 3 | NA18959.hp1 NA18999.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.118+5601A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633521 | ||||||
| chr17:62633659
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.118+5739C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633659 | ||||||
| chr17:62633660
|
G | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+5740G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633660 | ||||||
| chr17:62633693
|
A | AT | 4 | a0001c0001t0001g0011a0001c0001t0001g0305a0001c0001t0006g0163others(1): Show | 4 | HG02055.hp1 HG02148.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+5773_118+5774i others(3): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633693 | ||||||
| chr17:62633693
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 207 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.118+5773A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633693 | ||||||
| chr17:62633735
|
G | A | 1 | a0013c0027t0001g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.118+5815G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633735 | ||||||
| chr17:62633840
|
C | CA | 28 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0067others(25): Show | 28 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.118+5962dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
C | CAA | 11 | a0001c0001t0001g0050a0001c0002t0001g0004a0001c0002t0001g0047others(8): Show | 11 | HG00733.hp2 HG01433.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.118+5961_118+5962d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
C | CAAAAAAA others(3): Show |
1 | a0004c0005t0001g0045 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.118+5953_118+5962d others(12): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CA | C | 11 | a0001c0001t0001g0128a0001c0002t0001g0100a0001c0013t0001g0043others(8): Show | 11 | HG01884.hp2 HG02647.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+5962delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(3): Show |
C | 39 | a0001c0001t0001g0002a0001c0001t0001g0107a0001c0001t0001g0166others(36): Show | 39 | HG00609.hp2 HG00639.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.118+5953_118+5962d others(12): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(4): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(81): Show | 85 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.118+5952_118+5962d others(13): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(5): Show |
C | 43 | a0001c0001t0001g0029a0001c0001t0001g0112a0001c0001t0001g0116others(40): Show | 43 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.118+5951_118+5962d others(14): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(6): Show |
C | 38 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0121others(35): Show | 38 | HG01261.hp2 HG01433.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.118+5950_118+5962d others(15): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0002t0001g0104others(2): Show | 5 | HG01255.hp1 HG02040.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+5949_118+5962d others(16): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0002t0001g0101a0001c0002t0001g0153a0002c0006t0002g0152others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+5948_118+5962d others(17): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(9): Show |
C | 5 | a0001c0002t0001g0102a0001c0031t0001g0156a0002c0003t0001g0154others(2): Show | 5 | HG01243.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+5947_118+5962d others(18): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0281a0002c0007t0001g0282 | 2 | NA20300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.118+5945_118+5962d others(20): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633840
|
CAAAAAAA others(12): Show |
C | 1 | a0012c0035t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118+5944_118+5962d others(21): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62633840 | |||||
| chr17:62633962
|
C | T | 2 | a0001c0001t0001g0250a0001c0025t0001g0164 | 2 | HG01099.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.118+6042C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62633962 | ||||||
| chr17:62634087
|
T | C | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+6167T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634087 | ||||||
| chr17:62634228
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.118+6308T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634228 | ||||||
| chr17:62634258
|
G | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+6338G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634258 | ||||||
| chr17:62634340
|
G | A | 1 | a0002c0006t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.118+6420G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634340 | ||||||
| chr17:62634343
|
C | G | 1 | a0003c0004t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.118+6423C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634343 | ||||||
| chr17:62634356
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.118+6436G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634356 | ||||||
| chr17:62634612
|
T | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(38): Show | 41 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.118+6692T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634612 | ||||||
| chr17:62634670
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.118+6750A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634670 | ||||||
| chr17:62634696
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.118+6776G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634696 | ||||||
| chr17:62634707
|
C | T | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+6787C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634707 | ||||||
| chr17:62634783
|
C | G | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+6863C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634783 | ||||||
| chr17:62634787
|
T | C | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+6867T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634787 | ||||||
| chr17:62634795
|
A | C | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+6875A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634795 | ||||||
| chr17:62634797
|
G | GGAGTTCC others(26): Show |
1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+6882_118+6883i others(35): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62634797 | |||||
| chr17:62634812
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.118+6892T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634812 | ||||||
| chr17:62634830
|
CT | C | 10 | a0001c0001t0001g0121a0001c0001t0001g0188a0001c0001t0001g0288others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+6928delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62634830 | |||||
| chr17:62634850
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.118+6930G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634850 | ||||||
| chr17:62634987
|
C | T | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0235 | 3 | NA18963.hp2 NA18984.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.118+7067C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62634987 | ||||||
| chr17:62635191
|
C | CT | 17 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0183others(14): Show | 17 | HG00438.hp1 HG00733.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.118+7292dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635191
|
C | CTT | 13 | a0001c0001t0001g0011a0001c0001t0001g0116a0001c0001t0001g0123others(10): Show | 13 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+7291_118+7292d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635191
|
C | CTTT | 8 | a0001c0001t0001g0107a0002c0003t0001g0006a0002c0003t0001g0108others(5): Show | 8 | HG01069.hp2 HG02300.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+7290_118+7292d others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635191
|
CT | C | 117 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0060others(114): Show | 117 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.118+7292delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635191
|
CTT | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0294a0001c0002t0001g0076others(3): Show | 6 | HG01069.hp1 HG01109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+7291_118+7292d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635191
|
CTTTTT | C | 13 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0143others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+7288_118+7292d others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62635191 | |||||
| chr17:62635212
|
T | C | 1 | a0001c0002t0001g0255 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.118+7292T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635212 | ||||||
| chr17:62635247
|
G | A | 7 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0101others(4): Show | 7 | HG00280.hp1 HG01928.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+7327G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635247 | ||||||
| chr17:62635325
|
A | T | 1 | a0002c0006t0004g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.118+7405A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635325 | ||||||
| chr17:62635384
|
A | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 169 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.118+7464A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635384 | ||||||
| chr17:62635461
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118+7541G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635461 | ||||||
| chr17:62635521
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.118+7601G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635521 | ||||||
| chr17:62635608
|
C | A | 4 | a0001c0002t0001g0237a0001c0002t0001g0245a0001c0002t0001g0256others(1): Show | 4 | NA18950.hp2 NA18952.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+7688C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635608 | ||||||
| chr17:62635716
|
C | T | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+7796C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635716 | ||||||
| chr17:62635717
|
G | A | 2 | a0001c0002t0001g0153a0002c0006t0002g0152 | 2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118+7797G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635717 | ||||||
| chr17:62635810
|
C | T | 1 | a0002c0006t0001g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118+7890C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62635810 | ||||||
| chr17:62636014
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.118+8094C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636014 | ||||||
| chr17:62636023
|
G | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+8103G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636023 | ||||||
| chr17:62636082
|
C | T | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118+8162C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636082 | ||||||
| chr17:62636250
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 202 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.118+8344delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62636250 | |||||
| chr17:62636250
|
CAA | C | 6 | a0001c0002t0001g0153a0001c0031t0001g0156a0002c0003t0001g0154others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+8343_118+8344d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62636250 | |||||
| chr17:62636329
|
G | T | 1 | a0001c0002t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.118+8409G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636329 | ||||||
| chr17:62636461
|
A | AT | 17 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(14): Show | 17 | HG00741.hp2 HG01109.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.118+8566dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62636461 | |||||
| chr17:62636461
|
AT | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.118+8566delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62636461 | |||||
| chr17:62636461
|
ATT | A | 36 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0116others(33): Show | 36 | HG00639.hp2 HG00738.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.118+8565_118+8566d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62636461 | |||||
| chr17:62636462
|
T | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0213a0001c0002t0001g0158others(1): Show | 4 | HG00621.hp1 HG01928.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+8542T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636462 | ||||||
| chr17:62636463
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0166others(39): Show | 43 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.118+8543T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636463 | ||||||
| chr17:62636507
|
C | T | 35 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0264others(32): Show | 35 | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.118+8587C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636507 | ||||||
| chr17:62636562
|
A | G | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.118+8642A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636562 | ||||||
| chr17:62636563
|
G | A | 2 | a0003c0012t0001g0070a0003c0012t0001g0071 | 2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.118+8643G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636563 | ||||||
| chr17:62636645
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118+8725T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636645 | ||||||
| chr17:62636647
|
A | T | 10 | a0001c0001t0001g0180a0001c0001t0001g0233a0002c0003t0001g0231others(7): Show | 10 | HG01168.hp1 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.118+8727A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636647 | ||||||
| chr17:62636674
|
G | A | 1 | a0001c0017t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118+8754G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636674 | ||||||
| chr17:62636824
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.118+8904T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636824 | ||||||
| chr17:62636844
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.118+8924C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636844 | ||||||
| chr17:62636934
|
C | T | 1 | a0005c0010t0001g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.118+9014C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636934 | ||||||
| chr17:62636970
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+9050C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636970 | ||||||
| chr17:62636977
|
T | C | 1 | a0002c0006t0001g0258 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118+9057T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62636977 | ||||||
| chr17:62637129
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.118+9209G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62637129 | ||||||
| chr17:62637535
|
C | CA | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.118+9630dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62637535 | |||||
| chr17:62637535
|
C | CAA | 7 | a0001c0001t0001g0194a0001c0002t0001g0254a0005c0010t0001g0161others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+9629_118+9630d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62637535 | |||||
| chr17:62637535
|
CA | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(49): Show | 52 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.118+9630delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62637535 | |||||
| chr17:62638017
|
C | A | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.118+10097C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638017 | ||||||
| chr17:62638101
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.118+10181G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638101 | ||||||
| chr17:62638111
|
C | T | 2 | a0001c0001t0001g0250a0001c0025t0001g0164 | 2 | HG01099.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.118+10191C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638111 | ||||||
| chr17:62638143
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.118+10223G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638143 | ||||||
| chr17:62638178
|
AGTAAATA others(6): Show |
A | 5 | a0005c0010t0001g0161a0005c0010t0001g0246a0005c0010t0001g0270others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+10260_118+1027 others(17): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62638178 | |||||
| chr17:62638465
|
C | T | 1 | a0005c0010t0001g0272 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118+10545C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638465 | ||||||
| chr17:62638544
|
C | T | 1 | a0008c0016t0001g0293 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.118+10624C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638544 | ||||||
| chr17:62638652
|
