| geneid | 341883 |
|---|---|
| ensemblid | ENSG00000131951.12 |
| hgncid | 19848 |
| symbol | LRRC9 |
| name | leucine rich repeat containing 9 |
| refseq_nuc | NM_001395648.1 |
| refseq_prot | NP_001382577.1 |
| ensembl_nuc | ENST00000570145.2 |
| ensembl_prot | ENSP00000457773.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 59920144 |
| end | 60066817 |
| strand | + |
| ver | v1.2 |
| region | chr14:59920144-60066817 |
| region5000 | chr14:59915144-60071817 |
| regionname0 | LRRC9_chr14_59920144_60066817 |
| regionname5000 | LRRC9_chr14_59915144_60071817 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1494 | 280 | 61 | 54 | 125 | 10 | 28 | 95 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0002 | 0/0 | 1494 | 21 | 0 | 0 | 21 | 0 | 0 | 21 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0003 | 0/0 | 1494 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0004 | 0/0 | 1494 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0005 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0006 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0007 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0008 | 0/0 | 1037 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0009 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0010 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0011 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0012 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0013 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0014 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4485 | 158 | 28 | 36 | 70 | 9 | 14 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0002 | 1/0 | 4485 | 97 | 28 | 14 | 46 | 0 | 8 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0003 | 0/0 | 4485 | 21 | 0 | 0 | 21 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0004 | 0/0 | 4485 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0005 | 0/0 | 4485 | 8 | 5 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0006 | 0/0 | 4485 | 5 | 0 | 0 | 5 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0007 | 0/0 | 4485 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0008 | 0/0 | 4485 | 3 | 0 | 0 | 2 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0009 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0010 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0011 | 0/0 | 4485 | 2 | 0 | 0 | 0 | 2 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0012 | 0/0 | 4485 | 2 | 0 | 0 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0013 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0014 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0015 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0016 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0017 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0018 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| c0019 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3941 | 52 | 17 | 3 | 27 | 1 | 3 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0002 | 0/0 | 3618 | 44 | 9 | 12 | 14 | 0 | 9 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0003 | 0/0 | 3942 | 35 | 3 | 16 | 9 | 5 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0004 | 0/0 | 3618 | 29 | 4 | 1 | 24 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0005 | 0/0 | 3617 | 24 | 0 | 0 | 24 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0006 | 0/0 | 3943 | 12 | 1 | 4 | 3 | 1 | 3 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0007 | 0/0 | 3618 | 11 | 0 | 0 | 11 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0008 | 0/0 | 3941 | 11 | 1 | 5 | 0 | 3 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0009 | 0/0 | 3619 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0010 | 0/0 | 3941 | 9 | 0 | 1 | 8 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0011 | 0/0 | 3929 | 8 | 4 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0012 | 0/0 | 3618 | 8 | 8 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0013 | 0/0 | 3618 | 7 | 4 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0014 | 0/0 | 3943 | 7 | 1 | 2 | 3 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0015 | 0/0 | 3942 | 6 | 0 | 0 | 5 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0016 | 0/0 | 3940 | 4 | 0 | 2 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0017 | 0/0 | 3618 | 4 | 3 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0018 | 0/0 | 3618 | 3 | 3 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0019 | 0/0 | 3942 | 3 | 1 | 0 | 1 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0020 | 0/0 | 3617 | 3 | 0 | 0 | 3 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0021 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0022 | 0/0 | 3619 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0023 | 0/0 | 3930 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0024 | 1/0 | 3619 | 2 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0025 | 0/0 | 3619 | 2 | 1 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0026 | 0/0 | 3618 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0027 | 0/0 | 3940 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0028 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0029 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0030 | 0/0 | 3942 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0031 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0032 | 0/0 | 3941 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0033 | 0/0 | 3941 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0034 | 0/0 | 3944 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0035 | 0/0 | 3619 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0036 | 0/0 | 3943 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0037 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0038 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0039 | 0/0 | 3943 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0040 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0041 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0042 | 0/0 | 3942 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0043 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0044 | 0/0 | 3940 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| t0045 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4485 | 158 | 28 | 36 | 70 | 9 | 14 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002 | 1/0 | 4485 | 97 | 28 | 14 | 46 | 0 | 8 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0004 | 0/0 | 4485 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0005 | 0/0 | 4485 | 8 | 5 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0006 | 0/0 | 4485 | 5 | 0 | 0 | 5 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0012 | 0/0 | 4485 | 2 | 0 | 0 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0002c0003 | 0/0 | 4485 | 21 | 0 | 0 | 21 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0003c0007 | 0/0 | 4485 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0004c0008 | 0/0 | 4485 | 3 | 0 | 0 | 2 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0005c0013 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0006c0009 | 0/0 | 4485 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0007c0010 | 0/0 | 4485 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0008c0011 | 0/0 | 4485 | 2 | 0 | 0 | 0 | 2 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0009c0018 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0010c0017 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0011c0016 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0012c0015 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0013c0014 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0014c0019 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8425 | 52 | 17 | 3 | 27 | 1 | 3 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0003 | 0/0 | 8426 | 31 | 2 | 14 | 9 | 4 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0006 | 0/0 | 8427 | 10 | 1 | 4 | 3 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0008 | 0/0 | 8425 | 11 | 1 | 5 | 0 | 3 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0010 | 0/0 | 8425 | 8 | 0 | 1 | 7 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0011 | 0/0 | 8413 | 8 | 4 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0014 | 0/0 | 8427 | 7 | 1 | 2 | 3 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0015 | 0/0 | 8426 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0016 | 0/0 | 8424 | 4 | 0 | 2 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0019 | 0/0 | 8426 | 3 | 1 | 0 | 1 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0023 | 0/0 | 8414 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0027 | 0/0 | 8424 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0028 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0030 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0031 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0032 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0033 | 0/0 | 8425 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0034 | 0/0 | 8428 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0035 | 0/0 | 8103 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0036 | 0/0 | 8427 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0037 | 0/0 | 8426 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0039 | 0/0 | 8427 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0040 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0041 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0042 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0043 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0044 | 0/0 | 8424 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0001t0045 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0002 | 0/0 | 8102 | 37 | 9 | 12 | 9 | 0 | 7 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0004 | 0/0 | 8102 | 24 | 4 | 1 | 19 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0007 | 0/0 | 8102 | 11 | 0 | 0 | 11 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0012 | 0/0 | 8102 | 8 | 8 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0017 | 0/0 | 8102 | 4 | 3 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0020 | 0/0 | 8101 | 3 | 0 | 0 | 3 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0021 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0022 | 0/0 | 8103 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0024 | 1/0 | 8103 | 2 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0025 | 0/0 | 8103 | 2 | 1 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0026 | 0/0 | 8102 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0002t0029 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0004t0009 | 0/0 | 8103 | 10 | 0 | 3 | 4 | 1 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0005t0013 | 0/0 | 8102 | 7 | 4 | 1 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0005t0038 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0006t0002 | 0/0 | 8102 | 5 | 0 | 0 | 5 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0001c0012t0002 | 0/0 | 8102 | 2 | 0 | 0 | 0 | 0 | 2 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0002c0003t0005 | 0/0 | 8101 | 21 | 0 | 0 | 21 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0003c0007t0004 | 0/0 | 8102 | 4 | 0 | 0 | 4 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0004c0008t0010 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0004c0008t0015 | 0/0 | 8426 | 2 | 0 | 0 | 1 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0005c0013t0018 | 0/0 | 8102 | 2 | 2 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0006c0009t0005 | 0/0 | 8101 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0007c0010t0018 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0007c0010t0021 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0008c0011t0003 | 0/0 | 8426 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0008c0011t0006 | 0/0 | 8427 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0009c0018t0003 | 0/0 | 8426 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0010c0017t0003 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0011c0016t0004 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0012c0015t0003 | 0/0 | 8426 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0013c0014t0006 | 0/0 | 8427 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| a0014c0019t0005 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | copy fasta | chr14 | 59915144 | 60071817 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0016g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0019g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0023g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0023g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0027g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0028g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0030g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0031g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0032g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0033g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0034g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0035g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0036g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0039g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0040g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0041g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0042g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0043g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0044g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0001t0045g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0017g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0020g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0021g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0022g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0022g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0024g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0024g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0025g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0025g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0026g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0026g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0002t0029g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0004t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0005t0038g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0006t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0012t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0001c0012t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0002c0003t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0003c0007t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0015g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0004c0008t0015g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0005c0013t0018g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0005c0013t0018g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0006c0009t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0006c0009t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0007c0010t0018g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0007c0010t0021g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0008c0011t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0008c0011t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0009c0018t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0010c0017t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0011c0016t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0012c0015t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0013c0014t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| a0014c0019t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0011 | t0003 | g0212 | EUR | GBR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | GBR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0041 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00280 | hp2 | a0008 | c0011 | t0006 | g0211 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00323 | hp2 | a0001 | c0004 | t0009 | g0304 | EUR | FIN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00423 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00558 | hp2 | a0001 | c0002 | t0020 | g0282 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0319 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00621 | hp1 | a0001 | c0001 | t0016 | g0051 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00621 | hp2 | a0001 | c0001 | t0016 | g0206 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00642 | hp1 | a0001 | c0004 | t0009 | g0309 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00673 | hp2 | a0001 | c0001 | t0014 | g0250 | EAS | CHS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00735 | hp1 | a0001 | c0004 | t0009 | g0302 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0258 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0067 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG00741 | hp2 | a0001 | c0001 | t0043 | g0012 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01074 | hp1 | a0001 | c0001 | t0016 | g0105 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01074 | hp2 | a0001 | c0001 | t0016 | g0023 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01109 | hp2 | a0001 | c0002 | t0017 | g0141 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01169 | hp2 | a0010 | c0017 | t0003 | g0065 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0176 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0102 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01358 | hp2 | a0001 | c0005 | t0013 | g0151 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01361 | hp1 | a0001 | c0001 | t0034 | g0098 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01361 | hp2 | a0001 | c0004 | t0009 | g0303 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01496 | hp1 | a0001 | c0001 | t0039 | g0068 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01496 | hp2 | a0001 | c0001 | t0035 | g0156 | AMR | CLM | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0255 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0155 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0261 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0260 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01517 | hp2 | a0001 | c0001 | t0044 | g0008 | EUR | IBS | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0099 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01934 | hp1 | a0012 | c0015 | t0003 | g0164 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01934 | hp2 | a0001 | c0001 | t0014 | g0249 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02015 | hp2 | a0001 | c0002 | t0007 | g0275 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0289 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02040 | hp2 | a0001 | c0001 | t0014 | g0035 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02055 | hp1 | a0001 | c0005 | t0013 | g0179 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0273 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02074 | hp1 | a0001 | c0006 | t0002 | g0114 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02074 | hp2 | a0001 | c0001 | t0023 | g0049 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02080 | hp1 | a0001 | c0006 | t0002 | g0109 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02080 | hp2 | a0001 | c0002 | t0022 | g0270 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02132 | hp1 | a0001 | c0002 | t0022 | g0269 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02132 | hp2 | a0001 | c0006 | t0002 | g0116 | EAS | KHV | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02145 | hp1 | a0001 | c0005 | t0013 | g0180 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02145 | hp2 | a0001 | c0002 | t0025 | g0113 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0076 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02165 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | CDX | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02257 | hp1 | a0001 | c0002 | t0021 | g0161 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02258 | hp1 | a0001 | c0001 | t0033 | g0063 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02273 | hp2 | a0001 | c0001 | t0040 | g0104 | AMR | PEL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02280 | hp1 | a0001 | c0005 | t0013 | g0181 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0310 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02602 | hp1 | a0001 | c0001 | t0042 | g0184 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02602 | hp2 | a0001 | c0012 | t0002 | g0106 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02622 | hp2 | a0001 | c0002 | t0012 | g0122 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02683 | hp1 | a0001 | c0002 | t0025 | g0135 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02683 | hp2 | a0001 | c0001 | t0008 | g0031 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02717 | hp2 | a0001 | c0002 | t0012 | g0147 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02735 | hp1 | a0013 | c0014 | t0006 | g0162 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02735 | hp2 | a0001 | c0005 | t0013 | g0172 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02738 | hp2 | a0004 | c0008 | t0015 | g0167 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0121 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02818 | hp1 | a0001 | c0002 | t0017 | g0117 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02895 | hp1 | a0001 | c0002 | t0012 | g0123 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02896 | hp2 | a0001 | c0002 | t0012 | g0125 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0079 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03139 | hp1 | a0005 | c0013 | t0018 | g0110 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03195 | hp1 | a0009 | c0018 | t0003 | g0230 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03195 | hp2 | a0001 | c0002 | t0017 | g0142 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03209 | hp1 | a0001 | c0002 | t0012 | g0148 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03453 | hp1 | a0001 | c0002 | t0029 | g0017 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0120 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0083 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03516 | hp2 | a0001 | c0002 | t0024 | g0157 | AFR | ESN | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03540 | hp1 | a0001 | c0005 | t0013 | g0182 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | GWD | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03579 | hp1 | a0001 | c0002 | t0017 | g0174 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0066 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0163 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03688 | hp1 | a0001 | c0001 | t0019 | g0315 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0175 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0320 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03710 | hp2 | a0001 | c0004 | t0009 | g0308 | SAS | PJL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0233 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03834 | hp2 | a0001 | c0012 | t0002 | g0140 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03927 | hp1 | a0001 | c0001 | t0014 | g0046 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0127 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03942 | hp1 | a0001 | c0005 | t0013 | g0171 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03942 | hp2 | a0001 | c0001 | t0030 | g0160 | SAS | BEB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0240 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04204 | hp1 | a0001 | c0004 | t0009 | g0307 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0154 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0053 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18612 | hp2 | a0001 | c0006 | t0002 | g0115 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18747 | hp1 | a0001 | c0001 | t0037 | g0247 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18747 | hp2 | a0001 | c0001 | t0023 | g0059 | EAS | CHB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0214 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18939 | hp1 | a0001 | c0001 | t0041 | g0229 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18939 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18941 | hp2 | a0002 | c0003 | t0005 | g0205 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18942 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18942 | hp2 | a0001 | c0002 | t0020 | g0283 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18945 | hp2 | a0002 | c0003 | t0005 | g0202 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18946 | hp2 | a0001 | c0004 | t0009 | g0306 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18948 | hp1 | a0001 | c0004 | t0009 | g0305 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0278 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18960 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18961 | hp2 | a0003 | c0007 | t0004 | g0276 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18962 | hp1 | a0003 | c0007 | t0004 | g0277 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18962 | hp2 | a0001 | c0004 | t0009 | g0209 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18964 | hp1 | a0001 | c0002 | t0004 | g0318 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18964 | hp2 | a0002 | c0003 | t0005 | g0199 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18966 | hp1 | a0011 | c0016 | t0004 | g0267 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18966 | hp2 | a0001 | c0001 | t0015 | g0052 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18975 | hp2 | a0002 | c0003 | t0005 | g0190 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18977 | hp1 | a0002 | c0003 | t0005 | g0188 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18977 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18978 | hp2 | a0004 | c0008 | t0010 | g0055 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18980 | hp1 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0300 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18983 | hp2 | a0006 | c0009 | t0005 | g0191 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18984 | hp1 | a0002 | c0003 | t0005 | g0186 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18986 | hp2 | a0003 | c0007 | t0004 | g0280 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18988 | hp1 | a0002 | c0003 | t0005 | g0196 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18989 | hp1 | a0001 | c0002 | t0007 | g0290 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18989 | hp2 | a0001 | c0001 | t0011 | g0075 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18992 | hp1 | a0002 | c0003 | t0005 | g0195 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18992 | hp2 | a0001 | c0002 | t0020 | g0301 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18993 | hp1 | a0001 | c0001 | t0028 | g0030 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18994 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0268 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18995 | hp1 | a0002 | c0003 | t0005 | g0187 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18995 | hp2 | a0001 | c0001 | t0031 | g0219 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18998 | hp1 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18999 | hp2 | a0002 | c0003 | t0005 | g0201 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19002 | hp1 | a0001 | c0001 | t0045 | g0232 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19004 | hp1 | a0002 | c0003 | t0005 | g0197 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19006 | hp1 | a0001 | c0002 | t0007 | g0266 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19006 | hp2 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19007 | hp2 | a0001 | c0002 | t0007 | g0294 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19011 | hp2 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19012 | hp2 | a0002 | c0003 | t0005 | g0185 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19055 | hp1 | a0001 | c0004 | t0009 | g0210 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19055 | hp2 | a0002 | c0003 | t0005 | g0189 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19057 | hp2 | a0001 | c0002 | t0007 | g0274 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19059 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19059 | hp2 | a0001 | c0001 | t0014 | g0040 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19065 | hp1 | a0001 | c0002 | t0026 | g0132 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19065 | hp2 | a0002 | c0003 | t0005 | g0192 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19066 | hp1 | a0001 | c0002 | t0026 | g0130 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19067 | hp1 | a0004 | c0008 | t0015 | g0036 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19067 | hp2 | a0001 | c0002 | t0007 | g0317 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19068 | hp2 | a0002 | c0003 | t0005 | g0198 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19070 | hp1 | a0002 | c0003 | t0005 | g0200 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19075 | hp2 | a0001 | c0002 | t0007 | g0292 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19078 | hp1 | a0001 | c0002 | t0004 | g0316 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19078 | hp2 | a0001 | c0001 | t0036 | g0314 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19079 | hp1 | a0002 | c0003 | t0005 | g0194 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19079 | hp2 | a0001 | c0001 | t0015 | g0096 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19081 | hp1 | a0014 | c0019 | t0005 | g0042 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19081 | hp2 | a0001 | c0002 | t0007 | g0291 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19082 | hp1 | a0001 | c0006 | t0002 | g0108 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0271 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19084 | hp2 | a0001 | c0002 | t0007 | g0002 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19085 | hp2 | a0002 | c0003 | t0005 | g0193 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19086 | hp1 | a0002 | c0003 | t0005 | g0204 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19087 | hp2 | a0003 | c0007 | t0004 | g0279 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19088 | hp1 | a0006 | c0009 | t0005 | g0203 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19088 | hp2 | a0001 | c0001 | t0027 | g0234 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19090 | hp1 | a0001 | c0001 | t0019 | g0311 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19090 | hp2 | a0001 | c0002 | t0007 | g0293 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA19240 | hp2 | a0001 | c0005 | t0038 | g0150 | AFR | YRI | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | ASW | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02486 | hp1 | a0001 | c0002 | t0012 | g0124 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02486 | hp2 | a0007 | c0010 | t0021 | g0033 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0153 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0097 | AFR | ACB | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03471 | hp1 | a0007 | c0010 | t0018 | g0166 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | MSL | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18955 | hp1 | a0001 | c0001 | t0027 | g0246 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA18955 | hp2 | a0001 | c0001 | t0011 | g0050 | EAS | JPT | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA20300 | hp2 | a0005 | c0013 | t0018 | g0111 | AFR | USA | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0078 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | LWK | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0248 | REF | REF | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0024 | g0103 | REF | REF | LRRC9_chr14_59915144_60071817 | LRRC9 | chr14 | 59915144 | 60071817 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59931987
|
A | G | 2 | a0004a0014 | 4 | HG02738.hp2 NA18978.hp2 NA19067.hp1 others(1): Show |
missense_variant | MODERATE | c.491A>G | p.Asn164Ser | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/33 | 654/8103 | 491/4485 | 164/1494 | chr14 | 59931987 | ||
| chr14:59960963
|
G | A | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1129G>A | p.Gly377Ser | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/33 | 1292/8103 | 1129/4485 | 377/1494 | chr14 | 59960963 | ||
| chr14:59981854
|
G | C | 1 | a0012 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1885G>C | p.Ala629Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2048/8103 | 1885/4485 | 629/1494 | chr14 | 59981854 | ||
| chr14:59981881
|
A | C | 1 | a0005 | 2 | HG03139.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1912A>C | p.Asn638His | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2075/8103 | 1912/4485 | 638/1494 | chr14 | 59981881 | ||
| chr14:59982016
|
A | G | 1 | a0006 | 2 | NA18983.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.2047A>G | p.Thr683Ala | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/33 | 2210/8103 | 2047/4485 | 683/1494 | chr14 | 59982016 | ||
| chr14:59985158
|
A | T | 1 | a0003 | 4 | NA18961.hp2 NA18962.hp1 NA18986.hp2 others(1): Show |
missense_variant | MODERATE | c.2145A>T | p.Leu715Phe | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/33 | 2308/8103 | 2145/4485 | 715/1494 | chr14 | 59985158 | ||
| chr14:60001972
|
C | T | 1 | a0009 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2536C>T | p.Leu846Phe | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/33 | 2699/8103 | 2536/4485 | 846/1494 | chr14 | 60001972 | ||
| chr14:60002045
|
C | A | 1 | a0007 | 2 | HG02486.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2609C>A | p.Thr870Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/33 | 2772/8103 | 2609/4485 | 870/1494 | chr14 | 60002045 | ||
| chr14:60006505
|
T | C | 1 | a0011 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.2951T>C | p.Leu984Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/33 | 3114/8103 | 2951/4485 | 984/1494 | chr14 | 60006505 | ||
| chr14:60008141
|
G | A | 1 | a0008 | 2 | HG00099.hp1 HG00280.hp2 |
stop_gained | HIGH | c.3113G>A | p.Trp1038* | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/33 | 3276/8103 | 3113/4485 | 1038/1494 | chr14 | 60008141 | ||
| chr14:60057944
|
G | A | 3 | a0002a0006a0014 | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
missense_variant | MODERATE | c.4198G>A | p.Glu1400Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/33 | 4361/8103 | 4198/4485 | 1400/1494 | chr14 | 60057944 | ||
| chr14:60062015
|
A | C | 1 | a0010 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.4281A>C | p.Lys1427Asn | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/33 | 4444/8103 | 4281/4485 | 1427/1494 | chr14 | 60062015 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59928369
|
A | G | 1 | a0001c0005 | 8 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
synonymous_variant | LOW | c.150A>G | p.Leu50Leu | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/33 | 313/8103 | 150/4485 | 50/1494 | chr14 | 59928369 | ||
| chr14:59938560
|
G | A | 1 | a0001c0004 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
synonymous_variant | LOW | c.714G>A | p.Lys238Lys | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/33 | 877/8103 | 714/4485 | 238/1494 | chr14 | 59938560 | ||
| chr14:59977331
|
T | C | 3 | a0002c0003a0006c0009a0014c0019 | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
synonymous_variant | LOW | c.1746T>C | p.Pro582Pro | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/33 | 1909/8103 | 1746/4485 | 582/1494 | chr14 | 59977331 | ||
| chr14:60032021
|
C | T | 1 | a0001c0006 | 5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
synonymous_variant | LOW | c.3948C>T | p.Asp1316Asp | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/33 | 4111/8103 | 3948/4485 | 1316/1494 | chr14 | 60032021 | ||
| chr14:60053202
|
C | T | 10 | a0001c0001a0002c0003a0004c0008others(7): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
synonymous_variant | LOW | c.4128C>T | p.Asn1376Asn | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/33 | 4291/8103 | 4128/4485 | 1376/1494 | chr14 | 60053202 | ||
| chr14:60057997
|
C | T | 1 | a0001c0012 | 2 | HG02602.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.4251C>T | p.Asp1417Asp | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/33 | 4414/8103 | 4251/4485 | 1417/1494 | chr14 | 60057997 | ||
| chr14:60062039
|
G | A | 1 | a0001c0004 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
synonymous_variant | LOW | c.4305G>A | p.Leu1435Leu | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/33 | 4468/8103 | 4305/4485 | 1435/1494 | chr14 | 60062039 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59920168
|
C | T | 1 | a0001c0001t0045 | 1 | NA19002.hp1 | 5_prime_UTR_variant | MODIFIER | c.-139C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/33 | 7776 | chr14 | 59920168 | |||||
| chr14:60063389
|
C | T | 4 | a0001c0001t0008a0001c0001t0042a0001c0001t0043others(1): Show | 14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*27C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 27 | chr14 | 60063389 | |||||
| chr14:60063442
|
TA | T | 7 | a0001c0001t0027a0001c0001t0041a0001c0001t0044others(4): Show | 31 | HG00558.hp2 HG01517.hp2 NA18939.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*96delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 96 | INFO_REALIGN_3_PRIME | chr14 | 60063442 | ||||
| chr14:60063596
|
T | C | 1 | a0001c0005t0013 | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*234T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 234 | chr14 | 60063596 | |||||
| chr14:60063627
|
C | T | 6 | a0001c0001t0010a0001c0001t0015a0001c0001t0039others(3): Show | 17 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*265C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 265 | chr14 | 60063627 | |||||
| chr14:60064004
|
G | A | 1 | a0001c0001t0028 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 642 | chr14 | 60064004 | |||||
| chr14:60064108
|
C | A | 3 | a0002c0003t0005a0006c0009t0005a0014c0019t0005 | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 746 | chr14 | 60064108 | |||||
| chr14:60064120
|
T | C | 53 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(50): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*758T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 758 | chr14 | 60064120 | |||||
| chr14:60064369
|
A | G | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(37): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1007A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1007 | chr14 | 60064369 | |||||
| chr14:60064541
|
C | A | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(37): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1179C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1179 | chr14 | 60064541 | |||||
| chr14:60064587
|
T | C | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1225 | chr14 | 60064587 | |||||
| chr14:60065083
|
T | A | 1 | a0001c0001t0031 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1721 | chr14 | 60065083 | |||||
| chr14:60065111
|
G | A | 1 | a0001c0002t0012 | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1749 | chr14 | 60065111 | |||||
| chr14:60065241
|
G | A | 1 | a0001c0002t0029 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1879G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1879 | chr14 | 60065241 | |||||
| chr14:60065257
|
G | A | 4 | a0001c0002t0021a0005c0013t0018a0007c0010t0018others(1): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1895G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 1895 | chr14 | 60065257 | |||||
| chr14:60065433
|
A | C | 3 | a0002c0003t0005a0006c0009t0005a0014c0019t0005 | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2071A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2071 | chr14 | 60065433 | |||||
| chr14:60065440
|
G | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2078G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2078 | chr14 | 60065440 | |||||
| chr14:60065573
|
G | A | 1 | a0001c0001t0033 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2211G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2211 | chr14 | 60065573 | |||||
| chr14:60065647
|
CA | C | 48 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(45): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*2304delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2304 | INFO_REALIGN_3_PRIME | chr14 | 60065647 | ||||
| chr14:60065670
|
T | TAAAAGAG others(304): Show |
2 | a0001c0001t0011a0001c0001t0023 | 10 | HG02074.hp2 HG02559.hp2 HG02922.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(307): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | ||||
| chr14:60065670
|
T | TAAAAGAG others(315): Show |
1 | a0001c0001t0016 | 4 | HG00621.hp1 HG00621.hp2 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(318): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | ||||
| chr14:60065670
|
T | TAAAAGAG others(316): Show |
14 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(11): Show | 85 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(319): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | ||||
| chr14:60065670
|
T | TAAAAGAG others(317): Show |
12 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(9): Show | 52 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(320): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | ||||
| chr14:60065670
|
T | TAAAAGAG others(318): Show |
6 | a0001c0001t0006a0001c0001t0034a0001c0001t0036others(3): Show | 15 | HG00280.hp2 HG00423.hp2 HG00735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2326_*2327insGGCC others(321): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2327 | INFO_REALIGN_3_PRIME | chr14 | 60065670 | ||||
| chr14:60065806
|
T | C | 1 | a0001c0001t0040 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2444 | chr14 | 60065806 | |||||
| chr14:60065847
|
T | C | 1 | a0001c0002t0026 | 2 | NA19065.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2485T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2485 | chr14 | 60065847 | |||||
| chr14:60065893
|
G | A | 1 | a0001c0004t0009 | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2531 | chr14 | 60065893 | |||||
| chr14:60065994
|
T | A | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2632T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2632 | chr14 | 60065994 | |||||
| chr14:60066319
|
G | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | NA18747.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2957G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 2957 | chr14 | 60066319 | |||||
| chr14:60066512
|
G | A | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(34): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*3150G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3150 | chr14 | 60066512 | |||||
| chr14:60066526
|
A | G | 1 | a0001c0001t0034 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3164A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3164 | chr14 | 60066526 | |||||
| chr14:60066577
|
T | C | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(34): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*3215T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3215 | chr14 | 60066577 | |||||
| chr14:60066641
|
C | T | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(34): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*3279C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3279 | chr14 | 60066641 | |||||
| chr14:60066648
|
C | T | 58 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(55): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*3286C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3286 | chr14 | 60066648 | |||||
| chr14:60066797
|
A | C | 1 | a0001c0002t0007 | 11 | HG02015.hp2 NA18989.hp1 NA18998.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3435A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 33/33 | 3435 | chr14 | 60066797 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:59920466
|
A | G | 1 | a0001c0001t0032g0320 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-34+193A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920466 | ||||||
| chr14:59920500
|
T | C | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-34+227T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920500 | ||||||
| chr14:59920622
|
C | T | 116 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(113): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-34+349C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59920622 | ||||||
| chr14:59921015
|
C | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+742C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921015 | ||||||
| chr14:59921023
|
A | C | 116 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(113): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-34+750A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921023 | ||||||
| chr14:59921149
|
A | C | 2 | a0001c0002t0004g0318a0001c0002t0004g0319 | 2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-34+876A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59921149 | ||||||
| chr14:59921186
|
T | TC | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+915dupC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921186 | |||||
| chr14:59921717
|
A | AT | 41 | a0001c0001t0001g0165a0001c0001t0001g0313a0001c0001t0003g0168others(38): Show | 41 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-34+1465dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921717 | |||||
| chr14:59921717
|
A | ATTTTT | 20 | a0002c0003t0005g0001a0002c0003t0005g0187a0002c0003t0005g0188others(17): Show | 21 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.-34+1461_-34+1465d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59921717 | |||||
| chr14:59922083
|
C | CA | 9 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(6): Show | 9 | HG00621.hp2 HG00639.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+1820dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59922083 | |||||
| chr14:59922090
|
A | T | 65 | a0001c0001t0001g0299a0001c0002t0002g0003a0001c0002t0002g0296others(62): Show | 67 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-34+1817A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922090 | ||||||
| chr14:59922094
|
T | A | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-34+1821T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922094 | ||||||
| chr14:59922215
|
C | T | 2 | a0001c0002t0002g0158a0001c0002t0002g0159 | 2 | HG02738.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-34+1942C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922215 | ||||||
| chr14:59922278
|
G | C | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+2005G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922278 | ||||||
| chr14:59922802
|
T | A | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-34+2529T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59922802 | ||||||
| chr14:59923246
|
T | C | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-34+2973T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923246 | ||||||
| chr14:59923353
|
G | C | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-34+3080G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923353 | ||||||
| chr14:59923514
|
C | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+3241C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923514 | ||||||
| chr14:59923647
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34+3374T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923647 | ||||||
| chr14:59923864
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34+3591C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923864 | ||||||
| chr14:59923895
|
C | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-34+3622C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923895 | ||||||
| chr14:59923924
|
A | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34+3651A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59923924 | ||||||
| chr14:59924185
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-33-3726G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924185 | ||||||
| chr14:59924256
|
G | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33-3655G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924256 | ||||||
| chr14:59924309
|
G | A | 116 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(113): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-33-3602G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924309 | ||||||
| chr14:59924455
|
A | G | 11 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(8): Show | 11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33-3456A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924455 | ||||||
| chr14:59924458
|
G | A | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-33-3453G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924458 | ||||||
| chr14:59924704
|
A | G | 66 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(63): Show | 66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.-33-3207A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924704 | ||||||
| chr14:59924789
|
C | G | 117 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(114): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-33-3122C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924789 | ||||||
| chr14:59924899
|
C | CT | 6 | a0001c0001t0019g0315a0001c0001t0035g0156a0001c0002t0002g0183others(3): Show | 6 | HG01496.hp2 HG02559.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2998dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr14 | 59924899 | |||||
| chr14:59924977
|
C | A | 208 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(205): Show | 210 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-33-2934C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924977 | ||||||
| chr14:59924986
|
G | A | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-33-2925G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59924986 | ||||||
| chr14:59925001
|
G | C | 2 | a0001c0005t0013g0171a0001c0005t0013g0172 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-33-2910G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925001 | ||||||
| chr14:59925043
|
T | C | 312 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(309): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.-33-2868T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925043 | ||||||
| chr14:59925056
|
G | C | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-33-2855G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925056 | ||||||
| chr14:59925592
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33-2319G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925592 | ||||||
| chr14:59925673
|
A | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-33-2238A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925673 | ||||||
| chr14:59925954
|
G | A | 1 | a0001c0002t0004g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-33-1957G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925954 | ||||||
| chr14:59925976
|
C | G | 1 | a0001c0002t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1935C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59925976 | ||||||
| chr14:59926151
|
G | A | 2 | a0008c0011t0003g0212a0008c0011t0006g0211 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.-33-1760G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926151 | ||||||
| chr14:59926232
|
T | C | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-33-1679T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926232 | ||||||
| chr14:59926506
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33-1405A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926506 | ||||||
| chr14:59926567
|
T | A | 213 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(210): Show | 215 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.-33-1344T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926567 | ||||||
| chr14:59926658
|
C | T | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-33-1253C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926658 | ||||||
| chr14:59926785
|
G | A | 2 | a0001c0001t0011g0021a0001c0001t0011g0097 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-33-1126G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926785 | ||||||
| chr14:59926842
|
A | T | 1 | a0001c0001t0015g0096 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-33-1069A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926842 | ||||||
| chr14:59926852
|
C | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-1059C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926852 | ||||||
| chr14:59926864
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-33-1047A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926864 | ||||||
| chr14:59926946
|
T | A | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-33-965T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59926946 | ||||||
| chr14:59927651
|
C | T | 9 | a0001c0002t0024g0157a0001c0005t0013g0151a0001c0005t0013g0171others(6): Show | 9 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-260C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59927651 | ||||||
| chr14:59927762
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-33-149C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 1/32 | chr14 | 59927762 | ||||||
| chr14:59928110
|
G | T | 232 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0081others(229): Show | 234 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.48+119G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 2/32 | chr14 | 59928110 | ||||||
| chr14:59929311
|
A | G | 2 | a0001c0002t0012g0147a0001c0002t0012g0148 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.267+825A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929311 | ||||||
| chr14:59929338
|
T | C | 69 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(66): Show | 69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.267+852T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929338 | ||||||
| chr14:59929390
|
A | T | 1 | a0001c0001t0001g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.267+904A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929390 | ||||||
| chr14:59929414
|
C | CA | 190 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(187): Show | 192 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.267+938dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr14 | 59929414 | |||||
| chr14:59929428
|
CAG | C | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.267+944_267+945del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr14 | 59929428 | |||||
| chr14:59929629
|
A | G | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.267+1143A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929629 | ||||||
| chr14:59929903
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.268-1015G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59929903 | ||||||
| chr14:59930027
|
T | C | 3 | a0001c0001t0001g0213a0001c0001t0001g0259a0001c0001t0016g0105 | 3 | HG00323.hp1 HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.268-891T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930027 | ||||||
| chr14:59930072
|
T | A | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.268-846T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930072 | ||||||
| chr14:59930295
|
C | A | 54 | a0001c0002t0002g0003a0001c0002t0002g0207a0001c0002t0002g0215others(51): Show | 55 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-623C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930295 | ||||||
| chr14:59930322
|
A | T | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.268-596A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930322 | ||||||
| chr14:59930765
|
TA | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.268-152delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930765 | ||||||
| chr14:59930824
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.268-94T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 3/32 | chr14 | 59930824 | ||||||
| chr14:59931168
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.408+110G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 4/32 | chr14 | 59931168 | ||||||
| chr14:59931320
|
T | G | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.408+262T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 4/32 | chr14 | 59931320 | ||||||
| chr14:59931947
|
T | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.473-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 5/32 | chr14 | 59931947 | ||||||
| chr14:59932364
|
T | C | 66 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(63): Show | 66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.543+325T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932364 | ||||||
| chr14:59932677
|
A | G | 1 | a0001c0001t0010g0076 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.543+638A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932677 | ||||||
| chr14:59932825
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.543+786C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932825 | ||||||
| chr14:59932925
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+886T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59932925 | ||||||
| chr14:59933028
|
G | A | 1 | a0001c0001t0003g0025 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.543+989G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933028 | ||||||
| chr14:59933126
|
G | A | 1 | a0001c0001t0010g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.543+1087G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933126 | ||||||
| chr14:59933171
|
T | C | 2 | a0001c0002t0004g0318a0001c0002t0004g0319 | 2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.543+1132T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933171 | ||||||
| chr14:59933328
|
G | T | 3 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0075 | 3 | NA18942.hp1 NA18950.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.543+1289G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933328 | ||||||
| chr14:59933330
|
T | C | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.543+1291T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933330 | ||||||
| chr14:59933333
|
A | G | 3 | a0001c0001t0003g0070a0001c0001t0006g0071a0001c0001t0006g0072 | 3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.543+1294A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933333 | ||||||
| chr14:59933370
|
A | G | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.543+1331A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933370 | ||||||
| chr14:59933378
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.543+1339A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933378 | ||||||
| chr14:59933382
|
A | G | 2 | a0001c0001t0003g0095a0001c0001t0006g0169 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.543+1343A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933382 | ||||||
| chr14:59933478
|
G | A | 1 | a0001c0005t0013g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+1439G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59933478 | ||||||
| chr14:59934082
|
T | C | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.543+2043T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934082 | ||||||
| chr14:59934119
|
G | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.543+2080G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934119 | ||||||
| chr14:59934399
|
A | G | 45 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(42): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+2360A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934399 | ||||||
| chr14:59934452
|
T | C | 69 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(66): Show | 69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.543+2413T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934452 | ||||||
| chr14:59934490
|
C | T | 61 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.543+2451C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934490 | ||||||
| chr14:59934752
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.543+2713G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59934752 | ||||||
| chr14:59935023
|
C | T | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.543+2984C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935023 | ||||||
| chr14:59935052
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.543+3013G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935052 | ||||||
| chr14:59935123
|
T | TA | 30 | a0001c0001t0001g0027a0001c0001t0003g0029a0001c0001t0008g0006others(27): Show | 31 | HG00423.hp1 HG02055.hp2 HG02572.hp2 others(28): Show |
intron_variant | MODIFIER | c.543+3105dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935123 | |||||
| chr14:59935123
|
TA | T | 136 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.543+3105delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935123 | |||||
| chr14:59935165
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.543+3126C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935165 | ||||||
| chr14:59935293
|
CA | C | 126 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(123): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.544-3083delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935293 | |||||
| chr14:59935293
|
CAA | C | 67 | a0001c0001t0001g0257a0001c0001t0030g0160a0001c0002t0002g0005others(64): Show | 67 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.544-3084_544-3083d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59935293 | |||||
| chr14:59935375
|
C | T | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-3015C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935375 | ||||||
| chr14:59935412
|
C | T | 1 | a0001c0002t0002g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-2978C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935412 | ||||||
| chr14:59935418
|
T | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.544-2972T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935418 | ||||||
| chr14:59935436
|
T | C | 1 | a0001c0001t0008g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.544-2954T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935436 | ||||||
| chr14:59935902
|
G | A | 1 | a0001c0002t0012g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.544-2488G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59935902 | ||||||
| chr14:59936342
|
G | A | 2 | a0001c0002t0022g0269a0001c0002t0022g0270 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.544-2048G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936342 | ||||||
| chr14:59936389
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-2001C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936389 | ||||||
| chr14:59936408
|
A | G | 2 | a0001c0002t0017g0141a0001c0002t0017g0142 | 2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.544-1982A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936408 | ||||||
| chr14:59936596
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.544-1794T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936596 | ||||||
| chr14:59936678
|
C | A | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.544-1712C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936678 | ||||||
| chr14:59936815
|
C | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-1575C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59936815 | ||||||
| chr14:59937195
|
T | TA | 37 | a0001c0001t0001g0027a0001c0001t0001g0217a0001c0001t0001g0218others(34): Show | 38 | HG01175.hp2 HG01243.hp2 HG02040.hp2 others(35): Show |
intron_variant | MODIFIER | c.544-1172dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59937195 | |||||
| chr14:59937195
|
TA | T | 66 | a0001c0001t0008g0013a0001c0001t0030g0160a0001c0002t0002g0112others(63): Show | 66 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.544-1172delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr14 | 59937195 | |||||
| chr14:59937197
|
A | G | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-1193A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937197 | ||||||
| chr14:59937225
|
T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-1165T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937225 | ||||||
| chr14:59937280
|
T | A | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.544-1110T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937280 | ||||||
| chr14:59937290
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-1100T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937290 | ||||||
| chr14:59937318
|
C | T | 1 | a0001c0002t0020g0301 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.544-1072C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937318 | ||||||
| chr14:59937322
|
T | G | 319 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.544-1068T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937322 | ||||||
| chr14:59937386
|
A | G | 44 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0118others(41): Show | 44 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.544-1004A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937386 | ||||||
| chr14:59937472
|
A | G | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.544-918A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937472 | ||||||
| chr14:59937566
|
T | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.544-824T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937566 | ||||||
| chr14:59937829
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-561A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59937829 | ||||||
| chr14:59938121
|
T | C | 2 | a0001c0002t0004g0318a0001c0002t0004g0319 | 2 | HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.544-269T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938121 | ||||||
| chr14:59938191
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.544-199G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938191 | ||||||
| chr14:59938285
|
G | A | 67 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0081others(64): Show | 68 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.544-105G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938285 | ||||||
| chr14:59938369
|
T | C | 2 | a0001c0002t0022g0269a0001c0002t0022g0270 | 2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.544-21T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 6/32 | chr14 | 59938369 | ||||||
| chr14:59938667
|
G | A | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.726+95G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938667 | ||||||
| chr14:59938732
|
A | G | 1 | a0001c0002t0025g0113 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.726+160A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938732 | ||||||
| chr14:59938777
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.726+205G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938777 | ||||||
| chr14:59938848
|
T | A | 1 | a0001c0002t0004g0272 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.726+276T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938848 | ||||||
| chr14:59938856
|
A | ATAAT | 208 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(205): Show | 210 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.726+286_726+287ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938856 | |||||
| chr14:59938904
|
CATATATA others(11): Show |
C | 5 | a0001c0006t0002g0108a0001c0006t0002g0109a0001c0006t0002g0114others(2): Show | 5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.726+347_726+364del others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938904 | |||||
| chr14:59938914
|
C | CAT | 160 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(157): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.726+345_726+346dup others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | |||||
| chr14:59938914
|
C | CATATATG others(23): Show |
1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.726+346_726+347ins others(30): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | |||||
| chr14:59938914
|
CATATGCA others(1): Show |
C | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+347_726+354del others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | |||||
| chr14:59938914
|
CATATGCA others(3): Show |
C | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+347_726+356del others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938914 | |||||
| chr14:59938929
|
A | G | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+357A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938929 | ||||||
| chr14:59938930
|
C | T | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+358C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938930 | ||||||
| chr14:59938931
|
A | G | 1 | a0001c0001t0006g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.726+359A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938931 | ||||||
| chr14:59938932
|
C | T | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.726+360C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938932 | ||||||
| chr14:59938938
|
T | C | 2 | a0001c0001t0006g0258a0001c0002t0004g0310 | 2 | HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.726+366T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938938 | ||||||
| chr14:59938940
|
C | T | 2 | a0001c0001t0006g0258a0001c0002t0004g0310 | 2 | HG00735.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.726+368C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938940 | ||||||
| chr14:59938942
|
TATAC | T | 88 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0118others(85): Show | 89 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.726+378_726+381del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938942 | |||||
| chr14:59938946
|
C | CATAT | 94 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.726+377_726+378ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938946 | |||||
| chr14:59938948
|
T | C | 3 | a0001c0001t0006g0258a0001c0002t0002g0003a0001c0002t0004g0310 | 3 | HG00735.hp2 HG02572.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.726+376T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938948 | ||||||
| chr14:59938952
|
T | C | 94 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.726+380T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938952 | ||||||
| chr14:59938954
|
T | C | 94 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.726+382T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938954 | ||||||
| chr14:59938956
|
TACAC | T | 3 | a0001c0001t0006g0258a0001c0002t0002g0003a0001c0002t0004g0310 | 3 | HG00735.hp2 HG02572.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.726+388_726+391del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59938956 | |||||
| chr14:59938958
|
C | T | 94 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.726+386C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938958 | ||||||
| chr14:59938960
|
C | T | 95 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.726+388C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938960 | ||||||
| chr14:59938961
|
A | G | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.726+389A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938961 | ||||||
| chr14:59938979
|
A | G | 3 | a0001c0001t0003g0070a0001c0001t0006g0071a0001c0001t0006g0072 | 3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.726+407A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59938979 | ||||||
| chr14:59939020
|
T | TAC | 3 | a0001c0001t0035g0156a0001c0002t0004g0214a0001c0002t0024g0157 | 3 | HG01496.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.726+449_726+450ins others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939020 | |||||
| chr14:59939020
|
T | TATAC | 207 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(204): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.726+451_726+452ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939020 | |||||
| chr14:59939042
|
T | C | 1 | a0001c0002t0004g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.726+470T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939042 | ||||||
| chr14:59939064
|
C | T | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.726+492C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939064 | ||||||
| chr14:59939092
|
CAT | C | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.726+528_726+529del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59939092 | |||||
| chr14:59939100
|
T | C | 179 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(176): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.726+528T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939100 | ||||||
| chr14:59939106
|
C | T | 179 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(176): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.726+534C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939106 | ||||||
| chr14:59939114
|
T | C | 179 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(176): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.726+542T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939114 | ||||||
| chr14:59939116
|
C | T | 179 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(176): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.726+544C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939116 | ||||||
| chr14:59939639
|
C | A | 56 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0112others(53): Show | 56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.726+1067C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939639 | ||||||
| chr14:59939700
|
A | G | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.726+1128A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59939700 | ||||||
| chr14:59940030
|
G | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.726+1458G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940030 | ||||||
| chr14:59940378
|
G | T | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.726+1806G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940378 | ||||||
| chr14:59940430
|
T | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.726+1858T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940430 | ||||||
| chr14:59940665
|
TG | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.726+2098delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59940665 | |||||