C | T | 40 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(37): Show | 40 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.118+10732C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638652 | ||||||
| chr17:62638737
|
CA | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.118+10837delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62638737 | |||||
| chr17:62638737
|
CAA | C | 7 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(4): Show | 7 | HG01934.hp1 HG01943.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+10836_118+1083 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62638737 | |||||
| chr17:62638754
|
A | G | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118+10834A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638754 | ||||||
| chr17:62638776
|
G | T | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118+10856G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638776 | ||||||
| chr17:62638794
|
T | C | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118+10874T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638794 | ||||||
| chr17:62638827
|
T | C | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118+10907T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62638827 | ||||||
| chr17:62639106
|
A | T | 2 | a0001c0001t0001g0250a0001c0025t0001g0164 | 2 | HG01099.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.118+11186A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639106 | ||||||
| chr17:62639138
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.118+11218C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639138 | ||||||
| chr17:62639162
|
C | T | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+11242C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639162 | ||||||
| chr17:62639342
|
TTAAA | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.118+11435_118+1143 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62639342 | |||||
| chr17:62639507
|
G | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.118+11587G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639507 | ||||||
| chr17:62639551
|
A | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.118+11631A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639551 | ||||||
| chr17:62639670
|
G | C | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.118+11750G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639670 | ||||||
| chr17:62639677
|
T | G | 2 | a0001c0001t0006g0195a0001c0002t0002g0172 | 2 | NA18966.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.118+11757T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639677 | ||||||
| chr17:62639801
|
T | A | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118+11881T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639801 | ||||||
| chr17:62639826
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.118+11906C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62639826 | ||||||
| chr17:62639903
|
GAGTGCAA others(23): Show |
G | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.118+11985_118+1201 others(34): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62639903 | |||||
| chr17:62640017
|
C | CT | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0069others(126): Show | 130 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.118+12121dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62640017 | |||||
| chr17:62640017
|
C | CTT | 48 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.118+12120_118+1212 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62640017 | |||||
| chr17:62640017
|
C | CTTT | 8 | a0001c0002t0001g0289a0002c0003t0001g0303a0002c0006t0004g0007others(5): Show | 8 | HG01891.hp1 HG01952.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+12119_118+1212 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62640017 | |||||
| chr17:62640032
|
T | TG | 7 | a0001c0001t0001g0011a0001c0001t0003g0008a0001c0001t0003g0009others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+12112_118+1211 others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640032 | ||||||
| chr17:62640034
|
T | A | 8 | a0001c0001t0001g0011a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+12114T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640034 | ||||||
| chr17:62640042
|
G | T | 2 | a0003c0004t0001g0292a0003c0011t0001g0291 | 2 | HG01978.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.118+12122G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640042 | ||||||
| chr17:62640058
|
C | CA | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 197 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.118+12138_118+1213 others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640058 | ||||||
| chr17:62640059
|
G | A | 11 | a0001c0002t0001g0153a0001c0020t0001g0302a0001c0031t0001g0156others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+12139G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640059 | ||||||
| chr17:62640123
|
G | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+12203G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640123 | ||||||
| chr17:62640183
|
C | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.118+12263C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640183 | ||||||
| chr17:62640273
|
G | A | 1 | a0003c0004t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.118+12353G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640273 | ||||||
| chr17:62640320
|
T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 231 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.118+12400T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640320 | ||||||
| chr17:62640330
|
TG | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0112others(24): Show | 27 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.118+12411delG | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640330 | ||||||
| chr17:62640337
|
G | A | 2 | a0001c0002t0001g0153a0002c0006t0002g0152 | 2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118+12417G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640337 | ||||||
| chr17:62640433
|
G | C | 8 | a0001c0001t0001g0011a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+12513G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640433 | ||||||
| chr17:62640507
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.118+12587G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640507 | ||||||
| chr17:62640576
|
A | G | 34 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0264others(31): Show | 34 | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.118+12656A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640576 | ||||||
| chr17:62640685
|
A | AT | 14 | a0001c0001t0001g0233a0001c0002t0001g0104a0001c0002t0001g0153others(11): Show | 14 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.118+12782dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62640685 | |||||
| chr17:62640685
|
A | ATT | 8 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(5): Show | 8 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+12781_118+1278 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62640685 | |||||
| chr17:62640723
|
C | T | 1 | a0003c0004t0001g0292 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.118+12803C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640723 | ||||||
| chr17:62640977
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 226 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.118+13057A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640977 | ||||||
| chr17:62640993
|
C | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+13073C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62640993 | ||||||
| chr17:62641023
|
T | A | 4 | a0001c0002t0001g0153a0002c0006t0002g0152a0002c0006t0004g0109others(1): Show | 4 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+13103T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641023 | ||||||
| chr17:62641315
|
G | GA | 11 | a0001c0001t0001g0069a0001c0017t0001g0307a0001c0019t0001g0048others(8): Show | 11 | HG00438.hp1 HG01884.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.118+13412dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62641315 | |||||
| chr17:62641364
|
C | T | 2 | a0001c0001t0001g0250a0001c0025t0001g0164 | 2 | HG01099.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.118+13444C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641364 | ||||||
| chr17:62641430
|
A | G | 3 | a0001c0002t0001g0186a0001c0002t0001g0187a0001c0002t0001g0235 | 3 | NA18963.hp2 NA18984.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.118+13510A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641430 | ||||||
| chr17:62641460
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.118+13540C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641460 | ||||||
| chr17:62641496
|
A | G | 2 | a0002c0003t0001g0139a0002c0003t0001g0140 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.118+13576A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641496 | ||||||
| chr17:62641621
|
T | G | 4 | a0001c0002t0001g0237a0001c0002t0001g0245a0001c0002t0001g0256others(1): Show | 4 | NA18950.hp2 NA18952.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+13701T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641621 | ||||||
| chr17:62641772
|
A | G | 1 | a0002c0003t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.118+13852A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641772 | ||||||
| chr17:62641848
|
A | G | 1 | a0001c0008t0001g0284 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.118+13928A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641848 | ||||||
| chr17:62641895
|
C | CTCTG | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(2): Show | 5 | HG02622.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+13976_118+1397 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62641895 | |||||
| chr17:62641895
|
C | CTG | 3 | a0001c0001t0001g0073a0001c0002t0002g0267a0002c0006t0004g0007 | 3 | HG01952.hp2 HG02698.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.118+13998_118+1399 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62641895 | |||||
| chr17:62641895
|
C | CTGTG | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.118+13996_118+1399 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62641895 | |||||
| chr17:62641895
|
C | CTGTGTG | 12 | a0001c0001t0001g0226a0001c0001t0001g0283a0001c0002t0001g0266others(9): Show | 12 | HG01243.hp1 HG01255.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+13994_118+1399 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62641895 | |||||
| chr17:62641895
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118+13975C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641895 | ||||||
| chr17:62641897
|
G | C | 4 | a0001c0002t0001g0074a0001c0013t0001g0043a0001c0013t0001g0098others(1): Show | 4 | HG01175.hp1 NA18948.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+13977G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62641897 | ||||||
| chr17:62642207
|
T | C | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+14287T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642207 | ||||||
| chr17:62642479
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.118+14559C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642479 | ||||||
| chr17:62642513
|
C | T | 5 | a0005c0010t0001g0161a0005c0010t0001g0246a0005c0010t0001g0270others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+14593C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642513 | ||||||
| chr17:62642563
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118+14643C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642563 | ||||||
| chr17:62642697
|
T | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 85 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.118+14777T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642697 | ||||||
| chr17:62642967
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.118+15047C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62642967 | ||||||
| chr17:62643001
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.118+15081C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643001 | ||||||
| chr17:62643068
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+15148C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643068 | ||||||
| chr17:62643126
|
G | A | 6 | a0001c0002t0001g0047a0001c0002t0001g0051a0001c0002t0001g0082others(3): Show | 6 | HG01074.hp1 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+15206G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643126 | ||||||
| chr17:62643190
|
T | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(2): Show | 5 | HG02622.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+15270T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643190 | ||||||
| chr17:62643238
|
G | A | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118+15318G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643238 | ||||||
| chr17:62643297
|
C | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0190 | 3 | NA18950.hp1 NA18954.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.118+15377C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643297 | ||||||
| chr17:62643327
|
C | CA | 7 | a0001c0002t0001g0047a0001c0002t0001g0055a0001c0002t0001g0063others(4): Show | 7 | HG01106.hp1 HG01358.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+15427dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62643327 | |||||
| chr17:62643327
|
C | CAAAAAAA | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0073others(19): Show | 22 | HG01175.hp1 HG01258.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+15421_118+1542 others(11): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62643327 | |||||
| chr17:62643327
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0029a0002c0003t0001g0020a0002c0003t0001g0025others(3): Show | 6 | HG00438.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+15420_118+1542 others(12): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62643327 | |||||
| chr17:62643336
|
AAAAAAAA others(5): Show |
A | 2 | a0002c0003t0001g0019a0002c0003t0001g0024 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.118+15422_118+1543 others(16): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62643336 | |||||
| chr17:62643341
|
A | AAG | 36 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0264others(33): Show | 36 | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.118+15422_118+1542 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62643341 | |||||
| chr17:62643341
|
A | AG | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.118+15421_118+1542 others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643341 | ||||||
| chr17:62643341
|
A | G | 39 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0116others(36): Show | 39 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.118+15421A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643341 | ||||||
| chr17:62643568
|
T | C | 1 | a0002c0003t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.118+15648T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643568 | ||||||
| chr17:62643997
|
G | T | 1 | a0002c0006t0004g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118+16077G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62643997 | ||||||
| chr17:62644081
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.118+16161T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644081 | ||||||
| chr17:62644194
|
G | A | 1 | a0001c0002t0001g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.118+16274G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644194 | ||||||
| chr17:62644250
|
C | A | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+16330C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644250 | ||||||
| chr17:62644309
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.118+16389C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644309 | ||||||
| chr17:62644402
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.118+16482G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644402 | ||||||
| chr17:62644413
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.118+16493C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644413 | ||||||
| chr17:62644748
|
C | T | 1 | a0001c0002t0002g0275 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.118+16828C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62644748 | ||||||
| chr17:62645062
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.118+17142C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645062 | ||||||
| chr17:62645480
|
A | ATG | 30 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0112others(27): Show | 31 | HG00621.hp1 HG00639.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.118+17570_118+1757 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645480 | |||||
| chr17:62645480
|
ATG | A | 3 | a0001c0001t0003g0037a0002c0003t0001g0025a0016c0029t0002g0016 | 3 | HG01891.hp2 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.118+17570_118+1757 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645480 | |||||
| chr17:62645490
|