| chr14:59940708
|
T | A | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.726+2136T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940708 | ||||||
| chr14:59940933
|
T | A | 1 | a0001c0001t0008g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.726+2361T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940933 | ||||||
| chr14:59940983
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.726+2411C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59940983 | ||||||
| chr14:59941042
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.726+2470T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941042 | ||||||
| chr14:59941068
|
C | CA | 27 | a0001c0001t0001g0027a0001c0002t0004g0004a0001c0002t0007g0266others(24): Show | 28 | HG01243.hp2 NA18939.hp2 NA18941.hp2 others(25): Show |
intron_variant | MODIFIER | c.726+2506dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59941068 | |||||
| chr14:59941326
|
T | C | 1 | a0001c0001t0028g0030 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.726+2754T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941326 | ||||||
| chr14:59941387
|
T | G | 44 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(41): Show | 45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.726+2815T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941387 | ||||||
| chr14:59941480
|
C | T | 3 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0006g0258 | 3 | HG00735.hp2 HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.726+2908C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941480 | ||||||
| chr14:59941696
|
A | G | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.727-2893A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941696 | ||||||
| chr14:59941771
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.727-2818A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59941771 | ||||||
| chr14:59942336
|
T | A | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.727-2253T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942336 | ||||||
| chr14:59942435
|
G | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.727-2154G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942435 | ||||||
| chr14:59942722
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.727-1867C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942722 | ||||||
| chr14:59942774
|
C | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.727-1815C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942774 | ||||||
| chr14:59942776
|
C | CT | 3 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0004g0153 | 3 | HG01243.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.727-1812dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59942776 | |||||
| chr14:59942777
|
TC | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1811delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942777 | ||||||
| chr14:59942778
|
C | T | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.727-1811C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942778 | ||||||
| chr14:59942912
|
G | GTA | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1676_727-1675i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59942912 | |||||
| chr14:59942916
|
G | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1673G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59942916 | ||||||
| chr14:59943019
|
GT | G | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.727-1563delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943019 | |||||
| chr14:59943048
|
G | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.727-1541G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943048 | ||||||
| chr14:59943097
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1492A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943097 | ||||||
| chr14:59943220
|
G | GTATTAGT others(7): Show |
24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-1365_727-1364i others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943220 | |||||
| chr14:59943232
|
A | T | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.727-1357A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943232 | ||||||
| chr14:59943247
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.727-1342T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943247 | ||||||
| chr14:59943470
|
G | GA | 11 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(8): Show | 11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.727-1110dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr14 | 59943470 | |||||
| chr14:59943504
|
T | C | 2 | a0001c0002t0002g0118a0001c0002t0002g0183 | 2 | NA18944.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.727-1085T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943504 | ||||||
| chr14:59943783
|
C | T | 56 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0112others(53): Show | 56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.727-806C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943783 | ||||||
| chr14:59943873
|
T | C | 2 | a0001c0002t0002g0119a0001c0002t0002g0178 | 2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.727-716T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59943873 | ||||||
| chr14:59944050
|
T | C | 4 | a0001c0001t0011g0021a0001c0001t0011g0078a0001c0001t0011g0079others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-539T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944050 | ||||||
| chr14:59944141
|
A | C | 1 | a0001c0006t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.727-448A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944141 | ||||||
| chr14:59944172
|
G | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.727-417G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944172 | ||||||
| chr14:59944211
|
T | C | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.727-378T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944211 | ||||||
| chr14:59944214
|
A | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.727-375A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944214 | ||||||
| chr14:59944539
|
C | T | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.727-50C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 7/32 | chr14 | 59944539 | ||||||
| chr14:59944831
|
AT | A | 5 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039others(2): Show | 5 | HG00099.hp2 HG00642.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+88delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944831 | ||||||
| chr14:59944860
|
ACACACT | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+122_882+127del others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59944860 | |||||
| chr14:59944866
|
T | A | 42 | a0001c0002t0002g0003a0001c0002t0002g0296a0001c0002t0002g0297others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.882+122T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944866 | ||||||
| chr14:59944866
|
TCA | T | 141 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(138): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.882+141_882+142del others(2): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59944866 | |||||
| chr14:59944868
|
A | T | 64 | a0001c0002t0002g0003a0001c0002t0002g0296a0001c0002t0002g0297others(61): Show | 66 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.882+124A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944868 | ||||||
| chr14:59944870
|
A | T | 3 | a0001c0002t0002g0215a0001c0002t0004g0015a0001c0002t0029g0017 | 3 | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+126A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944870 | ||||||
| chr14:59944992
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+248A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59944992 | ||||||
| chr14:59945025
|
T | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+281T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945025 | ||||||
| chr14:59945026
|
A | T | 2 | a0008c0011t0003g0212a0008c0011t0006g0211 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.882+282A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945026 | ||||||
| chr14:59945042
|
T | C | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+298T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945042 | ||||||
| chr14:59945061
|
T | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+317T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945061 | ||||||
| chr14:59945176
|
C | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+432C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945176 | ||||||
| chr14:59945289
|
T | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+545T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945289 | ||||||
| chr14:59945311
|
G | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+567G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945311 | ||||||
| chr14:59945463
|
G | GA | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+727dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59945463 | |||||
| chr14:59945729
|
C | T | 1 | a0001c0001t0014g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882+985C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945729 | ||||||
| chr14:59945907
|
G | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+1163G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59945907 | ||||||
| chr14:59946007
|
A | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1263A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946007 | ||||||
| chr14:59946038
|
C | G | 3 | a0001c0001t0003g0014a0001c0001t0003g0064a0010c0017t0003g0065 | 3 | HG01169.hp2 HG02148.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.882+1294C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946038 | ||||||
| chr14:59946120
|
A | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+1376A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946120 | ||||||
| chr14:59946208
|
A | C | 10 | a0001c0002t0002g0107a0001c0002t0002g0119a0001c0002t0002g0137others(7): Show | 10 | HG00639.hp1 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+1464A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946208 | ||||||
| chr14:59946333
|
T | G | 44 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0118others(41): Show | 44 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+1589T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946333 | ||||||
| chr14:59946380
|
T | C | 319 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.882+1636T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946380 | ||||||
| chr14:59946492
|
C | CT | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1757dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59946492 | |||||
| chr14:59946504
|
CT | C | 13 | a0001c0001t0035g0156a0001c0002t0007g0266a0001c0002t0024g0157others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+1772delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59946504 | |||||
| chr14:59946516
|
T | C | 61 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+1772T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946516 | ||||||
| chr14:59946622
|
C | T | 1 | a0002c0003t0005g0200 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.882+1878C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946622 | ||||||
| chr14:59946657
|
T | G | 1 | a0001c0001t0008g0007 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.882+1913T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946657 | ||||||
| chr14:59946662
|
A | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+1918A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946662 | ||||||
| chr14:59946667
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.882+1923T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946667 | ||||||
| chr14:59946696
|
C | T | 1 | a0001c0001t0008g0155 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.882+1952C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946696 | ||||||
| chr14:59946844
|
T | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+2100T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946844 | ||||||
| chr14:59946925
|
G | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+2181G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59946925 | ||||||
| chr14:59947283
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.882+2539T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947283 | ||||||
| chr14:59947310
|
G | T | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+2566G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947310 | ||||||
| chr14:59947333
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+2589C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947333 | ||||||
| chr14:59947334
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.882+2590G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947334 | ||||||
| chr14:59947431
|
C | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+2687C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947431 | ||||||
| chr14:59947432
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+2688A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947432 | ||||||
| chr14:59947471
|
A | G | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.882+2727A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947471 | ||||||
| chr14:59947768
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+3024C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947768 | ||||||
| chr14:59947948
|
T | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.882+3204T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947948 | ||||||
| chr14:59947983
|
C | T | 2 | a0001c0001t0016g0023a0001c0002t0002g0136 | 2 | HG01074.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.882+3239C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59947983 | ||||||
| chr14:59948039
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0016g0206 | 3 | HG00609.hp2 HG00621.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.882+3295G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948039 | ||||||
| chr14:59948073
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.882+3329T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948073 | ||||||
| chr14:59948130
|
C | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+3386C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948130 | ||||||
| chr14:59948268
|
C | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+3524C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948268 | ||||||
| chr14:59948268
|
C | T | 44 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(41): Show | 45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.882+3524C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948268 | ||||||
| chr14:59948392
|
C | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+3648C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948392 | ||||||
| chr14:59948446
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+3702A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948446 | ||||||
| chr14:59948461
|
C | A | 5 | a0001c0006t0002g0108a0001c0006t0002g0109a0001c0006t0002g0114others(2): Show | 5 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+3717C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948461 | ||||||
| chr14:59948503
|
T | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+3759T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948503 | ||||||
| chr14:59948594
|
A | C | 3 | a0001c0005t0013g0179a0001c0005t0013g0180a0001c0005t0013g0181 | 3 | HG02055.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.882+3850A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948594 | ||||||
| chr14:59948673
|
A | G | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+3929A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948673 | ||||||
| chr14:59948720
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.882+3976G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948720 | ||||||
| chr14:59948823
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0257a0001c0001t0003g0037others(1): Show | 4 | HG00642.hp2 HG01361.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+4079G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59948823 | ||||||
| chr14:59949066
|
A | T | 8 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(5): Show | 8 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+4322A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949066 | ||||||
| chr14:59949325
|
G | A | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+4581G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949325 | ||||||
| chr14:59949424
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882+4680G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949424 | ||||||
| chr14:59949572
|
G | GCTTTTCT others(4): Show |
24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+4833_882+4834i others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59949572 | |||||
| chr14:59949590
|
AG | A | 61 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+4849delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59949590 | |||||
| chr14:59949673
|
G | A | 3 | a0001c0001t0001g0213a0001c0002t0002g0005a0001c0002t0004g0004 | 3 | HG01081.hp1 HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.882+4929G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949673 | ||||||
| chr14:59949683
|
T | G | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.882+4939T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949683 | ||||||
| chr14:59949708
|
C | T | 1 | a0001c0002t0025g0135 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882+4964C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949708 | ||||||
| chr14:59949759
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+5015G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949759 | ||||||
| chr14:59949793
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+5049A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59949793 | ||||||
| chr14:59950014
|
C | T | 100 | a0001c0001t0030g0160a0001c0002t0002g0003a0001c0002t0002g0107others(97): Show | 101 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.882+5270C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950014 | ||||||
| chr14:59950079
|
C | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.882+5335C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950079 | ||||||
| chr14:59950119
|
T | C | 3 | a0002c0003t0005g0001a0002c0003t0005g0187a0002c0003t0005g0188 | 4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+5375T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950119 | ||||||
| chr14:59950122
|
G | T | 32 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0118others(29): Show | 32 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+5378G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950122 | ||||||
| chr14:59950178
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.882+5434T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950178 | ||||||
| chr14:59950439
|
G | A | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+5695G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950439 | ||||||
| chr14:59950481
|
A | C | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.882+5737A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950481 | ||||||
| chr14:59950482
|
A | G | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+5738A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950482 | ||||||
| chr14:59950491
|
A | G | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.882+5747A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950491 | ||||||
| chr14:59950501
|
A | G | 1 | a0001c0001t0003g0256 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.882+5757A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950501 | ||||||
| chr14:59950565
|
G | A | 188 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(185): Show | 189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.882+5821G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950565 | ||||||
| chr14:59950627
|
G | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+5883G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950627 | ||||||
| chr14:59950679
|
T | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+5935T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950679 | ||||||
| chr14:59950738
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.882+5994A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950738 | ||||||
| chr14:59950833
|
T | C | 5 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0304others(2): Show | 5 | HG00323.hp2 NA18946.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+6089T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950833 | ||||||
| chr14:59950866
|
T | C | 1 | a0001c0004t0009g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.882+6122T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950866 | ||||||
| chr14:59950907
|
C | A | 1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882+6163C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950907 | ||||||
| chr14:59950913
|
C | T | 1 | a0001c0001t0008g0155 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.882+6169C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950913 | ||||||
| chr14:59950937
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6193C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950937 | ||||||
| chr14:59950990
|
C | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.882+6246C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59950990 | ||||||
| chr14:59951053
|
G | A | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.882+6309G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951053 | ||||||
| chr14:59951080
|
T | C | 1 | a0001c0002t0002g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.882+6336T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951080 | ||||||
| chr14:59951116
|
G | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6372G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951116 | ||||||
| chr14:59951231
|
A | G | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.882+6487A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951231 | ||||||
| chr14:59951326
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.882+6582C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951326 | ||||||
| chr14:59951377
|
G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+6633G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951377 | ||||||
| chr14:59951414
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+6670A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951414 | ||||||
| chr14:59951430
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.882+6686G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951430 | ||||||
| chr14:59951431
|
A | C | 141 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(138): Show | 143 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.882+6687A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951431 | ||||||
| chr14:59951548
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882+6804C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951548 | ||||||
| chr14:59951578
|
G | A | 1 | a0002c0003t0005g0189 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.882+6834G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951578 | ||||||
| chr14:59951582
|
T | C | 1 | a0001c0002t0017g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.882+6838T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951582 | ||||||
| chr14:59951619
|
C | A | 1 | a0001c0002t0002g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+6875C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951619 | ||||||
| chr14:59951659
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+6915T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951659 | ||||||
| chr14:59951675
|
C | T | 27 | a0001c0001t0035g0156a0001c0002t0004g0015a0001c0002t0021g0161others(24): Show | 28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+6931C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951675 | ||||||
| chr14:59951756
|
T | C | 27 | a0001c0001t0035g0156a0001c0002t0004g0015a0001c0002t0021g0161others(24): Show | 28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7012T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951756 | ||||||
| chr14:59951832
|
C | T | 2 | a0001c0004t0009g0302a0001c0004t0009g0309 | 2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.882+7088C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951832 | ||||||
| chr14:59951854
|
C | T | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.882+7110C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951854 | ||||||
| chr14:59951855
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.882+7111G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951855 | ||||||
| chr14:59951877
|
T | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.882+7133T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951877 | ||||||
| chr14:59951945
|
G | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.882+7201G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951945 | ||||||
| chr14:59951959
|
C | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.882+7215C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951959 | ||||||
| chr14:59951970
|
C | T | 1 | a0001c0001t0011g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882+7226C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59951970 | ||||||
| chr14:59952005
|
C | T | 25 | a0001c0002t0004g0015a0001c0002t0021g0161a0001c0002t0029g0017others(22): Show | 26 | HG02257.hp1 HG03453.hp1 NA18939.hp2 others(23): Show |
intron_variant | MODIFIER | c.882+7261C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952005 | ||||||
| chr14:59952034
|
C | T | 61 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+7290C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952034 | ||||||
| chr14:59952043
|
C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+7299C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952043 | ||||||
| chr14:59952044
|
G | A | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.882+7300G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952044 | ||||||
| chr14:59952056
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.882+7312T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952056 | ||||||
| chr14:59952081
|
A | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.882+7337A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952081 | ||||||
| chr14:59952188
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.882+7444G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952188 | ||||||
| chr14:59952242
|
G | T | 27 | a0001c0001t0035g0156a0001c0002t0004g0015a0001c0002t0021g0161others(24): Show | 28 | HG01496.hp2 HG02257.hp1 HG03453.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+7498G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952242 | ||||||
| chr14:59952389
|
G | A | 44 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(41): Show | 45 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.883-7429G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952389 | ||||||
| chr14:59952423
|
G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.883-7395G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952423 | ||||||
| chr14:59952423
|
G | C | 1 | a0001c0002t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.883-7395G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952423 | ||||||
| chr14:59952483
|
G | T | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.883-7335G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952483 | ||||||
| chr14:59952774
|
C | T | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.883-7044C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952774 | ||||||
| chr14:59952879
|
G | A | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.883-6939G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952879 | ||||||
| chr14:59952943
|
G | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6875G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59952943 | ||||||
| chr14:59953061
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.883-6757A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953061 | ||||||
| chr14:59953262
|
T | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-6556T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953262 | ||||||
| chr14:59953270
|
C | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6548C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953270 | ||||||
| chr14:59953286
|
C | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-6532C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953286 | ||||||
| chr14:59953529
|
TG | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-6288delG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953529 | ||||||
| chr14:59953645
|
G | A | 3 | a0001c0001t0008g0031a0001c0001t0008g0032a0001c0001t0008g0041 | 3 | HG00280.hp1 HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.883-6173G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953645 | ||||||
| chr14:59953811
|
T | C | 2 | a0001c0001t0003g0064a0010c0017t0003g0065 | 2 | HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.883-6007T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953811 | ||||||
| chr14:59953842
|
G | C | 1 | a0001c0002t0002g0183 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.883-5976G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953842 | ||||||
| chr14:59953879
|
G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.883-5939G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953879 | ||||||
| chr14:59953985
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-5833A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59953985 | ||||||
| chr14:59954073
|
A | G | 2 | a0002c0003t0005g0199a0002c0003t0005g0204 | 2 | NA18964.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.883-5745A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954073 | ||||||
| chr14:59954218
|
T | C | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.883-5600T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954218 | ||||||
| chr14:59954303
|
G | T | 1 | a0002c0003t0005g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.883-5515G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954303 | ||||||
| chr14:59954304
|
T | G | 1 | a0001c0002t0029g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.883-5514T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954304 | ||||||
| chr14:59954321
|
T | C | 2 | a0001c0002t0002g0138a0001c0002t0002g0139 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.883-5497T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954321 | ||||||
| chr14:59954361
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.883-5457G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954361 | ||||||
| chr14:59954416
|
C | A | 1 | a0014c0019t0005g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.883-5402C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954416 | ||||||
| chr14:59954728
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-5090A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954728 | ||||||
| chr14:59954970
|
G | A | 16 | a0001c0002t0002g0005a0001c0002t0002g0112a0001c0002t0002g0173others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.883-4848G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59954970 | ||||||
| chr14:59955155
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-4663C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955155 | ||||||
| chr14:59955171
|
G | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-4647G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955171 | ||||||
| chr14:59955583
|
A | C | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.883-4235A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955583 | ||||||
| chr14:59955608
|
A | AT | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-4203dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59955608 | |||||
| chr14:59955700
|
CTT | C | 45 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(42): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-4117_883-4116d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955700 | ||||||
| chr14:59955987
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.883-3831C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59955987 | ||||||
| chr14:59956040
|
A | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-3778A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956040 | ||||||
| chr14:59956151
|
GT | G | 3 | a0001c0001t0003g0022a0001c0001t0006g0163a0013c0014t0006g0162 | 3 | HG02735.hp1 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.883-3666delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956151 | ||||||
| chr14:59956231
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.883-3587T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956231 | ||||||
| chr14:59956244
|
T | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.883-3574T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956244 | ||||||
| chr14:59956279
|
T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883-3539T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956279 | ||||||
| chr14:59956285
|
A | G | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.883-3533A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956285 | ||||||
| chr14:59956311
|
T | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-3507T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956311 | ||||||
| chr14:59956523
|
A | G | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-3295A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956523 | ||||||
| chr14:59956538
|
C | T | 45 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(42): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-3280C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956538 | ||||||
| chr14:59956548
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.883-3270G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956548 | ||||||
| chr14:59956684
|
T | C | 1 | a0001c0002t0022g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-3134T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956684 | ||||||
| chr14:59956685
|
G | A | 1 | a0001c0001t0003g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.883-3133G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956685 | ||||||
| chr14:59956760
|
T | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3058T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956760 | ||||||
| chr14:59956761
|
T | C | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3057T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956761 | ||||||
| chr14:59956762
|
G | T | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3056G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956762 | ||||||
| chr14:59956763
|
C | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-3055C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956763 | ||||||
| chr14:59956793
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-3025A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956793 | ||||||
| chr14:59956853
|
G | A | 1 | a0001c0004t0009g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-2965G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956853 | ||||||
| chr14:59956897
|
T | C | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.883-2921T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59956897 | ||||||
| chr14:59957108
|
G | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-2710G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957108 | ||||||
| chr14:59957219
|
G | A | 45 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(42): Show | 46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.883-2599G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957219 | ||||||
| chr14:59957733
|
G | C | 3 | a0001c0001t0003g0070a0001c0001t0006g0071a0001c0001t0006g0072 | 3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.883-2085G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957733 | ||||||
| chr14:59957739
|
G | T | 3 | a0001c0001t0003g0070a0001c0001t0006g0071a0001c0001t0006g0072 | 3 | HG00423.hp2 NA18998.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.883-2079G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957739 | ||||||
| chr14:59957761
|
A | T | 186 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(183): Show | 187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.883-2057A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957761 | ||||||
| chr14:59957780
|
A | T | 1 | a0001c0001t0014g0102 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-2038A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957780 | ||||||
| chr14:59957843
|
C | T | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-1975C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59957843 | ||||||
| chr14:59958022
|
G | A | 1 | a0001c0002t0002g0183 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.883-1796G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958022 | ||||||
| chr14:59958165
|
G | A | 66 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(63): Show | 66 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.883-1653G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958165 | ||||||
| chr14:59958286
|
T | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-1532T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958286 | ||||||
| chr14:59958367
|
A | T | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-1451A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958367 | ||||||
| chr14:59958524
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.883-1294C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958524 | ||||||
| chr14:59958684
|
C | A | 56 | a0001c0001t0030g0160a0001c0002t0002g0107a0001c0002t0002g0112others(53): Show | 56 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.883-1134C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958684 | ||||||
| chr14:59958722
|
G | A | 22 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0081others(19): Show | 22 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-1096G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958722 | ||||||
| chr14:59958796
|
C | T | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-1022C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958796 | ||||||
| chr14:59958860
|
G | A | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-958G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958860 | ||||||
| chr14:59958861
|
A | G | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-957A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958861 | ||||||
| chr14:59958881
|
C | T | 46 | a0001c0002t0002g0003a0001c0002t0002g0207a0001c0002t0002g0215others(43): Show | 47 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.883-937C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958881 | ||||||
| chr14:59958965
|
T | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-853T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59958965 | ||||||
| chr14:59959197
|
C | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-621C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959197 | ||||||
| chr14:59959210
|
T | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.883-608T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959210 | ||||||
| chr14:59959391
|
G | GTGGTGAA others(3): Show |
1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.883-425_883-416dup others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr14 | 59959391 | |||||
| chr14:59959510
|
G | A | 69 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(66): Show | 69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.883-308G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 8/32 | chr14 | 59959510 | ||||||
| chr14:59960044
|
G | C | 3 | a0001c0002t0002g0112a0001c0002t0002g0173a0001c0002t0025g0113 | 3 | HG01884.hp2 HG02145.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1079+30G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960044 | ||||||
| chr14:59960053
|
T | C | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1079+39T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960053 | ||||||
| chr14:59960088
|
C | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1079+74C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960088 | ||||||
| chr14:59960185
|
G | C | 61 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1079+171G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960185 | ||||||
| chr14:59960328
|
C | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1079+314C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960328 | ||||||
| chr14:59960406
|
A | G | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1079+392A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960406 | ||||||
| chr14:59960432
|
T | G | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1079+418T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960432 | ||||||
| chr14:59960533
|
G | T | 210 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(207): Show | 212 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1080-381G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960533 | ||||||
| chr14:59960621
|
A | T | 69 | a0001c0001t0030g0160a0001c0002t0002g0005a0001c0002t0002g0107others(66): Show | 69 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.1080-293A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 9/32 | chr14 | 59960621 | ||||||
| chr14:59961418
|
C | T | 2 | a0001c0002t0002g0175a0001c0002t0002g0176 | 2 | HG01255.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1211+373C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59961418 | ||||||
| chr14:59961443
|
G | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1211+398G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59961443 | ||||||
| chr14:59962086
|
T | A | 1 | a0001c0002t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1211+1041T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962086 | ||||||
| chr14:59962401
|
T | C | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1211+1356T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962401 | ||||||
| chr14:59962409
|
A | AT | 43 | a0001c0002t0002g0003a0001c0002t0002g0215a0001c0002t0002g0296others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1211+1376dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962409 | |||||
| chr14:59962410
|
T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1211+1365T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962410 | ||||||
| chr14:59962446
|
G | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1211+1401G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962446 | ||||||
| chr14:59962464
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1211+1419C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962464 | ||||||
| chr14:59962528
|
C | T | 1 | a0001c0002t0007g0275 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1211+1483C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962528 | ||||||
| chr14:59962616
|
T | C | 2 | a0001c0012t0002g0106a0001c0012t0002g0140 | 2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1211+1571T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962616 | ||||||
| chr14:59962717
|
T | A | 2 | a0003c0007t0004g0276a0003c0007t0004g0277 | 2 | NA18961.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1211+1672T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59962717 | ||||||
| chr14:59962780
|
G | GA | 69 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1211+1748dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962780 | |||||
| chr14:59962780
|
GA | G | 53 | a0001c0001t0035g0156a0001c0001t0043g0012a0001c0002t0002g0003others(50): Show | 54 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211+1748delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59962780 | |||||
| chr14:59963414
|
T | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1211+2369T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59963414 | ||||||
| chr14:59963511
|
T | TA | 21 | a0001c0001t0001g0082a0001c0001t0035g0156a0001c0002t0024g0157others(18): Show | 22 | HG01496.hp2 HG01884.hp1 HG03516.hp2 others(19): Show |
intron_variant | MODIFIER | c.1211+2479dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59963511 | |||||
| chr14:59963544
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1211+2499A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59963544 | ||||||
| chr14:59964171
|
G | A | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1212-2418G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964171 | ||||||
| chr14:59964366
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-2223A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964366 | ||||||
| chr14:59964511
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-2078A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964511 | ||||||
| chr14:59964665
|
T | C | 1 | a0001c0001t0010g0043 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1212-1924T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59964665 | ||||||
| chr14:59964802
|
A | ACTATTCA others(7): Show |
117 | a0001c0001t0001g0208a0001c0001t0001g0213a0001c0001t0001g0217others(114): Show | 118 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1212-1776_1212-177 others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59964802 | |||||
| chr14:59965150
|
A | G | 1 | a0001c0002t0004g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1212-1439A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965150 | ||||||
| chr14:59965362
|
C | T | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1212-1227C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965362 | ||||||
| chr14:59965401
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1212-1188G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965401 | ||||||
| chr14:59965434
|
A | G | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1212-1155A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965434 | ||||||
| chr14:59965457
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-1132A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965457 | ||||||
| chr14:59965469
|
T | C | 20 | a0001c0002t0004g0265a0001c0002t0004g0268a0001c0002t0004g0271others(17): Show | 20 | HG00558.hp2 HG02165.hp2 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.1212-1120T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965469 | ||||||
| chr14:59965580
|
A | G | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-1009A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965580 | ||||||
| chr14:59965634
|
C | T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-955C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965634 | ||||||
| chr14:59965640
|
C | CTT | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-948_1212-947i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965640 | |||||
| chr14:59965661
|
A | T | 1 | a0001c0001t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-928A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965661 | ||||||
| chr14:59965840
|
G | A | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1212-749G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59965840 | ||||||
| chr14:59965882
|
C | CA | 7 | a0001c0001t0003g0100a0001c0002t0002g0112a0001c0002t0002g0126others(4): Show | 7 | HG01361.hp2 HG01884.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-669dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAA | 17 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0077others(14): Show | 17 | HG00642.hp1 HG00735.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1212-671_1212-669d others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAA | 25 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0087others(22): Show | 25 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1212-672_1212-669d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAA | 17 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0003g0022others(14): Show | 17 | HG00423.hp1 HG00423.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1212-673_1212-669d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAA | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0003g0168others(6): Show | 9 | HG01175.hp2 HG01361.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1212-674_1212-669d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0008g0007a0001c0001t0008g0010a0001c0002t0004g0015 | 3 | HG01081.hp2 HG01258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1212-678_1212-669d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0008g0154a0001c0001t0011g0097a0001c0001t0014g0066 | 3 | HG02559.hp2 HG03579.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1212-679_1212-669d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0043g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1212-680_1212-669d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1212-681_1212-669d others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0084a0001c0001t0008g0009a0001c0001t0044g0008 | 3 | HG01433.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1212-682_1212-669d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1212-683_1212-669d others(17): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1212-684_1212-669d others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1212-689_1212-669d others(23): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0019g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1212-690_1212-669d others(24): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CA | C | 23 | a0001c0002t0002g0107a0001c0002t0002g0118a0001c0002t0002g0145others(20): Show | 23 | HG00323.hp2 HG01175.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1212-669delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAA | C | 13 | a0001c0001t0030g0160a0001c0002t0002g0133a0001c0002t0002g0136others(10): Show | 13 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1212-670_1212-669d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA | C | 19 | a0001c0001t0001g0089a0001c0001t0003g0255a0001c0001t0006g0024others(16): Show | 20 | HG00621.hp2 HG00735.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1212-675_1212-669d others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(1): Show |
C | 42 | a0001c0001t0001g0080a0001c0001t0001g0208a0001c0001t0001g0223others(39): Show | 42 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1212-676_1212-669d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(2): Show |
C | 43 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0213others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1212-677_1212-669d others(11): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0016a0001c0001t0001g0092a0001c0001t0001g0248others(4): Show | 7 | HG00673.hp2 HG01934.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212-678_1212-669d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0008g0011a0001c0001t0011g0075a0001c0002t0002g0119 | 3 | HG00639.hp2 HG01192.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1212-679_1212-669d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(5): Show |
C | 6 | a0001c0002t0002g0137a0001c0002t0002g0149a0001c0002t0002g0177others(3): Show | 6 | HG00639.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212-680_1212-669d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1212-681_1212-669d others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(7): Show |
C | 21 | a0002c0003t0005g0001a0002c0003t0005g0186a0002c0003t0005g0187others(18): Show | 22 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(19): Show |
intron_variant | MODIFIER | c.1212-682_1212-669d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1212-683_1212-669d others(17): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1212-685_1212-669d others(19): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59965882
|
CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0003g0101a0001c0001t0015g0096 | 2 | HG01993.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1212-688_1212-669d others(22): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr14 | 59965882 | |||||
| chr14:59966135
|
T | G | 3 | a0001c0001t0008g0031a0001c0001t0008g0032a0001c0001t0008g0041 | 3 | HG00280.hp1 HG01175.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1212-454T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59966135 | ||||||
| chr14:59966271
|
T | G | 4 | a0001c0002t0004g0271a0001c0002t0004g0278a0001c0002t0004g0281others(1): Show | 4 | HG00558.hp2 NA18950.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212-318T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 10/32 | chr14 | 59966271 | ||||||
| chr14:59967318
|
T | C | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+105T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967318 | ||||||
| chr14:59967757
|
C | T | 1 | a0001c0002t0004g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1506+544C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967757 | ||||||
| chr14:59967808
|
A | G | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+595A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967808 | ||||||
| chr14:59967886
|
G | A | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1506+673G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59967886 | ||||||
| chr14:59968350
|
G | A | 2 | a0001c0001t0035g0156a0001c0002t0024g0157 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1506+1137G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968350 | ||||||
| chr14:59968426
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1506+1213C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968426 | ||||||
| chr14:59968427
|
A | C | 109 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1506+1214A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968427 | ||||||
| chr14:59968507
|
T | C | 2 | a0001c0001t0003g0029a0001c0001t0003g0047 | 2 | NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1506+1294T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59968507 | ||||||
| chr14:59968770
|
G | GC | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+1560dupC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59968770 | |||||
| chr14:59968972
|
G | GA | 110 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1506+1767dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59968972 | |||||
| chr14:59969327
|
G | A | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+2114G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969327 | ||||||
| chr14:59969345
|
G | A | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1506+2132G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969345 | ||||||
| chr14:59969413
|
A | G | 24 | a0001c0001t0035g0156a0001c0002t0024g0157a0002c0003t0005g0001others(21): Show | 25 | HG01496.hp2 HG03516.hp2 NA18939.hp2 others(22): Show |
intron_variant | MODIFIER | c.1506+2200A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969413 | ||||||
| chr14:59969484
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1506+2271G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969484 | ||||||
| chr14:59969546
|
C | T | 25 | a0001c0001t0035g0156a0001c0002t0002g0207a0001c0002t0024g0157others(22): Show | 26 | HG01496.hp2 HG02922.hp1 HG03516.hp2 others(23): Show |
intron_variant | MODIFIER | c.1506+2333C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969546 | ||||||
| chr14:59969760
|
A | G | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1506+2547A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969760 | ||||||
| chr14:59969775
|
T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1506+2562T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969775 | ||||||
| chr14:59969930
|
A | G | 39 | a0001c0001t0036g0314a0001c0001t0037g0247a0001c0002t0002g0003others(36): Show | 40 | HG00609.hp1 HG00673.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.1506+2717A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59969930 | ||||||
| chr14:59970041
|
G | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1506+2828G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970041 | ||||||
| chr14:59970112
|
T | C | 3 | a0001c0002t0002g0005a0001c0002t0004g0015a0001c0002t0029g0017 | 3 | HG01081.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1506+2899T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970112 | ||||||
| chr14:59970155
|
C | T | 9 | a0001c0001t0011g0021a0001c0002t0004g0004a0001c0005t0013g0151others(6): Show | 9 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506+2942C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970155 | ||||||
| chr14:59970208
|
T | A | 3 | a0001c0001t0003g0048a0001c0001t0014g0040a0001c0002t0002g0136 | 3 | HG03654.hp1 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1506+2995T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970208 | ||||||
| chr14:59970851
|
A | C | 2 | a0005c0013t0018g0110a0005c0013t0018g0111 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1506+3638A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970851 | ||||||
| chr14:59970877
|
G | C | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1506+3664G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970877 | ||||||
| chr14:59970889
|
T | C | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1506+3676T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59970889 | ||||||
| chr14:59971054
|
G | T | 1 | a0010c0017t0003g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1507-3522G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971054 | ||||||
| chr14:59971056
|
TTTACATT others(7): Show |
T | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1507-3509_1507-349 others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59971056 | |||||
| chr14:59971193
|
C | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-3383C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971193 | ||||||
| chr14:59971311
|
C | T | 3 | a0001c0002t0002g0173a0001c0002t0002g0215a0001c0002t0025g0113 | 3 | HG02145.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1507-3265C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971311 | ||||||
| chr14:59971317
|
C | T | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1507-3259C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971317 | ||||||
| chr14:59971375
|
C | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1507-3201C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971375 | ||||||
| chr14:59971513
|
G | A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1507-3063G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971513 | ||||||
| chr14:59971524
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-3052A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971524 | ||||||
| chr14:59971628
|
C | T | 165 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1507-2948C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59971628 | ||||||
| chr14:59972094
|
A | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1507-2482A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972094 | ||||||
| chr14:59972401
|
G | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1507-2175G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972401 | ||||||
| chr14:59972457
|
G | A | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1507-2119G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972457 | ||||||
| chr14:59972681
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1507-1895C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59972681 | ||||||
| chr14:59973038
|
G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1507-1538G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973038 | ||||||
| chr14:59973323
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-1253A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973323 | ||||||
| chr14:59973346
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1507-1230G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973346 | ||||||
| chr14:59973349
|
C | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-1227C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973349 | ||||||
| chr14:59973486
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1507-1090A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973486 | ||||||
| chr14:59973536
|
T | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0011g0050others(3): Show | 6 | HG00621.hp1 HG02074.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-1040T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973536 | ||||||
| chr14:59973598
|
TCTAGA | T | 4 | a0001c0001t0001g0208a0001c0001t0001g0225a0001c0001t0001g0257others(1): Show | 4 | NA18944.hp1 NA18968.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1507-974_1507-970d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr14 | 59973598 | |||||
| chr14:59973604
|
C | G | 1 | a0001c0002t0012g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1507-972C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973604 | ||||||
| chr14:59973919
|
G | A | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1507-657G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973919 | ||||||
| chr14:59973929
|
C | T | 2 | a0001c0002t0002g0145a0001c0002t0002g0146 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1507-647C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973929 | ||||||
| chr14:59973930
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1507-646G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973930 | ||||||
| chr14:59973950
|
T | C | 1 | a0001c0001t0011g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1507-626T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973950 | ||||||
| chr14:59973969
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1507-607A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59973969 | ||||||
| chr14:59974067
|
C | T | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-509C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59974067 | ||||||
| chr14:59974139
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1507-437T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 12/32 | chr14 | 59974139 | ||||||
| chr14:59974874
|
A | G | 4 | a0001c0002t0002g0112a0001c0002t0002g0173a0001c0002t0002g0215others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+166A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59974874 | ||||||
| chr14:59974944
|
C | T | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1639+236C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59974944 | ||||||
| chr14:59975033
|
G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+325G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975033 | ||||||
| chr14:59975034
|
C | CATATAT | 9 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0094others(6): Show | 9 | HG01169.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+339_1639+344d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | CATATATA others(1): Show |
49 | a0001c0001t0001g0058a0001c0001t0001g0077a0001c0001t0001g0084others(46): Show | 49 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1639+337_1639+344d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | CATATATA others(3): Show |
29 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0081others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1639+335_1639+344d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | CATATATA others(5): Show |
51 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(48): Show | 51 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1639+333_1639+344d others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | CATATATA others(7): Show |
23 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(20): Show | 23 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1639+331_1639+344d others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | CATATATA others(9): Show |
1 | a0001c0001t0028g0030 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1639+329_1639+344d others(18): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
C | T | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+326C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975034 | ||||||
| chr14:59975034
|
CAT | C | 16 | a0001c0002t0002g0159a0001c0002t0004g0214a0001c0002t0004g0273others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1639+343_1639+344d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975034
|
CATAT | C | 15 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(12): Show | 15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1639+341_1639+344d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975034 | |||||
| chr14:59975038
|
T | TGTGTCAC others(3): Show |
1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1639+330_1639+331i others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975038 | ||||||
| chr14:59975047
|
ATATATGC others(35): Show |
A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+345_1639+386d others(44): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975047 | |||||
| chr14:59975063
|
ACTATGTG | A | 163 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1639+356_1639+362d others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975063 | ||||||
| chr14:59975063
|
ACTATGTG others(4): Show |
A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+356_1639+366d others(13): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975063 | ||||||
| chr14:59975066
|
A | G | 41 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(38): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.1639+358A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975066 | ||||||
| chr14:59975066
|
ATG | A | 4 | a0001c0002t0002g0136a0001c0002t0002g0144a0001c0002t0004g0015others(1): Show | 4 | HG03453.hp1 HG03654.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+376_1639+377d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975066 | |||||
| chr14:59975087
|
G | GTGTATAT others(31): Show |
3 | a0001c0001t0030g0160a0001c0002t0025g0135a0001c0002t0026g0132 | 3 | HG02683.hp1 HG03942.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1639+434_1639+471d others(40): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975087 | |||||
| chr14:59975087
|
GTGTATAT others(31): Show |
G | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1639+434_1639+471d others(40): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975087 | |||||
| chr14:59975090
|
TATATATA others(43): Show |
T | 1 | a0002c0003t0005g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1639+393_1639+442d others(52): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975090 | |||||
| chr14:59975091
|
ATATATAT others(53): Show |
A | 2 | a0001c0001t0001g0094a0009c0018t0003g0230 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1639+394_1639+453d others(62): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975091 | |||||
| chr14:59975092
|
TATATATA others(41): Show |
T | 4 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0014g0066others(1): Show | 4 | HG02818.hp2 HG03579.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639+394_1639+441d others(50): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975092 | |||||
| chr14:59975093
|
ATATATAT others(51): Show |
A | 83 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0058others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1639+394_1639+451d others(60): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975093 | |||||
| chr14:59975095
|
ATATATAC others(49): Show |
A | 49 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0224others(46): Show | 49 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1639+394_1639+449d others(58): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975095 | |||||
| chr14:59975097
|
ATATACAT others(47): Show |
A | 18 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(15): Show | 18 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1639+394_1639+447d others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975097 | |||||
| chr14:59975099
|
ATACATAT others(45): Show |
A | 9 | a0001c0001t0001g0077a0001c0001t0001g0237a0001c0001t0001g0299others(6): Show | 9 | HG01952.hp1 HG02559.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.1639+394_1639+445d others(54): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975099 | |||||
| chr14:59975101
|
ACATATAT others(43): Show |
A | 2 | a0001c0001t0001g0016a0001c0001t0001g0091 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1639+394_1639+443d others(52): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975101 | ||||||
| chr14:59975102
|
C | T | 2 | a0001c0002t0002g0112a0004c0008t0015g0167 | 2 | HG01884.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1639+394C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975102 | ||||||
| chr14:59975102
|
CAT | C | 3 | a0001c0002t0002g0138a0001c0002t0002g0139a0001c0002t0002g0215 | 3 | HG01257.hp2 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1639+403_1639+404d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975102 | |||||
| chr14:59975102
|
CATATATA others(45): Show |
C | 2 | a0001c0002t0002g0145a0001c0002t0017g0174 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1639+418_1639+469d others(54): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975102 | |||||
| chr14:59975104
|
T | C | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1639+396T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975104 | ||||||
| chr14:59975111
|
A | G | 29 | a0001c0002t0021g0161a0001c0005t0013g0151a0001c0005t0013g0171others(26): Show | 30 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1639+403A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975111 | ||||||
| chr14:59975112
|
TGTATATA others(21): Show |
T | 22 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(19): Show | 23 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.1639+405_1639+432d others(30): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975112 | ||||||
| chr14:59975113
|
G | A | 7 | a0001c0002t0021g0161a0001c0005t0013g0151a0001c0005t0013g0171others(4): Show | 7 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+405G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975113 | ||||||
| chr14:59975113
|
G | GTA | 39 | a0001c0002t0004g0015a0001c0002t0004g0153a0001c0002t0004g0265others(36): Show | 40 | HG00558.hp2 HG02015.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.1639+417_1639+418d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | |||||
| chr14:59975113
|
G | GTATATAT others(35): Show |
1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1639+418_1639+419i others(44): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | |||||
| chr14:59975113
|
G | GTATATAT others(47): Show |
1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1639+418_1639+419i others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | |||||
| chr14:59975113
|
G | GTATATAT others(47): Show |
1 | a0001c0002t0004g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1639+416_1639+469d others(56): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975113 | |||||
| chr14:59975114
|
T | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+406T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975114 | ||||||
| chr14:59975115
|
A | ATATATAT others(61): Show |
9 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1639+416_1639+417i others(70): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975115 | |||||
| chr14:59975115
|
A | ATATATAT others(61): Show |
1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1639+416_1639+417i others(70): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975115 | |||||
| chr14:59975115
|
A | G | 8 | a0001c0002t0012g0120a0001c0002t0012g0121a0001c0002t0012g0122others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+407A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975115 | ||||||
| chr14:59975115
|
A | T | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+407A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975115 | ||||||
| chr14:59975116
|
T | C | 2 | a0001c0005t0013g0180a0001c0005t0013g0181 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1639+408T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975116 | ||||||
| chr14:59975116
|
T | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+408T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975116 | ||||||
| chr14:59975116
|
T | TAC | 3 | a0001c0002t0002g0005a0001c0002t0004g0004a0001c0005t0013g0179 | 3 | HG01081.hp1 HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1639+409_1639+410i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975116 | |||||
| chr14:59975117
|
A | ATATATAT others(23): Show |
2 | a0001c0002t0002g0143a0001c0002t0002g0144 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1639+418_1639+419i others(32): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975117 | |||||
| chr14:59975118
|
T | A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+410T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975118 | ||||||
| chr14:59975118
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1639+410T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975118 | ||||||
| chr14:59975119
|
A | C | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+411A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975119 | ||||||
| chr14:59975122
|
T | A | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+414T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975122 | ||||||
| chr14:59975125
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+417A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975125 | ||||||
| chr14:59975127
|
G | A | 2 | a0001c0002t0002g0143a0001c0002t0002g0144 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1639+419G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975127 | ||||||
| chr14:59975129
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+421A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975129 | ||||||
| chr14:59975131
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+423A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975131 | ||||||
| chr14:59975133
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+425A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975133 | ||||||
| chr14:59975135
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+427A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975135 | ||||||
| chr14:59975137
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+429A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975137 | ||||||
| chr14:59975140
|
C | CAT | 5 | a0001c0002t0002g0005a0001c0002t0004g0004a0001c0002t0021g0161others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1639+441_1639+442d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975140 | |||||
| chr14:59975140
|
CAT | C | 8 | a0001c0002t0002g0107a0001c0002t0002g0138a0001c0002t0002g0139others(5): Show | 8 | HG01175.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1639+441_1639+442d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975140 | |||||
| chr14:59975143
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+435A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975143 | ||||||
| chr14:59975145
|
A | G | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1639+437A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975145 | ||||||
| chr14:59975147
|
A | ATG | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1639+440_1639+441i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975147 | |||||
| chr14:59975148
|
T | TAC | 4 | a0001c0004t0009g0302a0001c0004t0009g0307a0001c0004t0009g0308others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1639+441_1639+442i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975148 | |||||
| chr14:59975150
|
T | C | 6 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0303others(3): Show | 6 | HG00323.hp2 HG01361.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1639+442T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975150 | ||||||
| chr14:59975151
|
G | A | 15 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0014g0066others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1639+443G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975151 | ||||||
| chr14:59975152
|
T | C | 1 | a0001c0002t0004g0300 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1639+444T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975152 | ||||||
| chr14:59975154
|
T | TAC | 17 | a0001c0002t0002g0005a0001c0002t0002g0207a0001c0002t0004g0004others(14): Show | 17 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1639+447_1639+448i others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr14 | 59975154 | |||||
| chr14:59975165
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1639+457G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975165 | ||||||
| chr14:59975190
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1639+482G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975190 | ||||||
| chr14:59975228
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+520C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975228 | ||||||
| chr14:59975336
|
A | G | 16 | a0001c0002t0002g0005a0001c0002t0004g0004a0001c0002t0004g0015others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1639+628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975336 | ||||||
| chr14:59975725
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1639+1017G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59975725 | ||||||
| chr14:59976006
|
C | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1640-1219C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976006 | ||||||
| chr14:59976063
|
G | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1640-1162G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976063 | ||||||
| chr14:59976067
|
G | A | 5 | a0001c0002t0021g0161a0005c0013t0018g0110a0005c0013t0018g0111others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1640-1158G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976067 | ||||||
| chr14:59976083
|
G | T | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1640-1142G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976083 | ||||||
| chr14:59976253
|
G | C | 58 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0069others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1640-972G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976253 | ||||||
| chr14:59976356
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1640-869G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976356 | ||||||
| chr14:59976472
|
C | T | 208 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1640-753C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976472 | ||||||
| chr14:59976630
|
G | C | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1640-595G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976630 | ||||||
| chr14:59976691
|
C | T | 1 | a0001c0001t0019g0311 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1640-534C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976691 | ||||||
| chr14:59976706
|
C | T | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1640-519C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976706 | ||||||
| chr14:59976749
|
G | A | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1640-476G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976749 | ||||||
| chr14:59976785
|
C | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.1640-440C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976785 | ||||||
| chr14:59976945
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1640-280G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976945 | ||||||
| chr14:59976951
|
A | G | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1640-274A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59976951 | ||||||
| chr14:59977088
|
A | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1640-137A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 13/32 | chr14 | 59977088 | ||||||
| chr14:59977412
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1762+65C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977412 | ||||||
| chr14:59977495
|
T | C | 1 | a0001c0005t0013g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1762+148T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977495 | ||||||
| chr14:59977568
|
T | TTG | 86 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0077others(83): Show | 87 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1762+255_1762+256d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | |||||
| chr14:59977568
|
T | TTGTG | 9 | a0001c0001t0001g0165a0001c0001t0003g0018a0001c0001t0003g0019others(6): Show | 9 | HG01496.hp2 HG02257.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1762+253_1762+256d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | |||||
| chr14:59977568
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0003g0029a0001c0001t0003g0047a0001c0005t0038g0150 | 3 | NA18984.hp2 NA19082.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1762+249_1762+256d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | |||||
| chr14:59977568
|
TTG | T | 20 | a0001c0001t0001g0082a0001c0001t0003g0037a0001c0001t0003g0260others(17): Show | 20 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1762+255_1762+256d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | |||||
| chr14:59977568
|
TTGTG | T | 3 | a0001c0001t0001g0248a0001c0005t0013g0182a0004c0008t0010g0055 | 3 | HG03540.hp1 NA18978.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1762+253_1762+256d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr14 | 59977568 | |||||
| chr14:59977632
|
G | A | 1 | a0001c0004t0009g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1762+285G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977632 | ||||||
| chr14:59977707
|
G | C | 1 | a0001c0002t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1763-310G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977707 | ||||||
| chr14:59977840
|
T | A | 1 | a0001c0001t0001g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1763-177T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977840 | ||||||
| chr14:59977934
|
A | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1763-83A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 14/32 | chr14 | 59977934 | ||||||
| chr14:59978245
|
A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1878+113A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978245 | ||||||
| chr14:59978251
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1878+119G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978251 | ||||||
| chr14:59978492
|
C | T | 2 | a0001c0005t0013g0171a0001c0005t0013g0172 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1878+360C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978492 | ||||||
| chr14:59978502
|
A | G | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1878+370A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59978502 | ||||||
| chr14:59979291
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1878+1159A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979291 | ||||||
| chr14:59979344
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1878+1212T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979344 | ||||||
| chr14:59979372
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1878+1240A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979372 | ||||||
| chr14:59979484
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1878+1352C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979484 | ||||||
| chr14:59979536
|
CGGGAGGC others(10): Show |
C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1878+1406_1878+142 others(21): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59979536 | |||||
| chr14:59979640
|
C | T | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1878+1508C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979640 | ||||||
| chr14:59979658
|
T | G | 1 | a0001c0002t0012g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1878+1526T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979658 | ||||||
| chr14:59979716
|
G | A | 6 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(3): Show | 6 | HG00609.hp2 HG00621.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1878+1584G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979716 | ||||||
| chr14:59979947
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1878+1815C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979947 | ||||||
| chr14:59979979
|
TA | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1878+1855delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59979979 | |||||
| chr14:59979988
|
G | T | 1 | a0005c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1878+1856G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59979988 | ||||||
| chr14:59980018
|
C | A | 1 | a0001c0002t0004g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1879-1830C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980018 | ||||||
| chr14:59980040
|
G | GCT | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.1879-1798_1879-179 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr14 | 59980040 | |||||
| chr14:59980189
|
T | C | 1 | a0001c0001t0008g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1879-1659T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980189 | ||||||
| chr14:59980212
|
T | C | 1 | a0010c0017t0003g0065 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1879-1636T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980212 | ||||||
| chr14:59980248
|
C | A | 1 | a0001c0001t0003g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1879-1600C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980248 | ||||||
| chr14:59980825
|
C | G | 1 | a0001c0002t0002g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1879-1023C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980825 | ||||||
| chr14:59980964
|
G | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1879-884G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59980964 | ||||||
| chr14:59981036
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1879-812T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59981036 | ||||||
| chr14:59981725
|
T | C | 1 | a0001c0002t0007g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1879-123T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 15/32 | chr14 | 59981725 | ||||||
| chr14:59982061
|
G | A | 2 | a0008c0011t0003g0212a0008c0011t0006g0211 | 2 | HG00099.hp1 HG00280.hp2 |
splice_donor_variant&intron_variant | HIGH | c.2091+1G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982061 | ||||||
| chr14:59982297
|
T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2091+237T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982297 | ||||||
| chr14:59982300
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2091+240A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982300 | ||||||
| chr14:59982450
|
G | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2091+390G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982450 | ||||||
| chr14:59982549
|
T | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0239 | 2 | NA18975.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2091+489T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982549 | ||||||
| chr14:59982632
|
GT | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2091+575delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr14 | 59982632 | |||||
| chr14:59982965
|
A | G | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2091+905A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59982965 | ||||||
| chr14:59983110
|
G | A | 7 | a0001c0002t0004g0015a0001c0002t0021g0161a0001c0002t0029g0017others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2091+1050G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983110 | ||||||
| chr14:59983228
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2091+1168T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983228 | ||||||
| chr14:59983238
|
A | G | 2 | a0001c0001t0003g0260a0001c0001t0003g0261 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2091+1178A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983238 | ||||||
| chr14:59983325
|
T | G | 2 | a0001c0001t0003g0048a0001c0001t0014g0040 | 2 | NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2091+1265T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983325 | ||||||
| chr14:59983454
|
C | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2091+1394C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983454 | ||||||
| chr14:59983460
|
T | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2091+1400T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983460 | ||||||
| chr14:59983963
|
C | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2092-1142C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59983963 | ||||||
| chr14:59984067
|
A | G | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2092-1038A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984067 | ||||||
| chr14:59984427
|
T | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2092-678T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984427 | ||||||
| chr14:59984716
|
T | C | 1 | a0001c0001t0031g0219 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2092-389T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984716 | ||||||
| chr14:59984755
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2092-350T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984755 | ||||||
| chr14:59984861
|
T | A | 1 | a0001c0002t0004g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2092-244T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984861 | ||||||
| chr14:59984862
|
A | G | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2092-243A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59984862 | ||||||
| chr14:59985052
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2092-53G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59985052 | ||||||
| chr14:59985098
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
splice_region_variant&intron_variant | LOW | c.2092-7G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 16/32 | chr14 | 59985098 | ||||||
| chr14:59985314
|
T | C | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2211+90T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985314 | ||||||
| chr14:59985434
|
A | G | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2211+210A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985434 | ||||||
| chr14:59985718
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2211+494C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985718 | ||||||
| chr14:59985770
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2211+546C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985770 | ||||||
| chr14:59985808
|
T | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2211+584T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985808 | ||||||
| chr14:59985972
|
T | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2211+748T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59985972 | ||||||
| chr14:59986101
|
A | G | 7 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0168others(4): Show | 7 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+877A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986101 | ||||||
| chr14:59986182
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+958T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986182 | ||||||
| chr14:59986401
|
T | A | 1 | a0001c0004t0009g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2211+1177T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986401 | ||||||
| chr14:59986523
|
T | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0077a0001c0001t0011g0050others(3): Show | 6 | HG00621.hp1 HG02074.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+1299T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986523 | ||||||
| chr14:59986650
|
T | G | 2 | a0001c0002t0002g0119a0001c0002t0002g0178 | 2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2211+1426T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986650 | ||||||
| chr14:59986767
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+1543A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59986767 | ||||||
| chr14:59987174
|
C | T | 1 | a0001c0001t0003g0243 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2211+1950C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987174 | ||||||
| chr14:59987179
|
C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+1955C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987179 | ||||||
| chr14:59987223
|
T | A | 1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2211+1999T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987223 | ||||||
| chr14:59987245
|
A | C | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2211+2021A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987245 | ||||||
| chr14:59987330
|
A | G | 3 | a0001c0002t0017g0141a0001c0002t0017g0142a0001c0002t0024g0157 | 3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2211+2106A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987330 | ||||||
| chr14:59987356
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2211+2132G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987356 | ||||||
| chr14:59987406
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2211+2182C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987406 | ||||||
| chr14:59987437
|
T | TCAACCTT others(322): Show |
7 | a0001c0001t0001g0044a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 7 | HG00738.hp1 HG01517.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(333): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987437
|
T | TCAACCTT others(323): Show |
113 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0045others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(334): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987437
|
T | TCAACCTT others(324): Show |
1 | a0001c0001t0014g0040 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2211+2229_2211+223 others(335): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987437
|
T | TCAACCTT others(324): Show |
39 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0227others(36): Show | 39 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(335): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987437
|
T | TCAACCTT others(325): Show |
3 | a0001c0001t0001g0253a0001c0001t0014g0035a0001c0001t0028g0030 | 3 | HG02015.hp1 HG02040.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(336): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987437
|
T | TCAACCTT others(326): Show |
2 | a0001c0001t0001g0244a0001c0001t0031g0219 | 2 | NA18995.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2211+2229_2211+223 others(337): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59987437 | |||||
| chr14:59987555
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0231a0001c0001t0001g0313 | 3 | NA18961.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2211+2331G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987555 | ||||||
| chr14:59987600
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2211+2376C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987600 | ||||||
| chr14:59987954
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0091 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2211+2730G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987954 | ||||||
| chr14:59987955
|
T | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0091 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2211+2731T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987955 | ||||||
| chr14:59987999
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+2775C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59987999 | ||||||
| chr14:59988047
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2211+2823C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988047 | ||||||
| chr14:59988367
|
G | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2211+3143G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988367 | ||||||
| chr14:59988550
|
T | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2211+3326T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988550 | ||||||
| chr14:59988556
|
C | T | 2 | a0001c0001t0003g0064a0010c0017t0003g0065 | 2 | HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2211+3332C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988556 | ||||||
| chr14:59988612
|
G | T | 41 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(38): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.2211+3388G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988612 | ||||||
| chr14:59988697
|
C | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2211+3473C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988697 | ||||||
| chr14:59988700
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2211+3476C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988700 | ||||||
| chr14:59988705
|
G | A | 1 | a0001c0002t0002g0296 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2211+3481G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988705 | ||||||
| chr14:59988946
|
C | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2211+3722C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59988946 | ||||||
| chr14:59989149
|
T | C | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2211+3925T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989149 | ||||||
| chr14:59989176
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+3952T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989176 | ||||||
| chr14:59989222
|
T | C | 1 | a0009c0018t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2211+3998T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989222 | ||||||
| chr14:59989283
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2211+4059T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989283 | ||||||
| chr14:59989484
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2211+4260C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989484 | ||||||
| chr14:59989927
|
C | CT | 42 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(39): Show | 43 | HG00099.hp1 HG00280.hp2 HG01346.hp2 others(40): Show |
intron_variant | MODIFIER | c.2211+4720dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59989927 | |||||
| chr14:59989927
|
CT | C | 7 | a0001c0001t0003g0255a0001c0001t0011g0073a0001c0002t0002g0138others(4): Show | 7 | HG01257.hp2 HG01515.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2211+4720delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59989927 | |||||
| chr14:59989949
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+4725C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989949 | ||||||
| chr14:59989965
|
T | C | 5 | a0001c0001t0001g0226a0001c0001t0003g0255a0001c0001t0003g0256others(2): Show | 5 | HG00735.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2211+4741T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989965 | ||||||
| chr14:59989989
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2211+4765G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989989 | ||||||
| chr14:59989996
|
C | T | 2 | a0005c0013t0018g0110a0005c0013t0018g0111 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2211+4772C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59989996 | ||||||
| chr14:59990127
|
G | A | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2211+4903G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990127 | ||||||
| chr14:59990154
|
C | T | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2211+4930C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990154 | ||||||
| chr14:59990174
|
G | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2211+4950G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990174 | ||||||
| chr14:59990213
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+4989C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990213 | ||||||
| chr14:59990253
|
G | T | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2211+5029G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990253 | ||||||
| chr14:59990328
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2211+5104T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990328 | ||||||
| chr14:59990331
|
T | C | 8 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(5): Show | 8 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.2211+5107T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990331 | ||||||
| chr14:59990810
|
G | A | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2211+5586G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990810 | ||||||
| chr14:59990997
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2211+5773T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59990997 | ||||||
| chr14:59991211
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2211+5987C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991211 | ||||||
| chr14:59991440
|
A | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.2211+6216A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991440 | ||||||
| chr14:59991587
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-6069C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991587 | ||||||
| chr14:59991678
|
A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2212-5978A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991678 | ||||||
| chr14:59991758
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2212-5898A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991758 | ||||||
| chr14:59991779
|
GCCATTGC | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0058others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2212-5873_2212-586 others(11): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59991779 | |||||
| chr14:59991795
|
C | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0058others(77): Show | 80 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2212-5861C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991795 | ||||||
| chr14:59991802
|
T | TAAAC | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2212-5851_2212-585 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59991802 | |||||
| chr14:59991928
|
C | T | 20 | a0002c0003t0005g0185a0002c0003t0005g0186a0002c0003t0005g0189others(17): Show | 20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.2212-5728C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991928 | ||||||
| chr14:59991959
|
G | C | 8 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0084others(5): Show | 8 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-5697G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991959 | ||||||
| chr14:59991992
|
C | G | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2212-5664C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59991992 | ||||||
| chr14:59992099
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-5557T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992099 | ||||||
| chr14:59992197
|
A | G | 2 | a0001c0001t0010g0034a0001c0001t0015g0062 | 2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2212-5459A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992197 | ||||||
| chr14:59992255
|
A | T | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2212-5401A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992255 | ||||||
| chr14:59992314
|
G | A | 2 | a0001c0002t0002g0215a0001c0002t0025g0113 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2212-5342G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992314 | ||||||
| chr14:59992402
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-5254C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992402 | ||||||
| chr14:59992458
|
C | T | 3 | a0001c0001t0003g0029a0001c0001t0003g0047a0001c0001t0016g0023 | 3 | HG01074.hp2 NA18984.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2212-5198C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992458 | ||||||
| chr14:59992484
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-5172G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992484 | ||||||
| chr14:59992573
|
C | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-5083C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992573 | ||||||
| chr14:59992653
|
G | A | 44 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0006g0020others(41): Show | 45 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(42): Show |
intron_variant | MODIFIER | c.2212-5003G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992653 | ||||||
| chr14:59992738
|
C | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2212-4918C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992738 | ||||||
| chr14:59992739
|
G | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2212-4917G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992739 | ||||||
| chr14:59992959
|
C | T | 2 | a0001c0001t0001g0226a0009c0018t0003g0230 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2212-4697C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59992959 | ||||||
| chr14:59993100
|
A | G | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2212-4556A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993100 | ||||||
| chr14:59993227
|
G | A | 2 | a0001c0002t0002g0220a0001c0002t0002g0233 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2212-4429G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993227 | ||||||
| chr14:59993246
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2212-4410C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993246 | ||||||
| chr14:59993362
|
A | G | 5 | a0001c0002t0004g0268a0001c0002t0004g0285a0001c0002t0004g0288others(2): Show | 5 | NA18966.hp1 NA18968.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.2212-4294A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993362 | ||||||
| chr14:59993389
|
A | C | 7 | a0001c0002t0004g0015a0001c0002t0021g0161a0001c0002t0029g0017others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2212-4267A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993389 | ||||||
| chr14:59993553
|
G | A | 3 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0306 | 3 | NA18946.hp2 NA18962.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2212-4103G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993553 | ||||||
| chr14:59993572
|
C | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-4084C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993572 | ||||||
| chr14:59993575
|
G | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-4081G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993575 | ||||||
| chr14:59993727
|
G | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-3929G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993727 | ||||||
| chr14:59993979
|
G | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-3677G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59993979 | ||||||
| chr14:59994193
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2212-3463G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994193 | ||||||
| chr14:59994242
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2212-3414C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994242 | ||||||
| chr14:59994318
|
C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-3338C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994318 | ||||||
| chr14:59994327
|
G | C | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2212-3329G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994327 | ||||||
| chr14:59994554
|
A | T | 1 | a0005c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2212-3102A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994554 | ||||||
| chr14:59994626
|
C | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-3030C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994626 | ||||||
| chr14:59994947
|
A | T | 4 | a0001c0006t0002g0108a0001c0006t0002g0109a0001c0006t0002g0114others(1): Show | 4 | HG02074.hp1 HG02080.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-2709A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59994947 | ||||||
| chr14:59995008
|
T | TAA | 182 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.2212-2639_2212-263 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995008 | |||||
| chr14:59995009
|
A | AAT | 5 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2212-2646_2212-264 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995009 | |||||
| chr14:59995025
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2212-2631A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995025 | ||||||
| chr14:59995258
|
T | G | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2212-2398T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995258 | ||||||
| chr14:59995362
|
T | A | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-2294T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995362 | ||||||
| chr14:59995376
|
C | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-2280C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995376 | ||||||
| chr14:59995466
|
G | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-2190G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995466 | ||||||
| chr14:59995710
|
G | A | 1 | a0002c0003t0005g0185 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2212-1946G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995710 | ||||||
| chr14:59995725
|
G | GT | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-1921dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr14 | 59995725 | |||||
| chr14:59995853
|
C | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-1803C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995853 | ||||||
| chr14:59995986
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2212-1670C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59995986 | ||||||
| chr14:59996093
|
A | T | 2 | a0001c0001t0001g0213a0001c0001t0016g0105 | 2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2212-1563A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996093 | ||||||
| chr14:59996581
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2212-1075C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996581 | ||||||
| chr14:59996875
|
C | T | 1 | a0001c0001t0014g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2212-781C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59996875 | ||||||
| chr14:59997197
|
T | C | 1 | a0002c0003t0005g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2212-459T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997197 | ||||||
| chr14:59997276
|
T | C | 3 | a0001c0002t0017g0141a0001c0002t0017g0142a0001c0002t0024g0157 | 3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2212-380T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997276 | ||||||
| chr14:59997393
|
G | A | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2212-263G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997393 | ||||||
| chr14:59997427
|
G | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2212-229G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 17/32 | chr14 | 59997427 | ||||||
| chr14:59997973
|
T | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.2403+126T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59997973 | ||||||
| chr14:59998020
|
G | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0028 | 2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2403+173G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998020 | ||||||
| chr14:59998138
|
T | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2403+291T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998138 | ||||||
| chr14:59998798
|
T | A | 2 | a0001c0002t0004g0289a0001c0002t0004g0300 | 2 | HG02040.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2404-303T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998798 | ||||||
| chr14:59998803
|
A | G | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2404-298A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59998803 | ||||||
| chr14:59999078
|
A | T | 1 | a0001c0005t0013g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2404-23A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59999078 | ||||||
| chr14:59999079
|