G | A | 10 | a0002c0003t0001g0015a0002c0003t0001g0018a0002c0003t0001g0019others(7): Show | 10 | HG01346.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+17570G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645490 | ||||||
| chr17:62645491
|
TATATA | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0168a0001c0001t0001g0170others(19): Show | 22 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+17572_118+1757 others(9): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645491 | ||||||
| chr17:62645492
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(152): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.118+17572A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645492 | ||||||
| chr17:62645494
|
ATAT | A | 22 | a0001c0001t0001g0233a0001c0001t0001g0247a0001c0001t0001g0264others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+17578_118+1758 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645494 | |||||
| chr17:62645495
|
TATTA | T | 3 | a0002c0003t0001g0019a0002c0003t0001g0024a0002c0015t0002g0017 | 3 | HG01884.hp2 HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.118+17576_118+1757 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645495 | ||||||
| chr17:62645496
|
A | T | 7 | a0002c0003t0001g0015a0002c0003t0001g0018a0002c0003t0001g0020others(4): Show | 7 | HG01346.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+17576A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645496 | ||||||
| chr17:62645496
|
AT | A | 12 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0251others(9): Show | 12 | HG00408.hp2 HG01109.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+17578delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645496 | |||||
| chr17:62645497
|
T | G | 22 | a0001c0001t0001g0125a0001c0001t0001g0168a0001c0001t0001g0170others(19): Show | 22 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+17577T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645497 | ||||||
| chr17:62645497
|
TTA | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0073a0001c0002t0001g0076others(4): Show | 7 | HG00741.hp2 HG02273.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+17607_118+1760 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645497 | |||||
| chr17:62645498
|
T | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(118): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.118+17578T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645498 | ||||||
| chr17:62645499
|
A | G | 1 | a0002c0015t0002g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118+17579A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645499 | ||||||
| chr17:62645499
|
A | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.118+17579A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645499 | ||||||
| chr17:62645500
|
TA | T | 12 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0251others(9): Show | 12 | HG00408.hp2 HG01109.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+17581delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645500 | ||||||
| chr17:62645501
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.118+17581A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645501 | ||||||
| chr17:62645501
|
A | T | 16 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.118+17581A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645501 | ||||||
| chr17:62645502
|
TA | T | 22 | a0001c0001t0001g0233a0001c0001t0001g0247a0001c0001t0001g0264others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+17583delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645502 | ||||||
| chr17:62645504
|
TA | T | 22 | a0001c0001t0001g0125a0001c0001t0001g0168a0001c0001t0001g0170others(19): Show | 22 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.118+17585delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645504 | ||||||
| chr17:62645519
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0003 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118+17601_118+1761 others(14): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645519 | |||||
| chr17:62645519
|
ATATATAT others(7): Show |
A | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG02451.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.118+17601_118+1761 others(18): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645519 | |||||
| chr17:62645519
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118+17601_118+1761 others(21): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645519 | |||||
| chr17:62645520
|
TA | T | 3 | a0001c0001t0001g0075a0001c0019t0001g0038a0003c0004t0001g0053 | 3 | HG01258.hp2 NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.118+17601delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645520 | ||||||
| chr17:62645521
|
A | T | 4 | a0001c0019t0001g0048a0001c0020t0001g0302a0003c0012t0001g0070others(1): Show | 4 | HG00140.hp1 HG01081.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+17601A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645521 | ||||||
| chr17:62645521
|
ATATATAT | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0169others(10): Show | 13 | HG00733.hp1 HG01069.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.118+17603_118+1760 others(11): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645521 | |||||
| chr17:62645521
|
ATATATAT others(6): Show |
A | 1 | a0002c0006t0001g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.118+17603_118+1761 others(17): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645521 | |||||
| chr17:62645521
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.118+17603_118+1761 others(18): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645521 | |||||
| chr17:62645521
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.118+17603_118+1761 others(21): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645521 | |||||
| chr17:62645522
|
TA | T | 6 | a0001c0001t0001g0068a0001c0002t0001g0065a0001c0002t0001g0082others(3): Show | 6 | HG01106.hp2 HG01168.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+17603delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645522 | ||||||
| chr17:62645522
|
TATATA | T | 5 | a0001c0002t0001g0257a0001c0002t0002g0267a0002c0007t0001g0193others(2): Show | 5 | HG03239.hp2 HG03579.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+17603_118+1760 others(9): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645522 | ||||||
| chr17:62645523
|
A | AT | 4 | a0001c0002t0001g0061a0001c0002t0001g0074a0001c0008t0001g0040others(1): Show | 4 | HG01175.hp1 HG02083.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+17604dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645523 | |||||
| chr17:62645523
|
A | T | 18 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0251others(15): Show | 18 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.118+17603A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645523 | ||||||
| chr17:62645523
|
ATATATT | A | 10 | a0001c0001t0001g0180a0001c0001t0001g0216a0001c0001t0001g0286others(7): Show | 10 | HG01168.hp1 HG01978.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+17605_118+1761 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645523 | |||||
| chr17:62645523
|
ATATATTT others(3): Show |
A | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0002t0001g0142 | 3 | HG00738.hp1 HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.118+17605_118+1761 others(14): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645523 | |||||
| chr17:62645523
|
ATATATTT others(4): Show |
A | 2 | a0001c0002t0001g0141a0002c0003t0001g0140 | 2 | HG02293.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.118+17605_118+1761 others(15): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645523 | |||||
| chr17:62645524
|
TA | T | 6 | a0001c0001t0001g0162a0001c0002t0001g0051a0001c0002t0001g0089others(3): Show | 6 | HG01515.hp2 HG01934.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+17605delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645524 | ||||||
| chr17:62645524
|
TATA | T | 11 | a0001c0002t0002g0259a0002c0003t0001g0015a0002c0003t0001g0018others(8): Show | 11 | HG01346.hp2 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+17605_118+1760 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645524 | ||||||
| chr17:62645525
|
A | ATTT | 4 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0090others(1): Show | 4 | HG01106.hp1 HG01346.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+17606_118+1760 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645525
|
A | T | 53 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0060others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.118+17605A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645525 | ||||||
| chr17:62645525
|
ATAT | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0212others(5): Show | 8 | HG02970.hp1 HG02970.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+17607_118+1760 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645525
|
ATATT | A | 10 | a0001c0001t0001g0188a0001c0001t0001g0196a0001c0001t0001g0204others(7): Show | 10 | HG01934.hp1 HG02004.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+17607_118+1761 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645525
|
ATATTTT | A | 11 | a0001c0001t0001g0148a0001c0001t0001g0202a0001c0001t0001g0203others(8): Show | 11 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+17607_118+1761 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645525
|
ATATTTTT others(4): Show |
A | 3 | a0002c0003t0001g0138a0002c0003t0001g0139a0005c0010t0001g0246 | 3 | HG02615.hp1 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.118+17607_118+1761 others(15): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645525
|
ATATTTTT others(5): Show |
A | 3 | a0002c0003t0001g0006a0002c0003t0001g0108a0002c0003t0001g0120 | 3 | HG02630.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.118+17607_118+1761 others(16): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645525 | |||||
| chr17:62645526
|
TA | T | 7 | a0001c0002t0001g0047a0001c0002t0001g0101a0001c0002t0001g0243others(4): Show | 7 | HG01981.hp1 HG02027.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+17607delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645526 | ||||||
| chr17:62645527
|
A | T | 94 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0059others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.118+17607A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645527 | ||||||
| chr17:62645527
|
ATT | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0183others(3): Show | 6 | HG01928.hp2 HG01978.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+17630_118+1763 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTT | A | 8 | a0001c0001t0001g0201a0001c0001t0001g0269a0001c0001t0001g0279others(5): Show | 8 | HG01167.hp1 HG01943.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.118+17628_118+1763 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTTT | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0191a0001c0001t0001g0213others(8): Show | 12 | HG00621.hp1 HG03130.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.118+17627_118+1763 others(9): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTTTT | A | 10 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0173others(7): Show | 10 | HG01192.hp2 HG01993.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.118+17626_118+1763 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0116a0001c0001t0001g0136a0001c0001t0001g0137others(2): Show | 5 | HG00639.hp2 HG02965.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+17622_118+1763 others(14): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTTTTT others(5): Show |
A | 9 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0017t0001g0106others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.118+17620_118+1763 others(16): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645527
|
ATTTTTTT others(7): Show |
A | 1 | a0002c0003t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118+17618_118+1763 others(18): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62645527 | |||||
| chr17:62645529
|
T | A | 5 | a0001c0001t0001g0194a0001c0001t0003g0037a0001c0002t0001g0100others(2): Show | 5 | HG01891.hp2 HG03834.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+17609T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645529 | ||||||
| chr17:62645531
|
T | A | 3 | a0001c0002t0001g0094a0001c0002t0001g0187a0002c0006t0001g0258 | 3 | HG03834.hp1 NA18963.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.118+17611T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645531 | ||||||
| chr17:62645532
|
T | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0014c0038t0001g0206 | 3 | HG02165.hp2 NA18965.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.118+17612T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645532 | ||||||
| chr17:62645533
|
T | A | 1 | a0002c0006t0001g0258 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118+17613T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645533 | ||||||
| chr17:62645534
|
T | A | 2 | a0001c0001t0001g0213a0001c0002t0002g0172 | 2 | HG00621.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.118+17614T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645534 | ||||||
| chr17:62645539
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.118+17619T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645539 | ||||||
| chr17:62645803
|
G | T | 2 | a0001c0002t0001g0153a0002c0006t0002g0152 | 2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.118+17883G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645803 | ||||||
| chr17:62645949
|
A | G | 1 | a0003c0004t0001g0171 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.118+18029A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62645949 | ||||||
| chr17:62646023
|
A | AT | 43 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0112others(40): Show | 43 | HG00639.hp1 HG01071.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.118+18122dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62646023 | |||||
| chr17:62646023
|
A | ATT | 13 | a0001c0001t0001g0011a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+18121_118+1812 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62646023 | |||||
| chr17:62646023
|
A | ATTT | 6 | a0001c0001t0001g0143a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 6 | HG01358.hp2 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+18120_118+1812 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62646023 | |||||
| chr17:62646023
|
AT | A | 12 | a0001c0001t0001g0199a0001c0001t0001g0250a0001c0001t0001g0288others(9): Show | 12 | HG00140.hp2 HG01081.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+18122delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62646023 | |||||
| chr17:62646027
|
T | A | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118+18107T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646027 | ||||||
| chr17:62646149
|
C | T | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.118+18229C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646149 | ||||||
| chr17:62646311
|
A | C | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.119-18237A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646311 | ||||||
| chr17:62646319
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-18229C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646319 | ||||||
| chr17:62646350
|
G | C | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.119-18198G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646350 | ||||||
| chr17:62646516
|
C | T | 2 | a0001c0002t0001g0186a0001c0002t0001g0187 | 2 | NA18963.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.119-18032C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646516 | ||||||
| chr17:62646615
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.119-17933C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646615 | ||||||
| chr17:62646772
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-17776C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646772 | ||||||
| chr17:62646949
|
C | T | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.119-17599C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62646949 | ||||||
| chr17:62647008
|
C | T | 2 | a0002c0003t0001g0006a0002c0003t0001g0120 | 2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.119-17540C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647008 | ||||||
| chr17:62647049
|
C | T | 2 | a0001c0001t0001g0125a0003c0004t0001g0126 | 2 | HG00738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.119-17499C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647049 | ||||||
| chr17:62647186
|
C | CT | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.119-17347dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62647186 | |||||
| chr17:62647186
|
C | CTT | 11 | a0001c0001t0001g0148a0001c0001t0001g0298a0001c0001t0003g0008others(8): Show | 11 | HG00280.hp2 HG01109.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.119-17348_119-1734 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62647186 | |||||