T | A | 2 | a0001c0001t0031g0219a0001c0001t0035g0156 | 2 | HG01496.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2404-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 18/32 | chr14 | 59999079 | ||||||
| chr14:59999350
|
G | A | 1 | a0001c0002t0012g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2529+124G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999350 | ||||||
| chr14:59999424
|
C | CATACATG others(7): Show |
1 | a0001c0001t0041g0229 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2529+198_2529+199i others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999424 | ||||||
| chr14:59999841
|
A | G | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2529+615A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999841 | ||||||
| chr14:59999862
|
C | A | 1 | a0001c0002t0012g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2529+636C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 59999862 | ||||||
| chr14:60000016
|
A | T | 1 | a0001c0001t0003g0168 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2529+790A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000016 | ||||||
| chr14:60000290
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2529+1064G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000290 | ||||||
| chr14:60000301
|
G | C | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2529+1075G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000301 | ||||||
| chr14:60000503
|
T | C | 2 | a0001c0005t0013g0171a0001c0005t0013g0172 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2529+1277T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000503 | ||||||
| chr14:60000565
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2529+1339C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000565 | ||||||
| chr14:60000747
|
C | A | 1 | a0001c0001t0019g0311 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2530-1219C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60000747 | ||||||
| chr14:60001027
|
A | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2530-939A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001027 | ||||||
| chr14:60001116
|
G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2530-850G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001116 | ||||||
| chr14:60001188
|
T | TTGTG | 16 | a0001c0001t0014g0035a0001c0002t0002g0005a0001c0002t0002g0112others(13): Show | 16 | HG01081.hp1 HG01358.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2530-758_2530-755d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr14 | 60001188 | |||||
| chr14:60001309
|
T | C | 318 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2530-657T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001309 | ||||||
| chr14:60001444
|
T | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2530-522T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001444 | ||||||
| chr14:60001502
|
T | G | 201 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2530-464T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001502 | ||||||
| chr14:60001517
|
A | C | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2530-449A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001517 | ||||||
| chr14:60001640
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2530-326G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001640 | ||||||
| chr14:60001722
|
TTATAG | T | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2530-241_2530-237d others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr14 | 60001722 | |||||
| chr14:60001762
|
A | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2530-204A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001762 | ||||||
| chr14:60001943
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2530-23C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001943 | ||||||
| chr14:60001944
|
T | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-22T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001944 | ||||||
| chr14:60001945
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-21G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001945 | ||||||
| chr14:60001946
|
T | A | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2530-20T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 19/32 | chr14 | 60001946 | ||||||
| chr14:60002145
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2664+45T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002145 | ||||||
| chr14:60002577
|
A | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2664+477A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002577 | ||||||
| chr14:60002599
|
A | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2664+499A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002599 | ||||||
| chr14:60002614
|
A | G | 1 | a0001c0001t0011g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2664+514A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002614 | ||||||
| chr14:60002842
|
A | G | 1 | a0001c0012t0002g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2664+742A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002842 | ||||||
| chr14:60002863
|
A | T | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2665-758A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60002863 | ||||||
| chr14:60003075
|
G | T | 1 | a0001c0001t0014g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2665-546G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003075 | ||||||
| chr14:60003310
|
T | A | 1 | a0001c0002t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2665-311T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003310 | ||||||
| chr14:60003396
|
C | T | 1 | a0002c0003t0005g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2665-225C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 20/32 | chr14 | 60003396 | ||||||
| chr14:60003854
|
C | CA | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842+62dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60003854 | |||||
| chr14:60003893
|
A | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+95A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60003893 | ||||||
| chr14:60004083
|
A | G | 1 | a0001c0001t0006g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2842+285A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004083 | ||||||
| chr14:60004085
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2842+287C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004085 | ||||||
| chr14:60004140
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842+342G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004140 | ||||||
| chr14:60004420
|
T | C | 2 | a0001c0004t0009g0210a0001c0004t0009g0306 | 2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.2842+622T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004420 | ||||||
| chr14:60004836
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+1038A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004836 | ||||||
| chr14:60004857
|
A | C | 2 | a0001c0002t0002g0220a0001c0002t0002g0233 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2842+1059A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004857 | ||||||
| chr14:60004881
|
T | TAC | 15 | a0001c0002t0004g0004a0001c0002t0004g0214a0001c0002t0017g0117others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+1106_2842+110 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
T | TACAC | 27 | a0001c0002t0002g0005a0001c0002t0002g0112a0001c0002t0002g0207others(24): Show | 28 | HG01081.hp1 HG01884.hp2 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.2842+1104_2842+110 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
T | TACACAC | 37 | a0001c0002t0004g0265a0001c0002t0004g0268a0001c0002t0004g0271others(34): Show | 38 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(35): Show |
intron_variant | MODIFIER | c.2842+1102_2842+110 others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
T | TACACACA others(1): Show |
9 | a0001c0002t0004g0310a0001c0002t0007g0274a0001c0005t0013g0151others(6): Show | 9 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2842+1100_2842+110 others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
T | TACACACA others(3): Show |
3 | a0001c0002t0007g0317a0001c0002t0021g0161a0001c0005t0013g0171 | 3 | HG02257.hp1 HG03942.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2842+1098_2842+110 others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
T | TACACACA others(5): Show |
1 | a0001c0005t0013g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2842+1096_2842+110 others(16): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004881
|
TAC | T | 164 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.2842+1106_2842+110 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr14 | 60004881 | |||||
| chr14:60004911
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2842+1113T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004911 | ||||||
| chr14:60004991
|
C | T | 39 | a0001c0002t0004g0265a0001c0002t0004g0268a0001c0002t0004g0271others(36): Show | 40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.2842+1193C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60004991 | ||||||
| chr14:60005030
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2842+1232T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005030 | ||||||
| chr14:60005060
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2842+1262C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005060 | ||||||
| chr14:60005284
|
G | A | 1 | a0001c0001t0030g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2843-1113G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005284 | ||||||
| chr14:60005769
|
A | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.2843-628A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005769 | ||||||
| chr14:60005976
|
G | A | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2843-421G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005976 | ||||||
| chr14:60005981
|
A | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2843-416A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60005981 | ||||||
| chr14:60006035
|
T | C | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2843-362T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006035 | ||||||
| chr14:60006099
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2843-298T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006099 | ||||||
| chr14:60006144
|
C | T | 3 | a0001c0002t0002g0173a0001c0002t0002g0215a0001c0002t0025g0113 | 3 | HG02145.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2843-253C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 21/32 | chr14 | 60006144 | ||||||
| chr14:60006623
|
C | T | 1 | a0002c0003t0005g0190 | 1 | NA18975.hp2 | splice_region_variant&intron_variant | LOW | c.3063+6C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60006623 | ||||||
| chr14:60006959
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3063+342C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60006959 | ||||||
| chr14:60007016
|
A | G | 1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3063+399A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007016 | ||||||
| chr14:60007083
|
G | A | 6 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0145others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3063+466G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007083 | ||||||
| chr14:60007248
|
C | T | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3063+631C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007248 | ||||||
| chr14:60007443
|
C | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3064-649C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007443 | ||||||
| chr14:60007764
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3064-328G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007764 | ||||||
| chr14:60007926
|
C | T | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3064-166C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | chr14 | 60007926 | ||||||
| chr14:60007940
|
TA | T | 55 | a0001c0001t0001g0251a0001c0002t0002g0003a0001c0002t0002g0107others(52): Show | 55 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.3064-130delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | |||||
| chr14:60007940
|
TAA | T | 156 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(153): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.3064-131_3064-130d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | |||||
| chr14:60007940
|
TAAA | T | 103 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0058others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.3064-132_3064-130d others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr14 | 60007940 | |||||
| chr14:60008527
|
G | C | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3186+313G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008527 | ||||||
| chr14:60008625
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3186+411T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008625 | ||||||
| chr14:60008886
|
T | A | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3186+672T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60008886 | ||||||
| chr14:60009038
|
T | C | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3186+824T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009038 | ||||||
| chr14:60009120
|
T | C | 197 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.3186+906T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009120 | ||||||
| chr14:60009232
|
C | A | 174 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.3186+1018C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009232 | ||||||
| chr14:60009459
|
G | A | 2 | a0001c0001t0001g0226a0009c0018t0003g0230 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3186+1245G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009459 | ||||||
| chr14:60009473
|
T | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3186+1259T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009473 | ||||||
| chr14:60009614
|
TTCAAAAC others(3): Show |
T | 1 | a0001c0001t0001g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3186+1404_3186+141 others(14): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60009614 | |||||
| chr14:60009689
|
G | A | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3186+1475G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009689 | ||||||
| chr14:60009714
|
T | C | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3186+1500T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009714 | ||||||
| chr14:60009769
|
G | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+1555G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009769 | ||||||
| chr14:60009779
|
C | T | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3186+1565C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009779 | ||||||
| chr14:60009835
|
C | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3186+1621C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009835 | ||||||
| chr14:60009841
|
G | A | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3186+1627G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60009841 | ||||||
| chr14:60010226
|
C | T | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3186+2012C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010226 | ||||||
| chr14:60010241
|
A | T | 260 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.3186+2027A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010241 | ||||||
| chr14:60010287
|
T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3186+2073T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010287 | ||||||
| chr14:60010448
|
G | A | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3186+2234G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010448 | ||||||
| chr14:60010449
|
A | G | 1 | a0001c0002t0004g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3186+2235A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010449 | ||||||
| chr14:60010450
|
C | A | 1 | a0001c0002t0004g0295 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3186+2236C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010450 | ||||||
| chr14:60010462
|
AC | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3186+2250delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60010462 | |||||
| chr14:60010480
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3186+2266G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010480 | ||||||
| chr14:60010844
|
G | C | 1 | a0001c0001t0037g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3186+2630G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010844 | ||||||
| chr14:60010861
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3186+2647C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60010861 | ||||||
| chr14:60011211
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3186+2997A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011211 | ||||||
| chr14:60011409
|
G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3186+3195G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011409 | ||||||
| chr14:60011493
|
T | A | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3186+3279T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011493 | ||||||
| chr14:60011550
|
C | T | 1 | a0001c0002t0004g0298 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3186+3336C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011550 | ||||||
| chr14:60011591
|
T | C | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG00099.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3186+3377T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011591 | ||||||
| chr14:60011633
|
A | G | 318 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.3186+3419A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011633 | ||||||
| chr14:60011883
|
A | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0094 | 3 | HG02615.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3186+3669A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60011883 | ||||||
| chr14:60012077
|
T | A | 24 | a0001c0005t0038g0150a0002c0003t0005g0001a0002c0003t0005g0185others(21): Show | 25 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(22): Show |
intron_variant | MODIFIER | c.3186+3863T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012077 | ||||||
| chr14:60012117
|
G | T | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3186+3903G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012117 | ||||||
| chr14:60012325
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3186+4111T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012325 | ||||||
| chr14:60012335
|
T | C | 82 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3186+4121T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012335 | ||||||
| chr14:60012378
|
A | G | 1 | a0001c0002t0004g0272 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.3186+4164A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012378 | ||||||
| chr14:60012695
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3187-3965A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012695 | ||||||
| chr14:60012818
|
C | T | 1 | a0001c0001t0006g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3187-3842C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012818 | ||||||
| chr14:60012936
|
TTTTA | T | 189 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3187-3708_3187-370 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60012936 | |||||
| chr14:60012952
|
A | T | 7 | a0001c0004t0009g0209a0001c0004t0009g0302a0001c0004t0009g0303others(4): Show | 7 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.3187-3708A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60012952 | ||||||
| chr14:60013016
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3187-3644C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013016 | ||||||
| chr14:60013041
|
G | A | 1 | a0008c0011t0003g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3187-3619G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013041 | ||||||
| chr14:60013083
|
A | G | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3187-3577A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013083 | ||||||
| chr14:60013086
|
T | G | 41 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(38): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.3187-3574T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013086 | ||||||
| chr14:60013246
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3187-3414G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013246 | ||||||
| chr14:60013268
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3187-3392C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013268 | ||||||
| chr14:60013335
|
C | G | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3187-3325C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013335 | ||||||
| chr14:60013622
|
T | C | 10 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(7): Show | 10 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.3187-3038T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013622 | ||||||
| chr14:60013641
|
C | T | 8 | a0001c0002t0012g0120a0001c0002t0012g0121a0001c0002t0012g0122others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3187-3019C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013641 | ||||||
| chr14:60013643
|
G | A | 16 | a0001c0002t0002g0005a0001c0002t0004g0004a0001c0002t0004g0015others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3187-3017G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013643 | ||||||
| chr14:60013665
|
T | C | 1 | a0001c0001t0016g0023 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3187-2995T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013665 | ||||||
| chr14:60013677
|
G | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0058others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.3187-2983G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013677 | ||||||
| chr14:60013756
|
T | C | 2 | a0001c0001t0003g0260a0001c0001t0003g0261 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3187-2904T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60013756 | ||||||
| chr14:60014003
|
C | G | 1 | a0001c0002t0012g0147 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3187-2657C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014003 | ||||||
| chr14:60014054
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3187-2606A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014054 | ||||||
| chr14:60014199
|
A | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3187-2461A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014199 | ||||||
| chr14:60014386
|
T | C | 3 | a0002c0003t0005g0001a0002c0003t0005g0187a0002c0003t0005g0188 | 4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.3187-2274T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014386 | ||||||
| chr14:60014389
|
T | A | 1 | a0007c0010t0018g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3187-2271T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014389 | ||||||
| chr14:60014485
|
G | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0252a0001c0001t0027g0234 | 3 | NA18956.hp1 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3187-2175G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014485 | ||||||
| chr14:60014776
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3187-1884T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014776 | ||||||
| chr14:60014998
|
AC | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3187-1661delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60014998 | ||||||
| chr14:60015046
|
C | T | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0006g0020 | 3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3187-1614C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015046 | ||||||
| chr14:60015193
|
A | T | 2 | a0001c0002t0002g0005a0001c0002t0004g0004 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3187-1467A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015193 | ||||||
| chr14:60015259
|
TA | T | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3187-1395delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr14 | 60015259 | |||||
| chr14:60015421
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3187-1239G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015421 | ||||||
| chr14:60015714
|
G | A | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3187-946G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015714 | ||||||
| chr14:60015949
|
T | C | 1 | a0001c0001t0032g0320 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3187-711T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015949 | ||||||
| chr14:60015969
|
T | C | 2 | a0001c0005t0013g0171a0001c0005t0013g0172 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3187-691T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60015969 | ||||||
| chr14:60016010
|
A | G | 1 | a0001c0002t0020g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3187-650A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016010 | ||||||
| chr14:60016017
|
G | T | 1 | a0001c0001t0042g0184 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3187-643G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016017 | ||||||
| chr14:60016033
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3187-627G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016033 | ||||||
| chr14:60016255
|
G | T | 1 | a0001c0001t0006g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3187-405G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016255 | ||||||
| chr14:60016272
|
C | A | 1 | a0001c0001t0006g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3187-388C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016272 | ||||||
| chr14:60016277
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3187-383C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 23/32 | chr14 | 60016277 | ||||||
| chr14:60016837
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3317+47G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016837 | ||||||
| chr14:60016880
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3317+90C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016880 | ||||||
| chr14:60016960
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3317+170G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60016960 | ||||||
| chr14:60017058
|
A | G | 1 | a0001c0004t0009g0303 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3317+268A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017058 | ||||||
| chr14:60017273
|
T | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3317+483T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017273 | ||||||
| chr14:60017373
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3317+583G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017373 | ||||||
| chr14:60017605
|
C | T | 1 | a0001c0001t0006g0242 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3318-766C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017605 | ||||||
| chr14:60017700
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3318-671T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017700 | ||||||
| chr14:60017745
|
T | C | 2 | a0001c0002t0002g0175a0001c0002t0002g0176 | 2 | HG01255.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3318-626T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017745 | ||||||
| chr14:60017772
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3318-599C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60017772 | ||||||
| chr14:60018106
|
T | C | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3318-265T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018106 | ||||||
| chr14:60018147
|
G | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3318-224G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018147 | ||||||
| chr14:60018197
|
T | C | 4 | a0001c0001t0011g0021a0001c0001t0011g0078a0001c0001t0011g0079others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318-174T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018197 | ||||||
| chr14:60018210
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3318-161G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018210 | ||||||
| chr14:60018213
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3318-158C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | chr14 | 60018213 | ||||||
| chr14:60018308
|
AC | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3318-61delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr14 | 60018308 | |||||
| chr14:60018522
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3426+43G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018522 | ||||||
| chr14:60018550
|
G | A | 1 | a0001c0002t0002g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3426+71G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018550 | ||||||
| chr14:60018600
|
G | GT | 161 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.3426+130dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr14 | 60018600 | |||||
| chr14:60018600
|
G | T | 1 | a0001c0001t0015g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3426+121G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018600 | ||||||
| chr14:60018659
|
T | G | 46 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0077others(43): Show | 46 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.3426+180T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018659 | ||||||
| chr14:60018854
|
T | A | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3427-267T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018854 | ||||||
| chr14:60018862
|
T | A | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3427-259T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60018862 | ||||||
| chr14:60019046
|
G | T | 1 | a0001c0001t0003g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3427-75G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 25/32 | chr14 | 60019046 | ||||||
| chr14:60019325
|
C | T | 1 | a0001c0002t0007g0294 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3566+65C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019325 | ||||||
| chr14:60019499
|
G | A | 1 | a0001c0002t0004g0286 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3566+239G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019499 | ||||||
| chr14:60019513
|
A | G | 2 | a0001c0001t0008g0032a0001c0001t0008g0041 | 2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.3566+253A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019513 | ||||||
| chr14:60019585
|
T | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3566+325T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019585 | ||||||
| chr14:60019594
|
A | G | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3566+334A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019594 | ||||||
| chr14:60019699
|
C | CT | 8 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0168others(5): Show | 8 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.3566+447dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr14 | 60019699 | |||||
| chr14:60019708
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3566+448C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019708 | ||||||
| chr14:60019799
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3566+539A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019799 | ||||||
| chr14:60019860
|
CAT | C | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3566+603_3566+604d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr14 | 60019860 | |||||
| chr14:60019892
|
C | T | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3566+632C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60019892 | ||||||
| chr14:60020282
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3566+1022G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020282 | ||||||
| chr14:60020719
|
A | C | 1 | a0001c0001t0008g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3566+1459A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020719 | ||||||
| chr14:60020725
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3566+1465C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60020725 | ||||||
| chr14:60021067
|
A | C | 4 | a0001c0001t0011g0021a0001c0001t0011g0078a0001c0001t0011g0079others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3567-1667A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021067 | ||||||
| chr14:60021112
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3567-1622A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021112 | ||||||
| chr14:60021284
|
T | C | 2 | a0001c0001t0010g0034a0001c0001t0015g0062 | 2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3567-1450T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021284 | ||||||
| chr14:60021311
|
C | T | 1 | a0001c0001t0010g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3567-1423C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021311 | ||||||
| chr14:60021387
|
G | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0088others(3): Show | 6 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3567-1347G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021387 | ||||||
| chr14:60021625
|
G | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3567-1109G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021625 | ||||||
| chr14:60021678
|
G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3567-1056G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021678 | ||||||
| chr14:60021861
|
C | T | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3567-873C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60021861 | ||||||
| chr14:60022018
|
T | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3567-716T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60022018 | ||||||
| chr14:60022186
|
T | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3567-548T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 26/32 | chr14 | 60022186 | ||||||
| chr14:60022900
|
C | G | 1 | a0001c0001t0016g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3703+30C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60022900 | ||||||
| chr14:60022947
|
A | C | 1 | a0001c0002t0002g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3703+77A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60022947 | ||||||
| chr14:60023089
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3703+219A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023089 | ||||||
| chr14:60023096
|
T | C | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3703+226T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023096 | ||||||
| chr14:60023326
|
T | C | 1 | a0001c0004t0009g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3703+456T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023326 | ||||||
| chr14:60023393
|
T | A | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3703+523T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023393 | ||||||
| chr14:60023541
|
A | AAG | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3703+674_3703+675d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60023541 | |||||
| chr14:60023649
|
T | G | 16 | a0001c0002t0002g0005a0001c0002t0004g0004a0001c0002t0004g0015others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3703+779T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023649 | ||||||
| chr14:60023762
|
A | C | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3703+892A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60023762 | ||||||
| chr14:60023945
|
C | CT | 260 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.3703+1076dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60023945 | |||||
| chr14:60024398
|
TTA | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3703+1529_3703+153 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024398 | ||||||
| chr14:60024415
|
G | A | 14 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.3703+1545G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024415 | ||||||
| chr14:60024466
|
G | C | 1 | a0001c0001t0003g0170 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3703+1596G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024466 | ||||||
| chr14:60024495
|
A | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3703+1625A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024495 | ||||||
| chr14:60024734
|
T | A | 1 | a0001c0002t0002g0297 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3703+1864T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024734 | ||||||
| chr14:60024826
|
CATTCTCC others(4): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3703+1957_3703+196 others(15): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024826 | ||||||
| chr14:60024840
|
T | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3703+1970T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60024840 | ||||||
| chr14:60025069
|
G | T | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3703+2199G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025069 | ||||||
| chr14:60025088
|
T | G | 1 | a0001c0001t0027g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3703+2218T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025088 | ||||||
| chr14:60025156
|
T | C | 1 | a0009c0018t0003g0230 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3703+2286T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025156 | ||||||