| chr17:62647223
|
G | A | 2 | a0001c0001t0001g0309a0001c0002t0001g0310 | 2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.119-17325G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647223 | ||||||
| chr17:62647279
|
G | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-17269G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647279 | ||||||
| chr17:62647418
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-17130C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647418 | ||||||
| chr17:62647438
|
G | T | 1 | a0001c0002t0001g0310 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.119-17110G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647438 | ||||||
| chr17:62647503
|
A | T | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.119-17045A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647503 | ||||||
| chr17:62647565
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.119-16983A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647565 | ||||||
| chr17:62647906
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.119-16642G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62647906 | ||||||
| chr17:62648123
|
G | C | 10 | a0001c0001t0001g0180a0001c0001t0001g0233a0002c0003t0001g0231others(7): Show | 10 | HG01168.hp1 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-16425G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648123 | ||||||
| chr17:62648179
|
G | A | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.119-16369G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648179 | ||||||
| chr17:62648211
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0004c0005t0001g0236 | 3 | HG01934.hp1 HG01943.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.119-16337C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648211 | ||||||
| chr17:62648268
|
A | G | 3 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.119-16280A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648268 | ||||||
| chr17:62648277
|
G | A | 1 | a0002c0009t0001g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.119-16271G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648277 | ||||||
| chr17:62648367
|
G | A | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.119-16181G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648367 | ||||||
| chr17:62648379
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.119-16169T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648379 | ||||||
| chr17:62648539
|
T | G | 1 | a0001c0013t0001g0099 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.119-16009T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648539 | ||||||
| chr17:62648787
|
G | A | 1 | a0002c0006t0004g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.119-15761G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648787 | ||||||
| chr17:62648917
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.119-15631T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62648917 | ||||||
| chr17:62649121
|
A | T | 1 | a0002c0015t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.119-15427A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649121 | ||||||
| chr17:62649411
|
C | T | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.119-15137C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649411 | ||||||
| chr17:62649542
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.119-15006G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649542 | ||||||
| chr17:62649755
|
C | T | 13 | a0001c0001t0003g0037a0002c0003t0001g0015a0002c0003t0001g0018others(10): Show | 13 | HG01346.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.119-14793C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649755 | ||||||
| chr17:62649817
|
C | T | 1 | a0002c0003t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.119-14731C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649817 | ||||||
| chr17:62649883
|
C | CT | 6 | a0001c0001t0001g0033a0001c0001t0001g0180a0002c0006t0004g0012others(3): Show | 6 | HG02165.hp1 HG03225.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-14653dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62649883 | |||||
| chr17:62649890
|
T | TTTTTTAA others(329): Show |
1 | a0001c0002t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.119-14643_119-1464 others(340): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62649890 | |||||
| chr17:62649905
|
T | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0294 | 2 | HG01069.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.119-14643T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649905 | ||||||
| chr17:62649942
|
G | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 200 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.119-14606G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649942 | ||||||
| chr17:62649980
|
C | T | 1 | a0002c0015t0002g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.119-14568C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62649980 | ||||||
| chr17:62650196
|
T | TCATTCTA others(23): Show |
1 | a0002c0006t0004g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.119-14346_119-1434 others(34): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62650196 | |||||
| chr17:62650347
|
G | A | 1 | a0001c0017t0001g0106 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.119-14201G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650347 | ||||||
| chr17:62650430
|
T | C | 1 | a0003c0004t0001g0215 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.119-14118T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650430 | ||||||
| chr17:62650494
|
A | T | 8 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(5): Show | 8 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-14054A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650494 | ||||||
| chr17:62650527
|
C | T | 1 | a0004c0005t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.119-14021C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650527 | ||||||
| chr17:62650558
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.119-13990C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650558 | ||||||
| chr17:62650564
|
T | A | 1 | a0003c0004t0001g0296 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.119-13984T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650564 | ||||||
| chr17:62650822
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.119-13726G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650822 | ||||||
| chr17:62650858
|
C | T | 1 | a0001c0002t0001g0186 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.119-13690C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650858 | ||||||
| chr17:62650859
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.119-13689G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650859 | ||||||
| chr17:62650896
|
A | G | 1 | a0003c0004t0001g0215 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.119-13652A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62650896 | ||||||
| chr17:62651086
|
CT | C | 12 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0199others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.119-13445delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62651086 | |||||
| chr17:62651147
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.119-13401G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651147 | ||||||
| chr17:62651149
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.119-13399T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651149 | ||||||
| chr17:62651240
|
C | T | 2 | a0002c0006t0004g0109a0002c0006t0004g0147 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.119-13308C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651240 | ||||||
| chr17:62651260
|
T | C | 1 | a0002c0006t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-13288T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651260 | ||||||
| chr17:62651273
|
A | C | 1 | a0002c0006t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-13275A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651273 | ||||||
| chr17:62651330
|
C | A | 26 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0116others(23): Show | 26 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.119-13218C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651330 | ||||||
| chr17:62651364
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.119-13184G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651364 | ||||||
| chr17:62651592
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.119-12956C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651592 | ||||||
| chr17:62651862
|
G | A | 11 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0144others(8): Show | 11 | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-12686G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651862 | ||||||
| chr17:62651933
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 205 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.119-12615T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651933 | ||||||
| chr17:62651973
|
G | T | 1 | a0001c0002t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.119-12575G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651973 | ||||||
| chr17:62651993
|
A | G | 2 | a0003c0004t0001g0215a0003c0012t0001g0182 | 2 | HG01496.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.119-12555A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62651993 | ||||||
| chr17:62652071
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.119-12477A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652071 | ||||||
| chr17:62652106
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.119-12442C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652106 | ||||||
| chr17:62652230
|
CTCAA | C | 3 | a0001c0001t0001g0011a0001c0002t0001g0153a0002c0006t0002g0152 | 3 | HG01109.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.119-12313_119-1231 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62652230 | |||||
| chr17:62652580
|
G | A | 1 | a0002c0006t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-11968G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652580 | ||||||
| chr17:62652780
|
G | A | 1 | a0006c0018t0009g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.119-11768G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652780 | ||||||
| chr17:62652820
|
C | A | 1 | a0001c0002t0002g0083 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.119-11728C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652820 | ||||||
| chr17:62652828
|
GGGGGAGG others(33): Show |
G | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.119-11708_119-1166 others(44): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62652828 | |||||
| chr17:62652918
|
G | T | 2 | a0001c0017t0001g0307a0006c0018t0002g0306 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.119-11630G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652918 | ||||||
| chr17:62652979
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.119-11569C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62652979 | ||||||
| chr17:62653041
|
C | T | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(2): Show | 5 | HG02622.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-11507C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62653041 | ||||||
| chr17:62653109
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.119-11439C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62653109 | ||||||
| chr17:62653165
|
C | G | 1 | a0002c0009t0001g0277 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.119-11383C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62653165 | ||||||
| chr17:62653188
|
G | T | 1 | a0001c0002t0001g0260 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.119-11360G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62653188 | ||||||
| chr17:62654043
|
G | A | 3 | a0001c0002t0001g0248a0009c0022t0001g0218a0009c0022t0001g0234 | 3 | NA18612.hp1 NA18957.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.119-10505G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654043 | ||||||
| chr17:62654097
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.119-10451T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654097 | ||||||
| chr17:62654117
|
T | TCCCTGGG others(6): Show |
4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-10428_119-1041 others(17): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62654117 | |||||
| chr17:62654326
|
C | G | 1 | a0001c0008t0001g0225 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.119-10222C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654326 | ||||||
| chr17:62654443
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.119-10105G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654443 | ||||||
| chr17:62654484
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.119-10064C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654484 | ||||||
| chr17:62654525
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.119-10023G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654525 | ||||||
| chr17:62654575
|
G | A | 1 | a0002c0009t0001g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.119-9973G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654575 | ||||||
| chr17:62654970
|
T | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-9578T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62654970 | ||||||
| chr17:62655004
|
G | A | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-9544G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655004 | ||||||
| chr17:62655023
|
C | T | 4 | a0004c0005t0001g0039a0004c0005t0001g0045a0004c0005t0001g0046others(1): Show | 4 | HG00280.hp1 HG01928.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-9525C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655023 | ||||||
| chr17:62655037
|
G | T | 1 | a0001c0001t0001g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.119-9511G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655037 | ||||||
| chr17:62655072
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.119-9476T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655072 | ||||||
| chr17:62655102
|
G | T | 1 | a0019c0030t0001g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.119-9446G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655102 | ||||||
| chr17:62655315
|
GT | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-9232delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655315 | ||||||
| chr17:62655368
|
C | T | 5 | a0001c0001t0001g0011a0001c0002t0001g0153a0002c0006t0002g0152others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-9180C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655368 | ||||||
| chr17:62655398
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.119-9150C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655398 | ||||||
| chr17:62655477
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-9071G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655477 | ||||||
| chr17:62655497
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-9051G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655497 | ||||||
| chr17:62655521
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-9027A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655521 | ||||||
| chr17:62655721
|
T | TAAA | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-8812_119-8810d others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62655721 | |||||
| chr17:62655721
|
TA | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0060others(183): Show | 187 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.119-8810delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62655721 | |||||
| chr17:62655733
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.119-8815A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655733 | ||||||
| chr17:62655735
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.119-8813A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655735 | ||||||
| chr17:62655824
|
C | T | 10 | a0001c0001t0001g0180a0001c0001t0001g0233a0002c0003t0001g0231others(7): Show | 10 | HG01168.hp1 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-8724C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655824 | ||||||
| chr17:62655832
|
C | T | 1 | a0001c0031t0001g0156 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.119-8716C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62655832 | ||||||
| chr17:62656055
|
A | G | 1 | a0002c0009t0001g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.119-8493A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656055 | ||||||
| chr17:62656058
|
T | C | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.119-8490T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656058 | ||||||
| chr17:62656136
|
T | A | 2 | a0001c0002t0001g0158a0019c0030t0001g0244 | 2 | HG01167.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.119-8412T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656136 | ||||||
| chr17:62656208
|
C | T | 2 | a0001c0001t0001g0264a0001c0002t0001g0253 | 2 | HG02132.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.119-8340C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656208 | ||||||
| chr17:62656351
|
T | C | 2 | a0003c0004t0001g0292a0003c0011t0001g0291 | 2 | HG01978.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.119-8197T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656351 | ||||||
| chr17:62656397
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-8151A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656397 | ||||||
| chr17:62656678
|
A | C | 1 | a0006c0018t0009g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.119-7870A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656678 | ||||||
| chr17:62656688
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.119-7860C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656688 | ||||||
| chr17:62656927
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.119-7621A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656927 | ||||||
| chr17:62656929
|
C | T | 3 | a0001c0001t0001g0011a0001c0002t0001g0153a0002c0006t0002g0152 | 3 | HG01109.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.119-7619C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656929 | ||||||
| chr17:62656991
|
T | G | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.119-7557T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656991 | ||||||
| chr17:62656993
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.119-7555T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62656993 | ||||||
| chr17:62657018
|
C | G | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7530C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657018 | ||||||
| chr17:62657195
|
G | A | 1 | a0004c0005t0008g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.119-7353G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657195 | ||||||
| chr17:62657303
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.119-7245G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657303 | ||||||
| chr17:62657326
|
A | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0166others(42): Show | 46 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.119-7222A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657326 | ||||||
| chr17:62657455
|
C | A | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-7093C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657455 | ||||||
| chr17:62657670
|
T | C | 1 | a0005c0010t0001g0161 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.119-6878T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657670 | ||||||
| chr17:62657743
|
G | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.119-6805G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657743 | ||||||
| chr17:62657879
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-6669G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657879 | ||||||
| chr17:62657883
|
A | G | 5 | a0001c0002t0002g0160a0001c0002t0002g0242a0001c0002t0002g0263others(2): Show | 5 | NA18986.hp1 NA18992.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-6665A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657883 | ||||||
| chr17:62657883
|
A | T | 1 | a0002c0003t0001g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.119-6665A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657883 | ||||||
| chr17:62657940
|
C | T | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-6608C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657940 | ||||||
| chr17:62657999
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-6549G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62657999 | ||||||
| chr17:62658199
|
C | T | 1 | a0006c0018t0009g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.119-6349C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62658199 | ||||||
| chr17:62658341
|
C | T | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-6207C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62658341 | ||||||
| chr17:62658405
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.119-6143T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62658405 | ||||||
| chr17:62658586
|
G | A | 3 | a0002c0015t0002g0010a0006c0018t0009g0013a0007c0014t0005g0127 | 3 | HG02809.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.119-5962G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62658586 | ||||||
| chr17:62658634
|
T | G | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.119-5914T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62658634 | ||||||
| chr17:62659051
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.119-5497G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659051 | ||||||
| chr17:62659080
|
C | T | 1 | a0003c0004t0001g0217 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.119-5468C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659080 | ||||||
| chr17:62659207
|
A | G | 5 | a0001c0001t0001g0011a0001c0002t0001g0153a0002c0006t0002g0152others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-5341A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659207 | ||||||
| chr17:62659265
|
C | T | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-5283C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659265 | ||||||
| chr17:62659467
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-5081G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659467 | ||||||
| chr17:62659501
|
G | A | 5 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0190others(2): Show | 5 | NA18950.hp1 NA18952.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-5047G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659501 | ||||||
| chr17:62659545
|
C | CA | 49 | a0001c0001t0001g0011a0001c0001t0001g0060a0001c0001t0001g0175others(46): Show | 49 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.119-4988dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62659545 | |||||
| chr17:62659551
|
A | G | 1 | a0002c0006t0004g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.119-4997A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659551 | ||||||
| chr17:62659731
|
G | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-4817G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659731 | ||||||
| chr17:62659898
|
C | T | 4 | a0001c0031t0001g0156a0002c0003t0001g0154a0002c0003t0001g0155others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-4650C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62659898 | ||||||
| chr17:62660409
|
T | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-4139T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62660409 | ||||||
| chr17:62660744
|
A | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0166others(43): Show | 47 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.119-3804A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62660744 | ||||||
| chr17:62660864
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0116 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.119-3684T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62660864 | ||||||
| chr17:62661068
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.119-3480C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661068 | ||||||
| chr17:62661187
|
G | A | 10 | a0002c0003t0001g0015a0002c0003t0001g0018a0002c0003t0001g0020others(7): Show | 10 | HG01346.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.119-3361G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661187 | ||||||
| chr17:62661423
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.119-3125T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661423 | ||||||
| chr17:62661502
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.119-3046C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661502 | ||||||
| chr17:62661511
|
CTTTTCTT others(17): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.119-3022_119-2999d others(26): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661511 | |||||
| chr17:62661512
|
TTTTC | T | 19 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0116others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.119-3022_119-3019d others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661512 | |||||
| chr17:62661548
|
CTCTT | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(2): Show | 5 | HG02622.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-2988_119-2985d others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661548 | |||||
| chr17:62661577
|
A | ATTCC | 12 | a0001c0001t0001g0033a0001c0001t0001g0059a0001c0001t0001g0075others(9): Show | 12 | HG01099.hp2 HG01258.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.119-2935_119-2932d others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661577 | |||||
| chr17:62661577
|
ATTCC | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 144 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.119-2935_119-2932d others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661577 | |||||
| chr17:62661577
|
ATTCCTTC others(1): Show |
A | 44 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0247others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.119-2939_119-2932d others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661577 | |||||
| chr17:62661577
|
ATTCCTTC others(5): Show |
A | 23 | a0001c0001t0001g0011a0001c0001t0003g0037a0001c0002t0001g0153others(20): Show | 23 | HG01109.hp2 HG01346.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.119-2943_119-2932d others(14): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62661577 | |||||
| chr17:62661618
|
T | C | 1 | a0001c0002t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.119-2930T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661618 | ||||||
| chr17:62661701
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-2847A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661701 | ||||||
| chr17:62661755
|
T | C | 1 | a0002c0003t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.119-2793T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661755 | ||||||
| chr17:62661772
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.119-2776G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62661772 | ||||||
| chr17:62662121
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0166a0001c0001t0001g0173others(14): Show | 17 | HG00408.hp2 HG01192.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.119-2427G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662121 | ||||||
| chr17:62662237
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.119-2311G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662237 | ||||||
| chr17:62662238
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.119-2310G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662238 | ||||||
| chr17:62662249
|
C | CA | 40 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0107others(37): Show | 40 | HG00639.hp2 HG00738.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.119-2285dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62662249 | |||||
| chr17:62662249
|
CA | C | 6 | a0001c0002t0001g0065a0001c0017t0001g0307a0001c0020t0001g0302others(3): Show | 6 | HG01168.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-2285delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62662249 | |||||
| chr17:62662264
|
T | A | 1 | a0001c0002t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.119-2284T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662264 | ||||||
| chr17:62662321
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 194 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.119-2227C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662321 | ||||||
| chr17:62662555
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG02622.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-1993A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662555 | ||||||
| chr17:62662909
|
CAAAAAAG others(6): Show |
C | 1 | a0002c0006t0004g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.119-1623_119-1611d others(15): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62662909 | |||||
| chr17:62662958
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.119-1590G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662958 | ||||||
| chr17:62662987
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.119-1561T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62662987 | ||||||
| chr17:62663128
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.119-1420C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663128 | ||||||
| chr17:62663129
|
G | A | 1 | a0003c0004t0001g0215 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.119-1419G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663129 | ||||||
| chr17:62663187
|
C | A | 1 | a0002c0007t0001g0192 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-1361C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663187 | ||||||
| chr17:62663226
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.119-1322C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663226 | ||||||
| chr17:62663368
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.119-1180T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663368 | ||||||
| chr17:62663463
|
C | T | 1 | a0001c0025t0001g0164 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.119-1085C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663463 | ||||||
| chr17:62663603
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 246 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.119-945G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663603 | ||||||
| chr17:62663701
|
G | A | 1 | a0002c0003t0001g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.119-847G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663701 | ||||||
| chr17:62663778
|
A | C | 1 | a0002c0006t0004g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.119-770A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62663778 | ||||||
| chr17:62663958
|
C | CT | 48 | a0001c0001t0001g0029a0001c0001t0001g0112a0001c0001t0001g0116others(45): Show | 48 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.119-571dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62663958 | |||||
| chr17:62663958
|
C | CTT | 8 | a0001c0008t0001g0208a0001c0008t0001g0222a0001c0008t0001g0223others(5): Show | 8 | HG02074.hp1 HG02129.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.119-572_119-571dup others(2): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62663958 | |||||
| chr17:62663958
|
CT | C | 24 | a0001c0001t0003g0009a0001c0001t0003g0014a0001c0001t0003g0037others(21): Show | 24 | HG01346.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.119-571delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62663958 | |||||
| chr17:62664020
|
C | T | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.119-528C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664020 | ||||||
| chr17:62664022
|
G | T | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.119-526G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664022 | ||||||
| chr17:62664085
|
A | G | 1 | a0001c0002t0001g0076 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.119-463A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664085 | ||||||
| chr17:62664093
|
G | A | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-455G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664093 | ||||||
| chr17:62664098
|
T | C | 5 | a0001c0008t0001g0222a0001c0008t0001g0223a0001c0008t0001g0284others(2): Show | 5 | HG02129.hp2 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-450T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664098 | ||||||
| chr17:62664151
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-397G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | chr17 | 62664151 | ||||||
| chr17:62664314
|
G | GGAATAGC others(5): Show |
2 | a0001c0008t0001g0208a0001c0008t0001g0225 | 2 | HG02074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.119-233_119-232ins others(12): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr17 | 62664314 | |||||
| chr17:62664987
|
G | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.520+38G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62664987 | ||||||
| chr17:62665164
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.520+215C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665164 | ||||||
| chr17:62665313
|
G | A | 1 | a0001c0017t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520+364G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665313 | ||||||
| chr17:62665345
|
C | G | 5 | a0005c0010t0001g0161a0005c0010t0001g0246a0005c0010t0001g0270others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+396C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665345 | ||||||
| chr17:62665401
|
T | TC | 16 | a0001c0002t0002g0259a0001c0008t0001g0208a0001c0008t0001g0222others(13): Show | 16 | HG00438.hp1 HG01168.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.520+462dupC | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr17 | 62665401 | |||||
| chr17:62665401
|