| chr14:60025244
|
C | A | 1 | a0001c0001t0015g0060 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3703+2374C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025244 | ||||||
| chr14:60025250
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3703+2380C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025250 | ||||||
| chr14:60025290
|
A | C | 260 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(257): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.3703+2420A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025290 | ||||||
| chr14:60025317
|
G | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3703+2447G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025317 | ||||||
| chr14:60025382
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3704-2502G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025382 | ||||||
| chr14:60025384
|
G | A | 1 | a0001c0002t0004g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3704-2500G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025384 | ||||||
| chr14:60025455
|
T | G | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3704-2429T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025455 | ||||||
| chr14:60025597
|
A | G | 1 | a0001c0002t0002g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3704-2287A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025597 | ||||||
| chr14:60025611
|
T | C | 1 | a0003c0007t0004g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3704-2273T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60025611 | ||||||
| chr14:60025679
|
CA | C | 80 | a0001c0001t0014g0040a0001c0001t0035g0156a0001c0002t0002g0207others(77): Show | 82 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.3704-2190delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60025679 | |||||
| chr14:60025679
|
CAAA | C | 13 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(10): Show | 13 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3704-2192_3704-219 others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr14 | 60025679 | |||||
| chr14:60026229
|
A | G | 2 | a0005c0013t0018g0110a0005c0013t0018g0111 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3704-1655A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026229 | ||||||
| chr14:60026337
|
G | T | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3704-1547G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026337 | ||||||
| chr14:60026485
|
T | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3704-1399T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026485 | ||||||
| chr14:60026529
|
C | G | 15 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(12): Show | 15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.3704-1355C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026529 | ||||||
| chr14:60026779
|
T | C | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3704-1105T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026779 | ||||||
| chr14:60026956
|
A | C | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3704-928A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026956 | ||||||
| chr14:60026973
|
T | C | 4 | a0001c0002t0004g0271a0001c0002t0004g0278a0001c0002t0004g0281others(1): Show | 4 | HG00558.hp2 NA18950.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-911T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60026973 | ||||||
| chr14:60027567
|
C | T | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3704-317C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60027567 | ||||||
| chr14:60027663
|
G | C | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3704-221G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 27/32 | chr14 | 60027663 | ||||||
| chr14:60028344
|
T | C | 3 | a0001c0002t0017g0141a0001c0002t0017g0142a0001c0002t0024g0157 | 3 | HG01109.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3921+243T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028344 | ||||||
| chr14:60028401
|
G | C | 1 | a0001c0001t0016g0105 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3921+300G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028401 | ||||||
| chr14:60028424
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3921+323G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028424 | ||||||
| chr14:60028638
|
T | C | 1 | a0001c0006t0002g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3921+537T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028638 | ||||||
| chr14:60028712
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0231a0001c0001t0001g0313 | 3 | NA18961.hp1 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3921+611G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028712 | ||||||
| chr14:60028802
|
C | T | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3921+701C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60028802 | ||||||
| chr14:60029329
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3921+1228G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029329 | ||||||
| chr14:60029436
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3921+1335C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029436 | ||||||
| chr14:60029526
|
G | A | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3921+1425G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029526 | ||||||
| chr14:60029652
|
C | A | 3 | a0001c0002t0002g0003a0001c0002t0002g0296a0001c0002t0002g0297 | 3 | HG00673.hp1 NA18978.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3921+1551C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029652 | ||||||
| chr14:60029724
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3921+1623T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029724 | ||||||
| chr14:60029758
|
A | C | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3921+1657A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029758 | ||||||
| chr14:60029864
|
C | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3921+1763C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60029864 | ||||||
| chr14:60029951
|
GA | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3921+1859delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr14 | 60029951 | |||||
| chr14:60030040
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3921+1939C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030040 | ||||||
| chr14:60030109
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3922-1886A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030109 | ||||||
| chr14:60030257
|
C | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-1738C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030257 | ||||||
| chr14:60030263
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-1732G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030263 | ||||||
| chr14:60030341
|
A | G | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3922-1654A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030341 | ||||||
| chr14:60030367
|
A | G | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3922-1628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030367 | ||||||
| chr14:60030587
|
A | G | 5 | a0001c0001t0001g0226a0001c0001t0003g0255a0001c0001t0003g0256others(2): Show | 5 | HG00735.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.3922-1408A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030587 | ||||||
| chr14:60030691
|
A | G | 1 | a0001c0001t0003g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3922-1304A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030691 | ||||||
| chr14:60030794
|
A | G | 2 | a0001c0001t0010g0053a0001c0001t0010g0054 | 2 | NA18612.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3922-1201A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030794 | ||||||
| chr14:60030928
|
C | T | 5 | a0001c0002t0021g0161a0005c0013t0018g0110a0005c0013t0018g0111others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3922-1067C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60030928 | ||||||
| chr14:60031183
|
C | G | 1 | a0002c0003t0005g0187 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3922-812C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031183 | ||||||
| chr14:60031244
|
C | T | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3922-751C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031244 | ||||||
| chr14:60031291
|
A | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3922-704A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031291 | ||||||
| chr14:60031367
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3922-628T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031367 | ||||||
| chr14:60031407
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3922-588T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031407 | ||||||
| chr14:60031556
|
T | C | 1 | a0001c0002t0002g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3922-439T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031556 | ||||||
| chr14:60031563
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3922-432G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031563 | ||||||
| chr14:60031681
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3922-314T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031681 | ||||||
| chr14:60031861
|
C | A | 14 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.3922-134C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031861 | ||||||
| chr14:60031976
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3922-19C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 28/32 | chr14 | 60031976 | ||||||
| chr14:60032155
|
A | G | 1 | a0007c0010t0021g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3990+92A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032155 | ||||||
| chr14:60032158
|
C | T | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3990+95C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032158 | ||||||
| chr14:60032330
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+267T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032330 | ||||||
| chr14:60032567
|
A | G | 1 | a0001c0002t0004g0289 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3990+504A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032567 | ||||||
| chr14:60032620
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3990+557C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032620 | ||||||
| chr14:60032646
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+583T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032646 | ||||||
| chr14:60032791
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+728T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032791 | ||||||
| chr14:60032859
|
CT | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+797delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032859 | ||||||
| chr14:60032942
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+879A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032942 | ||||||
| chr14:60032978
|
C | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+915C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60032978 | ||||||
| chr14:60033240
|
T | C | 1 | a0001c0001t0008g0041 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3990+1177T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033240 | ||||||
| chr14:60033589
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+1526A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033589 | ||||||
| chr14:60033713
|
T | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+1650T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60033713 | ||||||
| chr14:60034015
|
C | CT | 43 | a0001c0002t0002g0003a0001c0002t0002g0137a0001c0002t0002g0215others(40): Show | 44 | HG00558.hp2 HG00609.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.3990+1975dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | |||||
| chr14:60034015
|
C | CTT | 14 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0004g0272others(11): Show | 14 | HG01243.hp2 HG02015.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3990+1974_3990+197 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | |||||
| chr14:60034015
|
CT | C | 10 | a0001c0002t0002g0112a0001c0002t0002g0207a0001c0004t0009g0209others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3990+1975delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034015 | |||||
| chr14:60034017
|
T | TTC | 9 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0003g0025others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3990+1955_3990+195 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60034017 | |||||
| chr14:60034018
|
T | TC | 153 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(150): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.3990+1955_3990+195 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034018 | ||||||
| chr14:60034019
|
T | C | 6 | a0001c0001t0006g0020a0001c0001t0008g0013a0001c0001t0010g0034others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3990+1956T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034019 | ||||||
| chr14:60034020
|
T | C | 8 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+1957T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034020 | ||||||
| chr14:60034021
|
T | C | 1 | a0001c0001t0023g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3990+1958T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034021 | ||||||
| chr14:60034084
|
A | G | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3990+2021A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034084 | ||||||
| chr14:60034103
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+2040C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034103 | ||||||
| chr14:60034142
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3990+2079C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034142 | ||||||
| chr14:60034195
|
T | C | 2 | a0001c0001t0003g0228a0001c0001t0003g0243 | 2 | HG01981.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.3990+2132T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034195 | ||||||
| chr14:60034503
|
C | A | 3 | a0001c0002t0021g0161a0007c0010t0018g0166a0007c0010t0021g0033 | 3 | HG02257.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3990+2440C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034503 | ||||||
| chr14:60034562
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3990+2499T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034562 | ||||||
| chr14:60034613
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3990+2550C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034613 | ||||||
| chr14:60034857
|
A | G | 3 | a0001c0001t0001g0044a0001c0001t0011g0050a0001c0001t0023g0049 | 3 | HG02074.hp2 NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3990+2794A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034857 | ||||||
| chr14:60034990
|
C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3990+2927C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60034990 | ||||||
| chr14:60035103
|
AT | A | 171 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.3990+3053delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60035103 | |||||
| chr14:60035128
|
G | A | 1 | a0001c0001t0003g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3990+3065G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035128 | ||||||
| chr14:60035638
|
T | C | 1 | a0001c0002t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3990+3575T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035638 | ||||||
| chr14:60035728
|
G | A | 1 | a0001c0002t0002g0003 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3990+3665G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035728 | ||||||
| chr14:60035834
|
G | A | 41 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(38): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.3990+3771G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035834 | ||||||
| chr14:60035897
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+3834T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035897 | ||||||
| chr14:60035956
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3990+3893A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60035956 | ||||||
| chr14:60035960
|
T | TG | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3990+3898dupG | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60035960 | |||||
| chr14:60036033
|
T | C | 1 | a0001c0001t0003g0100 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3990+3970T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036033 | ||||||
| chr14:60036042
|
T | TA | 7 | a0001c0002t0007g0002a0001c0002t0007g0275a0001c0002t0007g0290others(4): Show | 8 | HG02015.hp2 NA18989.hp1 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.3990+3980dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036042 | |||||
| chr14:60036074
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+4011G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036074 | ||||||
| chr14:60036152
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3990+4089C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036152 | ||||||
| chr14:60036400
|
C | T | 1 | a0001c0002t0002g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3990+4337C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036400 | ||||||
| chr14:60036432
|
T | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+4369T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036432 | ||||||
| chr14:60036512
|
G | A | 1 | a0001c0001t0006g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3990+4449G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036512 | ||||||
| chr14:60036567
|
T | A | 2 | a0005c0013t0018g0110a0005c0013t0018g0111 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3990+4504T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036567 | ||||||
| chr14:60036728
|
CT | C | 281 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.3990+4676delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036728 | |||||
| chr14:60036728
|
CTT | C | 7 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0145others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3990+4675_3990+467 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60036728 | |||||
| chr14:60036829
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3990+4766A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036829 | ||||||
| chr14:60036843
|
G | A | 1 | a0001c0001t0016g0206 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3990+4780G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036843 | ||||||
| chr14:60036880
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+4817A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036880 | ||||||
| chr14:60036887
|
G | T | 1 | a0001c0002t0002g0118 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3990+4824G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60036887 | ||||||
| chr14:60037304
|
C | T | 4 | a0001c0001t0011g0021a0001c0001t0011g0078a0001c0001t0011g0079others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3990+5241C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037304 | ||||||
| chr14:60037326
|
T | C | 8 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0002g0129others(5): Show | 8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+5263T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037326 | ||||||
| chr14:60037357
|
G | A | 11 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(8): Show | 11 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.3990+5294G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037357 | ||||||
| chr14:60037548
|
G | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+5485G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037548 | ||||||
| chr14:60037677
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+5614G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037677 | ||||||
| chr14:60037883
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+5820G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037883 | ||||||
| chr14:60037978
|
C | G | 2 | a0001c0002t0002g0143a0001c0002t0002g0144 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3990+5915C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037978 | ||||||
| chr14:60037991
|
C | T | 2 | a0002c0003t0005g0202a0002c0003t0005g0205 | 2 | NA18941.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.3990+5928C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60037991 | ||||||
| chr14:60038069
|
T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3990+6006T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038069 | ||||||
| chr14:60038120
|
T | C | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3990+6057T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038120 | ||||||
| chr14:60038247
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+6184G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038247 | ||||||
| chr14:60038353
|
G | A | 1 | a0001c0002t0025g0135 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3990+6290G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038353 | ||||||
| chr14:60038380
|
G | C | 1 | a0001c0002t0012g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3990+6317G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038380 | ||||||
| chr14:60038450
|
G | A | 1 | a0001c0002t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3990+6387G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038450 | ||||||
| chr14:60038463
|
C | T | 1 | a0001c0002t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3990+6400C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038463 | ||||||
| chr14:60038476
|
C | G | 4 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0090others(1): Show | 4 | HG01433.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.3990+6413C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038476 | ||||||
| chr14:60038505
|
G | T | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3990+6442G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038505 | ||||||
| chr14:60038625
|
C | A | 8 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0002g0129others(5): Show | 8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+6562C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038625 | ||||||
| chr14:60038666
|
G | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3990+6603G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038666 | ||||||
| chr14:60038899
|
G | T | 3 | a0001c0004t0009g0302a0001c0004t0009g0307a0001c0004t0009g0309 | 3 | HG00642.hp1 HG00735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3990+6836G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60038899 | ||||||
| chr14:60039018
|
T | C | 1 | a0001c0001t0011g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3990+6955T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039018 | ||||||
| chr14:60039096
|
G | A | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+7033G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039096 | ||||||
| chr14:60039159
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+7096G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039159 | ||||||
| chr14:60039243
|
G | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3990+7180G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039243 | ||||||
| chr14:60039259
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3990+7196G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039259 | ||||||
| chr14:60039278
|
A | G | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+7215A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039278 | ||||||
| chr14:60039365
|
A | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+7302A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039365 | ||||||
| chr14:60039741
|
G | A | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3990+7678G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039741 | ||||||
| chr14:60039772
|
G | C | 2 | a0001c0002t0002g0220a0001c0002t0002g0233 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.3990+7709G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039772 | ||||||
| chr14:60039779
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+7716T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039779 | ||||||
| chr14:60039811
|
G | GA | 5 | a0001c0002t0002g0005a0001c0002t0002g0112a0001c0002t0002g0173others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.3990+7750dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60039811 | |||||
| chr14:60039828
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+7765C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039828 | ||||||
| chr14:60039890
|
T | C | 8 | a0001c0002t0012g0120a0001c0002t0012g0121a0001c0002t0012g0122others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3990+7827T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60039890 | ||||||
| chr14:60039897
|
ATTTAGTG others(1226): Show |
A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+7841_3990+907 others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60039897 | |||||
| chr14:60040176
|
C | T | 1 | a0001c0002t0004g0284 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3990+8113C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040176 | ||||||
| chr14:60040201
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(3): Show | 6 | NA18946.hp1 NA18979.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.3990+8138A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040201 | ||||||
| chr14:60040206
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3990+8143C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040206 | ||||||
| chr14:60040210
|
G | A | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.3990+8147G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040210 | ||||||
| chr14:60040387
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3990+8324A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040387 | ||||||
| chr14:60040408
|
C | T | 1 | a0001c0001t0045g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3990+8345C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040408 | ||||||
| chr14:60040448
|
A | G | 5 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0304others(2): Show | 5 | HG00323.hp2 NA18946.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.3990+8385A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040448 | ||||||
| chr14:60040465
|
G | T | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3990+8402G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040465 | ||||||
| chr14:60040468
|
G | A | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3990+8405G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040468 | ||||||
| chr14:60040499
|
C | T | 1 | a0002c0003t0005g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3990+8436C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040499 | ||||||
| chr14:60040594
|
T | C | 82 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3990+8531T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040594 | ||||||
| chr14:60040607
|
C | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8544C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040607 | ||||||
| chr14:60040690
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8627C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040690 | ||||||
| chr14:60040691
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+8628A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60040691 | ||||||
| chr14:60041126
|
C | G | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+9063C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041126 | ||||||
| chr14:60041137
|
C | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9074C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041137 | ||||||
| chr14:60041178
|
C | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9115C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041178 | ||||||
| chr14:60041179
|
A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9116A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041179 | ||||||
| chr14:60041182
|
A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9119A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041182 | ||||||
| chr14:60041229
|
T | G | 3 | a0001c0002t0002g0107a0001c0002t0002g0138a0001c0002t0002g0139 | 3 | HG01175.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3990+9166T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041229 | ||||||
| chr14:60041230
|
A | T | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3990+9167A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041230 | ||||||
| chr14:60041481
|
T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+9418T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041481 | ||||||
| chr14:60041677
|
T | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(9): Show | 12 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3990+9614T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041677 | ||||||
| chr14:60041791
|
G | A | 7 | a0001c0002t0004g0015a0001c0002t0021g0161a0001c0002t0029g0017others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3990+9728G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041791 | ||||||
| chr14:60041797
|
C | A | 1 | a0001c0002t0002g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3990+9734C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041797 | ||||||
| chr14:60041817
|
A | T | 39 | a0001c0002t0004g0265a0001c0002t0004g0268a0001c0002t0004g0271others(36): Show | 40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.3990+9754A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60041817 | ||||||
| chr14:60042081
|
A | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+10018A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042081 | ||||||
| chr14:60042225
|
C | T | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3990+10162C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042225 | ||||||
| chr14:60042252
|
G | T | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3990+10189G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042252 | ||||||
| chr14:60042306
|
A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10243A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042306 | ||||||
| chr14:60042308
|
T | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10245T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042308 | ||||||
| chr14:60042320
|
G | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10257G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042320 | ||||||
| chr14:60042326
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10263C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042326 | ||||||
| chr14:60042327
|
A | G | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10264A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042327 | ||||||
| chr14:60042330
|
T | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3990+10267T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042330 | ||||||
| chr14:60042355
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3990+10292C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042355 | ||||||
| chr14:60042471
|
C | T | 2 | a0001c0005t0013g0171a0001c0005t0013g0172 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3990+10408C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042471 | ||||||
| chr14:60042551
|
T | C | 1 | a0001c0001t0033g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3990+10488T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042551 | ||||||
| chr14:60042560
|
T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3990+10497T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042560 | ||||||
| chr14:60042579
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3991-10486G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042579 | ||||||
| chr14:60042647
|
T | C | 1 | a0001c0002t0007g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3991-10418T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042647 | ||||||
| chr14:60042648
|
C | T | 1 | a0002c0003t0005g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3991-10417C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042648 | ||||||
| chr14:60042698
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-10367C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042698 | ||||||
| chr14:60042744
|
T | C | 2 | a0001c0002t0002g0145a0001c0002t0002g0146 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3991-10321T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042744 | ||||||
| chr14:60042757
|
C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-10308C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60042757 | ||||||
| chr14:60043284
|
C | A | 296 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(293): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.3991-9781C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60043284 | ||||||
| chr14:60043735
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3991-9330G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60043735 | ||||||
| chr14:60043745
|
GTTTTC | G | 12 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(9): Show | 12 | HG01433.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3991-9314_3991-931 others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043745 | |||||
| chr14:60043756
|
C | CT | 81 | a0001c0001t0001g0087a0001c0001t0001g0241a0001c0001t0001g0253others(78): Show | 83 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.3991-9287dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | |||||
| chr14:60043756
|
C | CTT | 11 | a0001c0001t0015g0060a0001c0002t0004g0004a0001c0002t0004g0265others(8): Show | 11 | HG01243.hp2 HG01358.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.3991-9288_3991-928 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | |||||
| chr14:60043756
|
CT | C | 13 | a0001c0001t0001g0085a0001c0001t0035g0156a0001c0002t0002g0220others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3991-9287delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60043756 | |||||
| chr14:60044030
|
T | C | 4 | a0001c0002t0004g0273a0001c0002t0004g0289a0001c0002t0004g0298others(1): Show | 4 | HG02040.hp1 HG02071.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3991-9035T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044030 | ||||||
| chr14:60044355
|
A | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3991-8710A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044355 | ||||||
| chr14:60044875
|
G | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3991-8190G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044875 | ||||||
| chr14:60044940
|
A | G | 1 | a0001c0001t0039g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3991-8125A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60044940 | ||||||
| chr14:60045006
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-8059C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045006 | ||||||
| chr14:60045043
|
T | G | 1 | a0001c0001t0001g0248 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3991-8022T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045043 | ||||||
| chr14:60045051
|
C | CT | 12 | a0001c0002t0002g0134a0001c0002t0002g0233a0001c0002t0012g0120others(9): Show | 12 | HG01109.hp2 HG02486.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3991-7997dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045051
|
C | CTT | 13 | a0001c0001t0035g0156a0001c0002t0004g0004a0001c0002t0021g0161others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.3991-7998_3991-799 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045051
|
C | CTTT | 36 | a0001c0002t0004g0015a0001c0002t0004g0214a0001c0002t0004g0272others(33): Show | 37 | HG02165.hp2 HG02486.hp2 HG03139.hp1 others(34): Show |
intron_variant | MODIFIER | c.3991-7999_3991-799 others(7): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045051
|
C | CTTTT | 32 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(29): Show | 33 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.3991-8000_3991-799 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045051
|
CT | C | 26 | a0001c0001t0001g0087a0001c0001t0001g0221a0001c0001t0001g0222others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3991-7997delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045051
|
CTT | C | 147 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.3991-7998_3991-799 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60045051 | |||||
| chr14:60045101
|
A | G | 2 | a0008c0011t0003g0212a0008c0011t0006g0211 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.3991-7964A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045101 | ||||||
| chr14:60045299
|
T | C | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3991-7766T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045299 | ||||||
| chr14:60045393
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-7672C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045393 | ||||||
| chr14:60045426
|
C | T | 30 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0168others(27): Show | 31 | HG01358.hp1 HG01361.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.3991-7639C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045426 | ||||||
| chr14:60045477
|
G | A | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.3991-7588G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045477 | ||||||
| chr14:60045738