TC | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0050others(128): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.520+462delC | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr17 | 62665401 | |||||
| chr17:62665408
|
C | CT | 3 | a0001c0008t0001g0040a0002c0009t0001g0026a0002c0009t0001g0277 | 3 | HG02083.hp2 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.520+459_520+460ins others(1): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665408 | ||||||
| chr17:62665411
|
C | A | 1 | a0017c0032t0001g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.520+462C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665411 | ||||||
| chr17:62665412
|
A | C | 1 | a0017c0032t0001g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.520+463A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665412 | ||||||
| chr17:62665413
|
C | A | 1 | a0017c0032t0001g0265 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.520+464C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665413 | ||||||
| chr17:62665413
|
C | CA | 52 | a0001c0001t0001g0069a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 52 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.520+475dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr17 | 62665413 | |||||
| chr17:62665413
|
C | CAA | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(15): Show | 18 | HG01346.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.520+474_520+475dup others(2): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr17 | 62665413 | |||||
| chr17:62665574
|
C | T | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.521-520C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665574 | ||||||
| chr17:62665785
|
C | T | 1 | a0005c0010t0001g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.521-309C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665785 | ||||||
| chr17:62665828
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-266G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665828 | ||||||
| chr17:62665863
|
C | G | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.521-231C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665863 | ||||||
| chr17:62665936
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.521-158C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 2/29 | chr17 | 62665936 | ||||||
| chr17:62666445
|
G | A | 52 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(49): Show | 52 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.695-10G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 3/29 | chr17 | 62666445 | ||||||
| chr17:62666647
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.859+28G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 4/29 | chr17 | 62666647 | ||||||
| chr17:62666662
|
G | A | 1 | a0001c0002t0001g0141 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.859+43G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 4/29 | chr17 | 62666662 | ||||||
| chr17:62666705
|
G | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG01099.hp2 HG02145.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-52G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 4/29 | chr17 | 62666705 | ||||||
| chr17:62666905
|
G | A | 2 | a0001c0017t0001g0106a0001c0017t0001g0307 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.973+35G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62666905 | ||||||
| chr17:62667019
|
C | T | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.973+149C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62667019 | ||||||
| chr17:62667045
|
C | A | 18 | a0001c0008t0001g0040a0001c0008t0001g0208a0001c0008t0001g0222others(15): Show | 18 | HG00438.hp1 HG01168.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.973+175C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62667045 | ||||||
| chr17:62667066
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0226 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.973+196A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62667066 | ||||||
| chr17:62667068
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+198A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62667068 | ||||||
| chr17:62667371
|
C | T | 5 | a0001c0017t0001g0106a0001c0017t0001g0307a0002c0015t0002g0010others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-19C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 5/29 | chr17 | 62667371 | ||||||
| chr17:62667603
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1117+70G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62667603 | ||||||
| chr17:62667782
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1117+249C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62667782 | ||||||
| chr17:62667879
|
A | C | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0169others(2): Show | 5 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+346A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62667879 | ||||||
| chr17:62667885
|
A | G | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0169others(2): Show | 5 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+352A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62667885 | ||||||
| chr17:62668016
|
C | T | 1 | a0008c0016t0001g0293 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1117+483C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668016 | ||||||
| chr17:62668079
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1117+546G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668079 | ||||||
| chr17:62668106
|
C | T | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1117+573C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668106 | ||||||
| chr17:62668135
|
T | C | 1 | a0001c0002t0001g0235 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1117+602T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668135 | ||||||
| chr17:62668356
|
C | CAAAAAA | 49 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(46): Show | 49 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1117+824_1117+829d others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62668356 | |||||
| chr17:62668359
|
A | AAAAAAT | 6 | a0001c0002t0001g0142a0001c0002t0001g0266a0002c0003t0001g0120others(3): Show | 6 | HG01175.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117+829_1117+830i others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62668359 | |||||
| chr17:62668363
|
T | A | 12 | a0001c0001t0001g0116a0001c0001t0003g0008a0001c0001t0003g0009others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117+830T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668363 | ||||||
| chr17:62668367
|
T | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(2): Show | 5 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+834T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668367 | ||||||
| chr17:62668371
|
T | A | 1 | a0001c0001t0003g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1117+838T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668371 | ||||||
| chr17:62668387
|
T | A | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1117+854T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668387 | ||||||
| chr17:62668510
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1117+977G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668510 | ||||||
| chr17:62668823
|
T | G | 1 | a0008c0016t0001g0293 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1117+1290T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668823 | ||||||
| chr17:62668913
|
G | A | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1117+1380G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62668913 | ||||||
| chr17:62669085
|
A | AAC | 32 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1117+1592_1117+159 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62669085 | |||||
| chr17:62669085
|
AAC | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0067others(56): Show | 59 | HG00438.hp1 HG00738.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.1117+1592_1117+159 others(6): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62669085 | |||||
| chr17:62669085
|
AACAC | A | 36 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0148others(33): Show | 36 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1117+1590_1117+159 others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62669085 | |||||
| chr17:62669085
|
AACACAC | A | 3 | a0001c0002t0001g0254a0002c0003t0001g0139a0003c0004t0001g0171 | 3 | HG01515.hp1 HG02615.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1117+1588_1117+159 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62669085 | |||||
| chr17:62669085
|
AACACACA others(1): Show |
A | 53 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(50): Show | 53 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1117+1586_1117+159 others(12): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr17 | 62669085 | |||||
| chr17:62669438
|
A | T | 1 | a0004c0005t0001g0045 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1117+1905A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669438 | ||||||
| chr17:62669439
|
C | A | 1 | a0004c0005t0001g0045 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1117+1906C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669439 | ||||||
| chr17:62669506
|
G | A | 7 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0121others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1117+1973G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669506 | ||||||
| chr17:62669561
|
G | A | 7 | a0001c0001t0001g0304a0002c0006t0001g0135a0005c0010t0001g0161others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117+2028G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669561 | ||||||
| chr17:62669592
|
C | A | 5 | a0002c0003t0001g0138a0002c0003t0001g0139a0002c0003t0001g0140others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118-2057C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669592 | ||||||
| chr17:62669643
|
T | C | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1118-2006T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669643 | ||||||
| chr17:62669667
|
T | C | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1118-1982T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669667 | ||||||
| chr17:62669669
|
C | T | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118-1980C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62669669 | ||||||
| chr17:62670378
|
G | T | 5 | a0001c0002t0002g0160a0001c0002t0002g0242a0001c0002t0002g0263others(2): Show | 5 | NA18986.hp1 NA18992.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1118-1271G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670378 | ||||||
| chr17:62670618
|
T | C | 59 | a0001c0001t0001g0029a0001c0001t0001g0136a0001c0001t0001g0137others(56): Show | 59 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1118-1031T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670618 | ||||||
| chr17:62670705
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0184a0001c0001t0001g0212 | 3 | NA18960.hp2 NA18971.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1118-944C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670705 | ||||||
| chr17:62670804
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1118-845A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670804 | ||||||
| chr17:62670830
|
T | C | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1118-819T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670830 | ||||||
| chr17:62670850
|
G | C | 1 | a0001c0002t0001g0235 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1118-799G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670850 | ||||||
| chr17:62670939
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118-710A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62670939 | ||||||
| chr17:62671059
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1118-590G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62671059 | ||||||
| chr17:62671163
|
C | T | 3 | a0001c0020t0001g0302a0002c0003t0001g0303a0022c0024t0005g0301 | 3 | HG02622.hp2 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1118-486C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62671163 | ||||||
| chr17:62671451
|
T | C | 55 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(52): Show | 55 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1118-198T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62671451 | ||||||
| chr17:62671565
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1118-84C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62671565 | ||||||
| chr17:62671566
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1118-83G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 6/29 | chr17 | 62671566 | ||||||
| chr17:62671873
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0116 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1306+36G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 7/29 | chr17 | 62671873 | ||||||
| chr17:62672172
|
A | G | 55 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(52): Show | 55 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1461+20A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62672172 | ||||||
| chr17:62672781
|
G | C | 55 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(52): Show | 55 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1461+629G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62672781 | ||||||
| chr17:62672784
|
G | A | 3 | a0003c0004t0001g0053a0003c0004t0001g0207a0010c0023t0001g0097 | 3 | NA18942.hp1 NA18963.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1461+632G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62672784 | ||||||
| chr17:62672787
|
T | C | 23 | a0001c0001t0006g0205a0001c0008t0001g0040a0001c0008t0001g0208others(20): Show | 23 | HG00438.hp1 HG01168.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.1461+635T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62672787 | ||||||
| chr17:62672874
|
C | A | 1 | a0001c0002t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1461+722C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62672874 | ||||||
| chr17:62672991
|
C | CA | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1461+852dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62672991 | |||||
| chr17:62672991
|
C | CAA | 11 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0121others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1461+851_1461+852d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62672991 | |||||
| chr17:62672991
|
C | CAAA | 43 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(40): Show | 43 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1461+850_1461+852d others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62672991 | |||||
| chr17:62673000
|
A | T | 20 | a0001c0001t0006g0205a0001c0008t0001g0040a0001c0008t0001g0208others(17): Show | 20 | HG00438.hp1 HG01168.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1461+848A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673000 | ||||||
| chr17:62673005
|
T | TAA | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461+856_1461+857d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62673005 | |||||
| chr17:62673007
|
A | T | 1 | a0002c0006t0004g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1461+855A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673007 | ||||||
| chr17:62673082
|
T | C | 1 | a0002c0003t0001g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1461+930T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673082 | ||||||
| chr17:62673507
|
CT | C | 57 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(54): Show | 57 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1462-537delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62673507 | |||||
| chr17:62673507
|
CTT | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1462-538_1462-537d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62673507 | |||||
| chr17:62673507
|
CTTT | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0149a0001c0001t0001g0188others(3): Show | 6 | HG01167.hp1 HG02602.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1462-539_1462-537d others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62673507 | |||||
| chr17:62673797
|
A | ACCGCGCC others(1): Show |
3 | a0001c0001t0001g0011a0001c0002t0001g0153a0002c0006t0002g0152 | 3 | HG01109.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1462-265_1462-258d others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr17 | 62673797 | |||||
| chr17:62673804
|
C | T | 1 | a0001c0002t0001g0268 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1462-259C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673804 | ||||||
| chr17:62673854
|
G | A | 5 | a0001c0017t0001g0106a0001c0017t0001g0307a0002c0015t0002g0010others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462-209G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673854 | ||||||
| chr17:62673888
|
C | A | 1 | a0002c0003t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1462-175C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673888 | ||||||
| chr17:62673911
|
C | T | 56 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1462-152C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62673911 | ||||||
| chr17:62674057
|
C | T | 3 | a0001c0013t0001g0043a0001c0013t0001g0098a0001c0013t0001g0099 | 3 | NA18948.hp1 NA18966.hp2 NA18974.hp1 |
splice_region_variant&intron_variant | LOW | c.1462-6C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 8/29 | chr17 | 62674057 | ||||||
| chr17:62674236
|
A | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0304a0001c0002t0001g0153others(17): Show | 20 | HG01109.hp2 HG01884.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.1569+66A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674236 | ||||||
| chr17:62674270
|
G | A | 1 | a0002c0006t0004g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1569+100G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674270 | ||||||
| chr17:62674331
|
T | C | 5 | a0002c0003t0001g0006a0002c0003t0001g0110a0002c0003t0001g0111others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1569+161T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674331 | ||||||
| chr17:62674337
|
A | G | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1569+167A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674337 | ||||||
| chr17:62674348
|
C | T | 2 | a0003c0004t0001g0167a0003c0004t0001g0219 | 2 | NA18952.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1569+178C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674348 | ||||||
| chr17:62674595
|
G | C | 1 | a0002c0015t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1569+425G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674595 | ||||||
| chr17:62674603
|
T | G | 1 | a0022c0024t0005g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1569+433T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674603 | ||||||
| chr17:62674699
|
TGA | T | 36 | a0001c0001t0001g0304a0001c0001t0006g0205a0001c0008t0001g0040others(33): Show | 36 | HG00438.hp1 HG01168.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.1569+531_1569+532d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr17 | 62674699 | |||||
| chr17:62674701
|
A | AG | 17 | a0001c0001t0001g0116a0001c0001t0001g0175a0001c0001t0001g0202others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1569+540dupG | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr17 | 62674701 | |||||
| chr17:62674704
|
G | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0103a0001c0001t0001g0177others(3): Show | 6 | HG01167.hp1 HG01978.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1569+534G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674704 | ||||||
| chr17:62674708
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0068others(16): Show | 19 | HG00408.hp2 HG01192.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1569+538G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674708 | ||||||
| chr17:62674798
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1569+628T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674798 | ||||||
| chr17:62674853
|
C | T | 1 | a0001c0001t0006g0205 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1569+683C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674853 | ||||||
| chr17:62674869
|
C | A | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1569+699C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62674869 | ||||||
| chr17:62675027
|
C | G | 50 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0247others(47): Show | 50 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1570-763C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675027 | ||||||
| chr17:62675097
|
AAG | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1570-690_1570-689d others(4): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr17 | 62675097 | |||||
| chr17:62675294
|
C | T | 23 | a0001c0001t0001g0011a0001c0001t0006g0205a0001c0002t0001g0153others(20): Show | 23 | HG00438.hp1 HG01109.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1570-496C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675294 | ||||||
| chr17:62675297
|
C | T | 2 | a0002c0006t0004g0007a0002c0006t0004g0147 | 2 | HG01952.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1570-493C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675297 | ||||||
| chr17:62675323
|
C | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1570-467C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675323 | ||||||
| chr17:62675409
|
T | G | 2 | a0001c0020t0001g0302a0002c0003t0001g0303 | 2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1570-381T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675409 | ||||||
| chr17:62675515
|
C | T | 14 | a0001c0001t0001g0304a0001c0017t0001g0106a0001c0017t0001g0307others(11): Show | 14 | HG01884.hp1 HG01952.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1570-275C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675515 | ||||||
| chr17:62675520
|
C | A | 1 | a0004c0005t0001g0039 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1570-270C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675520 | ||||||
| chr17:62675526
|
G | A | 14 | a0001c0001t0001g0304a0001c0017t0001g0106a0001c0017t0001g0307others(11): Show | 14 | HG01884.hp1 HG01952.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1570-264G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675526 | ||||||
| chr17:62675537
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1570-253C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675537 | ||||||
| chr17:62675566
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1570-224G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 9/29 | chr17 | 62675566 | ||||||
| chr17:62675991
|
A | ATCATGCC others(1): Show |
4 | a0001c0017t0001g0106a0001c0017t0001g0307a0006c0018t0009g0013others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685+87_1685+94dup others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr17 | 62675991 | |||||
| chr17:62676009
|
T | C | 1 | a0002c0015t0002g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1685+104T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 10/29 | chr17 | 62676009 | ||||||
| chr17:62676308
|
G | A | 1 | a0001c0002t0001g0238 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1686-75G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 10/29 | chr17 | 62676308 | ||||||
| chr17:62676317
|
T | C | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1686-66T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 10/29 | chr17 | 62676317 | ||||||
| chr17:62676543
|
A | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0059others(171): Show | 175 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1834+12A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676543 | ||||||
| chr17:62676586
|
C | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(2): Show | 5 | HG02451.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834+55C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676586 | ||||||
| chr17:62676673
|
A | C | 1 | a0001c0002t0001g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1834+142A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676673 | ||||||
| chr17:62676873
|
C | T | 1 | a0006c0026t0002g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1834+342C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676873 | ||||||
| chr17:62676933
|
A | C | 13 | a0001c0031t0001g0156a0002c0003t0001g0006a0002c0003t0001g0108others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1835-336A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676933 | ||||||
| chr17:62676978
|
T | A | 1 | a0001c0002t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1835-291T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676978 | ||||||
| chr17:62676979
|
C | G | 1 | a0001c0002t0001g0240 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1835-290C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62676979 | ||||||
| chr17:62677091
|
A | G | 1 | a0001c0002t0001g0260 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1835-178A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62677091 | ||||||
| chr17:62677140
|
G | T | 1 | a0002c0006t0004g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1835-129G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 11/29 | chr17 | 62677140 | ||||||
| chr17:62677555
|
G | T | 1 | a0001c0002t0001g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2052+69G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62677555 | ||||||
| chr17:62677602
|
G | T | 1 | a0006c0018t0002g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2052+116G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62677602 | ||||||
| chr17:62677789
|
C | A | 2 | a0001c0002t0001g0186a0001c0002t0001g0187 | 2 | NA18963.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2052+303C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62677789 | ||||||
| chr17:62677879
|
A | G | 1 | a0001c0020t0001g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2052+393A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62677879 | ||||||
| chr17:62678037
|
G | A | 1 | a0002c0021t0001g0280 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2053-467G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62678037 | ||||||
| chr17:62678155
|
G | A | 1 | a0004c0005t0001g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2053-349G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62678155 | ||||||
| chr17:62678385
|
T | G | 151 | a0001c0001t0001g0011a0001c0001t0001g0067a0001c0001t0001g0132others(148): Show | 151 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.2053-119T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 12/29 | chr17 | 62678385 | ||||||
| chr17:62678695
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2195+49G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62678695 | ||||||
| chr17:62678734
|
G | A | 1 | a0002c0003t0001g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2195+88G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62678734 | ||||||
| chr17:62678743
|
G | C | 74 | a0001c0001t0001g0011a0001c0001t0006g0205a0001c0002t0001g0153others(71): Show | 74 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.2195+97G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62678743 | ||||||
| chr17:62678744
|
A | G | 5 | a0001c0001t0001g0011a0007c0014t0005g0030a0007c0014t0005g0031others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2195+98A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62678744 | ||||||
| chr17:62678781
|
T | C | 5 | a0002c0006t0004g0007a0002c0006t0004g0012a0002c0006t0004g0109others(2): Show | 5 | HG01891.hp1 HG01952.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2195+135T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62678781 | ||||||
| chr17:62679450
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2196-350G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 13/29 | chr17 | 62679450 | ||||||
| chr17:62680106
|
C | T | 13 | a0001c0001t0001g0011a0001c0002t0001g0153a0001c0017t0001g0106others(10): Show | 13 | HG01109.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2299-64C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 14/29 | chr17 | 62680106 | ||||||
| chr17:62680115
|
G | A | 5 | a0001c0001t0001g0011a0007c0014t0005g0030a0007c0014t0005g0031others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2299-55G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 14/29 | chr17 | 62680115 | ||||||
| chr17:62680323
|
C | T | 1 | a0002c0006t0002g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2437+15C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 15/29 | chr17 | 62680323 | ||||||
| chr17:62680496
|
A | G | 5 | a0001c0017t0001g0106a0001c0017t0001g0307a0006c0018t0002g0306others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2473+43A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 16/29 | chr17 | 62680496 | ||||||
| chr17:62680554
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG02451.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2473+101G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 16/29 | chr17 | 62680554 | ||||||
| chr17:62680622
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(196): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.2473+169G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 16/29 | chr17 | 62680622 | ||||||
| chr17:62680757
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2474-43C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 16/29 | chr17 | 62680757 | ||||||
| chr17:62681215
|
C | T | 11 | a0001c0002t0002g0083a0001c0002t0002g0160a0001c0002t0002g0172others(8): Show | 11 | HG01943.hp1 HG01952.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.2702+86C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 18/29 | chr17 | 62681215 | ||||||
| chr17:62681287
|
C | A | 2 | a0001c0002t0001g0240a0001c0002t0001g0255 | 2 | HG00621.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.2702+158C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 18/29 | chr17 | 62681287 | ||||||
| chr17:62681470
|
G | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0085 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2702+341G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 18/29 | chr17 | 62681470 | ||||||
| chr17:62681527
|
A | G | 9 | a0002c0009t0001g0026a0002c0009t0001g0027a0002c0009t0001g0062others(6): Show | 9 | HG00438.hp1 HG01168.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.2703-310A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 18/29 | chr17 | 62681527 | ||||||
| chr17:62681594
|
G | A | 3 | a0001c0002t0001g0153a0001c0017t0001g0106a0001c0017t0001g0307 | 3 | HG01109.hp2 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2703-243G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 18/29 | chr17 | 62681594 | ||||||
| chr17:62681979
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2803+42A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 19/29 | chr17 | 62681979 | ||||||
| chr17:62681986
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2803+49A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 19/29 | chr17 | 62681986 | ||||||
| chr17:62682435
|
A | G | 2 | a0001c0002t0001g0290a0021c0037t0001g0049 | 2 | HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2946+58A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62682435 | ||||||
| chr17:62682490
|
C | T | 2 | a0002c0003t0001g0019a0002c0003t0001g0024 | 2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2946+113C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62682490 | ||||||
| chr17:62682583
|
G | A | 1 | a0019c0030t0001g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2946+206G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62682583 | ||||||
| chr17:62682591
|
A | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.2946+214A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62682591 | ||||||
| chr17:62682640
|
A | AT | 8 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0204others(5): Show | 8 | HG00733.hp2 HG01978.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2946+281dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62682640 | |||||
| chr17:62682640
|
AT | A | 11 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0281others(8): Show | 11 | HG00558.hp1 HG01069.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.2946+281delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62682640 | |||||
| chr17:62683029
|
T | C | 1 | a0001c0041t0001g0287 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2946+652T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62683029 | ||||||
| chr17:62683095
|
ATAT | A | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0041others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.2946+722_2946+724d others(5): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62683095 | |||||
| chr17:62683266
|
C | T | 12 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 12 | HG01099.hp2 HG01891.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.2946+889C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62683266 | ||||||
| chr17:62683292
|
A | G | 1 | a0007c0014t0005g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2946+915A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62683292 | ||||||
| chr17:62683510
|
C | CT | 22 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0173others(19): Show | 22 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2946+1155dupT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62683510 | |||||
| chr17:62683510
|
CT | C | 25 | a0001c0001t0001g0128a0001c0001t0001g0197a0001c0001t0003g0008others(22): Show | 25 | HG01167.hp2 HG01891.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.2946+1155delT | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62683510 | |||||
| chr17:62683545
|
A | G | 1 | a0001c0002t0001g0141 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2946+1168A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62683545 | ||||||
| chr17:62683865
|
CA | C | 8 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0121others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2946+1500delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62683865 | |||||