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-7327C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045738 | ||||||
| chr14:60045758
|
A | G | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3991-7307A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60045758 | ||||||
| chr14:60046145
|
A | G | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3991-6920A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046145 | ||||||
| chr14:60046250
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0165a0001c0001t0016g0023others(1): Show | 4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3991-6815C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046250 | ||||||
| chr14:60046364
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3991-6701G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046364 | ||||||
| chr14:60046428
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-6637C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046428 | ||||||
| chr14:60046445
|
T | G | 5 | a0001c0002t0021g0161a0005c0013t0018g0110a0005c0013t0018g0111others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3991-6620T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046445 | ||||||
| chr14:60046591
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-6474G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046591 | ||||||
| chr14:60046647
|
C | T | 2 | a0001c0001t0010g0034a0001c0001t0015g0062 | 2 | NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.3991-6418C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046647 | ||||||
| chr14:60046682
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-6383G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046682 | ||||||
| chr14:60046701
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-6364T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046701 | ||||||
| chr14:60046785
|
A | T | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3991-6280A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046785 | ||||||
| chr14:60046788
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-6277T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046788 | ||||||
| chr14:60046804
|
G | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-6261G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046804 | ||||||
| chr14:60046855
|
G | A | 1 | a0001c0002t0021g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3991-6210G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046855 | ||||||
| chr14:60046934
|
C | T | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3991-6131C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60046934 | ||||||
| chr14:60047248
|
C | A | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3991-5817C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047248 | ||||||
| chr14:60047307
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3991-5758T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047307 | ||||||
| chr14:60047353
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-5712C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047353 | ||||||
| chr14:60047414
|
C | T | 1 | a0001c0001t0006g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3991-5651C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047414 | ||||||
| chr14:60047418
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-5647T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047418 | ||||||
| chr14:60047569
|
T | C | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-5496T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047569 | ||||||
| chr14:60047580
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-5485T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047580 | ||||||
| chr14:60047644
|
T | C | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3991-5421T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047644 | ||||||
| chr14:60047794
|
A | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-5271A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047794 | ||||||
| chr14:60047825
|
C | T | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3991-5240C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047825 | ||||||
| chr14:60047854
|
C | T | 2 | a0001c0002t0004g0015a0001c0002t0029g0017 | 2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3991-5211C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60047854 | ||||||
| chr14:60048085
|
T | C | 1 | a0005c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3991-4980T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048085 | ||||||
| chr14:60048128
|
A | G | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3991-4937A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048128 | ||||||
| chr14:60048227
|
G | T | 1 | a0001c0002t0017g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3991-4838G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048227 | ||||||
| chr14:60048237
|
C | G | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-4828C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048237 | ||||||
| chr14:60048386
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-4679C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048386 | ||||||
| chr14:60048527
|
C | T | 7 | a0001c0002t0004g0015a0001c0002t0021g0161a0001c0002t0029g0017others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3991-4538C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048527 | ||||||
| chr14:60048564
|
G | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-4501G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048564 | ||||||
| chr14:60048713
|
G | A | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.3991-4352G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048713 | ||||||
| chr14:60048744
|
T | G | 1 | a0001c0002t0002g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3991-4321T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048744 | ||||||
| chr14:60048791
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-4274G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60048791 | ||||||
| chr14:60049321
|
G | A | 3 | a0001c0001t0003g0025a0001c0001t0003g0048a0001c0001t0014g0040 | 3 | NA18990.hp1 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3991-3744G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049321 | ||||||
| chr14:60049766
|
G | C | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0006g0020 | 3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3991-3299G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049766 | ||||||
| chr14:60049974
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3991-3091A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60049974 | ||||||
| chr14:60049990
|
C | CATTTT | 3 | a0001c0002t0021g0161a0007c0010t0018g0166a0007c0010t0021g0033 | 3 | HG02257.hp1 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-3055_3991-305 others(9): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr14 | 60049990 | |||||
| chr14:60050046
|
G | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-3019G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050046 | ||||||
| chr14:60050065
|
C | T | 4 | a0001c0002t0017g0117a0001c0002t0017g0141a0001c0002t0017g0142others(1): Show | 4 | HG01109.hp2 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3991-3000C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050065 | ||||||
| chr14:60050094
|
T | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2971T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050094 | ||||||
| chr14:60050097
|
A | AC | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2968_3991-296 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050097 | ||||||
| chr14:60050098
|
G | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2967G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050098 | ||||||
| chr14:60050100
|
G | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2965G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050100 | ||||||
| chr14:60050101
|
A | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2964A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050101 | ||||||
| chr14:60050102
|
T | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2963T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050102 | ||||||
| chr14:60050103
|
T | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.3991-2962T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050103 | ||||||
| chr14:60050155
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3991-2910C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050155 | ||||||
| chr14:60050174
|
T | G | 1 | a0001c0001t0019g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3991-2891T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050174 | ||||||
| chr14:60050192
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-2873C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050192 | ||||||
| chr14:60050292
|
G | A | 2 | a0001c0001t0006g0099a0001c0001t0006g0169 | 2 | HG01928.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3991-2773G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050292 | ||||||
| chr14:60050318
|
C | T | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3991-2747C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050318 | ||||||
| chr14:60050362
|
T | C | 1 | a0001c0002t0002g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3991-2703T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050362 | ||||||
| chr14:60050426
|
C | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3991-2639C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050426 | ||||||
| chr14:60050427
|
G | A | 2 | a0001c0001t0006g0240a0001c0001t0006g0242 | 2 | HG00741.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3991-2638G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050427 | ||||||
| chr14:60050481
|
T | C | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.3991-2584T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050481 | ||||||
| chr14:60050487
|
A | G | 1 | a0001c0006t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3991-2578A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050487 | ||||||
| chr14:60050701
|
T | C | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-2364T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050701 | ||||||
| chr14:60050839
|
T | G | 1 | a0001c0002t0004g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3991-2226T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050839 | ||||||
| chr14:60050953
|
G | T | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0006g0020 | 3 | NA18945.hp1 NA19007.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3991-2112G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60050953 | ||||||
| chr14:60051045
|
G | A | 1 | a0001c0001t0010g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3991-2020G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051045 | ||||||
| chr14:60051071
|
A | G | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3991-1994A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051071 | ||||||
| chr14:60051118
|
T | C | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3991-1947T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051118 | ||||||
| chr14:60051288
|
G | A | 8 | a0001c0002t0012g0120a0001c0002t0012g0121a0001c0002t0012g0122others(5): Show | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3991-1777G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051288 | ||||||
| chr14:60051308
|
G | A | 3 | a0001c0001t0003g0064a0001c0001t0003g0238a0010c0017t0003g0065 | 3 | HG01169.hp2 HG01952.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3991-1757G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051308 | ||||||
| chr14:60051467
|
A | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-1598A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051467 | ||||||
| chr14:60051640
|
C | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-1425C>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051640 | ||||||
| chr14:60051718
|
G | A | 1 | a0004c0008t0010g0055 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3991-1347G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051718 | ||||||
| chr14:60051720
|
C | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3991-1345C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051720 | ||||||
| chr14:60051835
|
C | T | 1 | a0003c0007t0004g0280 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3991-1230C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051835 | ||||||
| chr14:60051891
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0235a0001c0001t0027g0234 | 3 | NA18956.hp2 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3991-1174T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051891 | ||||||
| chr14:60051971
|
C | T | 1 | a0001c0002t0004g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3991-1094C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051971 | ||||||
| chr14:60051975
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3991-1090C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051975 | ||||||
| chr14:60051997
|
C | A | 1 | a0001c0001t0008g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3991-1068C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60051997 | ||||||
| chr14:60052315
|
G | A | 1 | a0001c0002t0004g0268 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3991-750G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052315 | ||||||
| chr14:60052398
|
T | C | 1 | a0002c0003t0005g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3991-667T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052398 | ||||||
| chr14:60052403
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3991-662T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052403 | ||||||
| chr14:60052506
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.3991-559C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052506 | ||||||
| chr14:60052827
|
C | A | 169 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.3991-238C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 29/32 | chr14 | 60052827 | ||||||
| chr14:60053247
|
TAATG | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+43_4131+46del others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053247 | ||||||
| chr14:60053301
|
C | A | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4131+96C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053301 | ||||||
| chr14:60053381
|
GCTCA | G | 20 | a0002c0003t0005g0185a0002c0003t0005g0186a0002c0003t0005g0189others(17): Show | 20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+178_4131+181d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053381 | |||||
| chr14:60053381
|
GCTCACA | G | 3 | a0002c0003t0005g0001a0002c0003t0005g0187a0002c0003t0005g0188 | 4 | NA18939.hp2 NA18960.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.4131+178_4131+183d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053381 | |||||
| chr14:60053383
|
T | TCA | 35 | a0001c0002t0002g0129a0001c0002t0002g0146a0001c0002t0002g0175others(32): Show | 35 | HG00558.hp2 HG00609.hp1 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.4131+215_4131+216d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
T | TCACA | 42 | a0001c0002t0002g0003a0001c0002t0002g0107a0001c0002t0002g0118others(39): Show | 43 | HG00673.hp1 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+213_4131+216d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
T | TCACACA | 17 | a0001c0002t0002g0127a0001c0002t0002g0133a0001c0002t0002g0143others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.4131+211_4131+216d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
T | TCACACAC others(1): Show |
7 | a0001c0002t0012g0124a0001c0005t0013g0172a0001c0006t0002g0109others(4): Show | 7 | HG02080.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4131+209_4131+216d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
T | TCACACAC others(3): Show |
1 | a0001c0005t0013g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4131+207_4131+216d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
TCA | T | 7 | a0001c0002t0002g0005a0001c0002t0002g0112a0001c0002t0002g0173others(4): Show | 7 | HG01081.hp1 HG01361.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.4131+215_4131+216d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053383
|
TCACA | T | 9 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.4131+213_4131+216d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053383 | |||||
| chr14:60053412
|
CACACACA others(3): Show |
C | 72 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(69): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.4131+209_4131+218d others(12): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053412 | |||||
| chr14:60053414
|
CACACACA others(1): Show |
C | 6 | a0001c0001t0003g0038a0001c0001t0003g0039a0001c0001t0003g0057others(3): Show | 6 | HG00099.hp2 HG01081.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+211_4131+218d others(10): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053414 | |||||
| chr14:60053416
|
CACACAT | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0058others(81): Show | 84 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.4131+213_4131+218d others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053416 | |||||
| chr14:60053418
|
C | T | 20 | a0002c0003t0005g0185a0002c0003t0005g0186a0002c0003t0005g0189others(17): Show | 20 | NA18941.hp2 NA18945.hp2 NA18964.hp2 others(17): Show |
intron_variant | MODIFIER | c.4131+213C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053418 | ||||||
| chr14:60053418
|
CACAT | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0094a0001c0001t0003g0018others(1): Show | 4 | HG01516.hp1 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4131+215_4131+218d others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60053418 | |||||
| chr14:60053420
|
C | T | 33 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(30): Show | 34 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.4131+215C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053420 | ||||||
| chr14:60053422
|
T | C | 6 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(3): Show | 6 | HG01358.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4131+217T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053422 | ||||||
| chr14:60053429
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+224G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053429 | ||||||
| chr14:60053493
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4131+288A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053493 | ||||||
| chr14:60053532
|
T | C | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+327T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053532 | ||||||
| chr14:60053535
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+330G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053535 | ||||||
| chr14:60053861
|
T | C | 8 | a0001c0002t0002g0126a0001c0002t0002g0128a0001c0002t0002g0129others(5): Show | 8 | HG02074.hp1 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.4131+656T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053861 | ||||||
| chr14:60053940
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4131+735G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60053940 | ||||||
| chr14:60054082
|
T | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+877T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054082 | ||||||
| chr14:60054084
|
A | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+879A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054084 | ||||||
| chr14:60054304
|
A | T | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4131+1099A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054304 | ||||||
| chr14:60054444
|
G | T | 1 | a0001c0002t0017g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4131+1239G>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054444 | ||||||
| chr14:60054527
|
A | G | 2 | a0001c0002t0004g0289a0001c0002t0004g0300 | 2 | HG02040.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.4131+1322A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054527 | ||||||
| chr14:60054545
|
C | T | 2 | a0001c0001t0003g0255a0001c0001t0003g0256 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.4131+1340C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054545 | ||||||
| chr14:60054620
|
T | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1415T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054620 | ||||||
| chr14:60054622
|
C | T | 40 | a0001c0002t0004g0153a0001c0002t0004g0265a0001c0002t0004g0268others(37): Show | 41 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(38): Show |
intron_variant | MODIFIER | c.4131+1417C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054622 | ||||||
| chr14:60054669
|
G | GA | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1465dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60054669 | |||||
| chr14:60054736
|
G | A | 15 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(12): Show | 15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4131+1531G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054736 | ||||||
| chr14:60054767
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1562C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60054767 | ||||||
| chr14:60055006
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+1801C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055006 | ||||||
| chr14:60055205
|
A | T | 1 | a0001c0001t0011g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4131+2000A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055205 | ||||||
| chr14:60055401
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4131+2196C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055401 | ||||||
| chr14:60055410
|
AT | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4131+2208delT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055410 | |||||
| chr14:60055488
|
T | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+2283T>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055488 | ||||||
| chr14:60055531
|
T | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4131+2326T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055531 | ||||||
| chr14:60055595
|
C | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4132-2283C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055595 | ||||||
| chr14:60055701
|
T | C | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4132-2177T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055701 | ||||||
| chr14:60055731
|
T | TA | 9 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0090others(6): Show | 9 | HG00621.hp1 HG01074.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4132-2132dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055731 | |||||
| chr14:60055739
|
A | C | 2 | a0001c0012t0002g0106a0001c0012t0002g0140 | 2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4132-2139A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055739 | ||||||
| chr14:60055740
|
A | T | 2 | a0001c0004t0009g0210a0001c0004t0009g0306 | 2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.4132-2138A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055740 | ||||||
| chr14:60055744
|
A | AC | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-2134_4132-213 others(5): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055744 | ||||||
| chr14:60055744
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.4132-2134A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055744 | ||||||
| chr14:60055745
|
A | C | 79 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(76): Show | 79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.4132-2133A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055745 | ||||||
| chr14:60055746
|
AC | A | 6 | a0001c0001t0001g0058a0001c0001t0001g0257a0001c0001t0011g0021others(3): Show | 6 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.4132-2131delC | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055746 | ||||||
| chr14:60055747
|
C | A | 159 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.4132-2131C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055747 | ||||||
| chr14:60055747
|
C | T | 2 | a0001c0004t0009g0210a0001c0004t0009g0306 | 2 | NA18946.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.4132-2131C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055747 | ||||||
| chr14:60055860
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4132-2018G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055860 | ||||||
| chr14:60055902
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-1976C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055902 | ||||||
| chr14:60055906
|
G | GA | 177 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0045others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.4132-1957dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055906 | |||||
| chr14:60055906
|
G | GAA | 6 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0248others(3): Show | 6 | HG01884.hp1 HG02738.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.4132-1958_4132-195 others(6): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60055906 | |||||
| chr14:60055907
|
A | G | 2 | a0001c0002t0002g0220a0001c0002t0002g0233 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4132-1971A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60055907 | ||||||
| chr14:60056058
|
C | T | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-1820C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056058 | ||||||
| chr14:60056073
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0003g0262 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4132-1805T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056073 | ||||||
| chr14:60056483
|
A | G | 1 | a0001c0002t0004g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4132-1395A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056483 | ||||||
| chr14:60056696
|
A | G | 1 | a0001c0002t0002g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4132-1182A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056696 | ||||||
| chr14:60056889
|
G | C | 1 | a0001c0002t0002g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4132-989G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056889 | ||||||
| chr14:60056952
|
A | C | 166 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.4132-926A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60056952 | ||||||
| chr14:60057008
|
C | T | 15 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(12): Show | 15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4132-870C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057008 | ||||||
| chr14:60057014
|
G | A | 2 | a0005c0013t0018g0110a0005c0013t0018g0111 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4132-864G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057014 | ||||||
| chr14:60057029
|
G | C | 190 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.4132-849G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057029 | ||||||
| chr14:60057164
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-714A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057164 | ||||||
| chr14:60057183
|
A | G | 319 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.4132-695A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057183 | ||||||
| chr14:60057237
|
A | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4132-641A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057237 | ||||||
| chr14:60057274
|
T | C | 1 | a0001c0002t0002g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4132-604T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057274 | ||||||
| chr14:60057569
|
T | G | 191 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.4132-309T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057569 | ||||||
| chr14:60057653
|
G | GA | 225 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.4132-209dupA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60057653 | |||||
| chr14:60057653
|
G | GAA | 27 | a0001c0001t0011g0021a0001c0001t0011g0078a0001c0001t0011g0079others(24): Show | 28 | HG02559.hp2 HG02922.hp2 HG03139.hp2 others(25): Show |
intron_variant | MODIFIER | c.4132-210_4132-209d others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr14 | 60057653 | |||||
| chr14:60057771
|
G | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4132-107G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057771 | ||||||
| chr14:60057796
|
C | T | 3 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0152 | 3 | HG02615.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4132-82C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 30/32 | chr14 | 60057796 | ||||||
| chr14:60058032
|
C | CAAAT | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+12_4276+13ins others(4): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60058032 | |||||
| chr14:60058037
|
T | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+15T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058037 | ||||||
| chr14:60058063
|
A | C | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+41A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058063 | ||||||
| chr14:60058080
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4276+58T>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058080 | ||||||
| chr14:60058234
|
C | A | 2 | a0007c0010t0018g0166a0007c0010t0021g0033 | 2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4276+212C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058234 | ||||||
| chr14:60058338
|
G | A | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4276+316G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058338 | ||||||
| chr14:60058506
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4276+484G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058506 | ||||||
| chr14:60058611
|
A | C | 15 | a0001c0002t0004g0004a0001c0002t0004g0015a0001c0002t0021g0161others(12): Show | 15 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4276+589A>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058611 | ||||||
| chr14:60058790
|
TA | T | 14 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0009others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.4276+776delA | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60058790 | |||||
| chr14:60058872
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+850A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058872 | ||||||
| chr14:60058897
|
A | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4276+875A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60058897 | ||||||
| chr14:60059029
|
A | G | 167 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.4276+1007A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059029 | ||||||
| chr14:60059153
|
T | C | 82 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0061others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.4276+1131T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059153 | ||||||
| chr14:60059245
|
T | C | 1 | a0001c0002t0007g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4276+1223T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059245 | ||||||
| chr14:60059282
|
C | T | 1 | a0001c0002t0004g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4276+1260C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059282 | ||||||
| chr14:60059534
|
G | A | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4276+1512G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059534 | ||||||
| chr14:60059609
|
G | A | 1 | a0001c0002t0002g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4276+1587G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059609 | ||||||
| chr14:60059613
|
G | A | 1 | a0002c0003t0005g0188 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4276+1591G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059613 | ||||||
| chr14:60059620
|
A | G | 1 | a0001c0002t0002g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4276+1598A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059620 | ||||||
| chr14:60059638
|
A | T | 48 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0069others(45): Show | 48 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.4276+1616A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059638 | ||||||
| chr14:60059773
|
C | T | 201 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.4276+1751C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60059773 | ||||||
| chr14:60060016
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4276+1994T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060016 | ||||||
| chr14:60060274
|
T | C | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4277-1737T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060274 | ||||||
| chr14:60060463
|
G | A | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4277-1548G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060463 | ||||||
| chr14:60060609
|
C | T | 7 | a0001c0005t0013g0151a0001c0005t0013g0171a0001c0005t0013g0172others(4): Show | 7 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4277-1402C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60060609 | ||||||
| chr14:60060762
|
T | TTAGA | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4277-1246_4277-124 others(8): Show |
LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr14 | 60060762 | |||||
| chr14:60061194
|
A | G | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4277-817A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061194 | ||||||
| chr14:60061265
|
A | T | 1 | a0004c0008t0015g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4277-746A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061265 | ||||||
| chr14:60061321
|
G | A | 258 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.4277-690G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061321 | ||||||
| chr14:60061404
|
G | A | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4277-607G>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061404 | ||||||
| chr14:60061444
|
A | G | 1 | a0001c0005t0038g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4277-567A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061444 | ||||||
| chr14:60061469
|
A | T | 1 | a0001c0001t0035g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4277-542A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061469 | ||||||
| chr14:60061523
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4277-488T>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061523 | ||||||
| chr14:60061699
|
C | A | 169 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.4277-312C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061699 | ||||||
| chr14:60061730
|
A | T | 1 | a0001c0002t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4277-281A>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061730 | ||||||
| chr14:60061770
|
A | G | 5 | a0001c0005t0013g0151a0001c0005t0013g0179a0001c0005t0013g0180others(2): Show | 5 | HG01358.hp2 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.4277-241A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061770 | ||||||
| chr14:60061772
|
C | T | 168 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.4277-239C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061772 | ||||||
| chr14:60061790
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4277-221A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061790 | ||||||
| chr14:60061909
|
C | A | 259 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.4277-102C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 31/32 | chr14 | 60061909 | ||||||
| chr14:60062255
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4445+76A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062255 | ||||||
| chr14:60062310
|
A | G | 42 | a0001c0002t0004g0153a0001c0002t0004g0214a0001c0002t0004g0265others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.4445+131A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062310 | ||||||
| chr14:60062577
|
C | T | 39 | a0001c0002t0004g0265a0001c0002t0004g0268a0001c0002t0004g0271others(36): Show | 40 | HG00558.hp2 HG00609.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.4445+398C>T | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062577 | ||||||
| chr14:60062749
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4445+570A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062749 | ||||||
| chr14:60062824
|
A | G | 23 | a0002c0003t0005g0001a0002c0003t0005g0185a0002c0003t0005g0186others(20): Show | 24 | NA18939.hp2 NA18941.hp2 NA18945.hp2 others(21): Show |
intron_variant | MODIFIER | c.4446-499A>G | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60062824 | ||||||
| chr14:60062894
|
A | AT | 193 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0044others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.4446-415dupT | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr14 | 60062894 | |||||
| chr14:60063231
|
G | C | 10 | a0001c0004t0009g0209a0001c0004t0009g0210a0001c0004t0009g0302others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.4446-92G>C | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60063231 | ||||||
| chr14:60063269
|
C | A | 1 | a0005c0013t0018g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4446-54C>A | LRRC9 | ENSG00000131951.12 | transcript | ENST00000570145.2 | protein_coding | 32/32 | chr14 | 60063269 |