| chr17:62683934
|
A | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0308 | 2 | HG02280.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2946+1557A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62683934 | ||||||
| chr17:62684329
|
G | T | 1 | a0002c0039t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2946+1952G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684329 | ||||||
| chr17:62684374
|
G | A | 1 | a0005c0010t0001g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2946+1997G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684374 | ||||||
| chr17:62684481
|
A | T | 4 | a0005c0010t0001g0161a0005c0010t0001g0246a0005c0010t0001g0270others(1): Show | 4 | HG02280.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2946+2104A>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684481 | ||||||
| chr17:62684828
|
C | T | 1 | a0002c0003t0001g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2946+2451C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684828 | ||||||
| chr17:62684867
|
G | A | 1 | a0002c0007t0001g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2946+2490G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684867 | ||||||
| chr17:62684883
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.2946+2506G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684883 | ||||||
| chr17:62684938
|
T | G | 1 | a0002c0009t0001g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2946+2561T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62684938 | ||||||
| chr17:62685054
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2946+2677A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62685054 | ||||||
| chr17:62685166
|
AC | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2946+2790delC | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62685166 | ||||||
| chr17:62685167
|
C | A | 42 | a0001c0031t0001g0156a0002c0003t0001g0006a0002c0003t0001g0015others(39): Show | 42 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2946+2790C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62685167 | ||||||
| chr17:62685715
|
T | A | 2 | a0001c0001t0001g0180a0002c0006t0001g0135 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2947-2574T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62685715 | ||||||
| chr17:62686039
|
G | C | 86 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0041others(83): Show | 86 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.2947-2250G>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686039 | ||||||
| chr17:62686149
|
G | A | 1 | a0002c0003t0001g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2947-2140G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686149 | ||||||
| chr17:62686286
|
C | G | 1 | a0001c0002t0001g0238 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2947-2003C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686286 | ||||||
| chr17:62686298
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2947-1991C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686298 | ||||||
| chr17:62686311
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2947-1978G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686311 | ||||||
| chr17:62686417
|
C | T | 5 | a0002c0006t0004g0007a0002c0006t0004g0012a0002c0006t0004g0109others(2): Show | 5 | HG01891.hp1 HG01952.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2947-1872C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686417 | ||||||
| chr17:62686451
|
T | TCAA | 18 | a0001c0002t0001g0153a0001c0017t0001g0106a0001c0017t0001g0307others(15): Show | 18 | HG01109.hp2 HG01346.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.2947-1804_2947-180 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62686451 | |||||
| chr17:62686451
|
T | TCAACAA | 3 | a0002c0003t0001g0025a0002c0009t0001g0062a0002c0009t0001g0088 | 3 | HG02647.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2947-1807_2947-180 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62686451 | |||||
| chr17:62686451
|
TCAA | T | 18 | a0001c0001t0001g0103a0001c0001t0001g0250a0001c0001t0001g0304others(15): Show | 18 | HG01099.hp2 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2947-1804_2947-180 others(7): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62686451 | |||||
| chr17:62686451
|
TCAACAA | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.2947-1807_2947-180 others(10): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62686451 | |||||
| chr17:62686486
|
A | G | 1 | a0002c0006t0001g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2947-1803A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686486 | ||||||
| chr17:62686550
|
C | T | 2 | a0001c0001t0001g0211a0001c0002t0001g0146 | 2 | HG01261.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2947-1739C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686550 | ||||||
| chr17:62686551
|
G | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0075others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.2947-1738G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686551 | ||||||
| chr17:62686556
|
T | TCACCTCC others(4): Show |
1 | a0018c0033t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2947-1732_2947-172 others(15): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr17 | 62686556 | |||||
| chr17:62686669
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2947-1620C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686669 | ||||||
| chr17:62686670
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2947-1619A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686670 | ||||||
| chr17:62686692
|
C | T | 1 | a0003c0004t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2947-1597C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686692 | ||||||
| chr17:62686731
|
A | C | 32 | a0001c0031t0001g0156a0002c0003t0001g0006a0002c0003t0001g0015others(29): Show | 32 | HG01069.hp2 HG01071.hp1 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.2947-1558A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686731 | ||||||
| chr17:62686893
|
C | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0014 | 3 | HG02622.hp1 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2947-1396C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686893 | ||||||
| chr17:62686934
|
G | A | 14 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0101others(11): Show | 14 | HG00280.hp1 HG01074.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.2947-1355G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62686934 | ||||||
| chr17:62687109
|
C | G | 5 | a0002c0006t0004g0007a0002c0006t0004g0012a0002c0006t0004g0109others(2): Show | 5 | HG01891.hp1 HG01952.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2947-1180C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687109 | ||||||
| chr17:62687464
|
C | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0116 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2947-825C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687464 | ||||||
| chr17:62687625
|
T | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.2947-664T>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687625 | ||||||
| chr17:62687682
|
T | C | 87 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0041others(84): Show | 87 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2947-607T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687682 | ||||||
| chr17:62687692
|
C | T | 1 | a0001c0002t0001g0253 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2947-597C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687692 | ||||||
| chr17:62687716
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2947-573T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687716 | ||||||
| chr17:62687808
|
T | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.2947-481T>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687808 | ||||||
| chr17:62687931
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2947-358A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62687931 | ||||||
| chr17:62688037
|
T | C | 2 | a0001c0001t0001g0067a0001c0002t0001g0078 | 2 | NA18954.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2947-252T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62688037 | ||||||
| chr17:62688109
|
C | A | 1 | a0001c0001t0001g0002 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2947-180C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 20/29 | chr17 | 62688109 | ||||||
| chr17:62688425
|
C | A | 1 | a0002c0034t0002g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3061+22C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 21/29 | chr17 | 62688425 | ||||||
| chr17:62688498
|
T | C | 1 | a0002c0006t0002g0152 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.3062-3T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 21/29 | chr17 | 62688498 | ||||||
| chr17:62689122
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3334+162A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689122 | ||||||
| chr17:62689170
|
G | A | 1 | a0002c0015t0002g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3334+210G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689170 | ||||||
| chr17:62689219
|
G | A | 2 | a0002c0009t0001g0026a0002c0009t0001g0277 | 2 | HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3334+259G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689219 | ||||||
| chr17:62689282
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0304 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3335-240C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689282 | ||||||
| chr17:62689372
|
G | A | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3335-150G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689372 | ||||||
| chr17:62689425
|
G | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3335-97G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689425 | ||||||
| chr17:62689443
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.3335-79C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 23/29 | chr17 | 62689443 | ||||||
| chr17:62689774
|
A | G | 96 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(93): Show | 96 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.3573+14A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/29 | chr17 | 62689774 | ||||||
| chr17:62689790
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.3573+30C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 24/29 | chr17 | 62689790 | ||||||
| chr17:62690100
|
C | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.3742+38C>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 25/29 | chr17 | 62690100 | ||||||
| chr17:62690326
|
C | T | 1 | a0002c0003t0001g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3892+21C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/29 | chr17 | 62690326 | ||||||
| chr17:62690435
|
C | T | 14 | a0002c0006t0002g0152a0002c0006t0004g0007a0002c0006t0004g0012others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.3892+130C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/29 | chr17 | 62690435 | ||||||
| chr17:62690480
|
GC | G | 9 | a0002c0015t0002g0010a0002c0015t0002g0017a0002c0015t0002g0230others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.3893-155delC | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr17 | 62690480 | |||||
| chr17:62690592
|
GC | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3893-42delC | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr17 | 62690592 | |||||
| chr17:62690613
|
G | T | 11 | a0001c0002t0002g0083a0001c0002t0002g0160a0001c0002t0002g0172others(8): Show | 11 | HG01943.hp1 HG01952.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.3893-29G>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 26/29 | chr17 | 62690613 | ||||||
| chr17:62690790
|
G | A | 13 | a0002c0006t0004g0007a0002c0006t0004g0012a0002c0006t0004g0109others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.4012+29G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 27/29 | chr17 | 62690790 | ||||||
| chr17:62690832
|
G | A | 1 | a0001c0001t0007g0224 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4012+71G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 27/29 | chr17 | 62690832 | ||||||
| chr17:62690871
|
T | C | 14 | a0002c0006t0002g0152a0002c0006t0004g0007a0002c0006t0004g0012others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.4013-78T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 27/29 | chr17 | 62690871 | ||||||
| chr17:62690882
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(299): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.4013-67A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 27/29 | chr17 | 62690882 | ||||||
| chr17:62691134
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18979.hp1 | splice_region_variant&intron_variant | LOW | c.4192+6C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691134 | ||||||
| chr17:62691221
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4192+93C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691221 | ||||||
| chr17:62691222
|
A | G | 3 | a0006c0018t0002g0306a0006c0018t0009g0013a0006c0026t0002g0271 | 3 | HG01884.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4192+94A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691222 | ||||||
| chr17:62691233
|
GA | G | 3 | a0001c0002t0001g0153a0001c0017t0001g0106a0001c0017t0001g0307 | 3 | HG01109.hp2 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4192+107delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr17 | 62691233 | |||||
| chr17:62691256
|
C | T | 3 | a0001c0002t0001g0153a0001c0017t0001g0106a0001c0017t0001g0307 | 3 | HG01109.hp2 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4192+128C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691256 | ||||||
| chr17:62691317
|
A | G | 9 | a0002c0015t0002g0010a0002c0015t0002g0017a0002c0015t0002g0230others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4192+189A>G | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691317 | ||||||
| chr17:62691485
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.4192+357T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691485 | ||||||
| chr17:62691560
|
A | C | 85 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0041others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.4192+432A>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691560 | ||||||
| chr17:62691595
|
C | A | 1 | a0018c0033t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4192+467C>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691595 | ||||||
| chr17:62691631
|
C | T | 9 | a0002c0015t0002g0010a0002c0015t0002g0017a0002c0015t0002g0230others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4193-481C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691631 | ||||||
| chr17:62691771
|
C | CA | 85 | a0001c0001t0001g0180a0001c0001t0001g0194a0001c0001t0001g0197others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.4193-318dupA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr17 | 62691771 | |||||
| chr17:62691771
|
CA | C | 22 | a0001c0001t0001g0060a0001c0001t0001g0103a0001c0001t0001g0145others(19): Show | 22 | HG00738.hp1 HG01069.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.4193-318delA | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr17 | 62691771 | |||||
| chr17:62691771
|
CAAAAAA | C | 11 | a0001c0002t0002g0083a0001c0002t0002g0160a0001c0002t0002g0172others(8): Show | 11 | HG01943.hp1 HG01952.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.4193-323_4193-318d others(8): Show |
MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr17 | 62691771 | |||||
| chr17:62691800
|
G | A | 1 | a0002c0015t0002g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4193-312G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691800 | ||||||
| chr17:62691861
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(5): Show | 8 | HG01099.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4193-251C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691861 | ||||||
| chr17:62691883
|
G | A | 9 | a0002c0015t0002g0010a0002c0015t0002g0017a0002c0015t0002g0230others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4193-229G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691883 | ||||||
| chr17:62691911
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4193-201G>A | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62691911 | ||||||
| chr17:62692045
|
T | C | 88 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0041others(85): Show | 88 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.4193-67T>C | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 28/29 | chr17 | 62692045 | ||||||
| chr17:62692159
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4219+21C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 29/29 | chr17 | 62692159 | ||||||
| chr17:62692220
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4220-11C>T | MRC2 | ENSG00000011028.14 | transcript | ENST00000303375.10 | protein_coding | 29/29 | chr17 | 62692220 |